Methyl Alcohol

Formula: CH₄O
Molecular weight: 32.0419
IUPAC Standard InChI: InChI=1S/CH4O/c1-2/h2H,1H3
IUPAC Standard InChIKey: OKKJLVBELUTLKV-UHFFFAOYSA-N
CAS Registry Number: 67-56-1
Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript.
Isotopologues:
Other names: Methanol; Carbinol; Methyl hydroxide; Methylol; Monohydroxymethane; Wood alcohol; CH3OH; Colonial spirit; Columbian spirit; Hydroxymethane; Wood naphtha; Alcool methylique; Alcool metilico; Columbian spirits; Metanolo; Methylalkohol; Metylowy alkohol; Pyroxylic spirit; Wood spirit; Rcra waste number U154; UN 1230; Pyro alcohol; Spirit of wood; Bieleski's solution; NSC 85232
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Information on this page:
Other data available:
- Gas phase thermochemistry data
- Condensed phase thermochemistry data
- Phase change data
- Reaction thermochemistry data: reactions 1 to 50, reactions 51 to 100, reactions 101 to 150, reactions 151 to 200, reactions 201 to 250, reactions 251 to 300
- Henry's Law data
- IR Spectrum
- Vibrational and/or electronic energy levels
- Fluid Properties
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- Gas Phase Kinetics Database
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Gas phase ion energetics data

Go To: Top, Ion clustering data, Mass spectrum (electron ionization), Gas Chromatography, References, Notes

Data evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias
L - Sharon G. Lias

Data compiled as indicated in comments:
B - John E. Bartmess
LL - Sharon G. Lias and Joel F. Liebman
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

View reactions leading to CH₄O⁺ (ion structure unspecified)

Quantity	Value	Units	Method	Reference	Comment
IE (evaluated)	10.84 ± 0.01	eV	N/A	N/A	L
Quantity	Value	Units	Method	Reference	Comment
Proton affinity (review)	180.3	kcal/mol	N/A	Hunter and Lias, 1998	HL
Quantity	Value	Units	Method	Reference	Comment
Gas basicity	173.2	kcal/mol	N/A	Hunter and Lias, 1998	HL

Ionization energy determinations

IE (eV)	Method	Reference	Comment
10.85 ± 0.03	PI	Tao, Klemm, et al., 1992	LL
10.82 ± 0.05	EI	Holmes and Lossing, 1991	LL
10.84 ± 0.07	EI	Bowen and Maccoll, 1984	LBLHLM
10.9	EI	Mishchanchuk, Pokrovskii, et al., 1982	LBLHLM
10.84 ± 0.08	EI	Allam, Migahed, et al., 1982	LBLHLM
10.90 ± 0.03	EI	Sahini, Constantin, et al., 1978	LLK
10.85 ± 0.01	PI	Berkowitz, 1978	LLK
10.846 ± 0.002	PE	MacNeil and Dixon, 1977	LLK
10.90 ± 0.12	EI	Finney and Harrison, 1972	LLK
10.83 ± 0.03	PI	Warneck, 1971	LLK
10.85 ± 0.02	PE	Cocksey, Eland, et al., 1971	LLK
10.85	PE	Baker, Betteridge, et al., 1971	LLK
10.85	PE	Baker, Betteridge, et al., 1971	LLK
10.829 ± 0.015	PI	Omura, Kaneko, et al., 1969	RDSH
10.85	EI	Lifshitz, Shapiro, et al., 1969	RDSH
10.83	PE	Dewar and Worley, 1969	RDSH
10.84 ± 0.02	PI	Refaey and Chupka, 1968	RDSH
10.85	CI	Cermak, 1968	RDSH
10.83	PE	Al-Joboury and Turner, 1964	RDSH
10.85 ± 0.02	PI	Watanabe, 1954	RDSH
10.96	EI	Vorob'ev, Furlei, et al., 1989	Vertical value; LL
11.0	PE	Von Niessen, Bieri, et al., 1980	Vertical value; LLK
10.95	PE	Utsunomiya, Kobayashi, et al., 1980	Vertical value; LLK
10.95	PE	Kobayashi, 1978	Vertical value; LLK
10.86	PE	Benoit and Harrison, 1977	Vertical value; LLK
10.97 ± 0.03	PE	Peel and Willett, 1975	Vertical value; LLK
10.96	PE	Robin and Kuebler, 1973	Vertical value; LLK
10.95	PE	Ogata, Onizuka, et al., 1973	Vertical value; LLK
10.94	PE	Katsumata, Iwai, et al., 1973	Vertical value; LLK
10.95	PE	Ogata, Onizuka, et al., 1972	Vertical value; LLK
10.96	PE	Baker, Betteridge, et al., 1971	Vertical value; LLK

Appearance energy determinations

Ion	AE (eV)	Other Products	Method	Reference	Comment
CH⁺	22.31 ± 0.09	?	EI	Reed and Snedden, 1956	RDSH
CHO⁺	13.06 ± 0.10	H₂+H	PI	Warneck, 1971	LLK
CHO⁺	14.0 ± 0.2	H₂+H	EI	Lifshitz, Shapiro, et al., 1969	RDSH
CH₂⁺	14.05 ± 0.05	H₂O	PI	Warneck, 1971	LLK
CH₂⁺	15.3	H₂O	EI	Haney and Franklin, 1968	RDSH
CH₂O⁺	10.9	H₂	EI	Mishchanchuk, Pokrovskii, et al., 1982	LBLHLM
CH₂O⁺	12.05 ± 0.12	H₂	PI	Warneck, 1971	LLK
CH₂O⁺	12.45	H₂	PI	Refaey and Chupka, 1968	RDSH
CH₃⁺	13.82 ± 0.04	OH	PI	Warneck, 1971	LLK
CH₃⁺	13.5	OH	EI	Friedman, Long, et al., 1957	RDSH
CH₃O⁺	11.67 ± 0.09	H	EI	Bowen and Maccoll, 1984	LBLHLM
CH₃O⁺	10.4	H	EI	Mishchanchuk, Pokrovskii, et al., 1982	LBLHLM
CH₃O⁺	11.85 ± 0.08	H	EI	Allam, Migahed, et al., 1982	LBLHLM
CH₃O⁺	11.88 ± 0.05	H	EI	Selim and Helal, 1981	LLK
CH₃O⁺	11.69	H	EI	Lossing, 1977	LLK
CH₃O⁺	11.76 ± 0.11	H	EI	Finney and Harrison, 1972	LLK
CH₃O⁺	11.55 ± 0.03	H	PI	Warneck, 1971	LLK
CH₃O⁺	11.66 ± 0.04	H	PI	Omura, Kaneko, et al., 1969	RDSH
CH₃O⁺	11.67	H	EI	Lifshitz, Shapiro, et al., 1969	RDSH
CH₃O⁺	11.67 ± 0.03	H	PI	Refaey and Chupka, 1968	RDSH
CH₃O⁺[CH₂OH⁺]	11.649 ± 0.003	H	PI	Berkowitz, Ellison, et al., 1994	Unpublished results of B. Ruscic and J. Berkowitz; LL
CO⁺	13.7	2H₂	EI	Friedman, Long, et al., 1957	RDSH
CO⁺	14.31 ± 0.05	2H₂	EI	Friedland and Strakna, 1956	RDSH

De-protonation reactions

CH₃O^- + = Methyl Alcohol

By formula: CH₃O^- + H⁺ = CH₄O

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	382. ± 2.	kcal/mol	AVG	N/A	Average of 6 values; Individual data points
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	376.02 ± 0.62	kcal/mol	H-TS	Nee, Osterwalder, et al., 2006	gas phase; B
Δ_rG°	376.04 ± 0.55	kcal/mol	H-TS	Osborn, Leahy, et al., 1998	gas phase; B
Δ_rG°	374.0 ± 2.0	kcal/mol	IMRE	Bartmess, Scott, et al., 1979	gas phase; The acidity is 1.2 kcal/mol stronger than that from the D-EA cycle, due to the multi-compound fit for the acidity scale.; value altered from reference due to change in acidity scale; B
Δ_rG°	374.6 ± 2.1	kcal/mol	H-TS	Haas and Harrison, 1993	gas phase; Both metastable and 50 eV collision energy.; B
Δ_rG°	375.10 ± 0.60	kcal/mol	TDEq	Meot-ner and Sieck, 1986	gas phase; Experimental entropy: 21.5 eu, 0.6 less than H2O; B

Ion clustering data

Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), Gas Chromatography, References, Notes

Data compiled as indicated in comments:
B - John E. Bartmess
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias
RCD - Robert C. Dunbar

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. Searches may be limited to ion clustering reactions. A general reaction search form is also available.

Clustering reactions

+ Methyl Alcohol = ( • )

By formula: Br^- + CH₄O = (Br^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	14.50 ± 0.10	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	13.9 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	17.6	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	8.00 ± 0.10	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	8.7 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B
Δ_rG°	8.4 ± 2.0	kcal/mol	IMRE	Tanabe, Morgon, et al., 1996	gas phase; Anchored to H2O..Br- of Hiraoka, Mizure, et al., 19882; B

( • Methyl Alcohol ) + = ( • 2)

By formula: (Br^- • CH₄O) + CH₄O = (Br^- • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	12.00 ± 0.20	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	12.5 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	20.7	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.62	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	6.3 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 2 Methyl Alcohol ) + = ( • 3)

By formula: (Br^- • 2CH₄O) + CH₄O = (Br^- • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.50 ± 0.50	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	10.6 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	21.6	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.25	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	4.2 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 3 Methyl Alcohol ) + = ( • 4)

By formula: (Br^- • 3CH₄O) + CH₄O = (Br^- • 4CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.9 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.2	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	3.0 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 4 Methyl Alcohol ) + = ( • 5)

By formula: (Br^- • 4CH₄O) + CH₄O = (Br^- • 5CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.8 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.2	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.3 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 5 Methyl Alcohol ) + = ( • 6)

By formula: (Br^- • 5CH₄O) + CH₄O = (Br^- • 6CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.1 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.6	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.1 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 6 Methyl Alcohol ) + = ( • 7)

By formula: (Br^- • 6CH₄O) + CH₄O = (Br^- • 7CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.5 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.9	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.7 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 7 Methyl Alcohol ) + = ( • 8)

By formula: (Br^- • 7CH₄O) + CH₄O = (Br^- • 8CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.4 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.1	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.5 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 8 Methyl Alcohol ) + = ( • 9)

By formula: (Br^- • 8CH₄O) + CH₄O = (Br^- • 9CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.2 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; Entropy estimated.; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.	cal/mol*K	N/A	Hiraoka and Yamabe, 1991	gas phase; Entropy change calculated or estimated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.3 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; Entropy estimated.; B

( • 9 Methyl Alcohol ) + = ( • 10)

By formula: (Br^- • 9CH₄O) + CH₄O = (Br^- • 10CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.0 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; Entropy estimated.; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.	cal/mol*K	N/A	Hiraoka and Yamabe, 1991	gas phase; Entropy change calculated or estimated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.1 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; Entropy estimated.; B

CHO^- + Methyl Alcohol = (CHO^- • )

By formula: CHO^- + CH₄O = (CHO^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	28.8	kcal/mol	PHPMS	Meot-ner and Sieck, 1986	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.7	cal/mol*K	PHPMS	Meot-ner and Sieck, 1986	gas phase; M

+ Methyl Alcohol = ( • )

By formula: CHO₂^- + CH₄O = (CHO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.6 ± 1.0	kcal/mol	N/A	Meot-Ner and Sieck, 1986	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.6	cal/mol*K	PHPMS	Meot-Ner and Sieck, 1986	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	10.5 ± 1.6	kcal/mol	TDAs	Meot-Ner and Sieck, 1986	gas phase; B

CH₃O^- + Methyl Alcohol = (CH₃O^- • )

By formula: CH₃O^- + CH₄O = (CH₃O^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	29.3 ± 1.0	kcal/mol	TDAs	Paul and Kebarle, 1990	gas phase; B,M
Δ_rH°	28.80 ± 0.30	kcal/mol	TDAs	Meot-ner and Sieck, 1986	gas phase; B,M
Δ_rH°	29.4 ± 2.5	kcal/mol	TDAs	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B
Δ_rH°	19.0 ± 2.0	kcal/mol	N/A	Moylan, Dodd, et al., 1985	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	31.8	cal/mol*K	PHPMS	Paul and Kebarle, 1990	gas phase; M
Δ_rS°	26.7	cal/mol*K	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	20.30	kcal/mol	IMRE	Mustanir, Matsuoka, et al., 2006	gas phase; B
Δ_rG°	19.8 ± 1.0	kcal/mol	TDAs	Paul and Kebarle, 1990	gas phase; B
Δ_rG°	20.80 ± 0.50	kcal/mol	TDAs	Meot-ner and Sieck, 1986	gas phase; B
Δ_rG°	20.3 ± 1.6	kcal/mol	TDAs	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
19.1	296.	FA	MacKay and Bohme, 1978	gas phase; From thermochemical cycle,switching reaction(CH3O-)H2O; Meot-Ner(Mautner), 1986; M

(CH₃O^- • Methyl Alcohol ) + = (CH₃O^- • 2)

By formula: (CH₃O^- • CH₄O) + CH₄O = (CH₃O^- • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.4	kcal/mol	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.8	cal/mol*K	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M

(CH₃O^- • 2 Methyl Alcohol ) + = (CH₃O^- • 3)

By formula: (CH₃O^- • 2CH₄O) + CH₄O = (CH₃O^- • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.0	kcal/mol	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.3	cal/mol*K	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M

(CH₃O^- • 3 Methyl Alcohol ) + = (CH₃O^- • 4)

By formula: (CH₃O^- • 3CH₄O) + CH₄O = (CH₃O^- • 4CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.4	kcal/mol	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.4	cal/mol*K	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M

(CH₃O^- • ) + Methyl Alcohol = (CH₃O^- • • )

By formula: (CH₃O^- • H₂O) + CH₄O = (CH₃O^- • CH₄O • H₂O)

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
13.7	296.	FA	MacKay and Bohme, 1978	gas phase; From thermochemical cycle,switching reaction(CH3O-)2H2O; Meot-Ner(Mautner), 1986; M

CH₅O⁺ + Methyl Alcohol = (CH₅O⁺ • )

By formula: CH₅O⁺ + CH₄O = (CH₅O⁺ • CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	32.6	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rH°	32.3	kcal/mol	PHPMS	Szulejko and McMahon, 1992	gas phase; M
Δ_rH°	32.1	kcal/mol	PHPMS	Meot-Ner(Mautner), 1986	gas phase; M
Δ_rH°	33.1	kcal/mol	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M
Δ_rH°	33.7	kcal/mol	ICR	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O; Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.0	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rS°	29.2	cal/mol*K	PHPMS	Szulejko and McMahon, 1992	gas phase; M
Δ_rS°	26.6	cal/mol*K	PHPMS	Meot-Ner(Mautner), 1986	gas phase; M
Δ_rS°	30.5	cal/mol*K	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M
Δ_rS°	28.5	cal/mol*K	N/A	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O; Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	25.2	kcal/mol	ICR	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O; Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M

(CH₅O⁺ • Methyl Alcohol ) + = (CH₅O⁺ • 2)

By formula: (CH₅O⁺ • CH₄O) + CH₄O = (CH₅O⁺ • 2CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.2	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rH°	21.0	kcal/mol	PHPMS	Meot-Ner(Mautner), 1986	gas phase; M
Δ_rH°	21.3	kcal/mol	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.0	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rS°	25.8	cal/mol*K	PHPMS	Meot-Ner(Mautner), 1986	gas phase; M
Δ_rS°	28.2	cal/mol*K	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M

(CH₅O⁺ • 2 Methyl Alcohol ) + = (CH₅O⁺ • 3)

By formula: (CH₅O⁺ • 2CH₄O) + CH₄O = (CH₅O⁺ • 3CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	14.0	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rH°	16.1	kcal/mol	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.0	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rS°	28.9	cal/mol*K	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M

(CH₅O⁺ • 3 Methyl Alcohol ) + = (CH₅O⁺ • 4)

By formula: (CH₅O⁺ • 3CH₄O) + CH₄O = (CH₅O⁺ • 4CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.3	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rH°	13.5	kcal/mol	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.3	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rS°	28.7	cal/mol*K	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M

(CH₅O⁺ • 4 Methyl Alcohol ) + = (CH₅O⁺ • 5)

By formula: (CH₅O⁺ • 4CH₄O) + CH₄O = (CH₅O⁺ • 5CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	10.2	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rH°	12.5	kcal/mol	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.5	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rS°	31.1	cal/mol*K	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M

(CH₅O⁺ • 5 Methyl Alcohol ) + = (CH₅O⁺ • 6)

By formula: (CH₅O⁺ • 5CH₄O) + CH₄O = (CH₅O⁺ • 6CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.3	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rH°	11.9	kcal/mol	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.5	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rS°	32.9	cal/mol*K	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M

(CH₅O⁺ • 6 Methyl Alcohol ) + = (CH₅O⁺ • 7)

By formula: (CH₅O⁺ • 6CH₄O) + CH₄O = (CH₅O⁺ • 7CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.0	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rH°	12.0	kcal/mol	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.7	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Δ_rS°	35.7	cal/mol*K	PHPMS	Grimsrud and Kebarle, 1973	gas phase; M

(CH₅O⁺ • 7 Methyl Alcohol ) + = (CH₅O⁺ • 8)

By formula: (CH₅O⁺ • 7CH₄O) + CH₄O = (CH₅O⁺ • 8CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.4	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.9	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

(CH₅O⁺ • 8 Methyl Alcohol ) + = (CH₅O⁺ • 9)

By formula: (CH₅O⁺ • 8CH₄O) + CH₄O = (CH₅O⁺ • 9CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.1	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
3.9	200.	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

(CH₅O⁺ • 9 Methyl Alcohol ) + = (CH₅O⁺ • 10)

By formula: (CH₅O⁺ • 9CH₄O) + CH₄O = (CH₅O⁺ • 10CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.7	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
3.5	200.	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

(CH₅O⁺ • 10 Methyl Alcohol ) + = (CH₅O⁺ • 11)

By formula: (CH₅O⁺ • 10CH₄O) + CH₄O = (CH₅O⁺ • 11CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.6	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
3.8	184.	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

(CH₅O⁺ • 11 Methyl Alcohol ) + = (CH₅O⁺ • 12)

By formula: (CH₅O⁺ • 11CH₄O) + CH₄O = (CH₅O⁺ • 12CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.5	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
3.7	184.	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

(CH₅O⁺ • 12 Methyl Alcohol ) + = (CH₅O⁺ • 13)

By formula: (CH₅O⁺ • 12CH₄O) + CH₄O = (CH₅O⁺ • 13CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.6	kcal/mol	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
3.8	184.	PHPMS	Meot-Ner (Mautner), 1992	gas phase; M

(CH₅O⁺ • Methyl Alcohol • ) + = (CH₅O⁺ • 2 • )

By formula: (CH₅O⁺ • CH₄O • H₂O) + CH₄O = (CH₅O⁺ • 2CH₄O • H₂O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	16.4	kcal/mol	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.5	cal/mol*K	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M

(CH₅O⁺ • ) + Methyl Alcohol = (CH₅O⁺ • • )

By formula: (CH₅O⁺ • H₂O) + CH₄O = (CH₅O⁺ • CH₄O • H₂O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	24.5	kcal/mol	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n, Entropy change calculated or estimated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.	cal/mol*K	N/A	Meot-Ner(Mautner), 1986	gas phase; n, Entropy change calculated or estimated; M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
11.6	452.	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n, Entropy change calculated or estimated; M

(CH₅O⁺ • 2) + Methyl Alcohol = (CH₅O⁺ • • 2)

By formula: (CH₅O⁺ • 2H₂O) + CH₄O = (CH₅O⁺ • CH₄O • 2H₂O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	18.0	kcal/mol	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.3	cal/mol*K	PHPMS	Meot-Ner(Mautner), 1986	gas phase; n; M

CH₆N⁺ + Methyl Alcohol = (CH₆N⁺ • )

By formula: CH₆N⁺ + CH₄O = (CH₆N⁺ • CH₄O)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	19.0	kcal/mol	PHPMS	Meot-Ner, 1984	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.2	cal/mol*K	PHPMS	Meot-Ner, 1984	gas phase; M

CN^- + Methyl Alcohol = (CN^- • )

By formula: CN^- + CH₄O = (CN^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.70 ± 0.80	kcal/mol	TDAs	Larson, Szulejko, et al., 1988	gas phase; B,M
Δ_rH°	16.6 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988	gas phase; B
Δ_rH°	16.5 ± 3.5	kcal/mol	IMRE	Larson and McMahon, 1987	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.	cal/mol*K	PHPMS	Larson, Szulejko, et al., 1988	gas phase; M
Δ_rS°	24.3	cal/mol*K	N/A	Larson and McMahon, 1987	gas phase; switching reaction,Thermochemical ladder(CN-)H2O, Entropy change calculated or estimated; Payzant, Yamdagni, et al., 1971; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	8.80 ± 0.20	kcal/mol	TDAs	Larson, Szulejko, et al., 1988	gas phase; B
Δ_rG°	10.4 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988	gas phase; B
Δ_rG°	9.2 ± 2.3	kcal/mol	IMRE	Larson and McMahon, 1987	gas phase; B,M

C₂H^- + Methyl Alcohol = C₃H₅O^-

By formula: C₂H^- + CH₄O = C₃H₅O^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.6 ± 2.0	kcal/mol	IMRE	Chabinyc and Brauman, 1999	gas phase; Anchored to MeOH ΔGacid=375.2; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	10.90	kcal/mol	IMRE	Mustanir, Matsuoka, et al., 2006	gas phase; B
Δ_rG°	11.6 ± 2.0	kcal/mol	IMRE	Chabinyc and Brauman, 1999	gas phase; Anchored to MeOH ΔGacid=375.2; B

+ Methyl Alcohol = ( • )

By formula: C₂H₃O₂^- + CH₄O = (C₂H₃O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.6 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	10.5 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988	gas phase; B

(C₂H₄N⁺ • Methyl Alcohol ) + = (C₂H₄N⁺ • 2)

By formula: (C₂H₄N⁺ • CH₄O) + CH₄O = (C₂H₄N⁺ • 2CH₄O)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	20.9	kcal/mol	PHPMS	El-Shall, Olafsdottir, et al., 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.0	cal/mol*K	PHPMS	El-Shall, Olafsdottir, et al., 1991	gas phase; M

(C₂H₄N⁺ • 2 Methyl Alcohol ) + = (C₂H₄N⁺ • 3)

By formula: (C₂H₄N⁺ • 2CH₄O) + CH₄O = (C₂H₄N⁺ • 3CH₄O)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.9	kcal/mol	PHPMS	El-Shall, Olafsdottir, et al., 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.4	cal/mol*K	PHPMS	El-Shall, Olafsdottir, et al., 1991	gas phase; M

(C₂H₄N⁺ • Methyl Alcohol • ) + = (C₂H₄N⁺ • 2 • )

By formula: (C₂H₄N⁺ • CH₄O • C₂H₃N) + CH₄O = (C₂H₄N⁺ • 2CH₄O • C₂H₃N)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.7	kcal/mol	PHPMS	El-Shall, Olafsdottir, et al., 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.1	cal/mol*K	PHPMS	El-Shall, Olafsdottir, et al., 1991	gas phase; M

C₂H₄NO₂^- + Methyl Alcohol = C₃H₈NO₃^-

By formula: C₂H₄NO₂^- + CH₄O = C₃H₈NO₃^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.00 ± 0.50	kcal/mol	TDAs	Nieckarz, Atkins, et al., 2008	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	9.5 ± 1.0	kcal/mol	TDAs	Nieckarz, Atkins, et al., 2008	gas phase; B

C₂H₅O⁺ + Methyl Alcohol = (C₂H₅O⁺ • )

By formula: C₂H₅O⁺ + CH₄O = (C₂H₅O⁺ • CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	30.3	kcal/mol	ICR	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O, Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.9	cal/mol*K	N/A	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O, Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	22.3	kcal/mol	ICR	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O, Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M

C₂H₅O^- + Methyl Alcohol = (C₂H₅O^- • )

By formula: C₂H₅O^- + CH₄O = (C₂H₅O^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	27.3 ± 2.9	kcal/mol	IMRE	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B,M
Δ_rH°	25.6 ± 1.9	kcal/mol	CIDT	DeTuri and Ervin, 1999	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.3	cal/mol*K	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; switching reaction(CH3O-)CH3OH, Entropy change calculated or estimated; re-evaluated using Meot-Ner(Mautner), 1986 and Paul and Kebarle, 1990; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	18.6 ± 2.0	kcal/mol	IMRE	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B,M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
13.4	296.	FA	Mackay, Rakshit, et al., 1982	gas phase; From thermochemical cycle,switching reaction(CH3O-)CH3OH; Caldwell and Kebarle, 1986, Taft, 1983; M

C₂H₇O⁺ + Methyl Alcohol = (C₂H₇O⁺ • )

By formula: C₂H₇O⁺ + CH₄O = (C₂H₇O⁺ • CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	26.3	kcal/mol	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.1	cal/mol*K	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M

(C₂H₇O⁺ • Methyl Alcohol ) + = (C₂H₇O⁺ • 2)

By formula: (C₂H₇O⁺ • CH₄O) + CH₄O = (C₂H₇O⁺ • 2CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	18.8	kcal/mol	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	28.9	cal/mol*K	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M

(C₂H₇O⁺ • 2 Methyl Alcohol ) + = (C₂H₇O⁺ • 3)

By formula: (C₂H₇O⁺ • 2CH₄O) + CH₄O = (C₂H₇O⁺ • 3CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.9	kcal/mol	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	31.2	cal/mol*K	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M

(C₂H₇O⁺ • 3 Methyl Alcohol ) + = (C₂H₇O⁺ • 4)

By formula: (C₂H₇O⁺ • 3CH₄O) + CH₄O = (C₂H₇O⁺ • 4CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.7	kcal/mol	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	30.8	cal/mol*K	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M

(C₂H₇O⁺ • Methyl Alcohol • ) + = (C₂H₇O⁺ • 2 • )

By formula: (C₂H₇O⁺ • CH₄O • C₂H₆O) + CH₄O = (C₂H₇O⁺ • 2CH₄O • C₂H₆O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.1	kcal/mol	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	30.6	cal/mol*K	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M

(C₂H₇O⁺ • 2 Methyl Alcohol • ) + = (C₂H₇O⁺ • 3 • )

By formula: (C₂H₇O⁺ • 2CH₄O • C₂H₆O) + CH₄O = (C₂H₇O⁺ • 3CH₄O • C₂H₆O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	12.2	kcal/mol	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.5	cal/mol*K	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M

(C₂H₇O⁺ • ) + Methyl Alcohol = (C₂H₇O⁺ • • )

By formula: (C₂H₇O⁺ • C₂H₆O) + CH₄O = (C₂H₇O⁺ • CH₄O • C₂H₆O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	18.1	kcal/mol	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	30.6	cal/mol*K	PHPMS	Hiraoka, Grimsrud, et al., 1974	gas phase; n; M

C₂H₇O⁺ + Methyl Alcohol = (C₂H₇O⁺ • )

By formula: C₂H₇O⁺ + CH₄O = (C₂H₇O⁺ • CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	29.6	kcal/mol	ICR	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O, Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.6	cal/mol*K	N/A	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O, Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	21.7	kcal/mol	ICR	Larson and McMahon, 1982	gas phase; switching reaction((CH3)2OH+)(CH3)2O, Entropy change calculated or estimated; Grimsrud and Kebarle, 1973, Lias, Liebman, et al., 1984, Keesee and Castleman, 1986; M

C₂H₇O₂^- + 2 Methyl Alcohol = C₃H₁₁O₃^-

By formula: C₂H₇O₂^- + 2CH₄O = C₃H₁₁O₃^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.4 ± 1.0	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	13.10 ± 0.50	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B

C₂H₇O₂^- + + Methyl Alcohol = C₂H₉O₃^-

By formula: C₂H₇O₂^- + H₂O + CH₄O = C₂H₉O₃^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.8 ± 1.0	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	10.10 ± 0.50	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B

C₂H₉O₃^- + 2 + Methyl Alcohol = C₂H₁₁O₄^-

By formula: C₂H₉O₃^- + 2H₂O + CH₄O = C₂H₁₁O₄^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.2 ± 1.0	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.90 ± 0.50	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B

+ Methyl Alcohol = ( • )

By formula: C₃H₃N₂^- + CH₄O = (C₃H₃N₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.1	kcal/mol	PHPMS	Meot-Ner (Mautner), 1988	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.2	cal/mol*K	PHPMS	Meot-Ner (Mautner), 1988	gas phase; M

C₃H₇O⁺ + Methyl Alcohol = (C₃H₇O⁺ • )

By formula: C₃H₇O⁺ + CH₄O = (C₃H₇O⁺ • CH₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.1	kcal/mol	PHPMS	Meot-Ner (Mautner), Ross, et al., 1985	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	21.3	cal/mol*K	PHPMS	Meot-Ner (Mautner), Ross, et al., 1985	gas phase; M

C₃H₇O^- + Methyl Alcohol = (C₃H₇O^- • )

By formula: C₃H₇O^- + CH₄O = (C₃H₇O^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	26.9 ± 2.9	kcal/mol	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.3	cal/mol*K	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; switching reaction(CH3O-)CH3OH, Entropy change calculated or estimated; re-evaluated using Meot-Ner(Mautner), 1986 and Paul and Kebarle, 1990; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	18.2 ± 2.0	kcal/mol	IMRE	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B,M

C₃H₉Si⁺ + Methyl Alcohol = (C₃H₉Si⁺ • )

By formula: C₃H₉Si⁺ + CH₄O = (C₃H₉Si⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	39.2	kcal/mol	PHPMS	Wojtyniak and Stone, 1986	gas phase; switching reaction,Thermochemical ladder((CH3)3Si+)H2O, Entropy change calculated or estimated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.7	cal/mol*K	N/A	Wojtyniak and Stone, 1986	gas phase; switching reaction,Thermochemical ladder((CH3)3Si+)H2O, Entropy change calculated or estimated; M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
25.3	468.	PHPMS	Wojtyniak and Stone, 1986	gas phase; switching reaction,Thermochemical ladder((CH3)3Si+)H2O, Entropy change calculated or estimated; M

C₃H₉Sn⁺ + Methyl Alcohol = (C₃H₉Sn⁺ • )

By formula: C₃H₉Sn⁺ + CH₄O = (C₃H₉Sn⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	32.6	kcal/mol	PHPMS	Stone and Splinter, 1984	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	32.	cal/mol*K	PHPMS	Stone and Splinter, 1984	gas phase; M

C₃H₁₀N⁺ + Methyl Alcohol = (C₃H₁₀N⁺ • )

By formula: C₃H₁₀N⁺ + CH₄O = (C₃H₁₀N⁺ • CH₄O)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.1	kcal/mol	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	21.0	cal/mol*K	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M

(C₃H₁₀N⁺ • Methyl Alcohol ) + = (C₃H₁₀N⁺ • 2)

By formula: (C₃H₁₀N⁺ • CH₄O) + CH₄O = (C₃H₁₀N⁺ • 2CH₄O)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.7	kcal/mol	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.8	cal/mol*K	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M

(C₃H₁₀N⁺ • 2 Methyl Alcohol ) + = (C₃H₁₀N⁺ • 3)

By formula: (C₃H₁₀N⁺ • 2CH₄O) + CH₄O = (C₃H₁₀N⁺ • 3CH₄O)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	10.5	kcal/mol	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.0	cal/mol*K	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M

(C₃H₁₀N⁺ • Methyl Alcohol • ) + = (C₃H₁₀N⁺ • 2 • )

By formula: (C₃H₁₀N⁺ • CH₄O • C₃H₉N) + CH₄O = (C₃H₁₀N⁺ • 2CH₄O • C₃H₉N)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.5	kcal/mol	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M

(C₃H₁₀N⁺ • ) + Methyl Alcohol = (C₃H₁₀N⁺ • • )

By formula: (C₃H₁₀N⁺ • C₃H₉N) + CH₄O = (C₃H₁₀N⁺ • CH₄O • C₃H₉N)

Bond type: Hydrogen bonds of the type NH+-O between organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	10.6	kcal/mol	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.2	cal/mol*K	PHPMS	El-Shall, Daly, et al., 1992	gas phase; M

C₃H₁₁O₃^- + 3 Methyl Alcohol = C₄H₁₅O₄^-

By formula: C₃H₁₁O₃^- + 3CH₄O = C₄H₁₅O₄^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.0 ± 1.0	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	7.20 ± 0.50	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B

C₃H₁₁O₃^- + + 2 Methyl Alcohol = C₃H₁₃O₄^-

By formula: C₃H₁₁O₃^- + H₂O + 2CH₄O = C₃H₁₃O₄^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.8 ± 1.0	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.40 ± 0.50	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B

C₄H₂O₃^- + Methyl Alcohol = (C₄H₂O₃^- • )

By formula: C₄H₂O₃^- + CH₄O = (C₄H₂O₃^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.7 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
4.7	343.	PHPMS	Chowdhury, 1987	gas phase; M

+ Methyl Alcohol = ( • )

By formula: C₄H₄N^- + CH₄O = (C₄H₄N^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	18.6 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988, 2	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.5	cal/mol*K	PHPMS	Meot-ner, 1988, 2	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	10.4 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988, 2	gas phase; B

C₄H₉O^- + Methyl Alcohol = (C₄H₉O^- • )

By formula: C₄H₉O^- + CH₄O = (C₄H₉O^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	25.5 ± 1.0	kcal/mol	TDEq	Meot-Ner and Sieck, 1986	gas phase; B,M
Δ_rH°	23.4 ± 2.2	kcal/mol	CIDT	DeTuri and Ervin, 1999	gas phase; B
Δ_rH°	26.0 ± 2.5	kcal/mol	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.9	cal/mol*K	N/A	Meot-Ner and Sieck, 1986	gas phase; Entropy change calculated or estimated; M
Δ_rS°	29.3	cal/mol*K	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; switching reaction(CH3O-)CH3OH, Entropy change calculated or estimated; re-evaluated using Meot-Ner(Mautner), 1986 and Paul and Kebarle, 1990; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	10.20	kcal/mol	IMRE	Mustanir, Matsuoka, et al., 2006	gas phase; B
Δ_rG°	17.1 ± 1.6	kcal/mol	TDEq	Meot-Ner and Sieck, 1986	gas phase; B
Δ_rG°	17.3 ± 1.6	kcal/mol	IMRE	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; B,M

C₄H₁₁O₂⁺ + Methyl Alcohol = (C₄H₁₁O₂⁺ • )

By formula: C₄H₁₁O₂⁺ + CH₄O = (C₄H₁₁O₂⁺ • CH₄O)

Bond type: Hydrogen bonds between protonated and neutral organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	22.0	kcal/mol	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	28.3	cal/mol*K	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M

(C₄H₁₁O₂⁺ • Methyl Alcohol ) + = (C₄H₁₁O₂⁺ • 2)

By formula: (C₄H₁₁O₂⁺ • CH₄O) + CH₄O = (C₄H₁₁O₂⁺ • 2CH₄O)

Bond type: Hydrogen bonds between protonated and neutral organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	14.4	kcal/mol	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.6	cal/mol*K	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M

(C₄H₁₁O₂⁺ • 2 Methyl Alcohol ) + = (C₄H₁₁O₂⁺ • 3)

By formula: (C₄H₁₁O₂⁺ • 2CH₄O) + CH₄O = (C₄H₁₁O₂⁺ • 3CH₄O)

Bond type: Hydrogen bonds between protonated and neutral organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	12.6	kcal/mol	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.0	cal/mol*K	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M

(C₄H₁₁O₂⁺ • 3 Methyl Alcohol ) + = (C₄H₁₁O₂⁺ • 4)

By formula: (C₄H₁₁O₂⁺ • 3CH₄O) + CH₄O = (C₄H₁₁O₂⁺ • 4CH₄O)

Bond type: Hydrogen bonds between protonated and neutral organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	10.2	kcal/mol	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.3	cal/mol*K	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M

(C₄H₁₁O₂⁺ • 4 Methyl Alcohol ) + = (C₄H₁₁O₂⁺ • 5)

By formula: (C₄H₁₁O₂⁺ • 4CH₄O) + CH₄O = (C₄H₁₁O₂⁺ • 5CH₄O)

Bond type: Hydrogen bonds between protonated and neutral organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.2	kcal/mol	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.2	cal/mol*K	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M

(C₄H₁₁O₂⁺ • 5 Methyl Alcohol ) + = (C₄H₁₁O₂⁺ • 6)

By formula: (C₄H₁₁O₂⁺ • 5CH₄O) + CH₄O = (C₄H₁₁O₂⁺ • 6CH₄O)

Bond type: Hydrogen bonds between protonated and neutral organics

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.9	kcal/mol	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.0	cal/mol*K	PHPMS	Meot-Ner (Mautner), Sieck, et al., 1994	gas phase; M

C₄H₁₅O₄^- + 4 Methyl Alcohol = C₅H₁₉O₅^-

By formula: C₄H₁₅O₄^- + 4CH₄O = C₅H₁₉O₅^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.4 ± 1.0	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.70 ± 0.50	kcal/mol	TDAs	Meot-Ner(Mautner), 1986	gas phase; B

+ Methyl Alcohol = ( • )

By formula: C₅H₅^- + CH₄O = (C₅H₅^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.2 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988, 2	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.9 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988, 2	gas phase; B

C₅H₁₁O^- + Methyl Alcohol = (C₅H₁₁O^- • )

By formula: C₅H₁₁O^- + CH₄O = (C₅H₁₁O^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	25.7 ± 2.9	kcal/mol	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	17.0 ± 2.0	kcal/mol	IMRE	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B

C₆F₄O₂^- + Methyl Alcohol = (C₆F₄O₂^- • )

By formula: C₆F₄O₂^- + CH₄O = (C₆F₄O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	3.0 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
3.0	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₄ClNO₂^- + Methyl Alcohol = (C₆H₄ClNO₂^- • )

By formula: C₆H₄ClNO₂^- + CH₄O = (C₆H₄ClNO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.4 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
5.4	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₄ClNO₂^- + Methyl Alcohol = (C₆H₄ClNO₂^- • )

By formula: C₆H₄ClNO₂^- + CH₄O = (C₆H₄ClNO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.4 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
5.4	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₄ClNO₂^- + Methyl Alcohol = (C₆H₄ClNO₂^- • )

By formula: C₆H₄ClNO₂^- + CH₄O = (C₆H₄ClNO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.6 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
5.6	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₄FNO₂^- + Methyl Alcohol = (C₆H₄FNO₂^- • )

By formula: C₆H₄FNO₂^- + CH₄O = (C₆H₄FNO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.8 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
5.8	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₄FNO₂^- + Methyl Alcohol = (C₆H₄FNO₂^- • )

By formula: C₆H₄FNO₂^- + CH₄O = (C₆H₄FNO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.0 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
6.0	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₄FNO₂^- + Methyl Alcohol = (C₆H₄FNO₂^- • )

By formula: C₆H₄FNO₂^- + CH₄O = (C₆H₄FNO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.8 ± 2.0	kcal/mol	N/A	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.8	cal/mol*K	PHPMS	Chowdhury, 1987	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.6 ± 2.0	kcal/mol	TDAs	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

C₆H₄NO₃^- + Methyl Alcohol = (C₆H₄NO₃^- • )

By formula: C₆H₄NO₃^- + CH₄O = (C₆H₄NO₃^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.0 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

C₆H₄NO₃^- + Methyl Alcohol = (C₆H₄NO₃^- • )

By formula: C₆H₄NO₃^- + CH₄O = (C₆H₄NO₃^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.8 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

C₆H₄N₂O₄^- + Methyl Alcohol = (C₆H₄N₂O₄^- • )

By formula: C₆H₄N₂O₄^- + CH₄O = (C₆H₄N₂O₄^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.3 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
2.3	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₄N₂O₄^- + Methyl Alcohol = (C₆H₄N₂O₄^- • )

By formula: C₆H₄N₂O₄^- + CH₄O = (C₆H₄N₂O₄^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	3.3 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
3.3	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₄N₂O₄^- + Methyl Alcohol = (C₆H₄N₂O₄^- • )

By formula: C₆H₄N₂O₄^- + CH₄O = (C₆H₄N₂O₄^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	3.8 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
3.8	343.	PHPMS	Chowdhury, 1987	gas phase; M

+ Methyl Alcohol = ( • )

By formula: C₆H₄O₂^- + CH₄O = (C₆H₄O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.5 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
5.5	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₆H₅NO₂^- + Methyl Alcohol = (C₆H₅NO₂^- • )

By formula: C₆H₅NO₂^- + CH₄O = (C₆H₅NO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.10 ± 0.20	kcal/mol	TDAs	Sieck, 1985	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.1	cal/mol*K	PHPMS	Sieck, 1985	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	7.30 ± 0.40	kcal/mol	TDAs	Sieck, 1985	gas phase; B
Δ_rG°	6.3 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
6.3	343.	PHPMS	Chowdhury, 1987	gas phase; M

+ Methyl Alcohol = ( • )

By formula: C₆H₅S^- + CH₄O = (C₆H₅S^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.4	kcal/mol	PHPMS	Sieck and Meot-ner, 1989	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.0	cal/mol*K	PHPMS	Sieck and Meot-ner, 1989	gas phase; M

+ Methyl Alcohol = C₇H₉OS^-

By formula: C₆H₅S^- + CH₄O = C₇H₉OS^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.40 ± 0.10	kcal/mol	TDAs	Sieck and Meot-ner, 1989	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.50 ± 0.30	kcal/mol	TDAs	Sieck and Meot-ner, 1989	gas phase; B

C₆H₉^- + Methyl Alcohol = C₇H₁₃O^-

By formula: C₆H₉^- + CH₄O = C₇H₁₃O^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	20.8 ± 2.0	kcal/mol	IMRE	Chabinyc and Brauman, 1999	gas phase; Anchored to MeOH ΔGacid=375.2; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	11.50	kcal/mol	IMRE	Mustanir, Matsuoka, et al., 2006	gas phase; B
Δ_rG°	10.7 ± 2.0	kcal/mol	IMRE	Chabinyc and Brauman, 1999	gas phase; Anchored to MeOH ΔGacid=375.2; B

C₆H₁₁S₂^- + Methyl Alcohol = (C₆H₁₁S₂^- • )

By formula: C₆H₁₁S₂^- + CH₄O = (C₆H₁₁S₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.9 ± 2.5	kcal/mol	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	13.2 ± 1.6	kcal/mol	IMRE	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B

+ Methyl Alcohol = ( • )

By formula: C₇F₁₄^- + CH₄O = (C₇F₁₄^- • CH₄O)

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
6.4	308.	PHPMS	Knighton, Zook, et al., 1990	gas phase; M

C₇H₄F₃NO₂^- + Methyl Alcohol = (C₇H₄F₃NO₂^- • )

By formula: C₇H₄F₃NO₂^- + CH₄O = (C₇H₄F₃NO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	14.6 ± 2.0	kcal/mol	N/A	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.9 ± 1.6	kcal/mol	TDAs	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

C₇H₄N₂O₂^- + Methyl Alcohol = (C₇H₄N₂O₂^- • )

By formula: C₇H₄N₂O₂^- + CH₄O = (C₇H₄N₂O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.7 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
4.7	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₇H₄N₂O₂^- + Methyl Alcohol = (C₇H₄N₂O₂^- • )

By formula: C₇H₄N₂O₂^- + CH₄O = (C₇H₄N₂O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.5 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
4.5	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₇H₄N₂O₂^- + Methyl Alcohol = (C₇H₄N₂O₂^- • )

By formula: C₇H₄N₂O₂^- + CH₄O = (C₇H₄N₂O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.9 ± 2.0	kcal/mol	N/A	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	28.6	cal/mol*K	PHPMS	Chowdhury, 1987	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.1 ± 2.0	kcal/mol	TDAs	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

C₇H₇NO₂^- + Methyl Alcohol = (C₇H₇NO₂^- • )

By formula: C₇H₇NO₂^- + CH₄O = (C₇H₇NO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.3 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
6.3	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₇H₇NO₂^- + Methyl Alcohol = (C₇H₇NO₂^- • )

By formula: C₇H₇NO₂^- + CH₄O = (C₇H₇NO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.5 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
6.5	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₇H₇NO₂^- + Methyl Alcohol = (C₇H₇NO₂^- • )

By formula: C₇H₇NO₂^- + CH₄O = (C₇H₇NO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.4 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

C₇H₇NO₃^- + Methyl Alcohol = (C₇H₇NO₃^- • )

By formula: C₇H₇NO₃^- + CH₄O = (C₇H₇NO₃^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.1 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
6.1	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₇H₇NO₃^- + Methyl Alcohol = (C₇H₇NO₃^- • )

By formula: C₇H₇NO₃^- + CH₄O = (C₇H₇NO₃^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	14.3 ± 2.0	kcal/mol	N/A	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.4	cal/mol*K	PHPMS	Chowdhury, 1987	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.3 ± 2.0	kcal/mol	TDAs	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

C₈H₅^- + Methyl Alcohol = (C₈H₅^- • )

By formula: C₈H₅^- + CH₄O = (C₈H₅^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.5 ± 2.0	kcal/mol	IMRE	Chabinyc and Brauman, 1999	gas phase; B
Δ_rH°	21.4 ± 2.9	kcal/mol	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.3	cal/mol*K	N/A	Caldwell, Rozeboom, et al., 1984	gas phase; switching reaction(CH3O-)CH3OH, Entropy change calculated or estimated; re-evaluated using Meot-Ner(Mautner), 1986 and Paul and Kebarle, 1990; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	11.0 ± 2.0	kcal/mol	IMRE	Chabinyc and Brauman, 1999	gas phase; B
Δ_rG°	12.7 ± 2.0	kcal/mol	IMRE	Caldwell, Rozeboom, et al., 1984	gas phase; Reanchored to average data from Paul and Kebarle, 1990 and Meot-ner and Sieck, 1986.; value altered from reference due to change in acidity scale; B,M

C₈H₉NO₂^- + Methyl Alcohol = (C₈H₉NO₂^- • )

By formula: C₈H₉NO₂^- + CH₄O = (C₈H₉NO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.3 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
6.3	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₈H₁₇O₄⁺ + Methyl Alcohol = (C₈H₁₇O₄⁺ • )

By formula: C₈H₁₇O₄⁺ + CH₄O = (C₈H₁₇O₄⁺ • CH₄O)

Bond type: Hydrogen bonds with polydentate bonding in positive ions

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	19.5	kcal/mol	PHPMS	Sharma and Kebarle, 1984	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	34.0	cal/mol*K	PHPMS	Sharma and Kebarle, 1984	gas phase; M

C₉H₇^- + Methyl Alcohol = C₁₀H₁₁O^-

By formula: C₉H₇^- + CH₄O = C₁₀H₁₁O^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.6 ± 2.0	kcal/mol	IMRE	Chabinyc and Brauman, 1999	gas phase; Anchored to MeOH ΔGacid=375.2; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	10.20	kcal/mol	IMRE	Mustanir, Matsuoka, et al., 2006	gas phase; B
Δ_rG°	11.1 ± 2.0	kcal/mol	IMRE	Chabinyc and Brauman, 1999	gas phase; Anchored to MeOH ΔGacid=375.2; B

C₁₀H₄Cl₂O₂^- + Methyl Alcohol = (C₁₀H₄Cl₂O₂^- • )

By formula: C₁₀H₄Cl₂O₂^- + CH₄O = (C₁₀H₄Cl₂O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	<1.5 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
1.5	343.	PHPMS	Chowdhury, 1987	gas phase; DG<; M

+ Methyl Alcohol = ( • )

By formula: C₁₀H₆O₂^- + CH₄O = (C₁₀H₆O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.6 ± 1.6	kcal/mol	IMRE	Chowdhury, Grimsrud, et al., 1987	gas phase; Free energy affinity at 70°C.; B

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
4.6	343.	PHPMS	Chowdhury, 1987	gas phase; M

C₁₀H₂₁O₅⁺ + Methyl Alcohol = (C₁₀H₂₁O₅⁺ • )

By formula: C₁₀H₂₁O₅⁺ + CH₄O = (C₁₀H₂₁O₅⁺ • CH₄O)

Bond type: Hydrogen bonds with polydentate bonding in positive ions

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	20.0	kcal/mol	PHPMS	Sharma and Kebarle, 1984	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	28.0	cal/mol*K	PHPMS	Sharma and Kebarle, 1984	gas phase; M

C₁₂H₂₅O₆⁺ + Methyl Alcohol = (C₁₂H₂₅O₆⁺ • )

By formula: C₁₂H₂₅O₆⁺ + CH₄O = (C₁₂H₂₅O₆⁺ • CH₄O)

Bond type: Hydrogen bonds with polydentate bonding in positive ions

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	20.0	kcal/mol	PHPMS	Sharma and Kebarle, 1984	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.5	cal/mol*K	PHPMS	Sharma and Kebarle, 1984	gas phase; M

+ Methyl Alcohol = ( • )

By formula: Cl^- + CH₄O = (Cl^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17. ± 3.	kcal/mol	AVG	N/A	Average of 8 values; Individual data points
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.6	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M
Δ_rS°	24.1	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Δ_rS°	22.0	cal/mol*K	PHPMS	Sieck, 1985	gas phase; M
Δ_rS°	22.9	cal/mol*K	N/A	Larson and McMahon, 1984	gas phase; switching reaction(Cl-)t-C4H9OH, Entropy change calculated or estimated; French, Ikuta, et al., 1982; M
Δ_rS°	14.8	cal/mol*K	PHPMS	Yamdagni, Payzant, et al., 1973	gas phase; Entropy change is questionable; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	10.1 ± 0.8	kcal/mol	AVG	N/A	Average of 10 values; Individual data points

( • Methyl Alcohol ) + = ( • 2)

By formula: (Cl^- • CH₄O) + CH₄O = (Cl^- • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	14.10 ± 0.40	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	13.70 ± 0.20	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; B,M
Δ_rH°	14.1 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Δ_rH°	13.00 ± 0.70	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.2	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Δ_rS°	22.0	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M
Δ_rS°	19.4	cal/mol*K	PHPMS	Yamdagni, Payzant, et al., 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	7.30	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	7.10	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; B
Δ_rG°	6.8 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B
Δ_rG°	7.20 ± 0.40	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B

( • 2 Methyl Alcohol ) + = ( • 3)

By formula: (Cl^- • 2CH₄O) + CH₄O = (Cl^- • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.50 ± 0.20	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	10.80 ± 0.30	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; B,M
Δ_rH°	11.8 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Δ_rH°	12.30 ± 0.60	kcal/mol	N/A	Yamdagni, Payzant, et al., 1973	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.9	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Δ_rS°	22.7	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M
Δ_rS°	23.6	cal/mol*K	PHPMS	Yamdagni, Payzant, et al., 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.06	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	4.00	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; B
Δ_rG°	4.9 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B
Δ_rG°	5.20 ± 0.30	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B

( • 3 Methyl Alcohol ) + = ( • 4)

By formula: (Cl^- • 3CH₄O) + CH₄O = (Cl^- • 4CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	10.5 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Δ_rH°	10.50	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; B
Δ_rH°	11.20 ± 0.60	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.9	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Δ_rS°	26.4	cal/mol*K	PHPMS	Yamdagni, Payzant, et al., 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	3.6 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B
Δ_rG°	3.70	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; B
Δ_rG°	3.30 ± 0.20	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B

( • 4 Methyl Alcohol ) + = ( • 5)

By formula: (Cl^- • 4CH₄O) + CH₄O = (Cl^- • 5CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.2 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Δ_rH°	10.50 ± 0.50	kcal/mol	N/A	Yamdagni, Payzant, et al., 1973	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	21.7	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Δ_rS°	25.5	cal/mol*K	PHPMS	Yamdagni, Payzant, et al., 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.7 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B
Δ_rG°	2.90 ± 0.10	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B

( • 5 Methyl Alcohol ) + = ( • 6)

By formula: (Cl^- • 5CH₄O) + CH₄O = (Cl^- • 6CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.9 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.2	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.2 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B

( • 6 Methyl Alcohol ) + = ( • 7)

By formula: (Cl^- • 6CH₄O) + CH₄O = (Cl^- • 7CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.0 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	20.1	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.0 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B

( • 7 Methyl Alcohol ) + = ( • 8)

By formula: (Cl^- • 7CH₄O) + CH₄O = (Cl^- • 8CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	7.6 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	19.7	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.7 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B

( • 8 Methyl Alcohol ) + = ( • 9)

By formula: (Cl^- • 8CH₄O) + CH₄O = (Cl^- • 9CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	7.6 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	20.6	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.4 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B

( • 9 Methyl Alcohol ) + = ( • 10)

By formula: (Cl^- • 9CH₄O) + CH₄O = (Cl^- • 10CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	7.4 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	20.1	cal/mol*K	PHPMS	Hiraoka and Mizuse, 1987	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.4 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; B

( • 10 Methyl Alcohol ) + = ( • 11)

By formula: (Cl^- • 10CH₄O) + CH₄O = (Cl^- • 11CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	7.3 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; Estimated entropy; single temperature measurement; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	20.	cal/mol*K	N/A	Hiraoka and Mizuse, 1987	gas phase; Entropy change calculated or estimated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.3 ± 1.0	kcal/mol	TDAs	Hiraoka and Mizuse, 1987	gas phase; Estimated entropy; single temperature measurement; B

( • Methyl Alcohol • ) + = ( • 2 • )

By formula: (Cl^- • CH₄O • H₂O) + CH₄O = (Cl^- • 2CH₄O • H₂O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	10.8	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	19.	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

( • ) + Methyl Alcohol = ( • • )

By formula: (Cl^- • H₂O) + CH₄O = (Cl^- • CH₄O • H₂O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.2	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	20.9	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

( • 2) + Methyl Alcohol = ( • • 2)

By formula: (Cl^- • 2H₂O) + CH₄O = (Cl^- • CH₄O • 2H₂O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.4	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	18.1	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

+ Methyl Alcohol = ( • )

By formula: Co⁺ + CH₄O = (Co⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	35.4 ± 1.9	kcal/mol	CIDT	Rodgers and Armentrout, 2000	RCD

+ Methyl Alcohol = ( • )

By formula: Cu⁺ + CH₄O = (Cu⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.4	kcal/mol	HPMS	El-Shall, Schriver, et al., 1989	gas phase; Entropy change calculated or estimated, Cu+ from laser desorption; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.	cal/mol*K	N/A	El-Shall, Schriver, et al., 1989	gas phase; Entropy change calculated or estimated, Cu+ from laser desorption; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.9	kcal/mol	HPMS	El-Shall, Schriver, et al., 1989	gas phase; Entropy change calculated or estimated, Cu+ from laser desorption; M

( • Methyl Alcohol ) + = ( • 2)

By formula: (Cu⁺ • CH₄O) + CH₄O = (Cu⁺ • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.8	kcal/mol	HPMS	El-Shall, Schriver, et al., 1989	gas phase; Entropy change calculated or estimated, Cu+ from laser desorption; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.	cal/mol*K	N/A	El-Shall, Schriver, et al., 1989	gas phase; Entropy change calculated or estimated, Cu+ from laser desorption; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	6.3	kcal/mol	HPMS	El-Shall, Schriver, et al., 1989	gas phase; Entropy change calculated or estimated, Cu+ from laser desorption; M

+ Methyl Alcohol = CH₃D₄FO^-

By formula: F^- + CH₄O = CH₃D₄FO^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	29.8 ± 2.0	kcal/mol	TDEq	Wilkinson, Szulejko, et al., 1992	gas phase; Reported relative to ROH..F-, 0.5 kcal/mol weaker.; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	22.4 ± 2.0	kcal/mol	TDEq	Wilkinson, Szulejko, et al., 1992	gas phase; Reported relative to ROH..F-, 0.5 kcal/mol weaker.; B

+ Methyl Alcohol = ( • )

By formula: F^- + CH₄O = (F^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	29.6 ± 2.0	kcal/mol	IMRE	Larson and McMahon, 1983	gas phase; B,M
Δ_rH°	29.4 ± 2.2	kcal/mol	CIDT	DeTuri and Ervin, 1999	gas phase; B
Δ_rH°	23.3 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.0	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Δ_rS°	22.6	cal/mol*K	N/A	Larson and McMahon, 1983	gas phase; switching reaction(F-)H2O, Entropy change calculated or estimated; Arshadi, Yamdagni, et al., 1970; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	22.8 ± 2.0	kcal/mol	IMRE	Larson and McMahon, 1983	gas phase; B,M
Δ_rG°	15.8 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • Methyl Alcohol ) + = ( • 2)

By formula: (F^- • CH₄O) + CH₄O = (F^- • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	20.30 ± 0.30	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	19.3 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.2	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	12.97	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	12.4 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 2 Methyl Alcohol ) + = ( • 3)

By formula: (F^- • 2CH₄O) + CH₄O = (F^- • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.10 ± 0.60	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	14.5 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	21.2	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	8.06	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	8.2 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 3 Methyl Alcohol ) + = ( • 4)

By formula: (F^- • 3CH₄O) + CH₄O = (F^- • 4CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	12.5 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.5	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.5 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 4 Methyl Alcohol ) + = ( • 5)

By formula: (F^- • 4CH₄O) + CH₄O = (F^- • 5CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.9 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.3	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	3.8 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 5 Methyl Alcohol ) + = ( • 6)

By formula: (F^- • 5CH₄O) + CH₄O = (F^- • 6CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.5 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.8	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.6 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 6 Methyl Alcohol ) + = ( • 7)

By formula: (F^- • 6CH₄O) + CH₄O = (F^- • 7CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.8 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.5	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.2 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 7 Methyl Alcohol ) + = ( • 8)

By formula: (F^- • 7CH₄O) + CH₄O = (F^- • 8CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.7 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.8	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.7 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 8 Methyl Alcohol ) + = ( • 9)

By formula: (F^- • 8CH₄O) + CH₄O = (F^- • 9CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.2 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.7	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.5 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 9 Methyl Alcohol ) + = ( • 10)

By formula: (F^- • 9CH₄O) + CH₄O = (F^- • 10CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.8 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.1	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.3 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 10 Methyl Alcohol ) + = ( • 11)

By formula: (F^- • 10CH₄O) + CH₄O = (F^- • 11CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.6 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.5	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.0 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 11 Methyl Alcohol ) + = ( • 12)

By formula: (F^- • 11CH₄O) + CH₄O = (F^- • 12CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	8.5 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; Entropy estimated.; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.	cal/mol*K	N/A	Hiraoka and Yamabe, 1991	gas phase; Entropy change calculated or estimated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.1 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; Entropy estimated.; B

F₆S^- + Methyl Alcohol = (F₆S^- • )

By formula: F₆S^- + CH₄O = (F₆S^- • CH₄O)

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
4.5	308.	PHPMS	Knighton, Zook, et al., 1990	gas phase; M

HS^- + Methyl Alcohol = (HS^- • )

By formula: HS^- + CH₄O = (HS^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.0 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988	gas phase; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	11.0 ± 1.0	kcal/mol	TDAs	Meot-ner, 1988	gas phase; B

H₄ClO₂^- + Methyl Alcohol + 2 = CH₈ClO₃^-

By formula: H₄ClO₂^- + CH₄O + 2H₂O = CH₈ClO₃^-

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	10.40 ± 0.20	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; B
Δ_rH°	11.40 ± 0.30	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; For solvation by MeOH of core ion; B
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.80	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; B
Δ_rG°	6.00	kcal/mol	TDAs	Evans and Keesee, 1991	gas phase; For solvation by MeOH of core ion; B

+ Methyl Alcohol = ( • )

By formula: I^- + CH₄O = (I^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	11.90 ± 0.20	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	11.3 ± 1.0	kcal/mol	TDAs	Caldwell and Kebarle, 1984	gas phase; B,M
Δ_rH°	11.2	kcal/mol	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Δ_rH°	11.	kcal/mol	PHPMS	Caldwell, Masucci, et al., 1989	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	17.1	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Δ_rS°	17.8	cal/mol*K	PHPMS	Caldwell and Kebarle, 1984	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.76	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	6.0 ± 1.0	kcal/mol	TDAs	Caldwell and Kebarle, 1984	gas phase; B
Δ_rG°	5.7 ± 2.0	kcal/mol	IMRE	Tanabe, Morgon, et al., 1996	gas phase; Anchored to H2O..I- of Caldwell and Kebarle, 1984; B

( • Methyl Alcohol ) + = ( • 2)

By formula: (I^- • CH₄O) + CH₄O = (I^- • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.50 ± 0.20	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	11.1 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.6	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	4.25	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	4.4 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 2 Methyl Alcohol ) + = ( • 3)

By formula: (I^- • 2CH₄O) + CH₄O = (I^- • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	7.70 ± 0.60	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rH°	9.8 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	22.4	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	3.41	kcal/mol	TDAs	Bogdanov, Peschke, et al., 1999	gas phase; B
Δ_rG°	3.1 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 3 Methyl Alcohol ) + = ( • 4)

By formula: (I^- • 3CH₄O) + CH₄O = (I^- • 4CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.7 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.8	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	2.3 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 4 Methyl Alcohol ) + = ( • 5)

By formula: (I^- • 4CH₄O) + CH₄O = (I^- • 5CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.6 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.1	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.5 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 5 Methyl Alcohol ) + = ( • 6)

By formula: (I^- • 5CH₄O) + CH₄O = (I^- • 6CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.6 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.4	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.4 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 6 Methyl Alcohol ) + = ( • 7)

By formula: (I^- • 6CH₄O) + CH₄O = (I^- • 7CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.4 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	28.0	cal/mol*K	PHPMS	Hiraoka and Yamabe, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	1.1 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; B

( • 7 Methyl Alcohol ) + = ( • 8)

By formula: (I^- • 7CH₄O) + CH₄O = (I^- • 8CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	9.1 ± 1.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; Entropy estimated.; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	28.	cal/mol*K	N/A	Hiraoka and Yamabe, 1991	gas phase; Entropy change calculated or estimated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	0.8 ± 2.0	kcal/mol	TDAs	Hiraoka and Yamabe, 1991	gas phase; Entropy estimated.; B

+ Methyl Alcohol = ( • )

By formula: K⁺ + CH₄O = (K⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.9	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; switching reaction,n(K+)H2O; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	31.6	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; switching reaction,n(K+)H2O; M

( • Methyl Alcohol ) + = ( • 2)

By formula: (K⁺ • CH₄O) + CH₄O = (K⁺ • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	18.0	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	35.	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

( • 2 Methyl Alcohol ) + = ( • 3)

By formula: (K⁺ • 2CH₄O) + CH₄O = (K⁺ • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	14.5	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	28.	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

( • 3 Methyl Alcohol ) + = ( • 4)

By formula: (K⁺ • 3CH₄O) + CH₄O = (K⁺ • 4CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	12.5	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	29.	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

( • Methyl Alcohol • ) + = ( • 2 • )

By formula: (K⁺ • CH₄O • H₂O) + CH₄O = (K⁺ • 2CH₄O • H₂O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.5	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.3	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

( • 2 Methyl Alcohol • ) + = ( • 3 • )

By formula: (K⁺ • 2CH₄O • H₂O) + CH₄O = (K⁺ • 3CH₄O • H₂O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	12.5	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.6	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

( • ) + Methyl Alcohol = ( • • )

By formula: (K⁺ • H₂O) + CH₄O = (K⁺ • CH₄O • H₂O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	19.6	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	32.5	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; M

( • 2) + Methyl Alcohol = ( • • 2)

By formula: (K⁺ • 2H₂O) + CH₄O = (K⁺ • CH₄O • 2H₂O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	16.6	kcal/mol	HPMS	Evans and Keesee, 1991	gas phase; switching reaction,n(K+)3H2O; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	30.9	cal/mol*K	HPMS	Evans and Keesee, 1991	gas phase; switching reaction,n(K+)3H2O; M

+ Methyl Alcohol = ( • )

By formula: Li⁺ + CH₄O = (Li⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	36.8 ± 1.9	kcal/mol	CIDT	Rodgers and Armentrout, 2000	RCD
Δ_rH°	38.1	kcal/mol	ICR	Woodin and Beauchamp, 1978	gas phase; switching reaction(Li+)H20, Entropy change calculated or estimated; Dzidic and Kebarle, 1970 interpolated; M
Δ_rH°	38.	kcal/mol	ICR	Staley and Beauchamp, 1975	gas phase; switching reaction(Li+)H2O, from graph; Dzidic and Kebarle, 1970 extrapolated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.	cal/mol*K	N/A	Woodin and Beauchamp, 1978	gas phase; switching reaction(Li+)H20, Entropy change calculated or estimated; Dzidic and Kebarle, 1970 interpolated; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	30.3	kcal/mol	ICR	Woodin and Beauchamp, 1978	gas phase; switching reaction(Li+)H20, Entropy change calculated or estimated; Dzidic and Kebarle, 1970 interpolated; M

+ Methyl Alcohol = ( • )

By formula: Mg⁺ + CH₄O = (Mg⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	34.7 ± 1.6	kcal/mol	CIDT	Andersen, Muntean, et al., 2000	RCD
Δ_rH°	61. ± 5.	kcal/mol	PDiss	Operti, Tews, et al., 1988	gas phase; M

( • Methyl Alcohol ) + = ( • 2)

By formula: (Mg⁺ • CH₄O) + CH₄O = (Mg⁺ • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	28.8 ± 1.6	kcal/mol	CIDT	Andersen, Muntean, et al., 2000	RCD

( • 2 Methyl Alcohol ) + = ( • 3)

By formula: (Mg⁺ • 2CH₄O) + CH₄O = (Mg⁺ • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	21.9 ± 2.1	kcal/mol	CIDT	Andersen, Muntean, et al., 2000	RCD

+ Methyl Alcohol = ( • )

By formula: NO₂^- + CH₄O = (NO₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.40 ± 0.20	kcal/mol	TDAs	Sieck, 1985	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.8	cal/mol*K	PHPMS	Sieck, 1985	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	9.70 ± 0.40	kcal/mol	TDAs	Sieck, 1985	gas phase; B

+ Methyl Alcohol = ( • )

By formula: Na⁺ + CH₄O = (Na⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	23.2 ± 1.3	kcal/mol	CIDC	Amicangelo and Armentrout, 2001	Anchor NH3=24.41; RCD
Δ_rH°	21.9 ± 1.4	kcal/mol	CIDT	Armentrout and Rodgers, 2000	RCD
Δ_rH°	24.0 ± 0.2	kcal/mol	HPMS	Hoyau, Norrman, et al., 1999	RCD
Δ_rH°	26.6 ± 0.2	kcal/mol	HPMS	Guo, Conklin, et al., 1989	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	20500.	cal/mol*K	HPMS	Hoyau, Norrman, et al., 1999	RCD
Δ_rS°	24.3	cal/mol*K	HPMS	Guo, Conklin, et al., 1989	gas phase; M

Free energy of reaction

Δ_rG° (kcal/mol)	T (K)	Method	Reference	Comment
17.3	298.	IMRE	McMahon and Ohanessian, 2000	Anchor alanine=39.89; RCD

( • Methyl Alcohol ) + = ( • 2)

By formula: (Na⁺ • CH₄O) + CH₄O = (Na⁺ • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	20.5 ± 1.4	kcal/mol	CIDC	Amicangelo and Armentrout, 2001	Anchor NH3=24.41; RCD
Δ_rH°	21.4 ± 1.6	kcal/mol	CIDC	Amicangelo and Armentrout, 2001	Anchor NH3=24.41; RCD
Δ_rH°	20.5 ± 1.6	kcal/mol	CIDC	Amicangelo and Armentrout, 2001	Anchor NH3=24.41; RCD
Δ_rH°	20.2 ± 0.2	kcal/mol	HPMS	Guo, Conklin, et al., 1989	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	21.7	cal/mol*K	HPMS	Guo, Conklin, et al., 1989	gas phase; M

( • 2 Methyl Alcohol ) + = ( • 3)

By formula: (Na⁺ • 2CH₄O) + CH₄O = (Na⁺ • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.4 ± 0.4	kcal/mol	HPMS	Guo, Conklin, et al., 1989	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	25.1	cal/mol*K	HPMS	Guo, Conklin, et al., 1989	gas phase; M

( • 3 Methyl Alcohol ) + = ( • 4)

By formula: (Na⁺ • 3CH₄O) + CH₄O = (Na⁺ • 4CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.7 ± 0.2	kcal/mol	HPMS	Guo, Conklin, et al., 1989	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	30.0	cal/mol*K	HPMS	Guo, Conklin, et al., 1989	gas phase; M

+ Methyl Alcohol = ( • )

By formula: O₂^- + CH₄O = (O₂^- • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	19.10	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	21.9	cal/mol*K	PHPMS	Yamdagni, Payzant, et al., 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	12.50	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B

( • Methyl Alcohol ) + = ( • 2)

By formula: (O₂^- • CH₄O) + CH₄O = (O₂^- • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	15.50 ± 0.80	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	24.8	cal/mol*K	PHPMS	Yamdagni, Payzant, et al., 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	8.10 ± 0.40	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B

( • 2 Methyl Alcohol ) + = ( • 3)

By formula: (O₂^- • 2CH₄O) + CH₄O = (O₂^- • 3CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	13.50 ± 0.70	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B,M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	27.9	cal/mol*K	PHPMS	Yamdagni, Payzant, et al., 1973	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rG°	5.20 ± 0.30	kcal/mol	TDAs	Yamdagni, Payzant, et al., 1973	gas phase; B

+ Methyl Alcohol = ( • )

By formula: Pb⁺ + CH₄O = (Pb⁺ • CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	23.3 ± 0.2	kcal/mol	HPMS	Guo and Castleman, 1990	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	23.3	cal/mol*K	HPMS	Guo and Castleman, 1990	gas phase; M

( • Methyl Alcohol ) + = ( • 2)

By formula: (Pb⁺ • CH₄O) + CH₄O = (Pb⁺ • 2CH₄O)

Quantity	Value	Units	Method	Reference	Comment
Δ_rH°	17.2 ± 0.3	kcal/mol	HPMS	Guo and Castleman, 1990	gas phase; M
Quantity	Value	Units	Method	Reference	Comment
Δ_rS°	26.6	cal/mol*K	HPMS	Guo and Castleman, 1990	gas phase; M

Mass spectrum (electron ionization)

Go To: Top, Gas phase ion energetics data, Ion clustering data, Gas Chromatography, References, Notes

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

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Origin	Japan AIST/NIMC Database- Spectrum MS-NW- 72
NIST MS number	229809

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Gas Chromatography

Go To: Top, Gas phase ion energetics data, Ion clustering data, Mass spectrum (electron ionization), References, Notes

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

View large format table.

Column type	Active phase	Temperature (C)	I	Reference	Comment
Capillary	SE-30	140.	340.	Haken and Korhonen, 1985	Column length: 25. m; Column diameter: 0.33 mm
Packed	SE-30	100.	384.	Winskowski, 1983	Gaschrom Q; Column length: 2. m
Packed	SE-30	150.	356.	Haken, Nguyen, et al., 1979	Celatom AW silanized; Column length: 3.7 m
Packed	Apiezon L	120.	336.	Bogoslovsky, Anvaer, et al., 1978	Celite 545
Packed	SE-30	100.	373.	Pías and Gascó, 1975	Ar, Chromosorb W AW DMCS HP (80-100 mesh); Column length: 1. m
Packed	Apiezon L	100.	355.	Brown, Chapman, et al., 1968	N2, DCMS-treated Chromosorb W; Column length: 2.3 m
Packed	SE-30	80.	330.	Viani, Müggler-Chavan, et al., 1965	He, Chromosorb P; Column length: 6. m

Kovats' RI, non-polar column, custom temperature program

View large format table.

Column type	Active phase	I	Reference	Comment
Capillary	Petrocol DH-100	380.	Haagen-Smit Laboratory, 1997	He; Column length: 100. m; Column diameter: 0.2 mm; Program: 5C(10min) => 5C/min => 50C(48min) => 1.5C/min => 195C(91min)

Kovats' RI, polar column, isothermal

View large format table.

Column type	Active phase	Temperature (C)	I	Reference	Comment
Capillary	OV-351	100.	917.	Haken and Korhonen, 1985	N2; Column length: 25. m; Column diameter: 0.32 mm
Capillary	OV-351	80.	891.	Haken and Korhonen, 1985	N2; Column length: 25. m; Column diameter: 0.32 mm
Packed	PEG-2000	152.	860.	Anderson, Jurel, et al., 1973	He, Celite 545 (44-60 mesh); Column length: 3. m
Packed	PEG-2000	179.	881.	Anderson, Jurel, et al., 1973	He, Celite 545 (44-60 mesh); Column length: 3. m
Packed	Carbowax 20M	100.	892.	Zarazir, Chovin, et al., 1970	Chromosorb W; Column length: 2. m
Packed	Polyethylene Glycol 4000	100.	904.	Bonastre and Grenier, 1968	Chromosorb P; Column length: 6. m
Packed	Polyethylene Glycol 4000	120.	897.	Bonastre and Grenier, 1968	Chromosorb P; Column length: 6. m
Packed	Polyethylene Glycol 4000	140.	886.	Bonastre and Grenier, 1968	Chromosorb P; Column length: 6. m
Packed	Polyethylene Glycol 4000	80.	914.	Bonastre and Grenier, 1968	Chromosorb P; Column length: 6. m

Kovats' RI, polar column, temperature ramp

View large format table.

Column type	Active phase	I	Reference	Comment
Capillary	CBP-20	899.	Shimadzu, 2003	25. m/0.2 mm/0.25 μm, He, 50. C @ 5. min, 4. K/min; T_end: 200. C
Capillary	DB-Wax	888.	Shimoda and Shibamoto, 1990	He, 40. C @ 6. min, 3. K/min; Column length: 60. m; Column diameter: 0.25 mm; T_end: 190. C

Kovats' RI, polar column, custom temperature program

View large format table.

Column type	Active phase	I	Reference	Comment
Packed	Carbowax 20M	869.	Kevei and Kozma, 1976	Chromosorb; Program: not specified

Van Den Dool and Kratz RI, non-polar column, temperature ramp

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Column type	Active phase	I	Reference	Comment
Capillary	Petrocol DH	372.7	Censullo, Jones, et al., 2003	50. m/0.25 mm/0.5 μm, He, 35. C @ 10. min, 3. K/min, 200. C @ 10. min
Capillary	Petrocol DH	378.2	Censullo, Jones, et al., 2003	50. m/0.25 mm/0.5 μm, He, 35. C @ 10. min, 3. K/min, 200. C @ 10. min
Capillary	SE-30	400.0	Golovnya, Kuz'menko, et al., 2000	25. m/0.32 mm/1. μm, He, 4. K/min; T_start: 60. C
Capillary	SE-30	400.0	Golovnya, Kuz'menko, et al., 2000, 2	25. m/0.32 mm/1. μm, He, 4. K/min; T_start: 60. C
Capillary	DB-1	361.	Bartelt, 1997	30. m/0.32 mm/5. μm, He, 35. C @ 1. min, 10. K/min; T_end: 270. C

Van Den Dool and Kratz RI, non-polar column, custom temperature program

View large format table.

Column type	Active phase	I	Reference	Comment
Packed	SE-30	368.	Peng, Ding, et al., 1988	Supelcoport; Chromosorb; Column length: 3.05 m; Program: 40C(5min) => 10C/min => 200C or 250C (60min)

Van Den Dool and Kratz RI, polar column, temperature ramp

View large format table.

Column type	Active phase	I	Reference	Comment
Capillary	Carbowax	910.4	Censullo, Jones, et al., 2003	60. m/0.25 mm/0.5 μm, He, 50. C @ 10. min, 5. K/min, 250. C @ 10. min
Capillary	FFAP	916.	Ott, Fay, et al., 1997	30. m/0.25 mm/0.25 μm, He, 20. C @ 1. min, 4. K/min, 200. C @ 1. min
Packed	Carbowax 20M	866.	van den Dool and Kratz, 1963	Celite 545, 4.6 K/min; T_start: 75. C; T_end: 228. C

Normal alkane RI, non-polar column, isothermal

View large format table.

Column type	Active phase	Temperature (C)	I	Reference	Comment
Capillary	DB-1	60.	382.	Shimadzu, 2003, 2	60. m/0.32 mm/1. μm, He
Packed	Squalane	100.	338.	Vernon, 1971	N2
Packed	DC-400	150.	370.	Anderson, 1968	Helium, Gas-Pak (60-80 mesh); Column length: 3.0 m
Packed	Squalane	125.	348.	Cremer and Nonn, 1964	H2, Chromosorb W (80-100 mesh); Column length: 3. m

Normal alkane RI, non-polar column, temperature ramp

View large format table.

Column type	Active phase	I	Reference	Comment
Capillary	Polydimethyl siloxane: CP-Sil 5 CB	395.	Bramston-Cook, 2013	60. m/0.25 mm/1.0 μm, Helium, 45. C @ 1.45 min, 3.6 K/min, 210. C @ 2.72 min
Capillary	Petrocol DH	379.	Supelco, 2012	100. m/0.25 mm/0.50 μm, Helium, 20. C @ 15. min, 15. K/min, 220. C @ 30. min
Capillary	HP-5	367.5	Leffingwell and Alford, 2005	60. m/0.32 mm/0.25 μm, He, 30. C @ 2. min, 2. K/min, 260. C @ 28. min
Capillary	OV-101	381.	Zenkevich, 2005	25. m/0.20 mm/0.10 μm, N2/He, 6. K/min; T_start: 50. C; T_end: 250. C
Capillary	BP-1	370.	Health Safety Executive, 2000	50. m/0.22 mm/0.75 μm, He, 5. K/min; T_start: 50. C; T_end: 200. C
Capillary	DB-5MS	353.5	Shoenmakers, Oomen, et al., 2000	30. m/0.25 mm/0.25 μm, He, 40. C @ 1. min, 3. K/min; T_end: 250. C

Normal alkane RI, non-polar column, custom temperature program

View large format table.

Column type	Active phase	I	Reference	Comment
Capillary	HP-5 MS	381.	Kotowska, Zalikowski, et al., 2012	30. m/0.25 mm/0.25 μm, Helium; Program: not specified
Capillary	Methyl Silicone	373.	Chen and Feng, 2007	Program: not specified
Capillary	Methyl Silicone	373.	Kou, Zhang, et al., 2006	Program: not specified
Capillary	Methyl Silicone	408.	Blunden, Aneja, et al., 2005	60. m/0.32 mm/1.0 μm, Helium; Program: -50 0C (2 min) 8 0C/min -> 200 0C (7.75 min) 25 0C -> 225 0C (8 min)
Capillary	Methyl Silicone	373.	Fu and Wang, 2004	Program: not specified
Capillary	Methyl Silicone	362.	N/A	Program: not specified
Capillary	Polydimethyl siloxanes	381.	Zenkevich, 2001	Program: not specified
Capillary	Polydimethyl siloxanes	381.	Zenkevich, 2001, 2	Program: not specified
Capillary	Methyl Silicone	381.	Zenkevich, 1999	Program: not specified
Capillary	SPB-1	353.	Flanagan, Streete, et al., 1997	60. m/0.53 mm/5. μm, He; Program: 40C(6min) => 5C/min => 80C => 10C/min => 200C
Capillary	Polydimethyl siloxanes	381.	Zenkevich and Chupalov, 1996	Program: not specified
Capillary	Methyl Silicone	381.	Zenkevich, Korolenko, et al., 1995	Program: not specified
Capillary	DB-1	348.	Schuberth, 1994	30. m/0.25 mm/1. μm, He; Program: 40C (4min) => 10C/min => 200C => 50C/min => 250C
Capillary	SPB-1	353.	Strete, Ruprah, et al., 1992	60. m/0.53 mm/5.0 μm, Helium; Program: 40 0C (6 min) 5 0C/min -> 80 0C 10 0C/min -> 200 0C
Capillary	SPB-1	391.	Strete, Ruprah, et al., 1992	60. m/0.53 mm/5.0 μm, Helium; Program: not specified
Capillary	CP Sil 8 CB	404.	Weller and Wolf, 1989	40. m/0.25 mm/0.25 μm, He; Program: 30 0C (1 min) 15 0C/min -> 45 0C 3 0C/min -> 120 0C
Capillary	OV-1, SE-30, Methyl silicone, SP-2100, OV-101, DB-1, etc.	384.	Waggott and Davies, 1984	Hydrogen; Column length: 50. m; Column diameter: 0.32 mm; Program: not specified

Normal alkane RI, polar column, isothermal

View large format table.

Column type	Active phase	Temperature (C)	I	Reference	Comment
Capillary	Carbowax 20M	100.	892.	Sun, Siepmann, et al., 2006	30. m/0.25 mm/0.25 μm, Helium
Capillary	Carbowax 20M	60.	899.	Sun, Siepmann, et al., 2006	30. m/0.25 mm/0.25 μm, Helium
Capillary	Carbowax 20M	80.	895.	Sun, Siepmann, et al., 2006	30. m/0.25 mm/0.25 μm, Helium
Capillary	DB-Wax	60.	921.	Shimadzu, 2003, 2	50. m/0.32 mm/1. μm, He

Normal alkane RI, polar column, temperature ramp

View large format table.

Column type	Active phase	I	Reference	Comment
Capillary	DB-Wax	911.	Shimadzu, 2012	30. m/0.32 mm/0.50 μm, Helium, 4. K/min; T_start: 40. C; T_end: 260. C
Capillary	DB-Wax	907.	Chida, Sone, et al., 2004	60. m/0.25 mm/0.5 μm, 35. C @ 5. min, 4. K/min, 240. C @ 10. min
Capillary	DB-Wax	911.	Shimadzu Corporation, 2003	30. m/0.32 mm/0.5 μm, He, 4. K/min; T_start: 40. C; T_end: 260. C
Capillary	DB-Wax	903.	Tanaka, Yamauchi, et al., 2003	30. m/0.25 mm/0.25 μm, 30. C @ 1. min, 4. K/min; T_end: 250. C
Capillary	DB-Wax	905.	Tanaka, Yamauchi, et al., 2003	30. m/0.25 mm/0.25 μm, 30. C @ 1. min, 4. K/min; T_end: 250. C
Capillary	TC-Wax	898.	Suhardi, Suzuki, et al., 2002	60. m/0.25 mm/0.25 μm, He, 40. C @ 10. min, 3. K/min, 230. C @ 10. min
Capillary	DB-Wax	905.	Duque, Bonilla, et al., 2001	30. m/0.25 mm/0.25 μm, Helium, 4. K/min, 220. C @ 30. min; T_start: 25. C

Normal alkane RI, polar column, custom temperature program

View large format table.

Column type	Active phase	I	Reference	Comment
Capillary	Carbowax 20M	920.	Vinogradov, 2004	Program: not specified
Capillary	Polyethylene Glycol	897.	Zenkevich, Korolenko, et al., 1995	Program: not specified
Capillary	DB-Wax	909.	Peng, Yang, et al., 1991	Program: not specified
Capillary	Carbowax 400, Carbowax 20M, Carbowax 1540, Carbowax 4000, Superox 06, PEG 20M, etc.	907.	Waggott and Davies, 1984	Hydrogen; Column length: 50. m; Column diameter: 0.32 mm; Program: not specified
Capillary	Carbowax 400, Carbowax 20M, Carbowax 1540, Carbowax 4000, Superox 06, PEG 20M, etc.	920.	Waggott and Davies, 1984	Hydrogen; Column length: 50. m; Column diameter: 0.32 mm; Program: not specified
Capillary	Carbowax 20M	883.	Ramsey and Flanagan, 1982	Program: not specified

References

Go To: Top, Gas phase ion energetics data, Ion clustering data, Mass spectrum (electron ionization), Gas Chromatography, Notes

Hunter and Lias, 1998
Hunter, E.P.; Lias, S.G., Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update, J. Phys. Chem. Ref. Data, 1998, 27, 3, 413-656, https://doi.org/10.1063/1.556018 . [all data]

Tao, Klemm, et al., 1992
Tao, W.; Klemm, R.B.; Nesbitt, F.L.; Stief, J.L., A discharge flow-photoionization mass spectrometric study of hydroxymethyl radicals (H₂COH and H₂COD): Photoionization spectrum and ionization energy, J. Phys. Chem., 1992, 96, 104. [all data]

Holmes and Lossing, 1991
Holmes, J.L.; Lossing, F.P., Ionization energies of homologous organic compounds and correlation with molecular size, Org. Mass Spectrom., 1991, 26, 537. [all data]

Bowen and Maccoll, 1984
Bowen, R.D.; Maccoll, A., Low energy, low temperature mass spectra, Org. Mass Spectrom., 1984, 19, 379. [all data]

Mishchanchuk, Pokrovskii, et al., 1982
Mishchanchuk, B.G.; Pokrovskii, V.A.; Shabel'nikov, V.P.; Korol, E.N., Mass spectrometric study of energy characteristics of methanol and ethanol ions during ionization by a strong electric field, Teor. Eksp. Khim., 1982, 18, 307. [all data]

Allam, Migahed, et al., 1982
Allam, S.H.; Migahed, M.D.; El-Khodary, A., Electron impact ionization and dissociation of deuterated and non-deuterated methanol, methyl cyanide, nitromethane and nitrobenzene, Egypt. J. Phys., 1982, 13, 167. [all data]

Sahini, Constantin, et al., 1978
Sahini, V.E.; Constantin, V.; Serban, I., Determination of ionization potentials using a MI-1305 mass spectrometer, Rev. Roum. Chim., 1978, 23, 479. [all data]

Berkowitz, 1978
Berkowitz, J., Photoionization of CH₃OH, CD₃OH, and CH₃OD: Dissociative ionization mechanisms and ionic structures, J. Chem. Phys., 1978, 69, 3044. [all data]

MacNeil and Dixon, 1977
MacNeil, K.A.G.; Dixon, R.N., High-resolution photoelectron spectroscopy of methanol and its deuterated derivatives: Internal rotation in the ground ionic state, J. Electron Spectrosc. Relat. Phenom., 1977, 11, 315. [all data]

Finney and Harrison, 1972
Finney, C.D.; Harrison, A.G., A third-derivative method for determining electron-impact onset potentials, Int. J. Mass Spectrom. Ion Phys., 1972, 9, 221. [all data]

Warneck, 1971
Warneck, P., Photoionisation von methanol und formaldehyd, Z. Naturforsch. A:, 1971, 26, 2047. [all data]

Cocksey, Eland, et al., 1971
Cocksey, B.J.; Eland, J.H.D.; Danby, C.J., The effect of alkyl substitution on ionisation potential, J. Chem. Soc., 1971, (B), 790. [all data]

Baker, Betteridge, et al., 1971
Baker, A.D.; Betteridge, D.; Kemp, N.R.; Kirby, R.E., Application of photoelectron spectrometry to pesticide analysis. II.Photoelectron spectra of hydroxy-, and halo-alkanes and halohydrins, Anal. Chem., 1971, 43, 375. [all data]

Omura, Kaneko, et al., 1969
Omura, I.; Kaneko, T.; Yamada, Y.; Tanaka, K., Mass spectrometric studies of photoionization. V. Methanol and methanol-d, J. Phys. Soc. Japan, 1969, 27, 981. [all data]

Lifshitz, Shapiro, et al., 1969
Lifshitz, C.; Shapiro, M.; Sternberg, R., Isotopic effects on metastable transitions. IV. Isotopic methanols, Israel J. Chem., 1969, 7, 391. [all data]

Dewar and Worley, 1969
Dewar, M.J.S.; Worley, S.D., Photoelectron spectra of molecules. I. Ionization potentials of some organic molecules and their interpretation, J. Chem. Phys., 1969, 50, 654. [all data]

Refaey and Chupka, 1968
Refaey, K.M.A.; Chupka, W.A., Photoionization of the lower aliphatic alcohols with mass analysis, J. Chem. Phys., 1968, 48, 5205. [all data]

Cermak, 1968
Cermak, V., Penning ionization electron spectroscopy. I. Determination of ionization potentials of polyatomic molecules, Collection Czech. Chem. Commun., 1968, 33, 2739. [all data]

Al-Joboury and Turner, 1964
Al-Joboury, M.I.; Turner, D.W., Molecular photoelectron spectroscopy. Part II. A summary of ionization potentials, J. Chem. Soc., 1964, 4434. [all data]

Watanabe, 1954
Watanabe, K., Photoionization and total absorption cross section of gases. I. Ionization potentials of several molecules. Cross sections of NH₃ and NO, J. Chem. Phys., 1954, 22, 1564. [all data]

Vorob'ev, Furlei, et al., 1989
Vorob'ev, A.S.; Furlei, I.I.; Sultanov, A.S.; Khvostenko, V.I.; Leplyanin, G.V.; Derzhinskii, A.R.; Tolstikov, G.A., Mass spectrometry of reasonance capture of electrons and photoelectron spectroscopy of molecules of ethylene oxide, ethylene sulfide, and their derivatives, Bull. Acad. Sci. USSR, Div. Chem. Sci., 1989, 1388. [all data]

Von Niessen, Bieri, et al., 1980
Von Niessen, W.; Bieri, G.; Asbrink, L., 30.4 nm He(II) photoelectron spectra of organic molecules. Part III. Oxo-compounds (C,H,O), J. Electron Spectrosc. Relat. Phenom., 1980, 21, 175. [all data]

Utsunomiya, Kobayashi, et al., 1980
Utsunomiya, C.; Kobayashi, T.; Nagakura, S., Photoelectron angular distribution measurements for some aliphatic alcohols, amines, halides, Bull. Chem. Soc. Jpn., 1980, 53, 1216. [all data]

Kobayashi, 1978
Kobayashi, T., A simple general tendency in photoelectron angular distributions of some monosubstituted benzenes, Phys. Lett., 1978, 69, 105. [all data]

Benoit and Harrison, 1977
Benoit, F.M.; Harrison, A.G., Predictive value of proton affinity. Ionization energy correlations involving oxygenated molecules, J. Am. Chem. Soc., 1977, 99, 3980. [all data]

Peel and Willett, 1975
Peel, J.B.; Willett, G.D., Photoelectron spectroscopic studies of the higher alcohols, Aust. J. Chem., 1975, 28, 2357. [all data]

Robin and Kuebler, 1973
Robin, M.B.; Kuebler, N.A., Excited electronic states of the simple alcohols, J. Electron Spectrosc. Relat. Phenom., 1973, 1, 13. [all data]

Ogata, Onizuka, et al., 1973
Ogata, H.; Onizuka, H.; Nihei, Y.; Kamada, H., The photoelectron spectra of alcohols, mercaptans and amines, Bull. Chem. Soc. Jpn., 1973, 46, 3036. [all data]

Katsumata, Iwai, et al., 1973
Katsumata, S.; Iwai, T.; Kimura, K., Photoelectron spectra and sum rule consideration. Higher alkyl amines and alcohols, Bull. Chem. Soc. Jpn., 1973, 46, 3391. [all data]

Ogata, Onizuka, et al., 1972
Ogata, H.; Onizuka, H.; Nihei, Y.; Kamada, H., On the first bands of the photoelectron spectra of amines, alcohols, and mercaptans, Chem. Lett., 1972, 895. [all data]

Reed and Snedden, 1956
Reed, R.I.; Snedden, W., Studies in electron impact methods. Part 6.-The formation of the methine and carbon ions, J. Chem. Soc. Faraday Trans., 1956, 55, 876. [all data]

Haney and Franklin, 1968
Haney, M.A.; Franklin, J.L., Correlation of excess energies of electron-impact dissociations with the translational energies of the products, J.Chem. Phys., 1968, 48, 4093. [all data]

Friedman, Long, et al., 1957
Friedman, L.; Long, F.A.; Wolfsberg, M., Study of the mass spectra of the lower aliphatic alcohols, J. Chem. Phys., 1957, 27, 613. [all data]

Selim and Helal, 1981
Selim, E.T.M.; Helal, A.I., Heat of formation of CH₂=OH⁺ fragment ion, Indian J. Pure Appl. Phys., 1981, 19, 977. [all data]

Lossing, 1977
Lossing, F.P., Heats of formation of some isomeric [C_nH_2n+1]⁺ ions. Substitutional effects on ion stability, J. Am. Chem. Soc., 1977, 99, 7526. [all data]

Berkowitz, Ellison, et al., 1994
Berkowitz, J.; Ellison, G.B.; Gutman, D., Three methods to measure RH bond energies, J. Phys. Chem., 1994, 98, 2744. [all data]

Friedland and Strakna, 1956
Friedland, S.S.; Strakna, R.E., Appearance potential studies. I, J. Phys. Chem., 1956, 60, 815. [all data]

Nee, Osterwalder, et al., 2006
Nee, M.J.; Osterwalder, A.; Zhou, J.; Neumark, D.M., Slow electron velocity-map imaging photoelectron spectra of the methoxide anion, J. Chem. Phys., 2006, 125, 1, 014306, https://doi.org/10.1063/1.2212411 . [all data]

Osborn, Leahy, et al., 1998
Osborn, D.L.; Leahy, D.J.; Kim, E.H.; deBeer, E.; Neumark, D.M., Photoelectron spectroscopy of CH3O- and CD3O-, Chem. Phys. Lett., 1998, 292, 4-6, 651-655, https://doi.org/10.1016/S0009-2614(98)00717-9 . [all data]

Bartmess, Scott, et al., 1979
Bartmess, J.E.; Scott, J.A.; McIver, R.T., Jr., The gas phase acidity scale from methanol to phenol, J. Am. Chem. Soc., 1979, 101, 6047. [all data]

Haas and Harrison, 1993
Haas, M.J.; Harrison, A.G., The Fragmentation of Proton-Bound Cluster Ions and the Gas-Phase Acidities of Alcohols, Int. J. Mass Spectrom. Ion Proc., 1993, 124, 2, 115, https://doi.org/10.1016/0168-1176(93)80003-W . [all data]

Meot-ner and Sieck, 1986
Meot-ner, M.; Sieck, L.W., Relative acidities of water and methanol, and the stabilities of the dimer adducts, J. Phys. Chem., 1986, 90, 6687. [all data]

Bogdanov, Peschke, et al., 1999
Bogdanov, B.; Peschke, M.; Tonner, D.S.; Szulejko, J.E.; McMahon, T.B., Stepwise solvation of halides by alcohol molecules in the gas phase, Int. J. Mass Spectrom., 1999, 187, 707-725, https://doi.org/10.1016/S1387-3806(98)14180-5 . [all data]

Hiraoka and Yamabe, 1991
Hiraoka, K.; Yamabe, S., Solvation of Halide Ions with CH3OH in the gas Phase, Int. J. Mass Spectrom. Ion Proc., 1991, 109, 133, https://doi.org/10.1016/0168-1176(91)85101-Q . [all data]

Tanabe, Morgon, et al., 1996
Tanabe, F.K.J.; Morgon, N.H.; Riveros, J.M., Relative Bromide and Iodide Affinity of Simple Solvent Molecules Determined by FT-ICR, J. Phys. Chem., 1996, 100, 8, 2862-2866, https://doi.org/10.1021/jp952290p . [all data]

Hiraoka, Mizure, et al., 1988
Hiraoka, K.; Mizure, S.; Yamabe, S.; Nakatsuji, Y., Gas Phase Clustering Reactions of CN^- and CH₂CN^- with MeCN, Chem. Phys. Lett., 1988, 148, 6, 497, https://doi.org/10.1016/0009-2614(88)80320-8 . [all data]

Meot-Ner and Sieck, 1986
Meot-Ner, M.; Sieck, L.W., The ionic hydrogen bond and ion solvation. 5. OH...O^- bonds. Gas phase solvation and clustering of alkoxide and carboxylate anions, J. Am. Chem. Soc., 1986, 108, 7525. [all data]

Paul and Kebarle, 1990
Paul, G.J.C.; Kebarle, P., Thermodynamics of the Association Reactions OH- - H2O = HOHOH- and CH3O- - CH3OH = CH3OHOCH3- in the Gas Phase, J. Phys. Chem., 1990, 94, 12, 5184, https://doi.org/10.1021/j100375a076 . [all data]

Caldwell, Rozeboom, et al., 1984
Caldwell, G.; Rozeboom, M.D.; Kiplinger, J.P.; Bartmess, J.E., Anion-alcohol hydrogen bond strengths in the gas phase, J. Am. Chem. Soc., 1984, 106, 4660. [all data]

Moylan, Dodd, et al., 1985
Moylan, C.R.; Dodd, J.A.; Brauman, J.I., Electron photodetachment spectroscopy of Sslvated anions. A probe of structure and energetics, Chem. Phys. Lett., 1985, 118, 38. [all data]

Meot-Ner(Mautner), 1986
Meot-Ner(Mautner), M., Comparative Stabilities of Cationic and Anionic Hydrogen-Bonded Networks. Mixed Clusters of Water-Methanol, J. Am. Chem. Soc., 1986, 108, 20, 6189, https://doi.org/10.1021/ja00280a014 . [all data]

Mustanir, Matsuoka, et al., 2006
Mustanir; Matsuoka, M.; Mishima, M.; Koch, H., Stability of complexes of phenylacetylides and benzyl alkoxides with methanol in the gas phase. Acid-base correlation in the ionic hydrogen-bond strength, Bull. Chem. Soc. Japan, 2006, 79, 7, 1118-1125, https://doi.org/10.1246/bcsj.79.1118 . [all data]

MacKay and Bohme, 1978
MacKay, G.I.; Bohme, D.K., Proton-Transfer Reactions in Nitromethane at 297K, Int. J. Mass Spectrom. Ion Phys., 1978, 26, 4, 327, https://doi.org/10.1016/0020-7381(78)80052-7 . [all data]

Meot-Ner (Mautner), 1992
Meot-Ner (Mautner), M., Intermolecular Forces in Organic Clusters, J. Am. Chem. Soc., 1992, 114, 9, 3312, https://doi.org/10.1021/ja00035a024 . [all data]

Szulejko and McMahon, 1992
Szulejko, J.; McMahon, T.B., personal communication, 1992. [all data]

Grimsrud and Kebarle, 1973
Grimsrud, E.P.; Kebarle, P., Gas Phase Ion Equilibria Studies of the Solvation of the Hydrogen Ion by Methanol, Dimethyl Ether and Water. Effect of Hydrogen Bonding, J. Am. Chem. Soc., 1973, 95, 24, 7939, https://doi.org/10.1021/ja00805a002 . [all data]

Larson and McMahon, 1982
Larson, J.W.; McMahon, T.B., Formation, Thermochemistry, and Relative Stabilities of Proton - Bound dimers of Oxygen n - Donor Bases from Ion Cyclotron Resonance Solvent - Exchange Equilibria Measurements, J. Am. Chem. Soc., 1982, 104, 23, 6255, https://doi.org/10.1021/ja00387a016 . [all data]

Lias, Liebman, et al., 1984
Lias, S.G.; Liebman, J.F.; Levin, R.D., Evaluated gas phase basicities and proton affinities of molecules heats of formation of protonated molecules, J. Phys. Chem. Ref. Data, 1984, 13, 695. [all data]

Keesee and Castleman, 1986
Keesee, R.G.; Castleman, A.W., Jr., Thermochemical data on Ggs-phase ion-molecule association and clustering reactions, J. Phys. Chem. Ref. Data, 1986, 15, 1011. [all data]

Meot-Ner, 1984
Meot-Ner, (Mautner)M., The Ionic Hydrogen Bond and Ion Solvation. 1. -NH+ O-, -NH+ N- and -OH+ O- Bonds. Correlations with Proton Affinity. Deviations Due to Structural Effects, J. Am. Chem. Soc., 1984, 106, 5, 1257, https://doi.org/10.1021/ja00317a015 . [all data]

Larson, Szulejko, et al., 1988
Larson, J.W.; Szulejko, J.E.; McMahon, T.B., Gas Phase Lewis Acid-Base Interactions. An Experimental Determination of Cyanide Binding Energies From Ion Cyclotron Resonance and High-Pressure Mass Spectrometric Equilibrium Measurements., J. Am. Chem. Soc., 1988, 110, 23, 7604, https://doi.org/10.1021/ja00231a004 . [all data]

Meot-ner, 1988
Meot-ner, M., Ionic Hydrogen Bond and Ion Solvation. ₆. Interaction Energies of the Acetate Ion with Organic Molecules. Comparison of CH₃COO^- with Cl^-, CN^-, and SH^-, J. Am. Chem. Soc., 1988, 110, 12, 3854, https://doi.org/10.1021/ja00220a022 . [all data]

Larson and McMahon, 1987
Larson, J.W.; McMahon, T.B., Hydrogen bonding in gas phase anions. The energetics of interaction between cyanide ion and bronsted acids, J. Am. Chem. Soc., 1987, 109, 6230. [all data]

Payzant, Yamdagni, et al., 1971
Payzant, J.D.; Yamdagni, R.; Kebarle, P., Hydration of CN-, NO₂-, NO₃-, and HO- in the gas phase, Can. J. Chem., 1971, 49, 3308. [all data]

Chabinyc and Brauman, 1999
Chabinyc, M.L.; Brauman, J.I., Hydrogen bond strength and acidity. Structural and energetic correlations for acetylides and alcohols, J. Phys. Chem. A, 1999, 103, 46, 9163-9166, https://doi.org/10.1021/jp992852v . [all data]

El-Shall, Olafsdottir, et al., 1991
El-Shall, M.S.; Olafsdottir, S.; Meot-ner (Mautner), M.; Sieck, L.W., Energy effects on cluster ion distributions: Beam expansion and thermochemical studies on mixed clusters of methanol and acetonitrile, Chem. Phys. Lett., 1991, 185, 3-4, 193, https://doi.org/10.1016/S0009-2614(91)85046-Y . [all data]

Nieckarz, Atkins, et al., 2008
Nieckarz, R.J.; Atkins, C.G.; McMahon, T.B., Effects of Isomerization on the Measured Thermochemical Properties of Deprotonated Glycine/Protic-Solvent Clusters, Chemphyschem, 2008, 9, 18, 2816-2825, https://doi.org/10.1002/cphc.200800525 . [all data]

DeTuri and Ervin, 1999
DeTuri, V.F.; Ervin, K.M., Competitive threshold collision-induced dissociation: Gas-phase acidities and bond dissociation energies for a series of alcohols, J. Phys. Chem. A, 1999, 103, 35, 6911-6920, https://doi.org/10.1021/jp991459m . [all data]

Mackay, Rakshit, et al., 1982
Mackay, G.I.; Rakshit, A.B.; Bohme, D.K., An Experimental Study of the Reactivity and Relative Basicity of the Methoxide Anion in the Gas Phase at Room Temperature, and their Perturbation by Methanol Solvent, Can. J. Chem., 1982, 60, 20, 2594, https://doi.org/10.1139/v82-373 . [all data]

Caldwell and Kebarle, 1986
Caldwell, G.; Kebarle, P., Mobility of Gaseous Ions in Weak Electric Fields in Unpublished results, 1986. [all data]

Taft, 1983
Taft, R.W., Protonic acidities and basicities in the gas phase and in solution: Substiuent and solvent effects, Prog. Phys. Org. Chem., 1983, 14, 247. [all data]

Hiraoka, Grimsrud, et al., 1974
Hiraoka, K.; Grimsrud, E.P.; Kebarle, P., Gas Phase Ion Equilibria Studies of the Hydrogen Ion in Water - Dimethyl Ether and Methanol - Dimethyl Ether Mixtures, J. Am. Chem. Soc., 1974, 96, 11, 3359, https://doi.org/10.1021/ja00818a004 . [all data]

Meot-Ner (Mautner), 1988
Meot-Ner (Mautner), M., Models for Strong Interactions in Proteins and Enzymes. 2. Interactions of Ions with the Peptide Link and Imidazole, J. Am. Chem. Soc., 1988, 110, 10, 3075, https://doi.org/10.1021/ja00218a014 . [all data]

Meot-Ner (Mautner), Ross, et al., 1985
Meot-Ner (Mautner), M.; Ross, M.M.; Campana, J.E., Stable Hydrogen - Bonded Isomers of Covalent Ions, J. Am. Chem. Soc., 1985, 107, 4835. [all data]

Wojtyniak and Stone, 1986
Wojtyniak, A.C.M.; Stone, A.J., A High-Pressure Mass Spectrometric Study of the Bonding of Trimethylsilylium to Oxygen and Aromatic Bases, Can. J. Chem., 1986, 74, 59. [all data]

Stone and Splinter, 1984
Stone, J.A.; Splinter, D.E., A high-pressure mass spectrometric study of the binding of (CH₃)₃Sn⁺ to lewis bases in the gas phase, Int. J. Mass Spectrom. Ion Processes, 1984, 59, 169. [all data]

El-Shall, Daly, et al., 1992
El-Shall, M.S.; Daly, G.M.; Gao, J.; Meot-Ner (Mautner), M.; Sieck, L.W., How Sensitive are Cluster Compositions to Energetics? A Joint Beam Expansion/ Thermochemical Study of Water - Methanol - Trimethylamine Clusters, J. Phys. Chem., 1992, 96, 2, 507, https://doi.org/10.1021/j100181a002 . [all data]

Chowdhury, Grimsrud, et al., 1987
Chowdhury, S.; Grimsrud, E.P.; Kebarle, P., Bonding of Charged Delocalized Anions to Protic and Dipolar Aprotic Solvent Molecules, J. Phys. Chem., 1987, 91, 10, 2551, https://doi.org/10.1021/j100294a021 . [all data]

Chowdhury, 1987
Chowdhury, S. Grimsrud, Bonding of Charge Delocalized Anions to Protic and Dipolar Aprotic Solvents, J. Phys. Chem., 1987, 91, 10, 2551, https://doi.org/10.1021/j100294a021 . [all data]

Meot-ner, 1988, 2
Meot-ner, M., The Ionic Hydrogen Bond and Solvation. 7. Interaction Energies of Carbanions with Solvent Molecules, J. Am. Chem. Soc., 1988, 110, 12, 3858, https://doi.org/10.1021/ja00220a022 . [all data]

Meot-Ner (Mautner), Sieck, et al., 1994
Meot-Ner (Mautner), M.; Sieck, L.W.; Liebman, J.F.; Scheiner, S.; Duan, X., The Ionic Hydrogen Bond. 5. Polydentate and Solvent-Bridged Structures. Complexing of the Proton and the Hydronium Ions by Polyethers, J. Am. Chem. Soc., 1994, 116, 17, 7848, https://doi.org/10.1021/ja00096a047 . [all data]

Sieck, 1985
Sieck, L.W., Thermochemistry of Solvation of NO₂^- and C₆H₅NO₂^- by Polar Molecules in the Vapor Phase. Comparison with Cl^- and Variation with Ligand Structure., J. Phys. Chem., 1985, 89, 25, 5552, https://doi.org/10.1021/j100271a049 . [all data]

Sieck and Meot-ner, 1989
Sieck, L.W.; Meot-ner, M., Ionic Hydrogen Bond and Ion Solvation. 8. RS-..HOR Bond Strengths. Correlation with Acidities., J. Phys. Chem., 1989, 93, 4, 1586, https://doi.org/10.1021/j100341a079 . [all data]

Knighton, Zook, et al., 1990
Knighton, W.B.; Zook, D.R.; Grimsrud, E.P., Cluster-Assisted Decomposition Reactions of the Molecular Anions of SF6 and C7F14, J. Am. Soc. Mass Spectrom., 1990, 1, 5, 372, https://doi.org/10.1016/1044-0305(90)85017-G . [all data]

Sharma and Kebarle, 1984
Sharma, R.B.; Kebarle, P., Stabilites and Hydrogen Bonding in Complexes of H3O+ and CH3OH2+ with Crown Ethers, from Measurements of Gas - Phase Ion - Molecule Equilibria, J. Am. Chem. Soc., 1984, 106, 14, 3913, https://doi.org/10.1021/ja00326a005 . [all data]

Evans and Keesee, 1991
Evans, D.H.; Keesee, R.G., Thermodynamics of Gas-Phase Mixed-Solvent Cluster Ions - Water and Methanol on K+ and Cl- and Comparison to Liquid Solutions, J. Phys. Chem., 1991, 95, 9, 3558, https://doi.org/10.1021/j100162a024 . [all data]

Hiraoka and Mizuse, 1987
Hiraoka, K.; Mizuse, S., Gas-Phase Solvation of Cl- with H2O, CH3OH, C2H4OH, i-C3H7OH, n-C3H7OH, and t-C4H9OH, Chem. Phys., 1987, 118, 3, 457, https://doi.org/10.1016/0301-0104(87)85078-4 . [all data]

Larson and McMahon, 1984
Larson, J.W.; McMahon, T.B., Gas phase negative ion chemistry of alkylchloroformates, Can. J. Chem., 1984, 62, 675. [all data]

French, Ikuta, et al., 1982
French, M.A.; Ikuta, S.; Kebarle, P., Hydrogen bonding of O-H and C-H hydrogen donors to Cl^-. Results from mass spectrometric measurement of the ion-molecule equilibria RH + Cl^- = RHCl^-, Can. J. Chem., 1982, 60, 1907. [all data]

Yamdagni, Payzant, et al., 1973
Yamdagni, R.; Payzant, J.D.; Kebarle, P., Solvation of Cl- and O₂- with H₂O, CH₃OH, and CH₃CN in the gas phase, Can. J. Chem., 1973, 51, 2507. [all data]

Rodgers and Armentrout, 2000
Rodgers, M.T.; Armentrout, P.B., Noncovalent Metal-Ligand Bond Energies as Studied by Threshold Collision-Induced Dissociation, Mass Spectrom. Rev., 2000, 19, 4, 215, https://doi.org/10.1002/1098-2787(200007)19:4<215::AID-MAS2>3.0.CO;2-X . [all data]

El-Shall, Schriver, et al., 1989
El-Shall, M.S.; Schriver, K.E.; Whetten, R.L.; Meot-Ner (Mautner), M., Ion/Molecule Clustering Thermochemistry by Laser Ionization High - Pressure Mass Spectrometry, J. Phys. Chem., 1989, 93, 24, 7969, https://doi.org/10.1021/j100361a002 . [all data]

Wilkinson, Szulejko, et al., 1992
Wilkinson, F.E.; Szulejko, J.E.; Allison, C.E.; Mcmahon, T.B., Fourier Transform Ion Cyclotron Resonance Investigation of the Deuterium Isotope Effect on Gas Phase Ion/Molecule Hydrogen Bonding Interactions in Alcohol-Fluoride Adduct Ions, Int. J. Mass Spectrom., 1992, 117, 487-505, https://doi.org/10.1016/0168-1176(92)80110-M . [all data]

Larson and McMahon, 1983
Larson, J.W.; McMahon, T.B., Strong hydrogen bonding in gas-phase anions. An ion cyclotron resonance determination of fluoride binding energetics to bronsted acids from gas-phase fluoride exchange equilibria measurements, J. Am. Chem. Soc., 1983, 105, 2944. [all data]

Arshadi, Yamdagni, et al., 1970
Arshadi, M.; Yamdagni, R.; Kebarle, P., Hydration of Halide Negative Ions in the Gas Phase. II. Comparison of Hydration Energies for the Alkali Positive and Halide Negative Ions, J. Phys. Chem., 1970, 74, 7, 1475, https://doi.org/10.1021/j100702a014 . [all data]

Caldwell and Kebarle, 1984
Caldwell, G.; Kebarle, P., Binding energies and structural effects in halide anion-ROH and -RCOOH complexes from gas phase equilibria measurements, J. Am. Chem. Soc., 1984, 106, 967. [all data]

Caldwell, Masucci, et al., 1989
Caldwell, G.W.; Masucci, J.A.; Ikonomou, M.G., Negative Ion Chemical Ionization Mass Spectrometry - Binding of Molecules to Bromide and Iodide Anions, Org. Mass Spectrom., 1989, 24, 1, 8, https://doi.org/10.1002/oms.1210240103 . [all data]

Woodin and Beauchamp, 1978
Woodin, R.L.; Beauchamp, J.L., Bonding of Li+ to Lewis Bases in the Gas Phase. Reversals in Methyl Substituent Effects for Different Reference Acids, J. Am. Chem. Soc., 1978, 100, 2, 501, https://doi.org/10.1021/ja00470a024 . [all data]

Dzidic and Kebarle, 1970
Dzidic, I.; Kebarle, P., Hydration of the Alkali Ions in the Gas Phase. Enthalpies and Entropies of Reactions M+(H2O)n-1 + H2O = M+(H2O)n, J. Phys. Chem., 1970, 74, 7, 1466, https://doi.org/10.1021/j100702a013 . [all data]

Staley and Beauchamp, 1975
Staley, R.H.; Beauchamp, J.L., Intrinsic Acid - Base Properties of Molecules. Binding Energies of Li+ to pi - and n - Donor Bases, J. Am. Chem. Soc., 1975, 97, 20, 5920, https://doi.org/10.1021/ja00853a050 . [all data]

Andersen, Muntean, et al., 2000
Andersen, A.; Muntean, F.; Walter, D.; Rue, C.; Armentrout, P.B., Collision-Induced Dissociation and Theoretical Studies of Mg+ Complexes with CO, CO2, NH3, CH4, CH3OH, and C6H6, J. Phys. Chem. A, 2000, 104, 4, 692, https://doi.org/10.1021/jp993031t . [all data]

Operti, Tews, et al., 1988
Operti, L.; Tews, E.C.; Freiser, B.S., Determination of Gas-Phase Ligand Binding Energies to Mg+ by FTMS Techniques, J. Am. Chem. Soc., 1988, 110, 12, 3847, https://doi.org/10.1021/ja00220a020 . [all data]

Amicangelo and Armentrout, 2001
Amicangelo, J.C.; Armentrout, P.B., Relative and Absolute Bond Dissociation Energies of Sodium Cation Complexes Determined Using Competitive Collision-Induced Dissociation Experiments, Int. J. Mass Spectrom., 2001, 212, 1-3, 301, https://doi.org/10.1016/S1387-3806(01)00494-8 . [all data]

Armentrout and Rodgers, 2000
Armentrout, P.B.; Rodgers, M.T., An Absolute Sodium Cation Affinity Scale: Threshold Collision-Induced Dissociation Experiments and ab Initio Theory, J. Phys. Chem A, 2000, 104, 11, 2238, https://doi.org/10.1021/jp991716n . [all data]

Hoyau, Norrman, et al., 1999
Hoyau, S.; Norrman, K.; McMahon, T.B.; Ohanessian, G., A Quantitative Basis for a Scale of Na+ Affinities of Organic and Small Biological Molecules in the Gas Phase, J. Am. Chem. Soc., 1999, 121, 38, 8864, https://doi.org/10.1021/ja9841198 . [all data]

Guo, Conklin, et al., 1989
Guo, B.C.; Conklin, B.J.; Castleman, A.W., Thermochemical Properties of Ion Complexes Na+(M)n in the Gas Phase, J. Am. Chem. Soc., 1989, 111, 17, 6506, https://doi.org/10.1021/ja00199a005 . [all data]

McMahon and Ohanessian, 2000
McMahon, T.B.; Ohanessian, G., An Experimental and Ab Initio Study of the Nature of the Binding in Gas-Phase Complexes of Sodium Ions, Chem. Eur. J., 2000, 6, 16, 2931, https://doi.org/10.1002/1521-3765(20000818)6:16<2931::AID-CHEM2931>3.0.CO;2-7 . [all data]

Guo and Castleman, 1990
Guo, B.C.; Castleman, A.W., The Association Reactions of Pb+ Ion with CH3OH and CH3NH2 in the Gas Phase, Int. J. Mass Spectrom. Ion Proc., 1990, 100, 665, https://doi.org/10.1016/0168-1176(90)85101-7 . [all data]

Haken and Korhonen, 1985
Haken, J.K.; Korhonen, I.O.O., Gas chromatography of homologous esters. XXVII. Retention increments of C₁-C₁₈ primary alkanols and their 2-chloropropanoyl and 3-chloropropanoyl derivatives on SE-30 and OV-351 capillary columns, J. Chromatogr., 1985, 319, 131-142, https://doi.org/10.1016/S0021-9673(01)90548-5 . [all data]

Winskowski, 1983
Winskowski, J., Gaschromatographische Identifizierung von Stoffen anhand von Indexziffem und unterschiedlichen Detektoren, Chromatographia, 1983, 17, 3, 160-165, https://doi.org/10.1007/BF02271041 . [all data]

Haken, Nguyen, et al., 1979
Haken, J.K.; Nguyen, A.; Wainwright, M.S., Application of linear extrathermodynamic relationships to alcohols, aldehydes, ketones, amd ethoxy alcohols, J. Chromatogr., 1979, 179, 1, 75-85, https://doi.org/10.1016/S0021-9673(00)80658-5 . [all data]

Bogoslovsky, Anvaer, et al., 1978
Bogoslovsky, Yu.N.; Anvaer, B.I.; Vigdergauz, M.S., Chromatographic constants in gas chromatography (in Russian), Standards Publ. House, Moscow, 1978, 192. [all data]

Pías and Gascó, 1975
Pías, J.B.; Gascó, L., GC Retention Data of Alcohols and Benzoyl Derivatives of Alcohols, J. Chromatogr. - Chrom. Data, 1975, d14-d16. [all data]

Brown, Chapman, et al., 1968
Brown, I.; Chapman, I.L.; Nicholson, G.J., Gas chromatography of polar solutes in electron acceptor stationary phases, Aust. J. Chem., 1968, 21, 5, 1125-1141, https://doi.org/10.1071/CH9681125 . [all data]

Viani, Müggler-Chavan, et al., 1965
Viani, R.; Müggler-Chavan, F.; Reymond, D.; Egli, R.H., 196. Sur la composition de l'arôme de café, Helv. Chim. Acta, 1965, 48, 195-196, 1809-1815, https://doi.org/10.1002/hlca.19650480743 . [all data]

Haagen-Smit Laboratory, 1997
Haagen-Smit Laboratory, Procedure for the detailed hydrocarbon analysis of gasolines by single column high efficiency (capillary) column gas chromatography, SOP NO. MLD 118, Revision No. 1.1, California Environmental Protection Agency, Air Resources Board, El Monte, California, 1997, 22. [all data]

Anderson, Jurel, et al., 1973
Anderson, A.; Jurel, S.; Shymanska, M.; Golender, L., Gas-liquid chromatography of some aliphatic and heterocyclic mono- and pollyfunctional amines. VII. Retention indices of amines in some polar and unpolar stationary phases, Latv. PSR Zinat. Akad. Vestis Kim. Ser., 1973, 1, 51-63. [all data]

Zarazir, Chovin, et al., 1970
Zarazir, D.; Chovin, P.; Guiochon, G., Identification of hydroxylic compounds and their derivatives by gas chromatography, Chromatographia, 1970, 3, 4, 180-195, https://doi.org/10.1007/BF02269018 . [all data]

Bonastre and Grenier, 1968
Bonastre, J.; Grenier, P., Contribution à l'étude de la polarité des phases stationnaires en chromatographie gaz-liquide. III. Calcul des coefficients d'activité relatifs et des indices de rétention de quelques alcools aliphatiques, Bull. Soc. Chim. Fr., 1968, 1, 118-125. [all data]

Shimadzu, 2003
Shimadzu, Gas chromatography analysis of organic solvents using capillary columns (No. 2), 2003, retrieved from http://www.shimadzu.com/apps/form.cfm. [all data]

Shimoda and Shibamoto, 1990
Shimoda, M.; Shibamoto, T., Isolation and identification of headspace volatiles from brewed coffee with an on-column GC/MS method, J. Agric. Food Chem., 1990, 38, 3, 802-804, https://doi.org/10.1021/jf00093a045 . [all data]

Kevei and Kozma, 1976
Kevei, E.; Kozma, E., Gaschromatographische Untersuchungsmethoden zur Aromaprüfung in gekochtem Schweinefleisch (M. semimembranosus), Nahrung, 1976, 20, 3, 243-252, https://doi.org/10.1002/food.19760200303 . [all data]

Censullo, Jones, et al., 2003
Censullo, A.C.; Jones, D.R.; Wills, M.T., Speciation of the volatile organic compounds (VOCs) in solventborne aerosol coatings by solid phase microextraction-gas chromatography, J. Coat. Technol., 2003, 75, 936, 47-53, https://doi.org/10.1007/BF02697922 . [all data]

Golovnya, Kuz'menko, et al., 2000
Golovnya, R.V.; Kuz'menko, T.e.; Samusenko, A.L., Method for prediction of the ability of analyte for self-association in pure liquid, Proceedings 23rd ISCC; CD-ROM, 2000, retrieved from http://www.richrom.com/assets/CD23PDF/a09.pdf. [all data]

Golovnya, Kuz'menko, et al., 2000, 2
Golovnya, R.V.; Kuz'menko, T.E.; Samusenko, A.L., Gas-chromatographic method of evaluation of n-alkanol ability for self-association in pure liquid, Russ. Chem. Bull. (Engl. Transl.), 2000, 49, 2, 317-320, https://doi.org/10.1007/BF02494680 . [all data]

Bartelt, 1997
Bartelt, R.J., Calibration of a commercial solid-phase microextraction device for measuring headspace concentrations of organic volatiles, Anal. Chem., 1997, 69, 3, 364-372, https://doi.org/10.1021/ac960820n . [all data]

Peng, Ding, et al., 1988
Peng, C.T.; Ding, S.F.; Hua, R.L.; Yang, Z.C., Prediction of Retention Indexes I. Structure-Retention Index Relationship on Apolar Columns, J. Chromatogr., 1988, 436, 137-172, https://doi.org/10.1016/S0021-9673(00)94575-8 . [all data]

Ott, Fay, et al., 1997
Ott, A.; Fay, L.B.; Chaintreau, A., Determination and origin of the aroma impact compounds of yogurt flavor, J. Agric. Food Chem., 1997, 45, 3, 850-858, https://doi.org/10.1021/jf960508e . [all data]

van den Dool and Kratz, 1963
van den Dool, H.; Kratz, P. Dec., A generalization of the retention index system including linear temperature programmed gas-liquid partition chromatography, J. Chromatogr., 1963, 11, 463-471, https://doi.org/10.1016/S0021-9673(01)80947-X . [all data]

Shimadzu, 2003, 2
Shimadzu, Gas chromatography analysis of organic solvents using capillary columns (No. 3), 2003, retrieved from http://www.shimadzu.com/apps/form.cfm. [all data]

Vernon, 1971
Vernon, F., An investigation into hydrogen bonding in gas-liquid chromatography, J. Chromatogr., 1971, 63, 249-257, https://doi.org/10.1016/S0021-9673(01)85637-5 . [all data]

Anderson, 1968
Anderson, D.G., USe of Kovats retention indices and response factors for the qualitative and quantitative analysis of coating solvents, J. Paint Technol., 1968, 40, 527, 549-557. [all data]

Cremer and Nonn, 1964
Cremer, E.; Nonn, H., Kennzahlen zur Identifizierung chromatographisch getrennter Komponenten, Monatsh. Chem., 1964, 3, 3, 910-921, https://doi.org/10.1007/BF00908804 . [all data]

Bramston-Cook, 2013
Bramston-Cook, R., Kovats indices for C2-C13 hydrocarbons and selected oxygenated/halocarbons with 100 % dimethylpolysiloxane columns, 2013, retrieved from http://lotusinstruments.com/monographs/List .... [all data]

Supelco, 2012
Supelco, CatalogNo. 24160-U, Petrocol DH Columns. Catalog No. 24160-U, 2012, retrieved from http://www.sigmaaldrich.com/etc/medialib/docs/Supelco/Datasheet/1/w97949.Par.0001.File.tmp/w97949.pdf. [all data]

Leffingwell and Alford, 2005
Leffingwell, J.C.; Alford, E.D., Volatile constituents of Perique tobacco, Electron. J. Environ. Agric. Food Chem., 2005, 4, 2, 899-915. [all data]

Zenkevich, 2005
Zenkevich, I.G., Experimentally measured retention indices., 2005. [all data]

Health Safety Executive, 2000
Health Safety Executive, MDHS 96 Volatile organic compounds in air - Laboratory method using pumed solid sorbent tubes, solvent desorption and gas chromatography in Methods for the Determination of Hazardous Substances (MDHS) guidance, Crown, Colegate, Norwich, 2000, 1-24, retrieved from http://www.hse.gov.uk/pubns/mdhs/pdfs/mdhs96.pdf. [all data]

Shoenmakers, Oomen, et al., 2000
Shoenmakers, P.J.; Oomen, J.L.M.M.; Blomberg, J.; Genuit, W.; van Velzen, G., Comparison of comprehensive two-dimensional gas chromatography and gas chromatography-mass spectrometry for the characterization of complex hydrocarbon mixtures, J. Chromatogr. A, 2000, 892, 1-2, 29-46, https://doi.org/10.1016/S0021-9673(00)00744-5 . [all data]

Kotowska, Zalikowski, et al., 2012
Kotowska, U.; Zalikowski, M.; Isidorov, V.A., HS-SPME/GC-MS analysis of volatile and semi-volatile organic compounds emitted from municipal sewage sludge, Environ. Monit. Asses., 2012, 184, 5, 2893-2907, https://doi.org/10.1007/s10661-011-2158-8 . [all data]

Chen and Feng, 2007
Chen, Y.; Feng, C., QSPR study on gas chromatography retention index of some organic pollutants, Comput. Appl. Chem. (China), 2007, 24, 10, 1404-1408. [all data]

Kou, Zhang, et al., 2006
Kou, J.; Zhang, S.; Hu, Y.; Qiao, H.; Li, J., Stidy on the relationships between structures and gas chromatographic retention indices of alcohols, Comput. Appl. Chem. (Chinese), 2006, 23, 7, 651-654. [all data]

Blunden, Aneja, et al., 2005
Blunden, J.; Aneja, V.P.; Lonneman, W.A., Characterization of non-methane volatile organic compounds at swine facilities in eastern North Carolina, Atm. Environ., 2005, 39, 36, 6707-6718, https://doi.org/10.1016/j.atmosenv.2005.03.053 . [all data]

Fu and Wang, 2004
Fu, S.-P.; Wang, Y.-Q., Estimation and prediction of gas chromatographic retention indices of alcohols by molecular electronegativity-distance vector, J. Chongqing Univ., 2004, 27, 6, 106-109. [all data]

Zenkevich, 2001
Zenkevich, I.G., Encyclopedia of Chromatography. Derivatization of Acids for GC Analysis, Marcel Dekker, Inc., New York - Basel, 2001, 221. [all data]

Zenkevich, 2001, 2
Zenkevich, I.G., Encyclopedia of Chromatography. Derivatization of Carbonyls for GC Analysis, MArcel Dekker, Inc., New York - Basel, 2001, 233. [all data]

Zenkevich, 1999
Zenkevich, I.G., New Application of the Retention Index Concept in Gas and High Performance Liquid Chromatography, Fresenius' J. Anal. Chem., 1999, 365, 4, 305-309, https://doi.org/10.1007/s002160051491 . [all data]

Flanagan, Streete, et al., 1997
Flanagan, R.J.; Streete, P.J.; Ramsey, J.D., Volatile Substance Abuse, UNODC Technical Series, No 5, United Nations, Office on Drugs and Crime, Vienna International Centre, PO Box 500, A-1400 Vienna, Austria, 1997, 56, retrieved from http://www.odccp.org/pdf/technical_series₁997-01-01₁.pdf. [all data]

Zenkevich and Chupalov, 1996
Zenkevich, I.G.; Chupalov, A.A., New Possibilities of Chromato Mass Pectrometric Identification of Organic Compounds Using Increments of Gas Chromatographic Retention Indices of Molecular Structural Fragments, Zh. Org. Khim. (Rus.), 1996, 32, 5, 656-666. [all data]

Zenkevich, Korolenko, et al., 1995
Zenkevich, I.G.; Korolenko, L.I.; Khralenkova, N.B., Desorption with solvent vapor as a method of sample preparation in the sorption preconcentration of organic-compounds from the air of a working area and from industrial-waste gases, J. Appl. Chem. USSR (Engl. Transl.), 1995, 50, 10, 937-944. [all data]

Schuberth, 1994
Schuberth, J., Joint use of retention index and mass spectrum in postmortem tests for volatile organics by headspace capillary gas chromatography with ion-trap detection, J. Chromatogr. A, 1994, 674, 1-2, 63-71, https://doi.org/10.1016/0021-9673(94)85217-0 . [all data]

Strete, Ruprah, et al., 1992
Strete, P.J.; Ruprah, M.; Ramsey, J.D.; Flanagan, R.J., Detection and identification of volatile substances by headspace capillary gas chromatography to aid the diagnosis of acute poisoning, Analyst, 1992, 117, 7, 1111-1127, https://doi.org/10.1039/an9921701111 . [all data]

Weller and Wolf, 1989
Weller, J.-P.; Wolf, M., Massenspektroskopie und Headspace-GC, Beitr. Gerichtl. Med., 1989, 47, 525-532. [all data]

Waggott and Davies, 1984
Waggott, A.; Davies, I.W., Identification of organic pollutants using linear temperature programmed retention indices (LTPRIs) - Part II, 1984, retrieved from http://dwi.defra.gov.uk/research/completed-research/reports/dwi0383.pdf. [all data]

Sun, Siepmann, et al., 2006
Sun, L.; Siepmann, J.I.; Klotz, W.L.; Schure, M.R., retention in gas-liquid chromatography with a polyethylene oxide stationary phase: molecular simulation and experiment, J. Chromatogr. A, 2006, 1126, 1-2, 373-380, https://doi.org/10.1016/j.chroma.2006.05.084 . [all data]

Shimadzu, 2012
Shimadzu, Pharmaceutical Related, Analysis of pharmaceutical residual solvent (observation of separation) (1) - GC, 2012, retrieved from www.shimadzu.ru/applications/Applications_pdf/GC/Pharma/Pharmaceutical residual solvents GC.pdf. [all data]

Chida, Sone, et al., 2004
Chida, M.; Sone, Y.; Tamura, H., Aroma characteristics of stored tobacco cut leaves analyzed by a high vacuum distillation and canister system, J. Agric. Food Chem., 2004, 52, 26, 7918-7924, https://doi.org/10.1021/jf049223p . [all data]

Shimadzu Corporation, 2003
Shimadzu Corporation, Analysis of pharmaceutical residual solvent (observation of separation), 2003, retrieved from http://www.shimadzu.com.br/analitica/aplicacoes/book/pharm69.pdf. [all data]

Tanaka, Yamauchi, et al., 2003
Tanaka, T.; Yamauchi, T.; Katsumata, R.; Kiuchi, K., Comparison of volatile components in commercial Itohiki-Natto by solid phase microextraction and gas chromatography, Nippon Shokuhin Kagaku Kogaku Kaishi, 2003, 50, 6, 278-285, https://doi.org/10.3136/nskkk.50.278 . [all data]

Suhardi, Suzuki, et al., 2002
Suhardi, S.; Suzuki, M.; Yoshida, K.; Muto, T.; Fujita, A.; Watanbe, N., Changes in the volatile compounds and in the chemical and physical properties of snake fruit (Salacca edulis Reinw) Cv. Pondoh during maturation, J. Agric. Food Chem., 2002, 50, 26, 7627-7633, https://doi.org/10.1021/jf020620e . [all data]

Duque, Bonilla, et al., 2001
Duque, C.; Bonilla, A.; Bautista, E.; Zea, S., Exudation of low molecular wight compounds (thiobismethane, methyl isocyanide, amd methyl isothiocyanate) as a possible chemical defense mechanism in the marine sponge Ircinia felix, Biochem. Systematics Ecol., 2001, 29, 5, 459-467, https://doi.org/10.1016/S0305-1978(00)00081-8 . [all data]

Vinogradov, 2004
Vinogradov, B.A., Production, composition, properties and application of essential oils, 2004, retrieved from http://viness.narod.ru. [all data]

Peng, Yang, et al., 1991
Peng, C.T.; Yang, Z.C.; Ding, S.F., Prediction of rentention idexes. II. Structure-retention index relationship on polar columns, J. Chromatogr., 1991, 586, 1, 85-112, https://doi.org/10.1016/0021-9673(91)80028-F . [all data]

Ramsey and Flanagan, 1982
Ramsey, J.D.; Flanagan, R.J., Detection and Identification of Volatile Organic Compounds in Blood by Headspace Gas Chromatography as an Aid to the Diagnosis of Solvent Abuse, J. Chromatogr., 1982, 240, 2, 423-444, https://doi.org/10.1016/S0021-9673(00)99622-5 . [all data]

Notes

Go To: Top, Gas phase ion energetics data, Ion clustering data, Mass spectrum (electron ionization), Gas Chromatography, References

Symbols used in this document:

AE	Appearance energy
IE (evaluated)	Recommended ionization energy
T	Temperature
Δ_rG°	Free energy of reaction at standard conditions
Δ_rH°	Enthalpy of reaction at standard conditions
Δ_rS°	Entropy of reaction at standard conditions

Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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Methyl Alcohol

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Gas phase ion energetics data

Ionization energy determinations

Appearance energy determinations

De-protonation reactions

Ion clustering data

Clustering reactions

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Free energy of reaction

Mass spectrum (electron ionization)

Spectrum

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Additional Data

Gas Chromatography

Kovats' RI, non-polar column, isothermal

Kovats' RI, non-polar column, custom temperature program

Kovats' RI, polar column, isothermal

Kovats' RI, polar column, temperature ramp

Kovats' RI, polar column, custom temperature program

Van Den Dool and Kratz RI, non-polar column, temperature ramp

Van Den Dool and Kratz RI, non-polar column, custom temperature program

Van Den Dool and Kratz RI, polar column, temperature ramp

Normal alkane RI, non-polar column, isothermal

Normal alkane RI, non-polar column, temperature ramp

Normal alkane RI, non-polar column, custom temperature program

Normal alkane RI, polar column, isothermal

Normal alkane RI, polar column, temperature ramp

Normal alkane RI, polar column, custom temperature program

References

Notes