Argon
- Formula: Ar
- Molecular weight: 39.948
- IUPAC Standard InChIKey: XKRFYHLGVUSROY-UHFFFAOYSA-N
- CAS Registry Number: 7440-37-1
- Chemical structure:
This structure is also available as a 2d Mol file - Other names: Ar; UN 1006; UN 1951; argon atom
- Permanent link for this species. Use this link for bookmarking this species for future reference.
- Information on this page:
- Other data available:
- Gas phase thermochemistry data
- Phase change data
- Reaction thermochemistry data: reactions 1 to 50, reactions 51 to 100, reactions 101 to 102
- Henry's Law data
- Fluid Properties
- Data at other public NIST sites:
- NIST Atomic Spectra Database - Lines Holdings (on physics web site)
- NIST Atomic Spectra Database - Levels Holdings (on physics web site)
- NIST Atomic Spectra Database - Ground states and ionization energies (on physics web site)
- Gas Phase Kinetics Database
- X-ray Photoelectron Spectroscopy Database, version 5.0
- X-ray Photoelectron Spectroscopy Database, version 5.0
- X-ray Photoelectron Spectroscopy Database, version 5.0
- X-ray Photoelectron Spectroscopy Database, version 5.0
- X-ray Photoelectron Spectroscopy Database, version 5.0
- X-ray Photoelectron Spectroscopy Database, version 5.0
- X-ray Photoelectron Spectroscopy Database, version 5.0
- X-ray Photoelectron Spectroscopy Database, version 5.0
- Options:
Data at NIST subscription sites:
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Gas phase ion energetics data
Go To: Top, Ion clustering data, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias
L - Sharon G. Lias
Data compiled as indicated in comments:
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
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 15.759 ± 0.001 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 88.24 | kcal/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 82.77 | kcal/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
15.763 | PIPECO | Weitzel, Mahnert, et al., 1994 | LL |
15.75962 | EVAL | Lide, 1992 | LL |
15.82 | EI | Wetzel, Baiocchi, et al., 1987 | LBLHLM |
15.760 | S | Kelly, 1987 | LBLHLM |
15.759 | PE | Kimura, Katsumata, et al., 1981 | LLK |
15.88 | EI | Clare and Sowerby, 1981 | LLK |
15.7 | EI | Freiser, 1980 | LLK |
15.75962 ± 0.00001 | S | Minnhagen, 1973 | LLK |
15.753 ± 0.002 | TE | Spohr, Guyon, et al., 1971 | LLK |
15.75962 ± 0.00001 | S | Yoshino, 1970 | RDSH |
15.759 | S | Yoshino, 1969 | RDSH |
15.713 ± 0.003 | CI | Hotop and Niehaus, 1969 | RDSH |
15.757 ± 0.005 | PE | Collin and Natalis, 1968 | RDSH |
15.74 ± 0.05 | EI | Gallegos and Klaver, 1967 | RDSH |
15.78 ± 0.03 | EI | Winters, Collins, et al., 1966 | RDSH |
15.79 | PE | Al-Joboury and Turner, 1963 | RDSH |
Ion clustering data
Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias
B - John E. Bartmess
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
By formula: Ar+ + Ar = (Ar+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 20. ± 20. | kcal/mol | AVG | N/A | Average of 5 out of 7 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 12.8 | cal/mol*K | PHPMS | Teng and Conway, 1973 | gas phase; switching reaction(N2+)Ar; Turner and Conway, 1979, Liu and Conway, 1975; M |
By formula: (Ar+ • Ar) + Ar = (Ar+ • 2Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 5.06 ± 0.08 | kcal/mol | PHPMS | Turner and Conway, 1979 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 20.3 | cal/mol*K | PHPMS | Turner and Conway, 1979 | gas phase; M |
By formula: (Ar+ • 2Ar) + Ar = (Ar+ • 3Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 4.9 ± 0.3 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.3 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Free energy of reaction
ΔrG° (kcal/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
2.0 | 77. | PHPMS | Teng and Conway, 1973 | gas phase; M |
By formula: (Ar+ • 3Ar) + Ar = (Ar+ • 4Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.7 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 13.9 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (Ar+ • 4Ar) + Ar = (Ar+ • 5Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 16.1 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (Ar+ • 5Ar) + Ar = (Ar+ • 6Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.0 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (Ar+ • 6Ar) + Ar = (Ar+ • 7Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.4 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (Ar+ • 7Ar) + Ar = (Ar+ • 8Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.4 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (Ar+ • 8Ar) + Ar = (Ar+ • 9Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.3 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (Ar+ • 9Ar) + Ar = (Ar+ • 10Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.55 ± 0.20 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.1 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: (Ar+ • 10Ar) + Ar = (Ar+ • 11Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.4 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
By formula: ArNO- + 2Ar = Ar2NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.50 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar2NO- + 3Ar = Ar3NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.30 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar3NO- + 4Ar = Ar4NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.30 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar4NO- + 5Ar = Ar5NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.30 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar5NO- + 6Ar = Ar6NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.20 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar6NO- + 7Ar = Ar7NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.90 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar7NO- + 8Ar = Ar8NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.90 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar8NO- + 9Ar = Ar9NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.70 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar9NO- + 10Ar = Ar10NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.70 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar10NO- + 11Ar = Ar11NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.60 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar11NO- + 12Ar = Ar12NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.70 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar12NO- + 13Ar = Ar13NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.30 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Ar13NO- + 14Ar = Ar14NO-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.20 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
By formula: Br- + Ar = (Br- • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.80 | kcal/mol | Ther | Zhao, Yourshaw, et al., 1994 | gas phase; B |
ΔrH° | 1.40 | kcal/mol | Mobl | Gatland, 1984 | gas phase; B,M |
By formula: CH3+ + Ar = (CH3+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11.3 ± 2.0 | kcal/mol | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 20.1 | cal/mol*K | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
By formula: (CH3+ • Ar) + Ar = (CH3+ • 2Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.3 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 15.7 | cal/mol*K | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
By formula: (CH3+ • 2Ar) + Ar = (CH3+ • 3Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.0 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 22.3 | cal/mol*K | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
By formula: (CH3+ • 3Ar) + Ar = (CH3+ • 4Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.0 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 21.1 | cal/mol*K | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
By formula: (CH3+ • 4Ar) + Ar = (CH3+ • 5Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.9 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 20.6 | cal/mol*K | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
By formula: (CH3+ • 5Ar) + Ar = (CH3+ • 6Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.9 ± 0.3 | kcal/mol | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 21.0 | cal/mol*K | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
By formula: (CH3+ • 6Ar) + Ar = (CH3+ • 7Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.9 ± 0.4 | kcal/mol | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 21.2 | cal/mol*K | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; M |
By formula: (CH3+ • 7Ar) + Ar = (CH3+ • 8Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.93 | kcal/mol | PHPMS | Hiraoka, Kudaka, et al., 1991 | gas phase; Entropy change calculated or estimated; M |
By formula: CO+ + Ar = (CO+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 16.1 ± 1.4 | kcal/mol | PIPECO | Norwood, Guo, et al., 1989 | gas phase; CO+(X) ground state; M |
By formula: CO2+ + Ar = (CO2+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 6.0 | kcal/mol | PI | Pratt and Dehmer, 1983 | gas phase; M |
By formula: Co+ + Ar = (Co+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11.8 | kcal/mol | PDis | Asher, Bellert, et al., 1994 | RCD |
By formula: Cr+ + Ar = (Cr+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 6.9 ± 0.4 | kcal/mol | SIDT | Kemper, Hsu, et al., 1991 | gas phase; ΔrH(0 K) = 6.55 kcal/mol, ΔrS(100 K) = 14.4 cal/mol*K; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 15.8 | cal/mol*K | SIDT | Kemper, Hsu, et al., 1991 | gas phase; ΔrH(0 K) = 6.55 kcal/mol, ΔrS(100 K) = 14.4 cal/mol*K; M |
By formula: Cs+ + Ar = (Cs+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.95 | kcal/mol | IMob | Gatland, 1984, 2 | gas phase; M |
ΔrH° | 1.46 | kcal/mol | SCATTERING | Gislason, 1984 | gas phase; M |
ΔrH° | 1.96 | kcal/mol | IMob | Viehland, 1984 | gas phase; M |
ΔrH° | 2.28 | kcal/mol | IMob | Takebe, 1983 | gas phase; M |
ΔrH° | 2.3 | kcal/mol | IMob | Takebe, 1983 | gas phase; values from this reference are consistently too high; M |
By formula: D3+ + Ar = (D3+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.0 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 14.5 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (D3+ • Ar) + Ar = (D3+ • 2Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 4.8 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.5 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (D3+ • 2Ar) + Ar = (D3+ • 3Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 4.4 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 18.4 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (D3+ • 3Ar) + Ar = (D3+ • 4Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.4 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 16.6 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (D3+ • 4Ar) + Ar = (D3+ • 5Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.3 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.4 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (D3+ • 5Ar) + Ar = (D3+ • 6Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.2 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 19.1 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (D3+ • 6Ar) + Ar = (D3+ • 7Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 25.2 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
+ = ArF-
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.00 | kcal/mol | TDAs | Wada, Kikkawa, et al., 2007 | gas phase; Entropy estimated; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | -3.96 | kcal/mol | TDAs | Wada, Kikkawa, et al., 2007 | gas phase; Entropy estimated; B |
By formula: Fe+ + Ar = (Fe+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.6 ± 1.9 | kcal/mol | CIDT | Rodgers and Armentrout, 2000 | RCD |
By formula: H2+ + Ar = (H2+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 24. | kcal/mol | SIFT | Bedford and Smith, 1990 | gas phase; switching reaction(Ar+)Ar, ΔrH>; M |
By formula: H3+ + Ar = (H3+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 6.7 ± 0.2 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
ΔrH° | 7.5 ± 0.8 | kcal/mol | SIFT | Bedford and Smith, 1990 | gas phase; switching reaction(H3+)H2, Hiraoka and Mori, 1989, 2; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 13.4 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (H3+ • Ar) + Ar = (H3+ • 2Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 4.6 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 16.0 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (H3+ • 2Ar) + Ar = (H3+ • 3Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 4.3 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.3 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (H3+ • 3Ar) + Ar = (H3+ • 4Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.5 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 16.1 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (H3+ • 4Ar) + Ar = (H3+ • 5Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.3 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 16.7 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (H3+ • 5Ar) + Ar = (H3+ • 6Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.2 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 18.7 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: (H3+ • 6Ar) + Ar = (H3+ • 7Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.1 | kcal/mol | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 23.0 | cal/mol*K | PHPMS | Hiraoka and Mori, 1989, 2 | gas phase; M |
By formula: Hg+ + Ar = (Hg+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 5.3 ± 0.4 | kcal/mol | PI | Linn, Brom, et al., 1985 | gas phase; M |
By formula: I- + Ar = (I- • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.60 | kcal/mol | Ther | Zhao, Yourshaw, et al., 1994 | gas phase; B |
By formula: K+ + Ar = (K+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.8 ± 0.7 | kcal/mol | AVG | N/A | Average of 9 values; Individual data points |
By formula: Kr+ + Ar = (Kr+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 12.2 | kcal/mol | PI | Dehmer and Pratt, 1982 | gas phase; M |
ΔrH° | 13.6 | kcal/mol | PI | Ng, Tiedemann, et al., 1977 | gas phase; M |
By formula: Li+ + Ar = (Li+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7. ± 1. | kcal/mol | AVG | N/A | Average of 4 out of 6 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 7. | cal/mol*K | DT | McKnight and Sawina, 1973 | gas phase; ΔrS approximate; M |
Free energy of reaction
ΔrG° (kcal/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
1.4 | 294. | IMob | Cassidy and Elford, 1985 | gas phase; M |
1.9 | 319. | DT | Keller, Beyer, et al., 1973 | gas phase; LOW E/N; M |
2.6 | 215. | DT | McKnight and Sawina, 1973 | gas phase; ΔrS approximate; M |
By formula: Mg+ + Ar = (Mg+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.3 ± 1.6 | kcal/mol | CIDT | Andersen, Muntean, et al., 2000 | RCD |
By formula: N+ + Ar = (N+ • Ar)
Enthalpy of reaction
ΔrH° (kcal/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
28. (+11.,-0.) | CID | Haynes, Freysinger, et al., 1995 | gas phase; giuded ion beam CID; M |
By formula: NO- + Ar = (NO- • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.30 ± 0.90 | kcal/mol | N/A | Hendricks, de Clercq, et al., 2002 | gas phase; B |
ΔrH° | 1.60 ± 0.30 | kcal/mol | N/A | Bowen and Eaton, 1988 | gas phase; B |
By formula: N2+ + Ar = (N2+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 26.8 | kcal/mol | PD/KERD | Kim and Bowers, 1990 | gas phase; switching reaction(N2+)N2; Hiraoka and Nakajima, 1988; M |
ΔrH° | 25.4 | kcal/mol | PHPMS | Teng and Conway, 1973 | gas phase; switching reaction(N2+)N2; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 19.5 | cal/mol*K | PD/KERD | Kim and Bowers, 1990 | gas phase; switching reaction(N2+)N2; Hiraoka and Nakajima, 1988; M |
ΔrS° | 13.7 | cal/mol*K | PHPMS | Teng and Conway, 1973 | gas phase; switching reaction(N2+)N2; M |
By formula: (N2+ • Ar) + Ar = (N2+ • 2Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 3.8 | kcal/mol | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; ΔrH>; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17. | cal/mol*K | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; ΔrH>; M |
By formula: (N2+ • 2Ar) + Ar = (N2+ • 3Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.7 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 13.7 | cal/mol*K | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
By formula: (N2+ • 3Ar) + Ar = (N2+ • 4Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.7 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.9 | cal/mol*K | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
By formula: (N2+ • 4Ar) + Ar = (N2+ • 5Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.0 | cal/mol*K | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
By formula: (N2+ • 5Ar) + Ar = (N2+ • 6Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.4 | cal/mol*K | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
By formula: (N2+ • 6Ar) + Ar = (N2+ • 7Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.5 ± 0.2 | kcal/mol | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17.3 | cal/mol*K | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; M |
By formula: (N2+ • 7Ar) + Ar = (N2+ • 8Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.53 | kcal/mol | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17. | cal/mol*K | N/A | Hiraoka, Mori, et al., 1992 | gas phase; Entropy change calculated or estimated; M |
By formula: (N2+ • 8Ar) + Ar = (N2+ • 9Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.52 | kcal/mol | PHPMS | Hiraoka, Mori, et al., 1992 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 17. | cal/mol*K | N/A | Hiraoka, Mori, et al., 1992 | gas phase; Entropy change calculated or estimated; M |
By formula: Na+ + Ar = (Na+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 3.7 ± 2.1 | kcal/mol | CIDT | Armentrout and Rodgers, 2000 | RCD |
ΔrH° | 3.70 | kcal/mol | SCATTERING | Gislason, 1984 | gas phase; M |
ΔrH° | 4.39 | kcal/mol | IMob | Viehland, 1984 | gas phase; M |
ΔrH° | 4.4 | kcal/mol | DT | McKnight and Sawina, 1973 | gas phase; M |
ΔrH° | 4.87 | kcal/mol | IMob | Takebe, 1983 | gas phase; M |
By formula: O- + Ar = (O- • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.2 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • Ar) + Ar = (O- • 2Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.0 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 2Ar) + Ar = (O- • 3Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.6 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 3Ar) + Ar = (O- • 4Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.4 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 4Ar) + Ar = (O- • 5Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.2 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 5Ar) + Ar = (O- • 6Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.2 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 6Ar) + Ar = (O- • 7Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.0 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 7Ar) + Ar = (O- • 8Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.9 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 8Ar) + Ar = (O- • 9Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.9 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 9Ar) + Ar = (O- • 10Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.7 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 10Ar) + Ar = (O- • 11Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.4 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 11Ar) + Ar = (O- • 12Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.8 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 12Ar) + Ar = (O- • 13Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.2 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 13Ar) + Ar = (O- • 14Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.2 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 14Ar) + Ar = (O- • 15Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.4 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 15Ar) + Ar = (O- • 16Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.1 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 16Ar) + Ar = (O- • 17Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.1 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 17Ar) + Ar = (O- • 18Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.2 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 18Ar) + Ar = (O- • 19Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.1 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 19Ar) + Ar = (O- • 20Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.1 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 20Ar) + Ar = (O- • 21Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.1 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 21Ar) + Ar = (O- • 22Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.1 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 22Ar) + Ar = (O- • 23Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.1 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 23Ar) + Ar = (O- • 24Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.1 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 24Ar) + Ar = (O- • 25Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.2 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: (O- • 25Ar) + Ar = (O- • 26Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 0.2 ± 2.0 | kcal/mol | N/A | Arnold, Hendricks, et al., 1995 | gas phase; EA given is Vertical Detachment Energy. Affinity: difference between successive EAs in (Y); B |
By formula: O2- + Ar = (O2- • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1.66 | kcal/mol | N/A | Bowen and Eaton, 1988 | gas phase; Bound by 70 meV relative to EA(O2-.); B |
By formula: Rb+ + Ar = (Rb+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 2.03 | kcal/mol | IMob | Gatland, 1984, 2 | gas phase; M |
ΔrH° | 1.98 | kcal/mol | IMob | Viehland, 1984 | gas phase; M |
ΔrH° | 2.84 | kcal/mol | IMob | Takebe, 1983 | gas phase; M |
By formula: Xe+ + Ar = (Xe+ • Ar)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 4.1 | kcal/mol | PI | Dehmer and Pratt, 1982 | gas phase; M |
ΔrH° | 6.0 | kcal/mol | SIFT | Jones, Lister, et al., 1980 | gas phase; M |
ΔrH° | 3.2 | kcal/mol | PI | Ng, Tiedemann, et al., 1977 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 19.4 | cal/mol*K | SIFT | Jones, Lister, et al., 1980 | gas phase; M |
Mass spectrum (electron ionization)
Go To: Top, Gas phase ion energetics data, Ion clustering data, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Spectrum
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Additional Data
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Owner | NIST Mass Spectrometry Data Center Collection (C) 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | DOW CHEMICAL COMPANY / ASTM E14-UNCERTIFIED SPECTRUM 1 |
NIST MS number | 34321 |
References
Go To: Top, Gas phase ion energetics data, Ion clustering data, Mass spectrum (electron ionization), Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
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]
Weitzel, Mahnert, et al., 1994
Weitzel, K.-M.; Mahnert, J.; Penno, M.,
ZEKE-PEPICO investigations of dissociation energies in ionic reactions,
Chem. Phys. Lett., 1994, 224, 371. [all data]
Lide, 1992
Lide, D.R. (Editor),
Ionization potentials of atoms and atomic ions
in Handbook of Chem. and Phys., 1992, 10-211. [all data]
Wetzel, Baiocchi, et al., 1987
Wetzel, R.C.; Baiocchi, F.A.; Hayes, T.R.; Freund, R.S.,
Absolute cross sections for electron-impact ionization of the rare-gas atoms by the fast-neutral-beam method,
Phys. Rev. A, 1987, 35, 559. [all data]
Kelly, 1987
Kelly, R.L.,
Atomic and ionic spectrum lines of hydrogen through kryton,
J. Phys. Chem. Ref. Data, 1987, 16. [all data]
Kimura, Katsumata, et al., 1981
Kimura, K.; Katsumata, S.; Achiba, Y.; Yamazaki, T.; Iwata, S.,
Ionization energies, Ab initio assignments, and valence electronic structure for 200 molecules
in Handbook of HeI Photoelectron Spectra of Fundamental Organic Compounds, Japan Scientific Soc. Press, Tokyo, 1981. [all data]
Clare and Sowerby, 1981
Clare, P.; Sowerby, D.B.,
Electron impact ionisation energies of some halo-cyclotriphosphazenes,
J. Inorg. Nucl. Chem., 1981, 43, 477. [all data]
Freiser, 1980
Freiser, B.S.,
Electron impact ionization of argon ions by trapped ion cyclotron resonanace spectroscopy,
Int. J. Mass Spectrom. Ion Phys., 1980, 33, 263. [all data]
Minnhagen, 1973
Minnhagen, L.,
Spectrum and the energy levels of neutral argon, Ar I,
J. Opt. Soc. Am., 1973, 63, 1185. [all data]
Spohr, Guyon, et al., 1971
Spohr, R.; Guyon, P.M.; Chupka, W.A.; Berkowitz, J.,
Threshold photoelectron detector for use in the vacuum ultraviolet,
Rev. Sci. Instrum., 1971, 42, 1872. [all data]
Yoshino, 1970
Yoshino, K.,
Absorption spectrum of the argon atom in the vacuum-ultraviolet region,
J. Opt. Soc. Am., 1970, 60, 1220. [all data]
Yoshino, 1969
Yoshino, K.,
Absorption spectrum of the argon atom in the vacuum-ultraviolet region,
J. Opt. Soc. Am., 1969, 59, 1525. [all data]
Hotop and Niehaus, 1969
Hotop, H.; Niehaus, A.,
Reactions of excited atoms molecules with atoms and molecules. II. Energy analysis of penning electrons,
Z. Phys., 1969, 228, 68. [all data]
Collin and Natalis, 1968
Collin, J.E.; Natalis, P.,
Vibrational and electronic ionic states of nitric oxide. An accurate method for measuring ionization potentials by photoelectron spectroscopy,
Intern. J. Mass Spectrom. Ion Phys., 1968, 1, 483. [all data]
Gallegos and Klaver, 1967
Gallegos, E.J.; Klaver, R.F.,
Automatic voltage scanner for a peak switching mass spectrometer,
J.Sci. Instr., 1967, 44, 427. [all data]
Winters, Collins, et al., 1966
Winters, R.E.; Collins, J.H.; Courchene, W.L.,
Resolution of fine structure in ionization-efficiency curves,
J. Chem. Phys., 1966, 45, 1931. [all data]
Al-Joboury and Turner, 1963
Al-Joboury, M.I.; Turner, D.W.,
Molecular photo-electron spectroscopy. Part I. The hydrogen and nitrogen molecules,
J. Chem. Soc., 1963, 5141. [all data]
Teng and Conway, 1973
Teng, H.H.; Conway, D.C.,
Ion - Molecule Equilibria in Mixtures of N2 and Ar,
J. Chem. Phys., 1973, 59, 5, 2316, https://doi.org/10.1063/1.1680338
. [all data]
Turner and Conway, 1979
Turner, D.L.; Conway, D.C.,
Study of the 2Ar + Ar2+ = Ar + Ar3+ Reaction,
J. Chem. Phys., 1979, 71, 4, 1899, https://doi.org/10.1063/1.438544
. [all data]
Liu and Conway, 1975
Liu, W.F.; Conway, D.C.,
Ion - Molecule Reactions in Ar at 296, 195, and 77 K,
J. Chem. Phys., 1975, 62, 8, 3070, https://doi.org/10.1063/1.430906
. [all data]
Hiraoka and Mori, 1989
Hiraoka, K.; Mori, T.,
Formation and Stabilities of Cluster Ions Arn+,
J. Chem. Phys., 1989, 90, 12, 7143, https://doi.org/10.1063/1.456245
. [all data]
Hendricks, de Clercq, et al., 2002
Hendricks, J.H.; de Clercq, H.L.; Freidhoff, C.B.; Arnold, S.T.; Eaton, J.G.; Fancher, C.; Lyapustina, S.A.; S.,
Anion solvation at the microscopic level: Photoelectron spectroscopy of the solvated anion clusters, NO-(Y)(n), where Y=Ar, Kr, Xe, N2O, H2S, NH3, H2O, and C2H4(OH)(2),
J. Chem. Phys., 2002, 116, 18, 7926-7938, https://doi.org/10.1063/1.1457444
. [all data]
Zhao, Yourshaw, et al., 1994
Zhao, Y.X.; Yourshaw, I.; Reiser, G.; Arnold, C.C.; Neumark, D.M.,
Study of the ArBr(-), ArI(-), and KrI(-) anions and the corresponding neutral van der Waals complexes by anion zero electron kinetic energy,
J. Chem. Phys., 1994, 101, 8, 6538, https://doi.org/10.1063/1.468500
. [all data]
Gatland, 1984
Gatland, I.R.,
Determination of Ion-Atom Potentials from Mobility Experiments.
in Swarms of Ions and Electrons In Gases, W. Lindinger, Ed., Springer-Verlag, NY,, 1984, 44. [all data]
Hiraoka, Kudaka, et al., 1991
Hiraoka, K.; Kudaka, I.; Yamabe, S.,
A Charge-Transfer Complex CH3+ Ar in the Gas Phase,
Chem. Phys. Lett., 1991, 178, 1, 103, https://doi.org/10.1016/0009-2614(91)85060-A
. [all data]
Norwood, Guo, et al., 1989
Norwood, K.; Guo, J.H.; Luo, G.; Ng, C.Y.,
A Study of Intramolecular Charge Transfer in Mixed Ar/Co Dimer and Trimer Ions Using the Photoion - Photoelectron Coincidence Method,
Chem. Phys., 1989, 129, 1, 109, https://doi.org/10.1016/0301-0104(89)80023-0
. [all data]
Pratt and Dehmer, 1983
Pratt, S.T.; Dehmer, P.M.,
On the Dissociation Energy of ArCO2+,
J. Chem. Phys., 1983, 78, 10, 6336, https://doi.org/10.1063/1.444561
. [all data]
Asher, Bellert, et al., 1994
Asher, R.L.; Bellert, D.; Buthelezi, T.; Brucat, P.J.,
The Bond Strength of Ni2+,
Chem. Phys. Lett., 1994, 224, 5-6, 529, https://doi.org/10.1016/0009-2614(94)00574-5
. [all data]
Kemper, Hsu, et al., 1991
Kemper, P.R.; Hsu, M.T.; Bowers, M.T.,
Transition - Metal Ion - Rare Gas Clusters: Bond Strengths and Molecular Parameters for Co+(He/Ne)n, Ni+(He/Ne)n, and Cr+(He/Ne/Ar),
J. Phys. Chem., 1991, 95, 26, 10600, https://doi.org/10.1021/j100179a022
. [all data]
Gatland, 1984, 2
Gatland, I.R.,
Swarms of Ions and Electrons in Gases, W. Lindinger, T. D. Mark and F. Howorka, eds. (Springer, New York, 1984, 1984, 44. [all data]
Gislason, 1984
Gislason, E.A.,
Quoted in I. R. Gatland in Swarms of Ions and Electrons in Gases, W. Lindinger, T. D. Mark and F. Howorka, eds. (Springer, New York, 1984, 1984, 44. [all data]
Viehland, 1984
Viehland, L.A.,
Interaction Potentials for Li+ - Rare - Gas Systems,
Chem. Phys., 1984, 78, 2, 279, https://doi.org/10.1016/0301-0104(83)85114-3
. [all data]
Takebe, 1983
Takebe, M.,
The Generalized Mobility Curve for Alkali Ions in Rare Gases: Clustering Reactions and Mobility Curves,
J. Chem. Phys., 1983, 78, 12, 7223, https://doi.org/10.1063/1.444763
. [all data]
Hiraoka and Mori, 1989, 2
Hiraoka, K.; Mori, T.,
Isotope Effect and Nature of Bonding in the Cluster Ions H3+(Ar)n and D3+(Ar)n,
J. Chem. Phys., 1989, 91, 8, 4821, https://doi.org/10.1063/1.456720
. [all data]
Wada, Kikkawa, et al., 2007
Wada, A.; Kikkawa, A.; Sugiyama, T.; Hiraoka, K.,
Thermochemical Stabilities of the Gas-phase Cluster Ions of Halide Ions with Rare Gas Atoms,
Int. J. Mass Spectrom.., 2007, 267, 1-3, 284-287, https://doi.org/10.1016/j.ijms.2007.02.053
. [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]
Bedford and Smith, 1990
Bedford, D.K.; Smith, D.,
Variable-temperature selected ion flow tube studies of the reactions of Ar+, Ar2+ and ArHn+ (n=1-3) ions with H2, HD and D2 at 300 K and 80 K,
Int. J. Mass Spectrom. Ion Proc., 1990, 98, 2, 179, https://doi.org/10.1016/0168-1176(90)85017-V
. [all data]
Linn, Brom, et al., 1985
Linn, S.H.; Brom, J.M., Jr.; Tzeng, W.-B.; Ng, C.Y.,
Photoionization study of HgAr,
J. Chem. Phys., 1985, 82, 648. [all data]
Dehmer and Pratt, 1982
Dehmer, P.M.; Pratt, S.T.,
Photoionization of ArKr, ArXe, and KrXe and bond dissociation energies of the rare gas dimer ions,
J. Chem. Phys., 1982, 77, 4804. [all data]
Ng, Tiedemann, et al., 1977
Ng, C.Y.; Tiedemann, P.W.; Mahan, B.H.; Lee, Y.T.,
Photoionization Studies of the Diatomic Internuclear Rare Gas Molecules XeKr, XeAr, and KrAr,
J. Chem. Phys., 1977, 66, 12, 5737, https://doi.org/10.1063/1.433848
. [all data]
McKnight and Sawina, 1973
McKnight, L.G.; Sawina, J.M.,
Equilibrium Constants and Binding Energies of Alkali Metal Ions with Inert Gases,
Bull. Am. Phys. Soc., 1973, 18, 804. [all data]
Cassidy and Elford, 1985
Cassidy, R.A.; Elford, M.T.,
The Mobility of Li+ Ions in Helium and Argon,
Aust. J. Phys., 1985, 38, 4, 587, https://doi.org/10.1071/PH850587
. [all data]
Keller, Beyer, et al., 1973
Keller, C.E.; Beyer, R.A.; Colonna-Romano, L.M.,
Clustering of Ar to Li+ and a Comparison of Drift - Tube Models,
Phys. Rev. A, 1973, 8, 3, 1446, https://doi.org/10.1103/PhysRevA.8.1446
. [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]
Haynes, Freysinger, et al., 1995
Haynes, C.L.; Freysinger, W.; Armentrout, P.B.,
Collision-induced dissociation of N3+(X3-) with Ne, Ar, Kr, and Xe,
Int. J. Mass Spectrom. Ion Processes, 1995, 149/150, 267. [all data]
Bowen and Eaton, 1988
Bowen, K.H.; Eaton, J.G.,
Photodetachment Spectroscopy of Negative Cluster Ions,
in The Structure of Small Molecules and Ions, Ed. R. Naaman, Z. Vager, Plenum NY, 1988, 1988, p.147-169. [all data]
Kim and Bowers, 1990
Kim, H.S.; Bowers, M.T.,
Energetics, Structure and Photodissociation Dynamics of the Cluster Ar.N2+,
J. Chem. Phys., 1990, 93, 2, 1158, https://doi.org/10.1063/1.459179
. [all data]
Hiraoka and Nakajima, 1988
Hiraoka, K.; Nakajima, G.,
A Determination of the Stabilities of N2+(N2)n and O2+(N2)n with n = 1 - 11 from Measurements of the Gas - Phase Ion Equilibria,
J. Chem. Phys., 1988, 88, 12, 7709, https://doi.org/10.1063/1.454285
. [all data]
Hiraoka, Mori, et al., 1992
Hiraoka, K.; Mori, T.; Yamabe, S.,
Gas-Phase Solvation of N2+ with Ar Atoms - A Charge Switch in the Reaction N2+(Ar)...Ar+(N2),
Chem. Phys. Lett., 1992, 189, 1, 7, https://doi.org/10.1016/0009-2614(92)85144-Y
. [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]
Arnold, Hendricks, et al., 1995
Arnold, S.T.; Hendricks, J.H.; Bowen, K.H.,
Photoelectron spectroscopy of the solvated anion clusters O-(Ar)(n=1-26,34): Energetics and structure,
J. Chem. Phys., 1995, 102, 1, 39, https://doi.org/10.1063/1.469415
. [all data]
Jones, Lister, et al., 1980
Jones, J.D.C.; Lister, D.G.; Twiddy, N.D.,
Equilibrium Constant for the Reaction Xe+ + 2Ar ---> XeAr+ + Ar in the Temperature Range 150 - 300 K and the Dissociation Energy of XeAr+,
Chem. Phys. Lett., 1980, 70, 3, 575, https://doi.org/10.1016/0009-2614(80)80128-X
. [all data]
Notes
Go To: Top, Gas phase ion energetics data, Ion clustering data, Mass spectrum (electron ionization), References
- Symbols used in this document:
IE (evaluated) Recommended ionization energy T Temperature ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions ΔrS° Entropy of reaction at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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