Propene

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Reaction thermochemistry data

Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), Gas Chromatography, 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:
B - John E. Bartmess
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
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. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

C3H5- + Hydrogen cation = Propene

By formula: C3H5- + H+ = C3H6

Quantity Value Units Method Reference Comment
Δr1636.4 ± 1.3kJ/molG+TSEllison, Davico, et al., 1996gas phase; calculated dSacid=24.2±1.0 eu; B
Δr1634. ± 4.2kJ/molD-EAWenthold, Polak, et al., 1996gas phase; B
Δr1635. ± 8.8kJ/molG+TSBartmess, Scott, et al., 1979gas phase; value altered from reference due to change in acidity scale; B
Δr1632.8 ± 2.7kJ/molG+TSMackay, Lien, et al., 1978gas phase; B
Quantity Value Units Method Reference Comment
Δr1605.8 ± 0.42kJ/molIMREEllison, Davico, et al., 1996gas phase; calculated dSacid=24.2±1.0 eu; B
Δr1606. ± 4.6kJ/molH-TSWenthold, Polak, et al., 1996gas phase; B
Δr1607. ± 8.4kJ/molIMREBartmess, Scott, et al., 1979gas phase; value altered from reference due to change in acidity scale; B
Δr1605.0 ± 2.1kJ/molIMREMackay, Lien, et al., 1978gas phase; B

Hydrogen bromide + Propene = Propane, 2-bromo-

By formula: HBr + C3H6 = C3H7Br

Quantity Value Units Method Reference Comment
Δr-85.48kJ/molCmLacher, Kianpour, et al., 1957gas phase; ALS
Δr-83.889kJ/molCmLacher, Lea, et al., 1950gas phase; Heat of hydrobromination at 367°K; ALS
Δr-84.10 ± 0.59kJ/molCmLacher, Walden, et al., 1950gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -84.4 ± 1.0 kJ/mol; Heat of hydrobromination; ALS

Propene + Hydrogen = Propane

By formula: C3H6 + H2 = C3H8

Quantity Value Units Method Reference Comment
Δr-123.4 ± 5.0kJ/molChydKistiakowsky and Nickle, 1951gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -124.9 ± 2.1 kJ/mol; ALS
Δr-125.0 ± 0.42kJ/molChydKistiakowsky, Ruhoff, et al., 1935gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -126.00 ± 0.054 kJ/mol; At 355 °K; ALS

C3H5- + Hydrogen cation = Propene

By formula: C3H5- + H+ = C3H6

Quantity Value Units Method Reference Comment
Δr1698. ± 8.4kJ/molBranDePuy, Gronert, et al., 1989gas phase; B
Δr>1693.5 ± 2.5kJ/molG+TSFroelicher, Freiser, et al., 1986gas phase; B
Quantity Value Units Method Reference Comment
Δr1665. ± 8.8kJ/molH-TSDePuy, Gronert, et al., 1989gas phase; B
Δr>1661.0kJ/molIMRBFroelicher, Freiser, et al., 1986gas phase; B

Hydrogen iodide + 1-Propene, 3-iodo- = Propene + Iodine

By formula: HI + C3H5I = C3H6 + I2

Quantity Value Units Method Reference Comment
Δr-33.3 ± 1.4kJ/molEqkRodgers, Golden, et al., 1966gas phase; ALS
Δr-39.7 ± 4.2kJ/molEqkRodgers, Golden, et al., 1966gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -34.9 ± 0.96 kJ/mol; At 527 K; ALS

Propane, 2-chloro- = Propene + Hydrogen chloride

By formula: C3H7Cl = C3H6 + HCl

Quantity Value Units Method Reference Comment
Δr72.4 ± 0.8kJ/molEqkNoren and Sunner, 1970gas phase; ALS
Δr73.72 ± 0.63kJ/molEqkKabo and Andreevskii, 1963gas phase; At 415.5 K; ALS
Δr73.0 ± 2.1kJ/molEqkHowlett, 1955gas phase; ALS

Cobalt ion (1+) + Propene = (Cobalt ion (1+) • Propene)

By formula: Co+ + C3H6 = (Co+ • C3H6)

Enthalpy of reaction

ΔrH° (kJ/mol) T (K) Method Reference Comment
180. (+7.1,-0.) CIDArmentrout and Kickel, 1994gas phase; guided ion beam CID; M
180. (+6.7,-0.) CIDHaynes and Armentrout, 1994gas phase; guided ion beam CID; M

C3H9Si+ + Propene = (C3H9Si+ • Propene)

By formula: C3H9Si+ + C3H6 = (C3H9Si+ • C3H6)

Quantity Value Units Method Reference Comment
Δr128.kJ/molPHPMSLi and Stone, 1989gas phase; condensation; M
Quantity Value Units Method Reference Comment
Δr178.J/mol*KPHPMSLi and Stone, 1989gas phase; condensation; M

Propene + Bromine = Propane, 1,2-dibromo-

By formula: C3H6 + Br2 = C3H6Br2

Quantity Value Units Method Reference Comment
Δr-122.5 ± 0.84kJ/molCmConn, Kistiakowsky, et al., 1938gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -123.1 ± 0.84 kJ/mol; At 355 °K; ALS

C3H5- + Hydrogen cation = Propene

By formula: C3H5- + H+ = C3H6

Quantity Value Units Method Reference Comment
Δr>1693.5 ± 3.8kJ/molG+TSFroelicher, Freiser, et al., 1986gas phase; B
Quantity Value Units Method Reference Comment
Δr>1661.0kJ/molIMRBFroelicher, Freiser, et al., 1986gas phase; B

Lithium ion (1+) + Propene = (Lithium ion (1+) • Propene)

By formula: Li+ + C3H6 = (Li+ • C3H6)

Quantity Value Units Method Reference Comment
Δr96.kJ/molICRStaley and Beauchamp, 1975gas phase; switching reaction(Li+)H2O, from graph; Dzidic and Kebarle, 1970 extrapolated; M

Rh+ + Propene = (Rh+ • Propene)

By formula: Rh+ + C3H6 = (Rh+ • C3H6)

Enthalpy of reaction

ΔrH° (kJ/mol) T (K) Method Reference Comment
118. CIDChen and Armetrout, 1995gas phase; ΔrH>=, guided ion beam CID; M

Iron ion (1+) + Propene = (Iron ion (1+) • Propene)

By formula: Fe+ + C3H6 = (Fe+ • C3H6)

Enthalpy of reaction

ΔrH° (kJ/mol) T (K) Method Reference Comment
145. (+7.1,-0.) CIDArmentrout and Kickel, 1994gas phase; guided ion beam CID; M

(CAS Reg. No. 25012-80-0 • 4294967295Propene) + Propene = CAS Reg. No. 25012-80-0

By formula: (CAS Reg. No. 25012-80-0 • 4294967295C3H6) + C3H6 = CAS Reg. No. 25012-80-0

Quantity Value Units Method Reference Comment
Δr45.2 ± 8.8kJ/molN/ADePuy, Gronert, et al., 1989gas phase; B

(CAS Reg. No. 59513-13-2 • 4294967295Propene) + Propene = CAS Reg. No. 59513-13-2

By formula: (CAS Reg. No. 59513-13-2 • 4294967295C3H6) + C3H6 = CAS Reg. No. 59513-13-2

Quantity Value Units Method Reference Comment
Δr61.1 ± 8.8kJ/molN/ADePuy, Gronert, et al., 1989gas phase; B

Propene + Hydrogen chloride = Propane, 2-chloro-

By formula: C3H6 + HCl = C3H7Cl

Quantity Value Units Method Reference Comment
Δr-73.39kJ/molEqkKabo and Andreevskii, 1963gas phase; At 385°K; ALS

Hydrogen iodide + Propene = Propane, 2-iodo-

By formula: HI + C3H6 = C3H7I

Quantity Value Units Method Reference Comment
Δr-86.27kJ/molEqkFuruyama, Golden, et al., 1969gas phase; ALS

Propene + Sulfuric Acid = isopropyl hydrogen sulphate

By formula: C3H6 + H2O4S = isopropyl hydrogen sulphate

Quantity Value Units Method Reference Comment
Δr-38. ± 0.8kJ/molEqkEntelis, Korovina, et al., 1960liquid phase; ALS

1,2-Diiodopropane = Propene + Iodine

By formula: C3H6I2 = C3H6 + I2

Quantity Value Units Method Reference Comment
Δr47. ± 2.kJ/molEqkBenson and Amano, 1962gas phase; ALS

Propane, 2-bromo- = Hydrogen bromide + Propene

By formula: C3H7Br = HBr + C3H6

Quantity Value Units Method Reference Comment
Δr81. ± 2.kJ/molEqkRozhnov and Andreevskii, 1962gas phase; ALS

Propene + 2-Propanone, 1,1,1,3,3,3-hexafluoro- = 4-Penten-2-ol, 1,1,1-trifluoro-2-(trifluoromethyl)-

By formula: C3H6 + C3F6O = C6H6F6O

Quantity Value Units Method Reference Comment
Δr-78.2 ± 4.2kJ/molEqkMoore, 1971gas phase; ALS

Gold ion (1+) + Propene = (Gold ion (1+) • Propene)

By formula: Au+ + C3H6 = (Au+ • C3H6)

Quantity Value Units Method Reference Comment
Δr>310.kJ/molIMRBSchroeder, Hrusak, et al., 1995RCD

Gas phase ion energetics data

Go To: Top, Reaction thermochemistry data, Mass spectrum (electron ionization), Gas Chromatography, 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:
B - John E. Bartmess
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 C3H6+ (ion structure unspecified)

Quantity Value Units Method Reference Comment
IE (evaluated)9.73 ± 0.01eVN/AN/AL
Quantity Value Units Method Reference Comment
Proton affinity (review)751.6kJ/molN/AHunter and Lias, 1998HL
Quantity Value Units Method Reference Comment
Gas basicity722.7kJ/molN/AHunter and Lias, 1998HL

Ionization energy determinations

IE (eV) Method Reference Comment
9.73PITraeger, 1984LBLHLM
9.69 ± 0.09EISelim, 1980LLK
9.73 ± 0.02PIWood and Taylor, 1979LLK
9.7 ± 0.1PEBieri, Burger, et al., 1977LLK
9.73 ± 0.01PIKrassig, Reinke, et al., 1974LLK
9.744 ± 0.003PEMasclet, Grosjean, et al., 1973LLK
9.72PEKatrib and Rabalais, 1973LLK
9.72EILossing, 1972LLK
9.74PEFrost and Sandhu, 1971LLK
9.74 ± 0.01PIPerson and Nicole, 1970RDSH
9.69PEDewar and Worley, 1969RDSH
9.76CICermak, 1968RDSH
9.727 ± 0.010PINicholson, 1965RDSH
9.74SSamson, Marmo, et al., 1962RDSH
9.73 ± 0.02PISteiner, Giese, et al., 1961RDSH
9.73PIBralsford, Harris, et al., 1960RDSH
9.73 ± 0.01PIWatanabe, 1957RDSH
9.91 ± 0.01PEKrause, Taylor, et al., 1978Vertical value; LLK
10.2PEKobayashi, 1978Vertical value; LLK
10.03PEKimura, Katsumata, et al., 1975Vertical value; LLK
10.2PEWhite, Carlson, et al., 1974Vertical value; LLK
9.70PEHentrich, Gunkel, et al., 1974Vertical value; LLK
9.9PEWeidner and Schweig, 1972Vertical value; LLK
9.86PEMollere, Bock, et al., 1972Vertical value; LLK

Appearance energy determinations

Ion AE (eV) Other Products MethodReferenceComment
C+24.5 ± 0.5?EIPeers and Vigny, 1968RDSH
CH+22.5 ± 0.5?EIPeers and Vigny, 1968RDSH
CH2+17.0 ± 0.5?EIPeers and Vigny, 1968RDSH
CH3+14.9C2H3EIHaney and Franklin, 1968RDSH
CH4+14.7 ± 0.5?EIPeers and Vigny, 1968RDSH
C2+28. ± 1.?EIPeers and Vigny, 1968RDSH
C2H+21. ± 1.?EIPeers and Vigny, 1968RDSH
C2H2+12.92 ± 0.05CH4PIKrassig, Reinke, et al., 1974LLK
C2H2+13.6 ± 0.5CH4EIPeers and Vigny, 1968RDSH
C2H2+14.1CH4EIHaney and Franklin, 1968RDSH
C2H3+13.78 ± 0.03CH3EISelim, 1980LLK
C2H3+13.20 ± 0.04CH3PIKrassig, Reinke, et al., 1974LLK
C2H3+13.7 ± 0.5CH3EIPeers and Vigny, 1968RDSH
C2H4+12.4 ± 0.5?EIPeers and Vigny, 1968RDSH
C2H5+12.6 ± 0.5?EIPeers and Vigny, 1968RDSH
C3+27. ± 1.?EIPeers and Vigny, 1968RDSH
C3H+20.5 ± 0.52H2+HEIPeers and Vigny, 1968RDSH
C3H+20.2 ± 0.52H2+HEIHarrison and Tait, 1962RDSH
C3H2+47. ± 1.?EIPeers and Vigny, 1968RDSH
C3H2+17. ± 1.2H2EIPeers and Vigny, 1968RDSH
C3H3+14.21 ± 0.09H2+HEISelim, 1980LLK
C3H3+13.19 ± 0.05H2+HPIKrassig, Reinke, et al., 1974LLK
C3H3+14.3 ± 0.5H2+HEIPeers and Vigny, 1968RDSH
C3H3+14.21H2+HEIOmura, 1962RDSH
C3H4+11.91 ± 0.03H2PIKrassig, Reinke, et al., 1974LLK
C3H4+12.3 ± 0.5H2EIPeers and Vigny, 1968RDSH
C3H4+12.52H2EIOmura, 1961RDSH
C3H5+11.86HPITraeger, 1984LBLHLM
C3H5+11.90 ± 0.05HEISelim, 1980LLK
C3H5+11.78HPIButtrill, Williamson, et al., 1975LLK
C3H5+11.88 ± 0.03HPIKrassig, Reinke, et al., 1974LLK
C3H5+11.88HEILossing, 1971LLK
C3H22+33.3 ± 0.5?EIPeers and Vigny, 1968RDSH
C3H52+31.1 ± 0.5HEIPeers and Vigny, 1968RDSH
H+20. ± 1.?EIPeers and Vigny, 1968RDSH
H2+16. ± 1.?EIPeers and Vigny, 1968RDSH

De-protonation reactions

C3H5- + Hydrogen cation = Propene

By formula: C3H5- + H+ = C3H6

Quantity Value Units Method Reference Comment
Δr1636.4 ± 1.3kJ/molG+TSEllison, Davico, et al., 1996gas phase; calculated dSacid=24.2±1.0 eu; B
Δr1634. ± 4.2kJ/molD-EAWenthold, Polak, et al., 1996gas phase; B
Δr1635. ± 8.8kJ/molG+TSBartmess, Scott, et al., 1979gas phase; value altered from reference due to change in acidity scale; B
Δr1632.8 ± 2.7kJ/molG+TSMackay, Lien, et al., 1978gas phase; B
Quantity Value Units Method Reference Comment
Δr1605.8 ± 0.42kJ/molIMREEllison, Davico, et al., 1996gas phase; calculated dSacid=24.2±1.0 eu; B
Δr1606. ± 4.6kJ/molH-TSWenthold, Polak, et al., 1996gas phase; B
Δr1607. ± 8.4kJ/molIMREBartmess, Scott, et al., 1979gas phase; value altered from reference due to change in acidity scale; B
Δr1605.0 ± 2.1kJ/molIMREMackay, Lien, et al., 1978gas phase; B

C3H5- + Hydrogen cation = Propene

By formula: C3H5- + H+ = C3H6

Quantity Value Units Method Reference Comment
Δr1698. ± 8.4kJ/molBranDePuy, Gronert, et al., 1989gas phase; B
Δr>1693.5 ± 2.5kJ/molG+TSFroelicher, Freiser, et al., 1986gas phase; B
Quantity Value Units Method Reference Comment
Δr1665. ± 8.8kJ/molH-TSDePuy, Gronert, et al., 1989gas phase; B
Δr>1661.0kJ/molIMRBFroelicher, Freiser, et al., 1986gas phase; B

C3H5- + Hydrogen cation = Propene

By formula: C3H5- + H+ = C3H6

Quantity Value Units Method Reference Comment
Δr>1693.5 ± 3.8kJ/molG+TSFroelicher, Freiser, et al., 1986gas phase; B
Quantity Value Units Method Reference Comment
Δr>1661.0kJ/molIMRBFroelicher, Freiser, et al., 1986gas phase; B

Mass spectrum (electron ionization)

Go To: Top, Reaction thermochemistry data, Gas phase ion energetics data, Gas Chromatography, 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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NIST MS number 50

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Gas Chromatography

Go To: Top, Reaction thermochemistry data, 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 by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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Column type Active phase Temperature (C) I Reference Comment
PackedPorapack Q100.292.Ji, Majors, et al., 1999 
CapillaryCP Sil 5 CB20.294.Do and Raulin, 199225. m/0.15 mm/2. μm, H2
CapillaryPoraPLOT Q160.300.Do and Raulin, 198910. m/0.32 mm/10. μm, H2
CapillaryOV-120.289.Nijs and Jacobs, 1981He; Column length: 150. m; Column diameter: 0.50 mm
CapillarySqualane50.283.3Schröder, 1980 
PackedSqualane80.287.Chrétien and Dubois, 1977 
CapillarySqualane40.289.Matukuma, 1969N2; Column length: 91.4 m; Column diameter: 0.25 mm
PackedSqualane27.287.Hively and Hinton, 1968He, Chromosorb P; Column length: 15. m; Column diameter: 0.25 mm
PackedSqualane49.287.Hively and Hinton, 1968He, Chromosorb P; Column length: 15. m; Column diameter: 0.25 mm
PackedSqualane67.288.Hively and Hinton, 1968He, Chromosorb P; Column length: 15. m; Column diameter: 0.25 mm
PackedSqualane86.288.Hively and Hinton, 1968He, Chromosorb P; Column length: 15. m; Column diameter: 0.25 mm
PackedSqualane26.289.Zulaïca and Guiochon, 1966Column length: 10. m

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

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Column type Active phase I Reference Comment
CapillaryPetrocol DH-100283.Haagen-Smit Laboratory, 1997He; Column length: 100. m; Column diameter: 0.2 mm; Program: 5C(10min) => 5C/min => 50C(48min) => 1.5C/min => 195C(91min)
CapillaryDB-1290.Hoekman, 199360. m/0.32 mm/1.0 μm, He; Program: -40 C for 12 min; -40 - 125 C at 3 deg.min; 125-185 C at 6 deg/min; 185 - 220 C at 20 deg/min; hold 220 C for 2 min

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

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Column type Active phase I Reference Comment
CapillaryChromosorb 101295.Voorhees, Hileman, et al., 197510. K/min; Tstart: 0. C; Tend: 220. C

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

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Column type Active phase I Reference Comment
PackedSE-30294.Peng, Ding, et al., 1988Supelcoport; Chromosorb; Column length: 3.05 m; Program: 40C(5min) => 10C/min => 200C or 250C (60min)

Normal alkane RI, non-polar column, temperature ramp

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Column type Active phase I Reference Comment
CapillaryPolydimethyl siloxane: CP-Sil 5 CB286.Bramston-Cook, 201360. m/0.25 mm/1.0 μm, Helium, 45. C @ 1.45 min, 3.6 K/min, 210. C @ 2.72 min
CapillaryPetrocol DH294.Supelco, 2012100. m/0.25 mm/0.50 μm, Helium, 20. C @ 15. min, 15. K/min, 220. C @ 30. min
CapillaryUltra-ALLOY-5295.Tsuge, Ohtan, et al., 201130. m/0.25 mm/0.25 μm, 40. C @ 2. min, 20. K/min, 320. C @ 13. min
CapillaryUltra-ALLOY-5295.Tsuge, Ohtan, et al., 201130. m/0.25 mm/0.25 μm, 40. C @ 2. min, 20. K/min, 320. C @ 13. min
CapillaryUltra-ALLOY-5295.Tsuge, Ohtan, et al., 201130. m/0.25 mm/0.25 μm, 40. C @ 2. min, 20. K/min, 320. C @ 13. min
CapillaryUltra-ALLOY-5295.Tsuge, Ohtan, et al., 201130. m/0.25 mm/0.25 μm, 40. C @ 2. min, 20. K/min, 320. C @ 13. min
CapillaryUltra-ALLOY-5298.Tsuge, Ohtan, et al., 201130. m/0.25 mm/0.25 μm, 40. C @ 2. min, 20. K/min, 320. C @ 13. min
CapillaryOV-101290.Chupalov and Zenkevich, 1996N2, 3. K/min; Column length: 52. m; Column diameter: 0.26 mm; Tstart: 50. C; Tend: 220. C

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

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Column type Active phase I Reference Comment
CapillaryMethyl Silicone288.Chen and Feng, 2007Program: not specified
CapillaryMethyl Silicone290.Blunden, Aneja, et al., 200560. 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)
CapillaryMethyl Silicone290.Zenkevich, 2000Program: not specified
CapillarySPB-1283.Flanagan, Streete, et al., 199760. m/0.53 mm/5. μm, He; Program: 40C(6min) => 5C/min => 80C => 10C/min => 200C
CapillaryPolydimethyl siloxanes290.Zenkevich, Chupalov, et al., 1996Program: not specified
CapillaryPolydimethyl siloxanes290.Zenkevich and Chupalov, 1996Program: not specified
CapillarySPB-1283.Strete, Ruprah, et al., 199260. m/0.53 mm/5.0 μm, Helium; Program: 40 0C (6 min) 5 0C/min -> 80 0C 10 0C/min -> 200 0C
CapillarySPB-1310.Strete, Ruprah, et al., 199260. m/0.53 mm/5.0 μm, Helium; Program: not specified
PackedApieson L280.Kojima, Fujii, et al., 1980Chromosorb W; Column length: 20. m; Program: not specified
PackedSE-30290.Robinson and Odell, 1971N2, Chromosorb W; Column length: 6.1 m; Program: 50C910min) => 20C/min => 90(6min) => 10C/min => 150C(hold)

References

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

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Ellison, Davico, et al., 1996
Ellison, G.B.; Davico, G.E.; Bierbaum, V.M.; DePuy, C.H., Thermochemistry of theb Benzyl and Allyl Radicals and Ions, Int. J. Mass Spectrom. Ion Proc., 1996, 156, 1-2, 109-131, https://doi.org/10.1016/S0168-1176(96)04383-2 . [all data]

Wenthold, Polak, et al., 1996
Wenthold, P.G.; Polak, M.L.; Lineberger, W.C., Photoelectron Spectroscopy of the Allyl and 2-Methylallyl Anions, J. Phys. Chem., 1996, 100, 17, 6920, https://doi.org/10.1021/jp953401n . [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]

Mackay, Lien, et al., 1978
Mackay, G.I.; Lien, M.H.; Hopkinson, A.C.; Bohme, D.K., Experimental and theoretical studies of proton removal from propene, Can. J. Chem., 1978, 56, 131. [all data]

Lacher, Kianpour, et al., 1957
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Notes

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