Formic acid

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Gas phase thermochemistry data

Go To: Top, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics 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 as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DRB - Donald R. Burgess, Jr.
GT - Glushko Thermocenter, Russian Academy of Sciences, Moscow

Quantity Value Units Method Reference Comment
Δfgas-378.6kJ/molCmGuthrie, 1974Heat of hydrolysis; ALS
Δfgas-379.0kJ/molN/ALebedeva, 1964Value computed using ΔfHliquid° value of -425.5±0.3 kj/mol from Lebedeva, 1964 and ΔvapH° value of 46.5 kj/mol from Guthrie, 1974.; DRB
Δfgas-379.2 ± 0.6kJ/molCcbLebedeva, 1964Value computed using ΔfHliquid° from Lebedeva, 1964 and ΔvapH° value of 46.3 kJ/mol from Konicek and Wadso, 1970.; DRB
Δfgas-378.3kJ/molN/ASinke, 1959Value computed using ΔfHliquid° value of -424.8±0.3 kj/mol from Sinke, 1959 and ΔvapH° value of 46.5 kj/mol from Guthrie, 1974.; DRB
Δfgas-378.5 ± 0.6kJ/molCcbSinke, 1959Value computed using ΔfHliquid° from Sinke, 1959 and ΔvapH° value of 46.3 kJ/mol from Konicek and Wadso, 1970.; DRB
Quantity Value Units Method Reference Comment
gas248.70 ± 0.42J/mol*KN/AMillikan R.C., 1957Other third-law S(298.15 K) value is 248.11(1.26) J/mol*K [ Halford J.O., 1942, Millikan R.C., 1957]. Please also see Waring W., 1952.; GT

Constant pressure heat capacity of gas

Cp,gas (J/mol*K) Temperature (K) Reference Comment
33.2650.Chao J., 1986p=1 bar. Selected entropies and heat capacities are in close agreement with statistically calculated values [ Fukushima K., 1971] and value of S(298.15 K) calculated by ab initio method [ East A.L.L., 1997]. Maximum discrepancies with other statistical calculations [ Waring W., 1952, Green J.H.S., 1961, Gurvich, Veyts, et al., 1989] amount to 1.1-3.9 J/mol*K for S(T) and 3.0-5.9 J/mol*K for Cp(T). Please also see Chao J., 1978.; GT
33.44100.
34.91150.
37.83200.
43.54273.15
45.68 ± 0.07298.15
45.84300.
54.52400.
62.63500.
69.81600.
76.04700.
81.34800.
85.77900.
89.401000.
92.331100.
94.651200.
96.481300.
97.911400.
99.021500.

Condensed phase thermochemistry data

Go To: Top, Gas phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics 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 as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing

Quantity Value Units Method Reference Comment
Δfliquid-425.09kJ/molCmGuthrie, 1974Heat of hydrolysis; ALS
Δfliquid-425.5 ± 0.3kJ/molCcbLebedeva, 1964ALS
Δfliquid-424.8 ± 0.3kJ/molCcbSinke, 1959ALS
Quantity Value Units Method Reference Comment
Δcliquid-253.8 ± 0.3kJ/molCcbLebedeva, 1964Corresponding Δfliquid = -425.51 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS
Δcliquid-254.6 ± 0.3kJ/molCcbSinke, 1959Corresponding Δfliquid = -424.72 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS
Quantity Value Units Method Reference Comment
liquid131.84J/mol*KN/AStout and Fisher, 1941Includes 2.89 J/mol*K for zero-point entropy.; DH
liquid128.4J/mol*KN/AParks, Kelley, et al., 1929Extrapolation below 90 K, 29.7 J/mol*K. Revision of previous data.; DH
liquid143.1J/mol*KN/AGibson, Latimer, et al., 1920Used Berthelot's value, 10125 J/mol for H fusion. Extrapolation below 70 K, no details.; DH

Constant pressure heat capacity of liquid

Cp,liquid (J/mol*K) Temperature (K) Reference Comment
99.04298.15Stout and Fisher, 1941T = 15 to 300 K.; DH
98.10298.15Glagoleva and Chervov, 1936Temperature range: 298.15, 333.15, 353.15 K.; DH
100.0290.Radulescu and Jula, 1934DH
98.3291.5Gibson, Latimer, et al., 1920T = 71 to 292 K. Value is unsmoothed experimental datum.; DH
95.4298.von Reis, 1881T = 291 to 385 K.; DH

Phase change data

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Reaction thermochemistry data, Gas phase ion energetics 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 as indicated in comments:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing

Quantity Value Units Method Reference Comment
Tboil373.9 ± 0.5KAVGN/AAverage of 25 out of 30 values; Individual data points
Quantity Value Units Method Reference Comment
Tfus281.5 ± 0.6KAVGN/AAverage of 9 values; Individual data points
Quantity Value Units Method Reference Comment
Ttriple281.45KN/AWilhoit, Chao, et al., 1985Uncertainty assigned by TRC = 0.1 K; TRC
Ttriple281.40KN/AStout and Fisher, 1941, 2Uncertainty assigned by TRC = 0.06 K; TRC
Quantity Value Units Method Reference Comment
Ptriple0.0236barN/ATaylor and Bruton, 1952Uncertainty assigned by TRC = 0.000067 bar; TRC
Quantity Value Units Method Reference Comment
Tc577.KN/AAnselme and Teja, 1990Uncertainty assigned by TRC = 30. K; Tc > 577 K, which was observed with decomposition; TRC
Tc588.KN/AAmbrose and Ghiassee, 1987Uncertainty assigned by TRC = 10. K; TRC
Tc580.KN/AMajer and Svoboda, 1985 
Quantity Value Units Method Reference Comment
Δvap46.3kJ/molN/AMajer and Svoboda, 1985 
Δvap36.0kJ/molAStephenson and Malanowski, 1987Based on data from 283. to 384. K.; AC
Δvap46.3 ± 0.5kJ/molCKonicek and Wadso, 1970ALS
Δvap46.3 ± 0.5kJ/molCKonicek, Wadsö, et al., 1970AC
Δvap19.9kJ/molN/AStout and Fisher, 1941, 3AC

Enthalpy of vaporization

ΔvapH (kJ/mol) Temperature (K) Method Reference Comment
22.69373.8N/AMajer and Svoboda, 1985 
35.2315.EBAmbrose and Ghiassee, 1987, 2Based on data from 300. to 392. K.; AC
35.2325.N/ADreisbach and Shrader, 1949Based on data from 310. to 374. K. See also Dreisbach and Martin, 1949.; AC
29.6303.N/ACampbell and Campbell, 1934AC
20.3315.N/ACoolidge, 1930Based on data from 273. to 373. K.; AC
20.9338.N/ACoolidge, 1930Based on data from 273. to 373. K.; AC
20.4315.CCoolidge, 1930AC
21.1338.CCoolidge, 1930AC
36.8288.N/AKahlbaum, 1894Based on data from 273. to 307. K.; AC
47.7374.N/AKahlbaum, 1883Based on data from 295. to 374. K.; AC

Enthalpy of vaporization

ΔvapH = A exp(-αTr) (1 − Tr)β
    ΔvapH = Enthalpy of vaporization (at saturation pressure) (kJ/mol)
    Tr = reduced temperature (T / Tc)

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Temperature (K) 298. to 374.
A (kJ/mol) 23.8
α 2.1043
β -1.2652
Tc (K) 580.
ReferenceMajer and Svoboda, 1985

Antoine Equation Parameters

log10(P) = A − (B / (T + C))
    P = vapor pressure (bar)
    T = temperature (K)

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Temperature (K) A B C Reference Comment
273.7 to 307.42.00121515.-139.408Kahlbaum, 1894, 2Coefficents calculated by NIST from author's data.

Enthalpy of sublimation

ΔsubH (kJ/mol) Temperature (K) Method Reference Comment
60.5275.N/AStephenson and Malanowski, 1987Based on data from 268. to 281. K.; AC
62. ± 1.213.TE,MECalis-Van Ginkel, Calis, et al., 1978Based on data from 203. to 218. K.; AC
60.1264.AStull, 1947Based on data from 253. to 275. K.; AC
60.7266.N/ACoolidge, 1930Based on data from 265. to 268. K. See also Jones, 1960.; AC

Enthalpy of fusion

ΔfusH (kJ/mol) Temperature (K) Reference Comment
12.678281.40Stout and Fisher, 1941DH

Entropy of fusion

ΔfusS (J/mol*K) Temperature (K) Reference Comment
45.05281.40Stout and Fisher, 1941DH

In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products:


Reaction thermochemistry data

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics 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 as indicated in comments:
B - John E. Bartmess
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias

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

Chlorine anion + Formic acid = (Chlorine anion • Formic acid)

By formula: Cl- + CH2O2 = (Cl- • CH2O2)

Quantity Value Units Method Reference Comment
Δr115. ± 8.4kJ/molTDAsFrench, Ikuta, et al., 1982gas phase; B,M
Δr116. ± 8.8kJ/molCIDTWalker and Sunderlin, 1999gas phase; B
Δr107. ± 8.4kJ/molIMRELarson and McMahon, 1984gas phase; B,M
Δr156. ± 8.4kJ/molTDAsYamdagni and Kebarle, 1971gas phase; In serious disagreement with other's values. Source of error not obvious.; B,M
Quantity Value Units Method Reference Comment
Δr103.J/mol*KPHPMSFrench, Ikuta, et al., 1982gas phase; M
Δr101.J/mol*KN/ALarson and McMahon, 1984, 2gas phase; switching reaction(Cl-)t-C4H9OH, Entropy change calculated or estimated; French, Ikuta, et al., 1982; M
Δr166.J/mol*KPHPMSYamdagni and Kebarle, 1971gas phase; M
Quantity Value Units Method Reference Comment
Δr84.1 ± 8.4kJ/molTDAsFrench, Ikuta, et al., 1982gas phase; B
Δr77.0 ± 8.4kJ/molIMRELarson and McMahon, 1984gas phase; B,M
Δr106. ± 8.4kJ/molTDAsYamdagni and Kebarle, 1971gas phase; In serious disagreement with other's values. Source of error not obvious.; B

HCO2 anion + Hydrogen cation = Formic acid

By formula: CHO2- + H+ = CH2O2

Quantity Value Units Method Reference Comment
Δr1449. ± 5.0kJ/molD-EAKim, Bradforth, et al., 1995gas phase; dHacid(0K) = 344.67±0.62 kcal/mol; B
Δr1445. ± 9.2kJ/molG+TSCaldwell, Renneboog, et al., 1989gas phase; B
Δr1445. ± 9.2kJ/molG+TSFujio, McIver, et al., 1981gas phase; value altered from reference due to change in acidity scale; B
Δr1444. ± 12.kJ/molG+TSCumming and Kebarle, 1978gas phase; B
Δr1423. ± 19.kJ/molEIAEMuftakhov, Vasil'ev, et al., 1999gas phase; B
Quantity Value Units Method Reference Comment
Δr1419. ± 6.3kJ/molH-TSKim, Bradforth, et al., 1995gas phase; dHacid(0K) = 344.67±0.62 kcal/mol; B
Δr1415. ± 8.4kJ/molIMRECaldwell, Renneboog, et al., 1989gas phase; B
Δr1416. ± 8.4kJ/molIMREFujio, McIver, et al., 1981gas phase; value altered from reference due to change in acidity scale; B
Δr1415. ± 8.4kJ/molIMRECumming and Kebarle, 1978gas phase; B

Fluorine anion + Formic acid = (Fluorine anion • Formic acid)

By formula: F- + CH2O2 = (F- • CH2O2)

Quantity Value Units Method Reference Comment
Δr190. ± 8.4kJ/molIMRELarson and McMahon, 1983gas phase; These relative affinities are ca. 10 kcal/mol weaker than threshold values (see Wenthold and Squires, 1995) for donors greater than ca. 27 kcal/mol in free energy. This discrepancy has not yet been resolved, though the stronger value appears preferable.; B,M
Quantity Value Units Method Reference Comment
Δr101.J/mol*KN/ALarson and McMahon, 1983gas phase; switching reaction(F-)H2O, Entropy change calculated or estimated; Arshadi, Yamdagni, et al., 1970; M
Quantity Value Units Method Reference Comment
Δr159. ± 8.4kJ/molIMRELarson and McMahon, 1983gas phase; These relative affinities are ca. 10 kcal/mol weaker than threshold values (see Wenthold and Squires, 1995) for donors greater than ca. 27 kcal/mol in free energy. This discrepancy has not yet been resolved, though the stronger value appears preferable.; B,M

CH5O+ + Formic acid = (CH5O+ • Formic acid)

By formula: CH5O+ + CH2O2 = (CH5O+ • CH2O2)

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

Quantity Value Units Method Reference Comment
Δr134.kJ/molICRLarson and McMahon, 1982gas 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
Δr116.J/mol*KN/ALarson and McMahon, 1982gas 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
Δr99.6kJ/molICRLarson and McMahon, 1982gas 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

Iodide + Formic acid = (Iodide • Formic acid)

By formula: I- + CH2O2 = (I- • CH2O2)

Quantity Value Units Method Reference Comment
Δr79.1 ± 4.2kJ/molTDAsCaldwell and Kebarle, 1984gas phase; B,M
Δr54.0 ± 8.8kJ/molCIDTWalker and Sunderlin, 1999gas phase; Authors suggest real value somewhere between this and Caldwell and Kebarle, 1984; B
Quantity Value Units Method Reference Comment
Δr86.6J/mol*KPHPMSCaldwell and Kebarle, 1984gas phase; M
Quantity Value Units Method Reference Comment
Δr53.1 ± 4.2kJ/molTDAsCaldwell and Kebarle, 1984gas phase; B

(Chlorine anion • Formic acid) + Formic acid = (Chlorine anion • 2Formic acid)

By formula: (Cl- • CH2O2) + CH2O2 = (Cl- • 2CH2O2)

Quantity Value Units Method Reference Comment
Δr46.9 ± 8.8kJ/molCIDTWalker and Sunderlin, 1999gas phase; B
Δr143. ± 13.kJ/molN/ALuczynski, Wlodek, et al., 1978gas phase; Buffer gas: H2. Value too bound based on French, Ikuta, et al., 1982, by Grimsrud fractionation factor ( Williamson, Knighton, et al., 1996).; B,M
Quantity Value Units Method Reference Comment
Δr230.J/mol*KHPMSLuczynski, Wlodek, et al., 1978gas phase; Entropy change is questionable; M

(Chlorine anion • 4Formic acid) + Formic acid = (Chlorine anion • 5Formic acid)

By formula: (Cl- • 4CH2O2) + CH2O2 = (Cl- • 5CH2O2)

Quantity Value Units Method Reference Comment
Δr42.3 ± 8.4kJ/molN/ALuczynski, Wlodek, et al., 1978gas phase; Buffer gas: H2. Value too bound based on French, Ikuta, et al., 1982, by Grimsrud fractionation factor ( Williamson, Knighton, et al., 1996).; B,M
Quantity Value Units Method Reference Comment
Δr48.1J/mol*KHPMSLuczynski, Wlodek, et al., 1978gas phase; Entropy change is questionable; M

(Chlorine anion • 2Formic acid) + Formic acid = (Chlorine anion • 3Formic acid)

By formula: (Cl- • 2CH2O2) + CH2O2 = (Cl- • 3CH2O2)

Quantity Value Units Method Reference Comment
Δr93. ± 11.kJ/molN/ALuczynski, Wlodek, et al., 1978gas phase; Buffer gas: H2. Value too bound based on French, Ikuta, et al., 1982, by Grimsrud fractionation factor ( Williamson, Knighton, et al., 1996).; B,M
Quantity Value Units Method Reference Comment
Δr150.J/mol*KHPMSLuczynski, Wlodek, et al., 1978gas phase; Entropy change is questionable; M

HCO2 anion + Formic acid = (HCO2 anion • Formic acid)

By formula: CHO2- + CH2O2 = (CHO2- • CH2O2)

Quantity Value Units Method Reference Comment
Δr154. ± 4.2kJ/molN/AMeot-Ner and Sieck, 1986gas phase; B,M
Quantity Value Units Method Reference Comment
Δr164.J/mol*KPHPMSMeot-Ner and Sieck, 1986gas phase; large ΔrH, ΔrS,; cyclic structure? pyrolysis?; M
Quantity Value Units Method Reference Comment
Δr105. ± 6.7kJ/molTDAsMeot-Ner and Sieck, 1986gas phase; B

(HCO2 anion • 4Formic acid) + Formic acid = (HCO2 anion • 5Formic acid)

By formula: (CHO2- • 4CH2O2) + CH2O2 = (CHO2- • 5CH2O2)

Quantity Value Units Method Reference Comment
Δr42.3 ± 8.4kJ/molN/ALuczynski, Wlodek, et al., 1978gas phase; Buffer gas H2. There may be appreciable fractionation of neutral gases: Williamson, Knighton, et al., 1996; B,M
Quantity Value Units Method Reference Comment
Δr50.J/mol*KHPMSLuczynski, Wlodek, et al., 1978gas phase; Entropy change is questionable; M

(Chlorine anion • 3Formic acid) + Formic acid = (Chlorine anion • 4Formic acid)

By formula: (Cl- • 3CH2O2) + CH2O2 = (Cl- • 4CH2O2)

Quantity Value Units Method Reference Comment
Δr59.0 ± 9.2kJ/molN/ALuczynski, Wlodek, et al., 1978gas phase; Buffer gas: H2. Value too bound based on French, Ikuta, et al., 1982, by Grimsrud fractionation factor ( Williamson, Knighton, et al., 1996).; B,M
Quantity Value Units Method Reference Comment
Δr84.J/mol*KHPMSLuczynski, Wlodek, et al., 1978gas phase; M

(HCO2 anion • 3Formic acid) + Formic acid = (HCO2 anion • 4Formic acid)

By formula: (CHO2- • 3CH2O2) + CH2O2 = (CHO2- • 4CH2O2)

Quantity Value Units Method Reference Comment
Δr59.4 ± 8.8kJ/molN/ALuczynski, Wlodek, et al., 1978gas phase; Buffer gas H2. There may be appreciable fractionation of neutral gases: Williamson, Knighton, et al., 1996; B,M
Quantity Value Units Method Reference Comment
Δr90.0J/mol*KHPMSLuczynski, Wlodek, et al., 1978gas phase; M

(HCO2 anion • 2Formic acid) + Formic acid = (HCO2 anion • 3Formic acid)

By formula: (CHO2- • 2CH2O2) + CH2O2 = (CHO2- • 3CH2O2)

Quantity Value Units Method Reference Comment
Δr84. ± 11.kJ/molN/ALuczynski, Wlodek, et al., 1978gas phase; Buffer gas H2. There may be appreciable fractionation of neutral gases: Williamson, Knighton, et al., 1996; B,M
Quantity Value Units Method Reference Comment
Δr130.J/mol*KHPMSLuczynski, Wlodek, et al., 1978gas phase; M

(HCO2 anion • Formic acid) + Formic acid = (HCO2 anion • 2Formic acid)

By formula: (CHO2- • CH2O2) + CH2O2 = (CHO2- • 2CH2O2)

Quantity Value Units Method Reference Comment
Δr109. ± 13.kJ/molN/ALuczynski, Wlodek, et al., 1978gas phase; Buffer gas H2. There may be appreciable fractionation of neutral gases: Williamson, Knighton, et al., 1996; B,M
Quantity Value Units Method Reference Comment
Δr140.J/mol*KHPMSLuczynski, Wlodek, et al., 1978gas phase; M

CH6N+ + Formic acid = (CH6N+ • Formic acid)

By formula: CH6N+ + CH2O2 = (CH6N+ • CH2O2)

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

Quantity Value Units Method Reference Comment
Δr79.5kJ/molPHPMSMeot-Ner, 1984gas phase; M
Quantity Value Units Method Reference Comment
Δr101.J/mol*KPHPMSMeot-Ner, 1984gas phase; M

CH2NO5- + Water + Formic acid = CH4NO6-

By formula: CH2NO5- + H2O + CH2O2 = CH4NO6-

Quantity Value Units Method Reference Comment
Δr18.4 ± 0.84kJ/molIMREViidanoja, Reiner, et al., 2000gas phase; B

Bromine anion + Formic acid = CH2BrO2-

By formula: Br- + CH2O2 = CH2BrO2-

Quantity Value Units Method Reference Comment
Δr72.0 ± 7.1kJ/molCIDTWalker and Sunderlin, 1999gas phase; B

CH2IO2- + 2Formic acid = C2H4IO4-

By formula: CH2IO2- + 2CH2O2 = C2H4IO4-

Quantity Value Units Method Reference Comment
Δr41.8 ± 8.8kJ/molCIDTWalker and Sunderlin, 1999gas phase; B

NO3 anion + Formic acid = CH2NO5-

By formula: NO3- + CH2O2 = CH2NO5-

Quantity Value Units Method Reference Comment
Δr47.70 ± 0.84kJ/molIMREViidanoja, Reiner, et al., 1998gas phase; B

CH2BrO2- + 2Formic acid = C2H4BrO4-

By formula: CH2BrO2- + 2CH2O2 = C2H4BrO4-

Quantity Value Units Method Reference Comment
Δr40. ± 7.1kJ/molCIDTWalker and Sunderlin, 1999gas phase; B

Gas phase ion energetics data

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, 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
LL - Sharon G. Lias and Joel F. Liebman

Quantity Value Units Method Reference Comment
IE (evaluated)11.33 ± 0.01eVN/AN/AL
Quantity Value Units Method Reference Comment
Proton affinity (review)742.0kJ/molN/AHunter and Lias, 1998HL
Quantity Value Units Method Reference Comment
Gas basicity710.3kJ/molN/AHunter and Lias, 1998HL

Ionization energy determinations

IE (eV) Method Reference Comment
11.31PITraeger, 1985LBLHLM
11.329 ± 0.002SBell, Ng, et al., 1975LLK
11.16 ± 0.03PIWarneck, 1974LLK
11.314 ± 0.002PIKnowles and Nicholson, 1974LLK
11.3PEWatanabe, Yokoyama, et al., 1973LLK
11.33PEWatanabe, Yokoyama, et al., 1973, 2LLK
11.35 ± 0.03PEThomas, 1972LLK
11.16 ± 0.03PIMatthews and Warneck, 1969RDSH
11.33PEBrundle, Turner, et al., 1969RDSH
11.05 ± 0.03PIVilesov, 1960RDSH
11.05 ± 0.01PIWatanabe, 1957RDSH
11.33SPrice and Evans, 1937RDSH
11.5PEVon Niessen, Bieri, et al., 1980Vertical value; LLK
11.34PEBenoit and Harrison, 1977Vertical value; LLK
10.7PERao, 1975Vertical value; LLK
11.51PEKimura, Katsumata, et al., 1975Vertical value; LLK

Appearance energy determinations

Ion AE (eV) Other Products MethodReferenceComment
C+22.7 ± 0.5O+H2OEIStepanov, Perov, et al., 1988LL
CHO+12.76OHPITraeger, 1985LBLHLM
CHO+13.0 ± 0.1OHPIGolovin, Akopyan, et al., 1979LLK
CHO+12.79 ± 0.03OHPIWarneck, 1974LLK
CHO+12.79 ± 0.03OHPIMatthews and Warneck, 1969RDSH
CHO2+12.4 ± 0.1HPIGolovin, Akopyan, et al., 1979LLK
CHO2+12.26HPIAkopyan and Villem, 1976LLK
CHO2+12.29 ± 0.03HPIWarneck, 1974LLK
HO+17.97 ± 0.06HCOPIWarneck, 1974LLK
O+20.0 ± 0.5CO+H2EIStepanov, Perov, et al., 1988LL

De-protonation reactions

HCO2 anion + Hydrogen cation = Formic acid

By formula: CHO2- + H+ = CH2O2

Quantity Value Units Method Reference Comment
Δr1449. ± 5.0kJ/molD-EAKim, Bradforth, et al., 1995gas phase; dHacid(0K) = 344.67±0.62 kcal/mol; B
Δr1445. ± 9.2kJ/molG+TSCaldwell, Renneboog, et al., 1989gas phase; B
Δr1445. ± 9.2kJ/molG+TSFujio, McIver, et al., 1981gas phase; value altered from reference due to change in acidity scale; B
Δr1444. ± 12.kJ/molG+TSCumming and Kebarle, 1978gas phase; B
Δr1423. ± 19.kJ/molEIAEMuftakhov, Vasil'ev, et al., 1999gas phase; B
Quantity Value Units Method Reference Comment
Δr1419. ± 6.3kJ/molH-TSKim, Bradforth, et al., 1995gas phase; dHacid(0K) = 344.67±0.62 kcal/mol; B
Δr1415. ± 8.4kJ/molIMRECaldwell, Renneboog, et al., 1989gas phase; B
Δr1416. ± 8.4kJ/molIMREFujio, McIver, et al., 1981gas phase; value altered from reference due to change in acidity scale; B
Δr1415. ± 8.4kJ/molIMRECumming and Kebarle, 1978gas phase; B

References

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, Notes

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

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Campbell and Campbell, 1934
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Jones, 1960
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Larson and McMahon, 1984
Larson, J.W.; McMahon, T.B., Hydrogen bonding in gas phase anions. An experimental investigation of the interaction between chloride ion and bronsted acids from ICR chloride exchange equilibria, J. Am. Chem. Soc., 1984, 106, 517. [all data]

Yamdagni and Kebarle, 1971
Yamdagni, R.; Kebarle, P., Hydrogen bonding energies to negative ions from gas phase measurements of ionic equilibria, J. Am. Chem. Soc., 1971, 93, 7139. [all data]

Larson and McMahon, 1984, 2
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Cumming and Kebarle, 1978
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Larson and McMahon, 1982
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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]

Lias, Liebman, et al., 1984
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Meot-Ner and Sieck, 1986
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Meot-Ner, 1984
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Bell, Ng, et al., 1975
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Watanabe, Yokoyama, et al., 1973, 2
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Watanabe, 1957
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Price and Evans, 1937
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Benoit and Harrison, 1977
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Rao, 1975
Rao, C.N.R., Lone-pair ionization bands of chromophores in the photoelectron spectra of organic molecules, Indian J. Chem., 1975, 13, 950. [all data]

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Golovin, Akopyan, et al., 1979
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Akopyan and Villem, 1976
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Notes

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, References