Hydrogen cation

• Formula: H⁺
• Molecular weight: 1.00739
• IUPAC Standard InChI: InChI=1S/p+1 Copy

  
• IUPAC Standard InChIKey: GPRLSGONYQIRFK-UHFFFAOYSA-N Copy
• CAS Registry Number: 12408-02-5
• Chemical structure:
  This structure is also available as a 2d Mol file
• Isotopologues:
  • Deuterium cation
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Reaction thermochemistry data (reactions 1251 to 1300)
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Reaction thermochemistry data: reactions 1 to 50, reactions 51 to 100, reactions 101 to 150, reactions 151 to 200, reactions 201 to 250, reactions 251 to 300, reactions 301 to 350, reactions 351 to 400, reactions 401 to 450, reactions 451 to 500, reactions 501 to 550, reactions 551 to 600, reactions 601 to 650, reactions 651 to 700, reactions 701 to 750, reactions 751 to 800, reactions 801 to 850, reactions 851 to 900, reactions 901 to 950, reactions 951 to 1000, reactions 1001 to 1050, reactions 1051 to 1100, reactions 1101 to 1150, reactions 1151 to 1200, reactions 1201 to 1250, reactions 1301 to 1350, reactions 1351 to 1375
  • Gas phase ion energetics data
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Reaction thermochemistry data

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

Data compiled by: John E. Bartmess

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.

Reactions 1251 to 1300

C₁₄H₆F₄N^- +  = C₁₄H₇F₄N

By formula: C₁₄H₆F₄N^- + H⁺ = C₁₄H₇F₄N

C₁₅H₅F₇N^- +  = C₁₅H₆F₇N

By formula: C₁₅H₅F₇N^- + H⁺ = C₁₅H₆F₇N

C₁₄ClF₉N^- +  = C₁₄HClF₉N

By formula: C₁₄ClF₉N^- + H⁺ = C₁₄HClF₉N

C₁₇H₅F₉NO₂^- +  = C₁₇H₆F₉NO₂

By formula: C₁₇H₅F₉NO₂^- + H⁺ = C₁₇H₆F₉NO₂

C₁₅H₃F₉N^- +  = C₁₅H₄F₉N

By formula: C₁₅H₃F₉N^- + H⁺ = C₁₅H₄F₉N

C₁₃F₉N₂^- +  = C₁₃HF₉N₂

By formula: C₁₃F₉N₂^- + H⁺ = C₁₃HF₉N₂

C₁₄BrF₉N^- +  = C₁₄HBrF₉N

By formula: C₁₄BrF₉N^- + H⁺ = C₁₄HBrF₉N

C₁₄HF₁₀O^- +  = C₁₄H₂F₁₀O

By formula: C₁₄HF₁₀O^- + H⁺ = C₁₄H₂F₁₀O

C₁₅HF₁₂O^- +  = C₁₅H₂F₁₂O

By formula: C₁₅HF₁₂O^- + H⁺ = C₁₅H₂F₁₂O

C₁₁H₆F₄NO₂^- +  = C₁₁H₇F₄NO₂

By formula: C₁₁H₆F₄NO₂^- + H⁺ = C₁₁H₇F₄NO₂

C₁₂H₈F₄NO₂^- +  = C₁₂H₉F₄NO₂

By formula: C₁₂H₈F₄NO₂^- + H⁺ = C₁₂H₉F₄NO₂

C₁₂H₅F₇NO₂^- +  = C₁₂H₆F₇NO₂

By formula: C₁₂H₅F₇NO₂^- + H⁺ = C₁₂H₆F₇NO₂

C₁₁H₅ClF₄NO₂^- +  = C₁₁H₆ClF₄NO₂

By formula: C₁₁H₅ClF₄NO₂^- + H⁺ = C₁₁H₆ClF₄NO₂

C₁₁H₅BrF₄NO₂^- +  = C₁₁H₆BrF₄NO₂

By formula: C₁₁H₅BrF₄NO₂^- + H⁺ = C₁₁H₆BrF₄NO₂

C₁₂H₅F₄N₂O₂^- +  = C₁₂H₆F₄N₂O₂

By formula: C₁₂H₅F₄N₂O₂^- + H⁺ = C₁₂H₆F₄N₂O₂

C₁₇F₁₆N^- +  = C₁₇HF₁₆N

By formula: C₁₇F₁₆N^- + H⁺ = C₁₇HF₁₆N

C₂H₅Sn^- +  = C₂H₆Sn

By formula: C₂H₅Sn^- + H⁺ = C₂H₆Sn

C₂H₃Sn^- +  = C₂H₄Sn

By formula: C₂H₃Sn^- + H⁺ = C₂H₄Sn

C₆H₁₁O₂^- +  =

By formula: C₆H₁₁O₂^- + H⁺ = C₆H₁₂O₂

C₂H₅Te^- +  = C₂H₆Te

By formula: C₂H₅Te^- + H⁺ = C₂H₆Te

C₁₂H₈ClN₂O₆S₂^- +  = C₁₂H₉ClN₂O₆S₂

By formula: C₁₂H₈ClN₂O₆S₂^- + H⁺ = C₁₂H₉ClN₂O₆S₂

C₁₂H₇ClN₃O₈S₂^- +  = C₁₂H₈ClN₃O₈S₂

By formula: C₁₂H₇ClN₃O₈S₂^- + H⁺ = C₁₂H₈ClN₃O₈S₂

C₁₁H₁₀NO₂^- +  =

By formula: C₁₁H₁₀NO₂^- + H⁺ = C₁₁H₁₁NO₂

C₁₄H₈N^- +  =

By formula: C₁₄H₈N^- + H⁺ = C₁₄H₉N

C₈H₈F₃N₂O₃S₂^- +  = C₈H₉F₃N₂O₃S₂

By formula: C₈H₈F₃N₂O₃S₂^- + H⁺ = C₈H₉F₃N₂O₃S₂

C₆H₇Ge^- +  = C₆H₈Ge

By formula: C₆H₇Ge^- + H⁺ = C₆H₈Ge

C₂H₇Sn^- +  = C₂H₈Sn

By formula: C₂H₇Sn^- + H⁺ = C₂H₈Sn

C₆H₇Sn^- +  = C₆H₈Sn

By formula: C₆H₇Sn^- + H⁺ = C₆H₈Sn

FS^- +  = HFS

By formula: FS^- + H⁺ = HFS

Pb^- +  = HPb

By formula: Pb^- + H⁺ = HPb

C₈H₁₂O₄^-2 +  = C₈H₁₃O₄^-2

By formula: C₈H₁₂O₄^-2 + H⁺ = C₈H₁₃O₄^-2

Rh^- +  = HRh

By formula: Rh^- + H⁺ = HRh

Pd^- +  = HPd

By formula: Pd^- + H⁺ = HPd

Ag^- +  = HAg

By formula: Ag^- + H⁺ = HAg

Sb^- +  = HSb

By formula: Sb^- + H⁺ = HSb

C₆H₂F₃^- +  =

By formula: C₆H₂F₃^- + H⁺ = C₆H₃F₃

C₆H₅Se^- +  =

By formula: C₆H₅Se^- + H⁺ = C₆H₆Se

C₁₀H₁₇NO₃^- +  = C₁₀H₁₈NO₃

By formula: C₁₀H₁₇NO₃^- + H⁺ = C₁₀H₁₈NO₃

Ti^- +  =

By formula: Ti^- + H⁺ = HTi

H₂Si^- +  =

By formula: H₂Si^- + H⁺ = H₃Si

As^- +  =

By formula: As^- + H⁺ = HAs

C₈H₃F₅NO^- +  = C₈H₄F₅NO

By formula: C₈H₃F₅NO^- + H⁺ = C₈H₄F₅NO

C₁₄H₁₀N^- +  =

By formula: C₁₄H₁₀N^- + H⁺ = C₁₄H₁₁N

C₃H₇S₂^- +  =

By formula: C₃H₇S₂^- + H⁺ = C₃H₈S₂

C₈H₄O₄^-2 +  = C₈H₅O₄^-2

By formula: C₈H₄O₄^-2 + H⁺ = C₈H₅O₄^-2

C₈H₄O₄^-2 +  = C₈H₅O₄^-2

By formula: C₈H₄O₄^-2 + H⁺ = C₈H₅O₄^-2

C₆H₃F₃NO₆S₃^- +  = C₆H₄F₃NO₆S₃

By formula: C₆H₃F₃NO₆S₃^- + H⁺ = C₆H₄F₃NO₆S₃

C₇H₅F₂O₄S₂^- +  = C₇H₆F₂O₄S₂

By formula: C₇H₅F₂O₄S₂^- + H⁺ = C₇H₆F₂O₄S₂

C₁₁H₄F₉O₇S₃^- +  = C₁₁H₅F₉O₇S₃

By formula: C₁₁H₄F₉O₇S₃^- + H⁺ = C₁₁H₅F₉O₇S₃

C₁₂H₄F₅N₂O₂^- +  = C₁₂H₅F₅N₂O₂

By formula: C₁₂H₄F₅N₂O₂^- + H⁺ = C₁₂H₅F₅N₂O₂

References

Go To: Top, Reaction thermochemistry data, Notes

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

Koppel, Koppel, et al., 2000
Koppel, I.A.; Koppel, J.; Pihl, V.; Leito, I.; Mishima, M.; Vlasov, V.M.; Yagupolskii, L.M.; Taft, R.W., Comparison of Bronsted acidities of neutral CH acids in gas phase and dimethyl sulfoxide, J. Chem. Soc. Perkin Trans., 2000, 2, 6, 1125-1133, https://doi.org/10.1039/b001792m . [all data]

Gal, Decouzon, et al., 2001
Gal, J.F.; Decouzon, M.; Maria, P.C.; Gonzalez, A.I.; Mo, O.; Yanez, M.; El Chaouch, S.; Guillemin, J.C., Acidity trends in alpha,beta-unsaturated alkanes, silanes, germanes, and stannanes, J. Am. Chem. Soc., 2001, 123, 26, 6353-6359, https://doi.org/10.1021/ja004079j . [all data]

Chen, Walthall, et al., 2004
Chen, X.; Walthall, D.A.; Brauman, J.I., Acidities in cyclohexanediols enhanced by intramolecular hydrogen bonds, J. Am. Chem. Soc., 2004, 126, 39, 12614-12620, https://doi.org/10.1021/ja049780s . [all data]

Guillemin, Riague, et al., 2005
Guillemin, J.C.; Riague, E.H.; Gal, J.F.; Maria, P.C.; Mo, O.; Yanez, M., Acidity trends in alpha,beta-unsaturated sulfur, selenium, and tellurium derivatives: Comparison with C-, Si-, Ge-, Sn-, N-, P-, As-, and Sb-containing analogues, Chem. Eur. J., 2005, 11, 7, 2145-2153, https://doi.org/10.1002/chem.200400989 . [all data]

Leito, Raamat, et al., 2009
Leito, I.; Raamat, E.; Kutt, A.; Saame, J.; Kipper, K.; Koppel, I.A.; Koppel, I.; Zhang, M.; Mishima, M.; Yagupolskii, L.M.; Garlyauskayte, R.Y.; Filatov, A.A., Revision of the Gas-Phase Acidity Scale below 300 kcal mol(-1), J. Phys. Chem. A, 2009, 113, 29, 8421-8424, https://doi.org/10.1021/jp903780k . [all data]

Koppel, Koppel, et al., 2001
Koppel, I.A.; Koppel, J.; Leito, I.; Koppel, I.; Mishima, M.; Yagupolskii, L.M., The enormous acidifying effect of the supersubstituent =NSO2CF3 on the acidity of derivatives of benzenesulfonamide and toluene-p-sulfonamide in the gas phase and in dimethyl sulfoxide, J. Chem. Soc. Perkin Trans., 2001, 2, 2, 229-232, https://doi.org/10.1039/b005765g . [all data]

Polak, Gilles, et al., 1992
Polak, M.L.; Gilles, M.K.; Lineberger, W.C., Photoelectron Spectroscopy of SF-, J. Chem. Phys., 1992, 96, 9, 7191, https://doi.org/10.1063/1.462526 . [all data]

Feigerle, Corderman, et al., 1981
Feigerle, C.S.; Corderman, R.R.; Lineberger, W.C., Electron affinities of B, Al, Bi, and Pb, J. Chem. Phys., 1981, 74, 2, 1513, https://doi.org/10.1063/1.441174 . [all data]

Yang, Fu, et al., 2004
Yang, X.; Fu, Y.J.; Wang, X.B.; Slavicek, P.; Mucha, M.; Jungwirth, P.; Wang, L.S., Solvent-mediated folding of a doubly charged anion, J. Am. Chem. Soc., 2004, 126, 3, 876-883, https://doi.org/10.1021/ja038108c . [all data]

Scheer, Brodie, et al., 1998
Scheer, M.; Brodie, C.A.; Bilodeau, R.C.; Haugen, H.K., Laser spectroscopic measurements of binding energies and fine-structure splittings of Co-, Ni-, Rh-, and Pd-, Phys. Rev. A, 1998, 58, 3, 2051-2062, https://doi.org/10.1103/PhysRevA.58.2051 . [all data]

Bilodeau, Scheer, et al., 1998
Bilodeau, R.C.; Scheer, M.; Haugen, H.K., Infrared Laser Photodetachment of Transition Metal Negative Ions: Studies on Cr-, Mo-, Cu-, and Ag-, J. Phys. B: Atom. Mol. Opt. Phys., 1998, 31, 17, 3885-3891, https://doi.org/10.1088/0953-4075/31/17/013 . [all data]

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Scheer, M.; Haugen, H.K.; Beck, D.R., Single- and Multiphoton Infrared Laser Spectroscopy of Sb-: A Case Study, Phys. Rev. Lett., 1997, 79, 21, 4104-4107, https://doi.org/10.1103/PhysRevLett.79.4104 . [all data]

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Buker, H.H.; Nibbering, N.M.M.; Espinosa, D.; Mongin, F.; Schlosser, M., Additivity of substituent effects in the fluoroarene series: Equilibrium acidity in the gas phase and deprotonation rates in ethereal solution, Tetrahed. Lett., 1997, 38, 49, 8519-8522, https://doi.org/10.1016/S0040-4039(97)10303-3 . [all data]

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Gryn'ova, G.; Marshall, D.L.; Blanksby, S.J.; Coote, M.L., Switching Radical Stability by pH-Induced Orbital Conversion, Nat. Chem., 2013, 5, 6, 474-481, https://doi.org/10.1038/nchem.1625 . [all data]

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Walter, C.W.; Gibson, N.D.; Field, R.L.; Snedden, A.P.; Shapiro, J.Z.; Janczak, C.M.; Hanstorp, D., Electron affinity of arsenic and the fine structure of As- measured using infrared photodetachment threshold spectroscopy, Phys. Rev. A, 2009, 80, 1, 014501, https://doi.org/10.1103/PhysRevA.80.014501 . [all data]

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Koppel, I.; Koppel, J.; Maria, P.C.; Gal, J.F.; Notario, R.; Vlasov, V.M.; Taft, R.W., Comparison of Bronsted acidities of neutral NH-acids in gas phase, dimethyl sulfoxide and water, Int. J. Mass Spectrom., 1998, 175, 1-2, 61-69, https://doi.org/10.1016/S0168-1176(98)00113-X . [all data]

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Koppel, I.A.; Taft, R.W.; Anvia, F.; Zhu, S.Z.; Hu, L.Q.; Sung, K.S.; Desmarteau, D.D.; Yagupolskii, L.M., The Gas-Phase Acidities of Very Strong Neutral Bronsted Acids, J. Am. Chem. Soc., 1994, 116, 7, 3047, https://doi.org/10.1021/ja00086a038 . [all data]

Notes

Go To: Top, Reaction thermochemistry data, References

• Symbols used in this document:
  

  ΔrG°	Free energy of reaction at standard conditions
  ΔrH°	Enthalpy of reaction at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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