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 1301 to 1350)
  • 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 1251 to 1300, reactions 1351 to 1375
  • Gas phase ion energetics data
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Reaction thermochemistry data

Go To: Top, 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: 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 1301 to 1350

C₈H₅F₆N₂O₃S₂^- +  = C₈H₆F₆N₂O₃S₂

By formula: C₈H₅F₆N₂O₃S₂^- + H⁺ = C₈H₆F₆N₂O₃S₂

C₁₂H₇F₄N₂^- +  = C₁₂H₈F₄N₂

By formula: C₁₂H₇F₄N₂^- + H⁺ = C₁₂H₈F₄N₂

C₁₁H₅F₄N₂^- +  = C₁₁H₆F₄N₂

By formula: C₁₁H₅F₄N₂^- + H⁺ = C₁₁H₆F₄N₂

C₁₃H₅F₄N₂^- +  = C₁₃H₆F₄N₂

By formula: C₁₃H₅F₄N₂^- + H⁺ = C₁₃H₆F₄N₂

C₁₃H₃F₉N^- +  = C₁₃H₄F₉N

By formula: C₁₃H₃F₉N^- + H⁺ = C₁₃H₄F₉N

C₁₂ClF₉N^- +  = C₁₂HClF₉N

By formula: C₁₂ClF₉N^- + H⁺ = C₁₂HClF₉N

C₁₃H₅F₅NO^- +  =

By formula: C₁₃H₅F₅NO^- + H⁺ = C₁₃H₆F₅NO

C₆H₁₁O₆^- +  =

By formula: C₆H₁₁O₆^- + H⁺ = C₆H₁₂O₆

C₉H₅CrO₃^- +  =

By formula: C₉H₅CrO₃^- + H⁺ = C₉H₆CrO₃

C₂H₇NO₂P^- +  = C₂H₈NO₂P

By formula: C₂H₇NO₂P^- + H⁺ = C₂H₈NO₂P

C₁₀H₇N₂O^- +  = C₁₀H₈N₂O

By formula: C₁₀H₇N₂O^- + H⁺ = C₁₀H₈N₂O

CHF₂O₄S₂^- +  =

By formula: CHF₂O₄S₂^- + H⁺ = CH₂F₂O₄S₂

C₁₀H₄F₉O₆S₃^- +  = C₁₀H₅F₉O₆S₃

By formula: C₁₀H₄F₉O₆S₃^- + H⁺ = C₁₀H₅F₉O₆S₃

C₁₀H₃F₉NO₈S₃^- +  = C₁₀H₄F₉NO₈S₃

By formula: C₁₀H₃F₉NO₈S₃^- + H⁺ = C₁₀H₄F₉NO₈S₃

C₁₁H₄F₉O₇S₃^- +  = C₁₁H₅F₉O₇S₃

By formula: C₁₁H₄F₉O₇S₃^- + H⁺ = C₁₁H₅F₉O₇S₃

C₈H₇F₃NO₂S^- +  =

By formula: C₈H₇F₃NO₂S^- + H⁺ = C₈H₈F₃NO₂S

C₁₄F₁₀N^- +  = C₁₄HF₁₀N

By formula: C₁₄F₁₀N^- + H⁺ = C₁₄HF₁₀N

C₁₀H₃F₄N₂^- +  = C₁₀H₄F₄N₂

By formula: C₁₀H₃F₄N₂^- + H⁺ = C₁₀H₄F₄N₂

C₁₅F₁₂N^- +  = C₁₅HF₁₂N

By formula: C₁₅F₁₂N^- + H⁺ = C₁₅HF₁₂N

C₇H₃F₆O₄^- +  = C₇H₄F₆O₄

By formula: C₇H₃F₆O₄^- + H⁺ = C₇H₄F₆O₄

C₁₀F₈N₃^- +  = C₁₀HF₈N₃

By formula: C₁₀F₈N₃^- + H⁺ = C₁₀HF₈N₃

C₉HF₄N₂^- +  = C₉H₂F₄N₂

By formula: C₉HF₄N₂^- + H⁺ = C₉H₂F₄N₂

C₉H₃F₉NO₆S₃^- +  = C₉H₄F₉NO₆S₃

By formula: C₉H₃F₉NO₆S₃^- + H⁺ = C₉H₄F₉NO₆S₃

C₇HF₄N₂^- +  =

By formula: C₇HF₄N₂^- + H⁺ = C₇H₂F₄N₂

C₁₃H₈NO^- +  =

By formula: C₁₃H₈NO^- + H⁺ = C₁₃H₉NO

C₇H₈NO₂S^- +  =

By formula: C₇H₈NO₂S^- + H⁺ = C₇H₉NO₂S

HP^- +  =

By formula: HP^- + H⁺ = H₂P

C₈H₅ClF₄O₂S^- +  = C₈H₆ClF₄O₂S

By formula: C₈H₅ClF₄O₂S^- + H⁺ = C₈H₆ClF₄O₂S

C₉H₅F₃NO₂S^- +  = C₉H₆F₃NO₂S

By formula: C₉H₅F₃NO₂S^- + H⁺ = C₉H₆F₃NO₂S

C₈H₅F₃NO₄S^- +  = C₈H₆F₃NO₄S

By formula: C₈H₅F₃NO₄S^- + H⁺ = C₈H₆F₃NO₄S

C₉H₄F₇O₄S₂^- +  = C₉H₅F₇O₄S₂

By formula: C₉H₄F₇O₄S₂^- + H⁺ = C₉H₅F₇O₄S₂

C₁₀H₄F₉O₄S₂^- +  = C₁₀H₅F₉O₄S₂

By formula: C₁₀H₄F₉O₄S₂^- + H⁺ = C₁₀H₅F₉O₄S₂

C₁₂H₁₁F₆O₅S₂^- +  = C₁₂H₁₂F₆O₅S₂

By formula: C₁₂H₁₁F₆O₅S₂^- + H⁺ = C₁₂H₁₂F₆O₅S₂

FeO^- +  = HFeO

By formula: FeO^- + H⁺ = HFeO

C₁₂HF₉N^- +  = C₁₂H₂F₉N

By formula: C₁₂HF₉N^- + H⁺ = C₁₂H₂F₉N

C₁₀F₇O^- +  = C₁₀HF₇O

By formula: C₁₀F₇O^- + H⁺ = C₁₀HF₇O

C₁₁H₅F₅NO₂^- +  = C₁₁H₆F₅NO₂

By formula: C₁₁H₅F₅NO₂^- + H⁺ = C₁₁H₆F₅NO₂

C₇H₇^- +  =

By formula: C₇H₇^- + H⁺ = C₇H₈

C₁₂H₉N₂O₂^- +  =

By formula: C₁₂H₉N₂O₂^- + H⁺ = C₁₂H₁₀N₂O₂

Tl^- +  = HTl

By formula: Tl^- + H⁺ = HTl

C₆H₇N₂O₂^- +  =

By formula: C₆H₇N₂O₂^- + H⁺ = C₆H₈N₂O₂

C₁₀H₄F₉O₂S^- +  = C₁₀H₅F₉O₂S

By formula: C₁₀H₄F₉O₂S^- + H⁺ = C₁₀H₅F₉O₂S

C₁₀H₄F₉O₄S₂^- +  = C₁₀H₅F₉O₄S₂

By formula: C₁₀H₄F₉O₄S₂^- + H⁺ = C₁₀H₅F₉O₄S₂

C₁₁H₃F₁₂O₄S₂^- +  = C₁₁H₄F₁₂O₄S₂

By formula: C₁₁H₃F₁₂O₄S₂^- + H⁺ = C₁₁H₄F₁₂O₄S₂

C₇H₅F₃NO₂S^- +  = C₇H₆F₃NO₂S

By formula: C₇H₅F₃NO₂S^- + H⁺ = C₇H₆F₃NO₂S

C₂F₆N^- +  =

By formula: C₂F₆N^- + H⁺ = C₂HF₆N

C₁₀F₇O^- +  = C₁₀HF₇O

By formula: C₁₀F₇O^- + H⁺ = C₁₀HF₇O

C₇H₉O₃^- +  =

By formula: C₇H₉O₃^- + H⁺ = C₇H₁₀O₃

C₁₀H₁₁O₂^- +  =

By formula: C₁₀H₁₁O₂^- + H⁺ = C₁₀H₁₂O₂

C₁₀H₁₁O₂^- +  =

By formula: C₁₀H₁₁O₂^- + H⁺ = C₁₀H₁₂O₂

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, Taft, et al., 1994
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]

Koppel, Koppel, et al., 1998
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]

Cai and Cole, 2002
Cai, Y.; Cole, R.B., Stabilization of anionic adducts in negative ion electrospray mass spectrometry, Anal. Chem., 2002, 74, 5, 985-991, https://doi.org/10.1021/ac0108818 . [all data]

Lane and Squires, 1985
Lane, K.R.; Squires, R.R., Formation of HCr(CO)₃^- from the remarkable reaction of hydride ion with benzenechromium tricarbonyl, J. Am. Chem. Soc., 1985, 107, 6403. [all data]

Anderson, DePuy, et al., 1984
Anderson, D.R.; DePuy, C.H.; Filley, J.; Bierbaum, V.M., Gas Phase Chemistry of Trimethyl Phosphite, J. Am. Chem. Soc., 1984, 106, 22, 6513, https://doi.org/10.1021/ja00334a009 . [all data]

Muftakhov, Vasil'ev, et al., 1999
Muftakhov, M.V.; Vasil'ev, Y.V.; Khatymov, R.V.; Mazunov, V.A.; Takhistov, V.V.; Travkin, O.V.; Yakovleva, E.V., Thermochemistry of negatively charged ions. II. Energetics of formation of negative ions from acridanone and some of its derivatives, Rapid Commun. Mass Spectrom., 1999, 13, 10, 912-923, https://doi.org/10.1002/(SICI)1097-0231(19990530)13:10<912::AID-RCM585>3.0.CO;2-W . [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]

Ervin and Lineberger, 2005
Ervin, K.M.; Lineberger, W.C., Photoelectron spectroscopy of phosphorus hydride anions, J. Chem. Phys., 2005, 122, 19, 194303, https://doi.org/10.1063/1.1881153 . [all data]

Zhang, Badal, et al., 2013
Zhang, M.; Badal, M.M.R.; Koppel, I.A.; Mishima, M., Gas-Phase Acidities of alpha- and alpha,alpha-SO2CF3-Substituted Toluenes. Varying Resonance Demand in the Electron-Rich System, Bull. Chem. Soc. Japan, 2013, 86, 7, 813-820, https://doi.org/10.1246/bcsj.20130052 . [all data]

Engelking and Lineberger, 1977
Engelking, P.C.; Lineberger, W.C., Laser photoelecton spectrometry of FeO-: Electron affinity, electronic state separations, and ground state vibrations of iron oxide, and a new ground state assignment, J. Chem. Phys., 1977, 66, 5054. [all data]

Gunion, Karney, et al., 1996
Gunion, R.F.; Karney, W.; Wenthold, P.G.; Borden, W.T.; Lineberger, W.C., Ultraviolet Photoelectron Spectroscopy of Some C7H7- Isomers: Quadricyclanide, Norbornadienide, Cycloheptatrienide, and 1,6-Heptadiynide, J. Am. Chem. Soc., 1996, 118, 21, 5074, https://doi.org/10.1021/ja954026f . [all data]

Carpenter, Covington, et al., 2000
Carpenter, D.L.; Covington, A.M.; Thompson J.S., Laser Photodetachment Electron Spectroscopy of Tl-, Phys. Rev. A, 2000, 61, 4, 42501, https://doi.org/10.1103/PhysRevA.61.042501 . [all data]

Lee, 2005
Lee, J.K., Insights into nucleic acid reactivity through gas-phase experimental and computational studies, Int. J. Mass Spectrom., 2005, 240, 3, 261-272, https://doi.org/10.1016/j.ijms.2004.09.020 . [all data]

Decouzon, Gal, et al., 1997
Decouzon, M.; Gal, J.-F.; Maria, P.-C.; Bohm, S.; Jimenez, P.; Roux, M.V.; Exner, O., Steric Effects in Crowded Molecules in the Gas Phase: Polymethyl Substituted Benzoic Acids, New J. Chem., 1997, 21, 561. [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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