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Biochemistry 46 (27), 7992-8003 (10 Jul 2007)
The Journal of biological chemistry 275 (28), 21754-60 (14 Jul 2000)
Proceedings of the National Academy of Sciences of the United States of America 88 (14), 6254-8 (15 Jul 1991)
Methods in enzymology 247, 215-27 (1994)
Biochemistry 32 (44), 11934-42 (09 Nov 1993)
Journal of bacteriology 172 (10), 6061-5 (Oct 1990)
Methods in enzymology 282, 333-46 (1997)
Chemical Society Reviews 37 (7), 1347 (2008)
Nucleic Acids Research 18 (1), 51 (1990)
Proton affinity measurements using ion mobility spectrometry
The Journal of Chemical Thermodynamics 35 (6), 863 (2003)
Abstract
Relative proton affinities are usually measured by means of high pressure mass spectrometry. In this work ion mobility spectrometry was used to determine proton affinities. The standard molar enthalpy change ΔH0M for the reaction MH++Nright harpoon over leftM+NH+ was found to be: −(56.3±0.8) kJ·mol−1, when M was ethyl acetate and N ethanol; −(27.8±0.5) kJ·mol−1, when M was acetophenone and N ethyl acetate; −(10.6±0.2) kJ·mol−1, when M was cycloheptanone and N ethyl acetate; −(66.1±1.2) kJ·mol−1, when M was dimethyl methyl phosphonate and N ethyl acetate; and, −(56.7±0.9) kJ·mol−1, when M was dimethyl methyl phosphonate and N cycloheptanone. These values are internally consistent and in good agreement with results obtained with high pressure mass spectrometry. On the basis of proton affinities of cycloheptanone and ethyl acetate, an absolute proton affinity of (902±1.2) kJ·mol−1 has been determined for dimethyl methyl phosphonate.
Author Keywords: Proton affinity; Ion mobility spectrometry
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