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The ionic hydrogen bond and ion solvation. 7. Interaction energies of carbanions with solvent molecules

Cite this: J. Am. Chem. Soc. 1988, 110, 12, 3858–3862
Publication Date (Print):June 1, 1988
https://doi.org/10.1021/ja00220a022
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    2. Michael Meot-Ner (Mautner) . Update 1 of: Strong Ionic Hydrogen Bonds. Chemical Reviews 2012, 112 (10) , PR22-PR103. https://doi.org/10.1021/cr200430n
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    13. Alexander N. Isaev. Two kinds of X H⋯C(sp 3 ) hydrogen bond formed by the methide anion: Syn- and anti- orientation of monomers. Computational and Theoretical Chemistry 2017, 1117 , 141-149. https://doi.org/10.1016/j.comptc.2017.08.013
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    15. Mustanir, Mio Matsuoka, Masaaki Mishima, Heinz Koch. Stability of Complexes of Phenylacetylides and Benzyl Alkoxides with Methanol in the Gas Phase. Acid–Base Correlation in the Ionic Hydrogen-Bond Strength. Bulletin of the Chemical Society of Japan 2006, 79 (7) , 1118-1125. https://doi.org/10.1246/bcsj.79.1118
    16. Keiko Takashima, José M. Riveros. Gas-phase solvated negative ions. Mass Spectrometry Reviews 1998, 17 (6) , 409-430. https://doi.org/10.1002/(SICI)1098-2787(1998)17:6<409::AID-MAS2>3.0.CO;2-J
    17. Silvia Bradamante, Giorgio A. Pagani. Benzyl and heteroarylmethyl carbanions: Structure and substitutent effects. 1997, 189-263. https://doi.org/10.1016/S1068-7394(96)80006-6
    18. Ben L.M. Van Baar. Chapter 2. Ionisation Methods in LC-MS and LC-MS-MS (TSP, APCI, ESP and cf-FAB). 1996, 71-133. https://doi.org/10.1016/S0301-4770(08)60779-4
    19. Andrew T. Pudzianowski. MP2/6-311++G( d , p ) study of ten ionic hydrogen-bonded binary systems: Structures, normal modes, thermodynamics, and counterpoise energies. The Journal of Chemical Physics 1995, 102 (20) , 8029-8039. https://doi.org/10.1063/1.469001
    20. Matthias Kolb, Walter Thiel. Beyond the MNDO model: Methodical considerations and numerical results. Journal of Computational Chemistry 1993, 14 (7) , 775-789. https://doi.org/10.1002/jcc.540140704
    21. Steve Scheiner. Calculating the Properties of Hydrogen Bonds by ab Initio Methods. 1991, 165-218. https://doi.org/10.1002/9780470125793.ch5
    22. Zofia Dega-Szafran, Andrzej Hrynio, Miroslaw Szafran. A quantitative comparison of spectroscopic and energy data, in solution, of NHO and OHO hydrogen bonds and gas-phase proton affinities: complexes of pyridines and pyridine N-oxides with acetic acids. Journal of Molecular Structure 1990, 240 , 159-174. https://doi.org/10.1016/0022-2860(90)80507-G
    23. M. MEOT‐NER. ChemInform Abstract: Ionic Hydrogen Bond and Ion Solvation. Part 6. Interaction Energies of the Acetate Ion with Organic Molecules. Comparison of CH3COO‐ with Cl‐, CN‐, and SH‐.. ChemInform 1988, 19 (39) https://doi.org/10.1002/chin.198839066
    24. M. MEOT‐NER. ChemInform Abstract: The Ionic Hydrogen Bond and Ion Solvation. Part 7. Interaction Energies of Carbanions with Solvent Molecules.. ChemInform 1988, 19 (39) https://doi.org/10.1002/chin.198839067

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