Additivity of Proton affinities: Theoretical studies of fluorine‐ and methyl‐substituted benzenes
- 1 June 1995
- journal article
- research article
- Published by Wiley in Journal of Physical Organic Chemistry
- Vol. 8 (6) , 435-441
- https://doi.org/10.1002/poc.610080608
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Protonation of fused aromatic systems: Ab initio study of some model Wheland intermediatesInternational Journal of Quantum Chemistry, 1994
- Combined ab initio MO and experimental studies on unimolecular hydrogen fluoride loss from protonated fluorobenzene in the gas phaseJournal of the American Chemical Society, 1993
- Thermodynamics of some proton-transfer reactions. Dynamic ion structures and the measurement of entropies of ‘internal translation’Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics, 1987
- A scale of directional substituent polarizability parameters from ab initio calculations of polarizability potentialsJournal of the American Chemical Society, 1986
- Substituent effects on the intrinsic basicity of benzene: proton affinities of substituted benzenesJournal of the American Chemical Society, 1976
- Gas-phase basicities and proton affinities of compounds between water and ammonia and substituted benzenes from a continuous ladder of proton transfer equilibria measurementsJournal of the American Chemical Society, 1976
- Directing, activating and deactivating effectsPublished by Wiley ,1973
- Stable carbocations. CXXXVI. Intramolecular 1,2-hydrogen shifts in difluoro- and dimethylbenzenium ionsJournal of the American Chemical Society, 1972
- Aromatic Substitution. XI.1 The AlCl3CH3NO2-Catalyzed Benzylation of Halobenzenes with Benzyl Chloride in Nitromethane SolutionJournal of the American Chemical Society, 1962
- 948. A quantitative treatment of electrophilic aromatic substitutionJournal of the Chemical Society, 1960