Theoretical Study of Carbon−Halogen Bond Dissociation Enthalpies of Substituted Benzyl Halides. How Important Are Polar Effects?1
- 1 May 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 121 (20) , 4877-4882
- https://doi.org/10.1021/ja982866z
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Carbon−Oxygen Bond Strength in Diphenyl Ether and Phenyl Vinyl Ether: An Experimental and Computational StudyThe Journal of Physical Chemistry A, 1997
- Energies of Activation. The Paradigm of Hydrogen Abstractions by RadicalsJournal of the American Chemical Society, 1995
- Electron transfer and bond breaking. Examples of passage from a sequential to a concerted mechanism in the electrochemical reductive cleavage of arylmethyl halidesJournal of the American Chemical Society, 1992
- Are relative bond energies a measure of radical stabilization energies?Journal of the American Chemical Society, 1991
- Stabilities of substituted benzyl radicals: dissociation rates of amino-, hydroxy-, and cyanoethylbenzenesThe Journal of Physical Chemistry, 1989
- Real-time reaction monitoring by continuous-introduction ion-spray tandem mass spectrometryJournal of the American Chemical Society, 1989
- Density-functional exchange-energy approximation with correct asymptotic behaviorPhysical Review A, 1988
- Synthesis, characterization, and x-ray crystal structure of a donor-stabilized bis(silylene)iron complexJournal of the American Chemical Society, 1988
- Quantitative relationship between bond dissociation energies, infrared stretching frequencies, and force constants in polyatomic moleculesThe Journal of Physical Chemistry, 1987
- Tricyclo[3.2.1.01.5]octane. 3,2,1-PropellaneJournal of the American Chemical Society, 1972