Mechanistic Crossover Induced by Steric Hindrance: A Theoretical Study of Electron Transfer and Substitution Mechanisms of Cyanoformaldehyde Anion Radical and Alkyl Halides-Reference-Cited by-同舟云学术

Mechanistic Crossover Induced by Steric Hindrance: A Theoretical Study of Electron Transfer and Substitution Mechanisms of Cyanoformaldehyde Anion Radical and Alkyl Halides

Published:1998-02-20 Issue:9 Volume:120 Page:2131-2145
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Sastry G. Narahari¹,Shaik Sason¹

Affiliation:

1. Contribution from the Institute of Physical Chemistry, University of Fribourg, Perolles, CH-1700 Fribourg, Switzerland, and The Department of Organic Chemistry and the Lise Meitner-Minerva Center for Computational Quantum Chemistry, The Hebrew University, Jerusalem 91904, Israel

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja972746b

Reference36 articles.

1. Towards the Definition of the Maximum Allowable Tightness of an Electron Transfer Transition State in the Reactions of Radical Anions and Alkyl Halides

2. Electron Transfer and Charge Transfer: Twin Themes in Unifying the Mechanisms of Organic and Organometallic Reactions

3. On the Occurrence of Electron Transfer in Aliphatic Nucleophilic Substitution.

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