Are Anion Radicals Nucleophiles and/or Outersphere Electron Donors? An Ab Initio Study of the Reaction of Ethylene and Formaldehyde Anion Radicals with Methyl Fluoride and Chloride-Reference-Cited by-同舟云学术

Are Anion Radicals Nucleophiles and/or Outersphere Electron Donors? An Ab Initio Study of the Reaction of Ethylene and Formaldehyde Anion Radicals with Methyl Fluoride and Chloride

Published:1996-01-01 Issue:24 Volume:118 Page:5737-5744
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Bertran Juan¹,Gallardo Iluminada¹,Moreno Miquel¹,Savéant Jean-Michel¹

Affiliation:

1. Contribution from the Departament de Quimica, Unitat de Quimica Fisica, Universitat Autonoma de Barcelona, 08193, Bellaterra, Barcelona, Spain, and the Laboratoire d'Electrochimie Moléculaire de l'Université Denis Diderot, Unité Associée au CNRS No 438, 2 place Jussieu, 75251 Paris Cedex 05, France

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja953679t

Reference41 articles.

1. On the Coupling of Anion Radicals with Sterically Hindered Alkyl Halides.

2. Dissociative electron transfer. Homogeneous and heterogeneous reductive cleavage of the carbon-halogen bond in simple aliphatic halides

3. Homogeneous redox catalysis of multielectron electrochemical reactions

4. Single Electron Transfer as Rate-Determining Step in an Aliphatic Nucleophilic Substitution.

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