A Theoretical Study of Chlorine Atom and Methyl Radical Addition to Nitrogen Bases: Why Do Cl Atoms Form Two-Center−Three-Electron Bonds Whereas CH3 Radicals Form Two-Center−Two-Electron Bonds?-Reference-Cited by-同舟云学术

A Theoretical Study of Chlorine Atom and Methyl Radical Addition to Nitrogen Bases: Why Do Cl Atoms Form Two-Center−Three-Electron Bonds Whereas CH3 Radicals Form Two-Center−Two-Electron Bonds?

Published:1996-01-01 Issue:43 Volume:118 Page:10571-10576
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

McKee Michael L.¹,Nicolaides Athanassios¹,Radom Leo¹

Affiliation:

1. Contribution from the Department of Chemistry, Auburn University, Auburn, Alabama 36849, and Research School of Chemistry, Australian National University, Canberra, ACT 0200, Australia

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9613973

Reference57 articles.

1. σ*-Radicals R3N — hal: electron paramagnetic resonance studies of the radiolysis of alkylammonium halides

2. Paramagnetic NH3Cl and NH3Br Color Centers in Irradiated Ammonium Halide Single Crystals

3. Pyridine complexes of chlorine atoms

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