Issue 7, 1997
From the journal:

Journal of Chemical Research, Synopses

EPR Studies on Carboxylic Esters. Part 14.1 Radical Anions of O-Phenyl Halobenzenecarbothioates

Jürgen Voss,   Thomas Behrens,   Manfred Krasmann,   Kai Osternack  and  Lilia Prangova  

Abstract

Radical anions of O-phenyl halobenzenecarbothioates are generated by in situ electroreduction and shown to be mostly persistent by their EPR spectra; in certain cases, dependent on the nature and position of the halogen substituent, elimination of halide anions occurs.

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Article information

DOI
https://doi.org/10.1039/A700763I
Article type
Paper

J. Chem. Res. (S), 1997, 252-253

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EPR Studies on Carboxylic Esters. Part 14.1 Radical Anions of O-Phenyl Halobenzenecarbothioates

J. Voss, T. Behrens, M. Krasmann, K. Osternack and L. Prangova, J. Chem. Res. (S), 1997, 252 DOI: 10.1039/A700763I

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