Fragmentation of intermediate radical anions determines the main features of the hydrodefluorination of isomeric perfluoroxylenes. Quantum chemical substantiation-Reference-Cited by-同舟云学术

Fragmentation of intermediate radical anions determines the main features of the hydrodefluorination of isomeric perfluoroxylenes. Quantum chemical substantiation

Published:2022-05 Issue: Volume:257-258 Page:109976
ISSN:0022-1139
Container-title:Journal of Fluorine Chemistry
language:en
Short-container-title:Journal of Fluorine Chemistry

Author:

Andreev R.V.^ORCID,Beregovaya I.V.,Shchegoleva L.N.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry

Reference26 articles.

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3. Potential energy surface and dissociative cleavage of chlorobenzene radical anion;Beregovaya;Chem. Phys. Letters.,2001

4. Dissociative attachment in vinyl and allyl chloride, chlorobenzene and benzyl chloride;Stricklett;Chem. Phys. Letters.,1986

5. Symmetry control in bond cleavage processes: dissociative electron attachment to unsaturated halocarbons;Dressler;Chimia,1985

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