Back to Search Start Over

Sydnon-äthylene. III. Chemische Reaktionen elektronisch angeregter 4-Styryl-sydnone

Authors :
Bernd‐Michael Neumann
D. Gloyna
H.‐G. Henning
Joachim Sauer
Source :
Journal für Praktische Chemie. 320:81-90
Publication Year :
1978
Publisher :
Wiley, 1978.

Abstract

Sydnone Ethylenes. III. Chemical Reactions of Excited 4-Styryl-sydnones Dependent on the character of the substituents in the photo reactions of 4-styryl sydnones Z/E-isomerism competes with CO2-elimination. Excited p-nitrostyryl sydnones exhibit a relatively strong degradation of the bond order in the CC region. Their quantum yields of Z/E-isomerism are therefore much higher than those of compounds with p-substituents of lower acceptor effect. In these compounds the cleavage of the sydnone ring with elimination of carbon dioxide is favoured especially if a methyl group is in 3-position of the sydnone.

Details

ISSN :
00218383
Volume :
320
Database :
OpenAIRE
Journal :
Journal für Praktische Chemie
Accession number :
edsair.doi...........df428a5d8fe2eaaac895852f236bde39
Full Text :
https://doi.org/10.1002/prac.19783200110