Synthesis and photochromic properties of novel nonsymmetric dihetarylethenes based on benzindole and thiophene View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-08

AUTHORS

A. V. Metelitsa, V. P. Rybalkin, N. I. Makarova, P. V. Levchenko, V. S. Kozyrev, E. N. Shepelenko, L. L. Popova, V. A. Bren’, V. I. Minkina

ABSTRACT

Novel nonsymmetric dihetarylethenes 3-(5-methoxy-1,2-dimethyl-1H-benzo[g]indol-3-yl)-4-(3-thienyl)-furan-2,5-dione and 1-alkyl- and 1-aryl-3-(5-methoxy-1,2-dimethyl-1H-benzo[g]indol-3-yl-4-(3-thienyl)-1(H)-pyrrole-2,5-diones were synthesized. The substitution of the furandione moiety for pyrroledione gives rise to the radiation and photochemical channels of deactivation of the electron excitation energy of dihetarylethenes. The products of photolysis of pyrrolediones undergo recyclization in both the ground and excited states.

PAGES

1639-1644

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-010-0288-8

DOI

http://dx.doi.org/10.1007/s11172-010-0288-8

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1037138087


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