Photochromic fluorescent indol-3-yl-substituted maleimides View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-03

AUTHORS

E. N. Shepelenko, N. I. Makarova, V. A. Podshibyakin, K. S. Tikhomirova, A. D. Dubonosov, A. V. Metelitsa, V. A. Bren, V. I. Minkin

ABSTRACT

New hetarylethenes, 3-(indol-3-yl)-4-thienyl(but-1-en-1-yl)-substituted pyrrole-2,5-diones containing coumarin or fluorene substituents on the pyrrole nitrogen atom, were synthesized by reactions of furan-2,5-diones with 9H-fluoren-2-amine and 6-amino-2H-chromen-2-one. Acyclic maleimide isomers showed fluorescence with quantum yields of 0.002 to 0.072. Their irradiation with UV light generates non-fluorescing cyclic isomer. The reverse ring opening occurs in the excited state. More... »

PAGES

366-370

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428017030095

DOI

http://dx.doi.org/10.1134/s1070428017030095

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1085138818


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