Synthesis, structures, and photochromic properties of N-aryl-3-indolylfulgides View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2008-07

AUTHORS

S. K. Balenko, V. P. Rybalkin, N. I. Makarova, S. O. Bezuglyi, E. N. Shepelenko, L. L. Popova, V. V. Tkachev, S. M. Aldoshin, A. V. Metelitsa, V. A. Bren’, V. I. Minkin

ABSTRACT

New 3-indolylfulgides, viz., 3-[1-(1-aryl-5-methoxy-2-methyl-1H-indol-3-yl)ethylidene]-4-(1-methylethylidene)tetrahydro-2,5-furandiones, were synthesized. These compounds were obtained as E-isomers, as demonstrated by X-ray diffraction, electronic spectroscopy, and 1H NMR spectroscopy. Fulgides exhibit photochromic properties in solution. The cyclic dihydrocarbazole photoisomers of indolylfulgides show fluorescence properties and are characterized by high thermal stability.

PAGES

1435-1443

References to SciGraph publications

  • 1998-09. Fluorescent photochromic fulgides in RESEARCH ON CHEMICAL INTERMEDIATES
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s11172-008-0186-5

    DOI

    http://dx.doi.org/10.1007/s11172-008-0186-5

    DIMENSIONS

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