E. V. Lukovskaya, N. V. Dyachenko, A. V. Khoroshutin, A. A. Bobyleva, A. V. Anisimov, V. A. Karnoukhova, G. Jonusauskas, Yu. V. Fedorov, O. A. Fedorova, “Annelated tricyclic thiophenes and their photophysical properties”, Mendeleev Commun., 2018, Volume 28, Issue 5,Pages <nobr>543

This article is cited in 7 papers

Communications

Annelated tricyclic thiophenes and their photophysical properties

E. V. Lukovskaya^a, N. V. Dyachenko^a, A. V. Khoroshutin^a, A. A. Bobyleva^a, A. V. Anisimov^a, V. A. Karnoukhova^b, G. Jonusauskas^c, Yu. V. Fedorov^b, O. A. Fedorova^ab

^a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
^b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
^c Centre de Physique Moléculaire Optique et Hetzienne, University Bordeaux 1, France

Abstract: Photochemical oxidative cyclization of 3-[(E)-2-(3,4-di-methoxyphenyl)vinyl]thiophene and its 15-crown-5-analogue (15-[(E)-2-(3-thienyl)vinyl]-2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecine) affords the isomeric thiophene-containing fused aromatic compounds demonstrating photophysical properties different from those of initial styryl derivatives. E-Configuration of the initial styryl dye, 3-[(E)-2-(3,4-dimethoxyphenyl)vinyl]thiophene, has been proved by X-ray analysis.

Language: English

DOI: 10.1016/j.mencom.2018.09.032

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