Luminescence Properties of 2-[2-Allyl(arenesulfonyl)oxyphenyl]- 5-(2,6-difluorophenyl)-1,3,4-oxadiazoles


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The alkylation of 2-(2,6-difluorophenyl)-5-(2-hydroxyphenyl)-1,3,4-oxadiazole with allyl bromide gave 2-(2-allyloxyphenyl)-5-(2,6-difluorophenyl)-1,3,4-oxadiazole, and sulfonylation of the same substrate with benzene- and p-toluenesulfonyl chlorides afforded the corresponding 2-(2-arenesulfonyloxyphenyl)-5-(2,6-difluorophenyl)-1,3,4-oxadiazoles. 2-(2-Allyloxyphenyl)- and 2-(2-tosyloxyphenyl)-5-(2,6-difluorophenyl)- 1,3,4-oxadiazoles showed strong luminescence in the ultraviolet region (λmaxfl 335–374 nm, φ = 0.12–0.80), whereas the luminescence quantum yield of 2-(2-benzenesulfonyloxyphenyl)-5-(2,6-difluorophenyl)- 1,3,4-oxadiazole was considerably lower (λmaxfl 334–338 nm, φ = 0.012–0.090).

作者简介

I. Mikhailov

Research Institute of Physical and Organic Chemistry; Southern Scientific Center

编辑信件的主要联系方式.
Email: mikhail@ipoc.sfedu.ru
俄罗斯联邦, pr. Stachki 194/2, Rostov-on-Don, 344090; ul. Chekhova 41, Rostov-on-Don, 344006

Yu. Artyushkina

Research Institute of Physical and Organic Chemistry

Email: mikhail@ipoc.sfedu.ru
俄罗斯联邦, pr. Stachki 194/2, Rostov-on-Don, 344090

G. Dushenko

Research Institute of Physical and Organic Chemistry

Email: mikhail@ipoc.sfedu.ru
俄罗斯联邦, pr. Stachki 194/2, Rostov-on-Don, 344090

O. Mikhailova

Research Institute of Physical and Organic Chemistry

Email: mikhail@ipoc.sfedu.ru
俄罗斯联邦, pr. Stachki 194/2, Rostov-on-Don, 344090

Yu. Revinskii

Southern Scientific Center

Email: mikhail@ipoc.sfedu.ru
俄罗斯联邦, ul. Chekhova 41, Rostov-on-Don, 344006

V. Minkin

Research Institute of Physical and Organic Chemistry

Email: mikhail@ipoc.sfedu.ru
俄罗斯联邦, pr. Stachki 194/2, Rostov-on-Don, 344090

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