Spectral luminescent properties of 2-aryl-5-(2,4,6-trimethylphenyl)-1Н-1,3,4-oxadiazoles


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Abstract

Reaction of aroylhydrazides with 2,4,6-trimethylbenzoyl chloride in the presence of Et3N afforded N-(mesityl)aroylhydrazides, which through subsequent cyclization at treatment with SOCl2 resulted in 2-aryl-5-(2,4,6-trimethylphenyl)-1Н-1,3,4-oxadiazoles. For 2-hydroxyphenyl derivative containing a stable O–H N intramolecular bond a low quantum luminescence yield is observed (φ 0.006–0.038) due to the nonradiative deactivation of the agitated state by ESPIT mechanism.

About the authors

Yu. M. Artyushkina

Southern Scientific Center of Russian Academy of Sciences; Southern Federal University

Email: mikhail@ipoc.sfedu.ru
Russian Federation, pr. Chekhova 41, Rostov-on-Don, 344006; Rostov-on-Don

I. E. Mikhailov

Southern Scientific Center of Russian Academy of Sciences; Research Institute of Physical and Organic Chemistry

Author for correspondence.
Email: mikhail@ipoc.sfedu.ru
Russian Federation, pr. Chekhova 41, Rostov-on-Don, 344006; Rostov-on-Don

G. A. Dushenko

Southern Scientific Center of Russian Academy of Sciences; Research Institute of Physical and Organic Chemistry

Email: mikhail@ipoc.sfedu.ru
Russian Federation, pr. Chekhova 41, Rostov-on-Don, 344006; Rostov-on-Don

O. I. Mikhailova

Research Institute of Physical and Organic Chemistry

Email: mikhail@ipoc.sfedu.ru
Russian Federation, Rostov-on-Don

Yu. V. Revinskii

Southern Scientific Center of Russian Academy of Sciences

Email: mikhail@ipoc.sfedu.ru
Russian Federation, pr. Chekhova 41, Rostov-on-Don, 344006

O. N. Burov

Southern Federal University

Email: mikhail@ipoc.sfedu.ru
Russian Federation, Rostov-on-Don

S. V. Kurbatov

Southern Federal University

Email: mikhail@ipoc.sfedu.ru
Russian Federation, Rostov-on-Don

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