2,5-Diaryl-1,3,4-oxadiazoles: synthesis, spectral-luminescent properties, and complexation with beryllium(ii)

Cyclization of aroylbenzohydrazides in SOCl 2 was used to obtain 2,5-diaryl-1,3,4-oxadiazoles, and to study their spectral-luminescent properties. Oxadiazoles with phenyl or 2-methoxyphenyl substituents at position 2 of the oxadiazole ring have a luminescence with a high quantum yield in polar and n...

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Bibliographic Details
Published inRussian chemical bulletin Vol. 69; no. 12; pp. 2302 - 2306
Main Authors Mikhailov, I. E., Artyushkina, Yu. M., Dushenko, G. A., Minkin, V. I.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.12.2020
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Summary:Cyclization of aroylbenzohydrazides in SOCl 2 was used to obtain 2,5-diaryl-1,3,4-oxadiazoles, and to study their spectral-luminescent properties. Oxadiazoles with phenyl or 2-methoxyphenyl substituents at position 2 of the oxadiazole ring have a luminescence with a high quantum yield in polar and nonpolar solvents (λ fl max = 378−424 nm, φ = 0.88−0.98). Replacement of these groups with a 2-phenol substituent results in a ligand with strong emission only in highly polar aprotic DMSO (λ fl max = 397 nm, φ = 0.18). Based on this ligand, a chelated beryllium complex with the composition L 2 Be was obtained, which has a strong luminescence in the violet region of the visible spectrum (λ fl max = 410−414 nm, φ = 0.34−0.48).
ISSN:1066-5285
1573-9171
DOI:10.1007/s11172-020-3039-5