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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Published in | Russian chemical bulletin Vol. 69; no. 12; pp. 2302 - 2306 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.12.2020
|
Subjects | |
Online Access | Get full text |
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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). |
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ISSN: | 1066-5285 1573-9171 |
DOI: | 10.1007/s11172-020-3039-5 |