Research output: Contribution to journal › Article › peer-review
Azo dyes containing 1,3,4-thiadiazole fragment: Synthesis and properties. / Selivanova, Galina; Skolyapova, Alexandrina; Wang, Jiaying et al.
In: New Journal of Chemistry, Vol. 46, No. 4, 28.01.2022, p. 1929-1942.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Azo dyes containing 1,3,4-thiadiazole fragment: Synthesis and properties
AU - Selivanova, Galina
AU - Skolyapova, Alexandrina
AU - Wang, Jiaying
AU - Karpova, Elena
AU - Shundrina, Inna
AU - Bagryanskaya, Irina
AU - Amosov, Evgeny
N1 - Funding Information: This work was supported by Ministry of Science and Higher Education of the Russian Federation (grant AAAA-A21-121011490017-5). Authors would like to acknowledge the Multi-Access Chemical Research Center SB RAS for spectral and analytical measurements (O. B. Stacenko). Publisher Copyright: © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
PY - 2022/1/28
Y1 - 2022/1/28
N2 - New 1,3,4-thiadiazole derivatives containing a diazenyl group, as well as both a diazenyl and an imino group, were synthesized and their optical and thermal properties were investigated. Initially, new azo compounds containing an azo group directly in the thiadiazole block were obtained by the coupling of diazonium bisulfates based on the previously known 5-derivatives of 2-amino-1,3,4-thiadiazoles with N,N-dialkyl anilines (N(n-Bu)2, NEt2, and NEt(EtOH)). Schiff bases were obtained by the interaction of p-toluidine, p-phenylenediamine and p-aminophenol with azo compounds containing an aldehyde group in the 1,3,4-thiadiazole ring. The new dyes were characterized by spectral (IR, UV, 1H NMR, 13C NMR and mass spectra) and X-ray analyses. This journal is
AB - New 1,3,4-thiadiazole derivatives containing a diazenyl group, as well as both a diazenyl and an imino group, were synthesized and their optical and thermal properties were investigated. Initially, new azo compounds containing an azo group directly in the thiadiazole block were obtained by the coupling of diazonium bisulfates based on the previously known 5-derivatives of 2-amino-1,3,4-thiadiazoles with N,N-dialkyl anilines (N(n-Bu)2, NEt2, and NEt(EtOH)). Schiff bases were obtained by the interaction of p-toluidine, p-phenylenediamine and p-aminophenol with azo compounds containing an aldehyde group in the 1,3,4-thiadiazole ring. The new dyes were characterized by spectral (IR, UV, 1H NMR, 13C NMR and mass spectra) and X-ray analyses. This journal is
UR - http://www.scopus.com/inward/record.url?scp=85123468477&partnerID=8YFLogxK
U2 - 10.1039/d1nj05084b
DO - 10.1039/d1nj05084b
M3 - Article
AN - SCOPUS:85123468477
VL - 46
SP - 1929
EP - 1942
JO - New Journal of Chemistry
JF - New Journal of Chemistry
SN - 1144-0546
IS - 4
ER -
ID: 35380550