175135-75-8Relevant articles and documents
Synthesis and characterization of linear 1,4-diazine-triphenylamine–based selective chemosensors for recognition of nitroaromatic compounds and aliphatic amines
Baranova, Anna A.,Charushin, Valery N.,Chupakhin, Oleg N.,Chuvashov, Roman D.,Khokhlov, Konstantin O.,Kvashnin, Yuriy A.,Makarova, Nadezhda I.,Metelitsa, Anatoly V.,Rusinov, Gennady L.,Schapov, Il'ya E.,Shchepochkin, Aleksandr V.,Verbitskiy, Egor V.,Vetrova, Elena V.,Yakovleva, Yuliya A.,Zhilina, Ekaterina F.
, (2020)
Novel 1,4-diazine-based dyes of the D–π–A type, possessing triphenylamine as an electron-donating group, have been developed. Fluorescence studies have demonstrated that emission of these fluorophores is sensitive towards different nitroaromatic compounds and aliphatic amines, both in solutions and in a vapor phase. Moreover, these compounds can be considered as “naked-eye” fluorescent probes for solution polarity because they possess pronounced solvatochromic properties. Therefore, these compounds have to be regarded as potential multifunctional chemosensors for monitoring hazardous organic substances.
Synthesis of new heterocycles festooned with thiophene and evaluating their antioxidant activity
Abed, Nader A.,Hammouda, Mohamed M.,Ismail, Mohamed A.,Abdel-Latif, Ehab
, p. 4153 - 4163 (2020/09/09)
The chemical performance of 5-bromo-2-(bromoacetyl)-thiophene (1) was tested toward the reaction with numerous bi-nucleophilic reagents (namely; 2-aminobenzothiazoles, 2-aminothiazole, 2-aminotetrazole, 2-aminotriazole, 2-aminopyridines, 2-aminobenzimidaz
