1217-99-8Relevant academic research and scientific papers
The nitro aromatic compounds detection by triazole carboxylic acid and its complex with the fluorescent property
Yan, Jie,Ni, Jue Chen,Zhao, Jin Xin,Sun, Li Xian,Bai, Feng Ying,Shi, Zhan,Xing, Yong Heng
, p. 2682 - 2689 (2017)
The 5-methyl-1-(4-nitrophenyl)-1H-1, 2, 3-triazole-4-carboxylic acid (1) was synthesized by an improved method. By using the compound 1 as ligand, a new complex [Cu(L)2][Cu(L)2(H2O)2] (2) was prepared firstly under hydrothermal condition. Both 1 and 2 were all used as exclusive fluorescence sensor for 2, 4, 6-trinitrophenol (TNP) for the first time. The fluorescence exploration demonstrated that they exhibit highly selective and sensitive (KSV?=?393685?M?1 and KSV?=?213269?M?1, respectively) sensing to TNP from other nitro aromatic compounds (NACs) with high quenching efficiency QP value of 96.76% and 93.37%, as well as low detection limit (0.68?μM and 0.37?μM, respectively). It means that complex 2 had higher selectivity due to the less interference by 4-NT and 2-NP compared with 1. Moreover, the fluorescence quenching phenomenon of sensor 1 with TNP was analyzed by density functional theory (DFT).
Synthesis and antibacterial activity of di-heteryl substitued [1,2,4]triazolo [3,4-b] [1,3,4]thiadiazoles
Sanjeeva Reddy,Vani Devi,Sunitha,Kalyani,Nagaraj
, p. 590 - 597 (2017/01/18)
A new series of 3-(5-methyl-1-phenyl-1H-4-pyrazolyl)-6-(5-methyl-1-aryl-1H-1,2,3-triazol-4-yl)[1,2,4]triazolo [3,4-b][1,3,4]thiadiazoles 12a-j have been prepared and assayed for their antibacterial activity against human pathogenic Gram-positive bacteria viz., Staphylococcus aureus, Bacillus subtilis and Gram-negative Escherichia coli. Among the screened compounds 12b, 12c and 12f, in which phenyl ring of triazole moiety bear 4-chloro, 4-nitro and 4-fluoro substituents respectively, showed high activity against all the micro-organisms employed. The activities of these compounds are almost equal to the standards.
The synthesis of some new (S)-1-aryl-N-(1-hydroxy-3-phenylpropan-2-yl)-5- methyl-1H-1,2,3-triazole-4-carboxamide
Shen,Chen,Wu,Dong
, p. 781 - 786 (2013/08/23)
Some new (S)-1-aryl-N-(1-hydroxy-3-phenylpropan-2-yl)-5-methyl-1 H-1,2,3-triazole-4-carboxamides 4a, 4b, 4c, 4d, 4e, 4f, 4g, 4h, 4i, 4j have been synthesized and established by 1H and 13C NMR, IR, MS spectra, CHN analyses, and x-ray
Synthesis and mesomorphic properties of novel [1,2,3]-triazole mesogenic based compounds
Benbayer, Chahinez,Kheddam, Narimane,Sa?di-Besbes, Salima,Givenchy, Elisabeth Taffin De,Guittard, Frédéric,Grelet, Eric,Safer, Abdel Mounaim,Derdour, A?cha
, p. 22 - 28 (2013/03/13)
A series of five-membered heterocyclic 1,2,3-triazole derivatives with different substituents in N1 position was synthesized. The heterocyclic moiety was connected through an ester function to a p-decyloxyphenyl or p-decyloxybiphenyl tails Polarized micro
Synthesis of 2,1-benzisoxazoles by nucleophilic substitution of hydrogen in nitroarenes activated by the azole ring
Pokhodylo, Nazariy T.,Teslenko, Yuriy O.,Matiychuk, Vasyl S.,Obushak, Mykola D.
experimental part, p. 2741 - 2748 (2010/02/28)
Reaction of 1-nitro-4-(1,2,3-triazolyl/tetrazolyl)benzenes with arylacetonitriles in an alcoholic medium in the presence of excess alkali gives novel 2,1-benzisoxazoles. These findings indicate a high reactivity of nitroarenes activated by the azole ring due to their electron-deficient character. Moreover, it was found that annulation of the isoxazole ring occurred regioselectively in disubstituted nitroarenes. In the case of 1-(4-nitrophenyl)-1H-tetrazole, the tetrazole ring cleaved faster than the sH-adduct was formed. Georg Thieme Verlag Stuttgart.
