3,3'-DISULFANIDILBIS (1H-1,2,4-TRIAZOL-5-AMIN) SINTEZI
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Annotatsiya
Ishdan maqsad 3-amino-5-merkapto-1,2,4-triazoldan yangi organik modda 3,3'-disulfanidilbis(1H-1,2,4-triazol-5-amin)ni sintez qilishdir. Maqolada 3-amino-5-merkapto-1,2,4-triazolning ahamiyati va undan 3,3'-disulfanidilbis(1H-1,2,4-triazol-5-amin)ning eng maqbul sintez usuli keltirilgan. 3-amino-5-merkapto-1,2,4-triazol va 3,3'-disulfanidilbis(1H-1,2,4-triazol-5-amin)ning infraqizil va Raman spektroskopik tahlillari keltirilgan.
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Foydalaniladigan adabiyotlar
A. Kamal, MA. Syed, & SM. Mohammed. “Theraputic Potential of Benzothaizole” A Patent Review (2010- 2104). Informa healthcare, 25 (3), 2015.
AK. Singh, & KR. Kandel, “Synthesis of Triazole Derivative: [4-(Benzylideneamino)-5-phenyl-4H-1,2,4- triazole-3-thiol],” J. Nepal Chem. Soc., 30, 2012.
Артемьев Г.А., Уломский Е.Н., Русинов В.Л. “Оптимизация промышленных методов получения 5-амино-3-меркапто-1,2,4-триазола и 5-амино-3-метилтио-1,2,4-триазола”
Frank Hipler, Manuela Winter, Roland A. Fischer N–S–H hydrogen bonding in 2-mercapto-5-methyl-1,3,4-thiadiazole. Synthesis and crystal structures of mercapto functionalised 1,3,4-thiadiazoles.
Potts K.T. The chemistry of 1,2,4-triazoles.
Yanli Gai, Xitong Chen, Huajun Yang, Yanxiang Wang, Xianhui Bu A new strategy for constructing a disulfidefunctionalized ZIF-8 analogue using structuredirecting ligand–ligand covalent interaction.
K. Bahgat, & S. Fraihat, “Normal Coordinate Analysis, Molecular Structure, Vibrational, Electronic Spectra and NMR Investigation of 4-Amino-3-phenyl-1H-1,2,4- triazole-5(4H)-thione by Ab initio HF and DFT Method,” Spectrochimica Acta Part A: Mol. Biomol. Spectro., 135, 2015.
А. В. Васильев, Е. В. Гриненко, А. О. Щукин, Т. Г. Федулина Инфракрасная спектроскопия органических и природных соединений. САНКТ-ПЕТЕРБУРГ СПбГЛТА 2007. Ст-16.