P-HOLATDA TURLI O'RINBOSARLAR BO'LGAN AMINLAR ASOSIDA 2-NAFTOL BILAN AZOBIRIKMALAR SINTEZI
Загрузки
В данной статье изучен синтез азосоединений на основе ароматических аминов с различными заместителями в пара-
положении и 2-нафтола. Были рассмотрены условия реакции, физико-химические свойства азосоединений и структура
полученных продуктов, определённая с помощью спектроскопических методов. На основе полученных результатов
исследовано влияние заместителей на выход продуктов реакции.
1. Valiulin R. Organic Chemistry: 100 Must-Know Mechanisms // Organic Chemistry: 100 Must-Know Mechanisms. – De Gruyter, – 2020. – P. 97-98.
2. Kareem A. F., Thejeel K. A., Ismael H. I. Review, Analyses of azo dyes' synthesis, characterization and biological activity // Texas Journal of Multidisciplinary Studies. – 2022. – V. 12. – P. 14-20.
3. Ju Y., Kumar D., Varma R. S. Revisiting nucleophilic substitution reactions: microwave-assisted synthesis of azides, thiocyanates, and sulfones in an aqueous medium // The Journal of organic chemistry. – 2006. – V. 71. – №. 17. – P. 6697-6700.
4. Iranpoor N. et al. Conversion of alcohols, thiols, carboxylic acids, trimethylsilyl ethers, and carboxylates to thiocyanates with triphenylphosphine / diethylazodicarboxylate / NH4SCN // Synthesis. – 2004. – V. 4. – №. 01. – P. 92-96.
5. Odey J. O. et al. Experimental and theoretical studies of the electrochemical properties of mono azo dyes derived from 2-nitroso-1-naphthol, 1-nitroso-2-naphthol, and CI disperse yellow 56 commercial dye in dye-sensitized solar cell //Journal of Molecular Structure. – 2021. – Т. 1241. – С. 130615.
6. Attoh C. N. D. et al. Antimicrobial, antioxidant, and anti-inflammatory evaluation of synthesised Azo compounds based on β-naphthol, Catechol and Quinol Nucleus //J Pharm Res Int. – 2022. – Т. 34. – С. 48-64
7. Zhang Y. et al. An environmentally friendly approach to the green synthesis of azo dyes with aryltriazenes via ionic liquid promoted CN bonds formation //Dyes and Pigments. – 2018. – Т. 158. – С. 438-444
8. Çanakçı D., Serin S. Synthesis of new azo dye polymers based on naphthol by oxidative polycondensation: antimicrobial activity and fastness studies //Journal of Polymer Research. – 2020. – Т. 27. – С. 1-23
9. Kocaokutgen H., Gümrükçüoğlu I. E. Thermal characterization of some azo dyes containing intermolecular hydrogen bonds and non-bonds //Journal of thermal analysis and calorimetry. – 2003. – Т. 71. – С. 675-679
10. Gür M., Kocaokutgen H., Taş M. Synthesis, spectral, and thermal characterisations of some azo-ester derivatives containing a 4-acryloyloxy group //Dyes and Pigments. – 2007. – Т. 72. – №. 1. – С. 101-108
11. Jin J. et al. One-pot diazo coupling reaction under microwave irradiation in the absence of solvent //Synthetic Communications. – 2000. – Т. 30. – №. 5. – С. 829-834.
12. B. Aslam, W. Wang, M. I. Arshad et al., “Antibiotic resistance: a rundown of a global crisis,” Infection and Drug Resistance, vol. 11, pp. 1645–1658, 2018
13. Shridhar A. H. et al. Synthesis and biological activities of Bis alkyl 1, 3, 4-oxadiazole incorporated azo dye derivatives //Arabian Journal of Chemistry. – 2016. – Т. 9. – С. S1643-S1648.
Copyright (c) 2025 «ВЕСТНИК НУУз»
Это произведение доступно по лицензии Creative Commons «Attribution-NonCommercial-ShareAlike» («Атрибуция — Некоммерческое использование — На тех же условиях») 4.0 Всемирная.
.jpg)
2.png)
