Synthesis and crystal strucrure of Bis-(2,6-diaminopyridine) tetrachlorid zinc(II)
- 作者: Nazarov Y.E.1, Turaev X.X.1, Ashurov J.M.2, Kasimov S.A.1, Suyunov J.R.1, Ermuratova N.A.3, Kornilov K.N.4
-
隶属关系:
- Termez State University
- Institute of Bioorganic Chemistry of the Academy of Sciences of the Republic of Uzbekistan
- Termez Engineering and Technology Institute
- Russian Biotechnological University
- 期: 卷 70, 编号 3 (2025)
- 页面: 486-494
- 栏目: STRUCTURE OF ORGANIC COMPOUNDS
- URL: https://journals.rcsi.science/0023-4761/article/view/293804
- DOI: https://doi.org/10.31857/S0023476125030154
- EDN: https://elibrary.ru/BCSFJL
- ID: 293804
如何引用文章
详细
In the presented work, the synthesis of a complex resulting from the reaction of 2,6-diaminopyridine with the Zn(II) ion in an alcohol solution of hydrochloric acid is described for the first time. The composition, molecular and crystal structure of the synthesized complex were determined by X-ray structural analysis. The structure of the new complex, its crystallographic data, and the geometry of hydrogen bonds in the crystal system were determined. The composition of the metal complex was confirmed by elemental analysis, and the existing chemical bonds were studied by IR spectroscopy. The surface of the crystals was studied according to Hirschfeld. To determine the stability of the obtained complex, its thermal analysis was carried out. The stability of the complex, caused by intramolecular hydrogen bonds, was confirmed.
全文:

作者简介
Y. Nazarov
Termez State University
Email: kornilovkn@mgupp.ru
乌兹别克斯坦, Termez
X. Turaev
Termez State University
Email: kornilovkn@mgupp.ru
乌兹别克斯坦, Termez
J. Ashurov
Institute of Bioorganic Chemistry of the Academy of Sciences of the Republic of Uzbekistan
Email: kornilovkn@mgupp.ru
乌兹别克斯坦, Tashkent
Sh. Kasimov
Termez State University
Email: kornilovkn@mgupp.ru
乌兹别克斯坦, Termez
J. Suyunov
Termez State University
Email: kornilovkn@mgupp.ru
乌兹别克斯坦, Termez
N. Ermuratova
Termez Engineering and Technology Institute
Email: kornilovkn@mgupp.ru
乌兹别克斯坦, Termez
K. Kornilov
Russian Biotechnological University
编辑信件的主要联系方式.
Email: kornilovkn@mgupp.ru
俄罗斯联邦, Moscow
参考
- Liu S.H., Chen J.-D., Liou L.-S., Wang J.-C. // Inorg. Chem. 2001. V. 40. № 25. P. 6499. https://doi.org/10.1021/ic010529c
- Moussa O.B., Chebbi H., Zid M.F. // J. Molec. Struct. 2019. V. 1180. P. 72. https://doi.org/10.1016/j.molstruc.2018.11.077
- Andreini C., Bertini I. // J. Inorg. Biochem. 2012. V. 111. P. 150. https://doi.org/10.1016/j.jinorgbio.2011.11.020
- Balan A.M., Ashoki R.F.N., Vasanthi M. et al. // Int. J. Life Sci. Pharm. Res. 2013. V. 3. № 2. P. 67. https://www.ijlpr.com/index.php/journal/article/view/376/278
- Crea F., De Stefano C., Milea D., Sammartano S. // J. Solution Chem. 2009. V. 38. P. 115. https://link.springer.com/article/10.1007/s10953-008-9357-0
- Cigala R.M., Crea F., De Stefano С. et al. // J. Mol. Liq. 2012. V. 165. P. 143. https://doi.org/10.1016/j.molliq.2011.11.002
- Cigala R.M., Crea F., De Stefano C. et al. // Monatch. Chem. 2015. V. 146. P. 527. https://doi.org/10.1007/s00706-014-1394-3
- Umirova G.A., Turaev Kh.Kh., Alimnazarov B.Kh. et al. // Acta Cryst. E. 2023. V. 79. № 9. P. 856. https://doi.org/10.1107/S2056989023007466
- Suyunov J.R., Turaev Kh.Kh., Alimnazarov B.Kh. et al. // IUCrData. 2023. V. 8. № 12. P. x231032. https://doi.org/10.1107/S2414314623010325
- Shoukry A.A., Al-Mhayawi S.R. // Eur. J. Chem. 2013. № 4. Р. 260. https://doi.org/10.5155/eurjchem.4.3.260-267.800
- Hall V.M., Bertke J.A., Swift J.A. // Acta Cryst. С. 2017. V. 73. № 11. P. 990. https://doi.org/10.1107/S2053229617014978
- Sakong C. // Dyes and Pigments. 2011. V. 88. № 2. P. 166. https://doi.org/10.1016/j.dyepig.2010.06.003
- Coelho P.J. // Dyes and Pigments. 2012. V. 92. № 1. P. 745. https://doi.org/10.1016/j.dyepig.2011.06.019
- Groom C.R. // Acta Cryst. B. 2016. V. 72. № 2. P. 171. https://doi.org/10.1107/S2052520616003954
- Raposo M.M. // Tetrahedron. 2011. V. 67. № 29. P. 5189. https://doi.org/10.1016/j.tet.2011.05.053
- Khanmohammadi H. // Dyes and Pigments. 2013. V. 98. № 3. P. 557. https://doi.org/10.1016/j.dyepig.2013.03.023
- Mahmoud W.H., Sayed F.N., Mohamed G.G. // Appl. Organometall. Chem. 2016. V. 30. № 11. P. 959. https://doi.org/10.1002/aoc.3529
- Merino E. // Chem. Soc. Rev. 2011. V. 40. № 7. P. 3835. https://doi.org/10.1039/C0CS00183J
- Rigaku Oxford Diffraction, CrysAlisPro Software System, Version 1.171.40.84a. 2020. Rigaku Corporation, Oxford, UK
- Sheldrick G.M. // Acta Cryst. А. 2015. V. 71. P. 3. https://doi.org/10.1107/S2053273314026370
- Sheldrick G.M. // Acta Cryst. C. 2015. V. 71. P. 3. https://dx.doi.org/10.1107/S2053229614024218
- Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Cryst. 2009. V. 42. P. 339. https://dx.doi.org/10.1107/S0021889808042726
- Nazarov Y.E., Turaev Kh.Kh., Alimnazarov B.Kh. et al. // IUCrData. 2024. V. 9. № 6. Р. x240570. https://doi.org/10.1107/S2414314624005704
- Ben Moussa O., Chebbi H., Zid M.F. // Acta Cryst. E. 2018. V. 74. № 4. P. 436. https://doi.org/10.1107/S2056989018003171
- Suyunov J.R., Turaev Kh.Kh., Alimnazarov B.Kh. et al. // Acta Cryst. E. 2023. V. 79. P. 1083. https://doi.org/10.1107/S2056989023009350
- Mghandef M., Boughzala H. // Acta Cryst. E. 2015. V. 71. № 5. P. 555. https://doi.org/10.1107/S2056989015007707
- Nasr M.B., Soudani S., Lefebvre F. et al. // J. Mol. Struct. 2017. V. 138. P. 71. https://doi.org/10.1016/j.molstruc.2017.02.098
- Spackman P.R., Byrom P.J. // Chem. Phys. Lett. 1997. V. 267. № 3–4. Р. 215. https://doi.org/10.1016/S0009-2614(97)00100-0
补充文件
