Second Example of a Cubane-Like Nickel(II) Complex in a Series of N-Derivatives of Taurine

E. O. Zemlyakova; Землякова Е. О.; L A. Khamidullina; Хамидуллина Л. А.; I. S. Puzyrev; Пузырев И. С.; P. D. Tobysheva; Тобышева П. Д.; Yu. S. Petrova; Петрова Ю. С.; L. K. Neudachina; Неудачина Л. К.; P. A. Slepukhin; Слепухин П. А.; A. V. Pestov; Пестов А. В.

doi:10.31857/S0132344X2260045X

Second Example of a Cubane-Like Nickel(II) Complex in a Series of N-Derivatives of Taurine

作者: Zemlyakova E.O.¹, Khamidullina LA.¹^,2, Puzyrev I.S.¹, Tobysheva P.D.¹, Petrova Y.S.², Neudachina L.K.², Slepukhin P.A.¹, Pestov A.V.¹^,2
隶属关系:
1. Postovskii Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences, Yekaterinburg, Russia
2. Ural Federal University named after the first President of Russia B.N. Yeltsin, Yekaterinburg, Russia
期: 卷 49, 编号 7 (2023)
页面: 441-448
栏目: Articles
URL: https://journal-vniispk.ru/0132-344X/article/view/137298
DOI: https://doi.org/10.31857/S0132344X2260045X
EDN: https://elibrary.ru/TUZEZI
ID: 137298

如何引用文章

全文:

开放存取

##reader.subscriptionAccessGranted##
受限制的访问

订阅存取

详细
作者简介
参考
补充文件
统计

详细

A new homometallic cubane-like nickel(II) complex based on N-2-(2-pyridyl)ethyl-2-aminoethanesulfonic acid [Ni4L4(OH)4]·2H2O (I) is synthesized, and its structure is studied by X-ray diffraction (XRD) (CIF file CCDC no. 2211359). In crystals of the complex, the metallocenters are joined into tetrahedra with the Ni…Ni distances (3.144–3.201 Å) supplemented to cubanes by the μ3-bridging oxygen atoms of the hydroxy groups. The coordination environment of each metallocenter is a distorted octahedron. The ligand is deprotonated, exists in the facial conformation, and performs the tridentate function to form two six-membered conjugated chelate cycles.

关键词

cubane-like nickel(II) complex, N-derivatives of taurine, complex formation, XRD

参考

Пестов А.В., Слепухин П.А., Чарушин В.Н. // Успехи химии. 2015. Т. 84. № 3. С. 310 (Pestov A.V, Slepukhin P.A., Charushin V.N. // Russ. Chem. Rev. 2015. V. 84. № 3. P. 310). https://doi.org/10.1070/RCR4461
Петрова Ю.С., Неудачина Л.К. // Журн. неорган. химии. 2013. Т. 58. № 5. С. 697 (Petrova Y.S., Neudachina L.K. // Russ. J. Inorg. Chem. 2013. V. 58. № 5. P. 617). https://doi.org/10.1134/S0036023613050173
Землякова Е.О., Пестов А.В., Слепухин П.А. и др. // Коорд. химия. 2018. Т. 44. № 11. С. 667 (Zemlyakova E.O., Pestov A.V., Slepukhin P.A. et al. // Russ. J. Coord. Chem. 2018. V. 44. № 11. P. 667). https://doi.org/10.1134/S107032841811009X
Ульянова М.И., Баскакова С.А., Аксенова Т.В. и др. // Коорд. химия. 2015. Т. 41. № 4. С. 213 (Ul’yanova, M.I., Baskakova, S.A., Aksenova, T.V. et al. // Russ. J. Coord. Chem. 2015. V. 41. P. 240). https://doi.org/10.1134/S1070328415040090
Пестов А.В., Слепухин П.А., Корякова О.В. и др. // Коорд. химия. 2014. Т. 40. № 4. С. 216 (Pestov A.V., Slepukhin P.A., Koryakova O.V. et al. // Russ. J. Coord. Chem. 2014. V. 40. P. 216). https://doi.org/10.1134/S107032841404006X
Yusuf M., Fariduddin Q., Hayat S. et al. // Bull. Environ. Contam. Toxicol. 2011. V. 86. № 1. P. 1.
Fabiano C.C., Tezotto T., Favarin J. et al. // Front. Plant Sci. 2015. V. 6. № 654.
Li J.X., Jiang Y.M., Chen M.J. // J. Coord. Chem. 2008. V. 61. № 11. P. 1765.
Hosler E.R., Herbst R.W., Maroney M.J. et al. // Dalton Trans. 2012. V. 41. № 3. P. 804.
Chohan B.S., Maroney M.J. // Inorg. Chem. 2006. V. 45. № 5. P. 1906.
Henderson R.K., Bouwman E., Spek A.L. et al. // Inorg. Chem. 1997. V. 36. № 21. P. 4616.
Пестов А.В., Слепухин П.А., Ятлук Ю.Г. // Коорд. химия. 2011. Т. 37. № 8. С. 619 (Pestov A. V., Slepukhin P.A., Yatluk Y.G. // Russ. J. Coord. Chem. 2011. V. 37. № 8. P. 619). https://doi.org/10.1134/S1070328411070116
Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. A-ppl. Crystallogr. 2009. V. 42. № 2. P. 339.
Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3.