Features of Cadmium(II) Complexation with N-Donor Heterocyclic Ligands in the Presence of the Octadecahydroeicosaborate Anion

V. V. Avdeeva; Авдеева В. В.; A. S. Kubasov; Кубасов А. С.; S. E. Nikiforova; Никифорова С. Е.; L. V. Goeva; Гоева Л. В.; E. A. Malinina; Малинина Е. А.; N. T. Kuznetsov; Кузнецов Н. Т.

doi:10.31857/S0044457X23601165

Features of Cadmium(II) Complexation with N-Donor Heterocyclic Ligands in the Presence of the Octadecahydroeicosaborate Anion

Autores: Avdeeva V.V.¹, Kubasov A.S.¹, Nikiforova S.E.¹, Goeva L.V.¹, Malinina E.A.¹, Kuznetsov N.T.¹
Afiliações:
1. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Edição: Volume 68, Nº 10 (2023)
Páginas: 1413-1421
Seção: КООРДИНАЦИОННЫЕ СОЕДИНЕНИЯ
URL: https://ogarev-online.ru/0044-457X/article/view/140307
DOI: https://doi.org/10.31857/S0044457X23601165
EDN: https://elibrary.ru/YRVHUS
ID: 140307

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Resumo

The process of cadmium(II) complexation with 1-ethyl-2-(4-methoxyphenyl)azobenzimidazole (L1), 2,2′-bipyridyl (L2), and 1,10-phenanthroline (L3) in the presence of the [trans-B20H18]2– anion has been studied. It has been found that the nature of the organic ligand affects the composition and structures of the resulting compounds. Complexation with ligand L1, a benzimidazole derivative, has yielded binuclear complex [CdL12NO3(μ-NO3)CdL1(NO3)2] (1), which contains no boron cluster anion. In the case of azaheterocyclic ligands L2 and L3, depending on the Cd : L ratio, heteroleptic complexes [CdL2NO3]2[trans-B20H18] (L = L2 (2); L3 (3)) with coordinated nitrate ions (Cd : L = 1 : 2) or tris-chelate complexes [CdL3][trans-B20H18] (L = L2 (4); L3 (5)) with the boron cluster anion as a counterion (Cd : L = 1 : 3) have been isolated. The structures of complexes [CdL12NO3(μ-NO3)CdL1(NO3)2] (1) and [Cd(L2)2NO3]2[trans-B20H18] (2) have been determined by X-ray diffraction.

Palavras-chave

cadmium(II), octadecahydroeicosaborate anion, azaheterocycles, benzimidazole derivatives

Bibliografia

Boron Science: New Technologies and Applications / Ed. Hosmane N.S. Boca Raton: CRC Press, 2012.
Handbook of Boron Science: with Applications in Organometallics, Catalysis, Materials and Medicine / Eds. Hosmane N.S., Eagling R.D. Singapore: World Scientific, 2018. V. 1–4. https://doi.org/10.1142/q0130
Matveev E.Y., Avdeeva V.V., Zhizhin K.Y. et al. // Inorganics. 2022. V. 10. P. 238. https://doi.org/10.3390/inorganics10120238
Laila Z., Yazbeck O., Ghaida F. et al. // J. Organomet. Chem. 2020. V. 910. P. 121132. https://doi.org/10.1016/j.jorganchem.2020.121132
Avdeeva V.V., Malinina E.A., Kuznetsov N.T. // Coord. Chem. Rev. 2022. V. 469. P. 214636. https://doi.org/10.1016/j.ccr.2022.214636
Paskevicius M., Hansen B.R.S., Jørgensen M. et al. // Nat. Commun. 2017. V. 8. P. 15136. https://doi.org/10.1038/ncomms15136
Stogniy M.Y., Bogdanova E.V., Anufriev S.A. et al. // Russ. J. Inorg. Chem. 2022. V. 67. P. 1537. https://doi.org/10.1134/S0036023622600848
Sivaev I.B. // Russ. J. Inorg. Chem. 2020. V. 65. P. 1854. https://doi.org/10.1134/S0036023620120165
Hu J.R., Wang J.H., Jin K.G. et al. // Russ. J. Coord. Chem. 2020. V. 46. P. 437. https://doi.org/10.1134/S1070328420060019
Saldin V.I., Slobodyuk A.B., Sukhovei V.V. // Russ. J. Inorg. Chem. 2022. V. 67. P. 1012. https://doi.org/10.1134/S003602362207021X
Kubasov A.S., Matveev E.Yu., Retivov V.M. et al. // Russ. Chem. Bull. 2014. V. 63. P. 187. https://doi.org/10.1007/s11172-014-0412-2
Matveev E.Y., Novikov I.V., Kubasov A.S. et al. // Russ. J. Inorg. Chem. 2021. V. 66. P. 187. https://doi.org/10.1134/S0036023621020121
Fei Cheng, Frieder Jäkle // Polym. Chem. 2011. V. 2. P. 2122. https://doi.org/10.1039/C1PY00123J
Avdeeva V.V., Kubasov A.S., Korolenko S.E. et al. // Russ. J. Inorg. Chem. 2022. V. 67. P. 628. https://doi.org/10.1134/S0036023622050023
Sivaev I.B. // Russ. J. Inorg. Chem. 2021. V. 66. P. 1289. https://doi.org/10.1134/S0036023621090151
Avdeeva V.V., Buzanov G.A., Goeva L.V. et al. // Inorg. Chim. Acta. 2019. V. 493. P. 38. https://doi.org/10.1016/j.ica.2019.04.055
Avdeeva V.V., Buzanov G.A., Malinina E.A. et al. // Crystals. 2020. V. 10. P. 389. https://doi.org/10.3390/cryst10050389
Korolenko S.E., Malinina E.A., Avdeeva V.V. et al. // Polyhedron. 2021. V. 194. P. 114902. https://doi.org/10.1016/j.poly.2020.114902
Nikiforova S.E., Kubasov A.S., Goeva L.V. et al. // Polyhedron. 2022. V. 226. P. 116108. https://doi.org/10.1016/j.poly.2022.116108
Korolenko S.E., Avdeeva V.V., Malinina E.A., Kuznetsov N.T. // Russ. J. Inorg. Chem. 2021. V. 66. P. 1350. https://doi.org/10.1134/S0036023621090047
Korolenko S.E., Kubasov A.S., Khan N.A. et al. // J. Clust. Sci. 2022. V. 34. P. 933. https://doi.org/10.1007/s10876-022-02263-0
Korolenko S.E., Kubasov A.S., Goeva L.V. et al. // Inorg. Chim. Acta. 2021. V. 527. P. 120587. https://doi.org/10.1016/j.ica.2021.120587
Chamberland B.L., Muetterties E.L. // Inorg. Chem. 1964. V. 3. P. 1450. https://doi.org/10.1021/ic50020a025
Hawthorne M.F., Pilling R.L. // J. Am. Chem. Soc. 1966. V. 88. P. 3873. https://doi.org/10.1021/ja00968a044
Li F., Shelly K., Knobler C.B., Hawthorne M.F. // Angew. Chem. 1998. V. 37. P. 1865.
Hawthorne M.F., Shelly K., Li F. // Chem. Commun. 2002. P. 547. https://doi.org/10.1039/B110076A
Curtis Z.B., Young C., Dickerson R., Kaczmarczyk A. // Inorg. Chem. 1974. V. 13. P. 1760. https://doi.org/10.1021/ic50137a046
Voinova V.V., Klyukin I.N., Novikov A.S. et al. // Russ. J. Inorg. Chem. 2021. V. 66. P. 295. https://doi.org/10.1134/S0036023621030190
Avdeeva V.V., Buzin M.I., Dmitrienko A.O. et al. // Chem. Eur. J. 2017. V. 23. P. 16819. https://doi.org/10.1002/chem.201703285
Avdeeva V.V., Malinina E.A., Zhizhin K.Y. et al. // J. Struct. Chem. 2019. V. 60. P. 692. https://doi.org/10.1134/S0022476619050020
Avdeeva V.V., Malinina E.A., Kuznetsov N.T. // Russ. J. Inorg. Chem. 2020. V. 65. P. 335. https://doi.org/10.1134/S003602362003002X
Avdeeva V.V., Buzin M.I., Malinina E.A. et al. // Cryst. Eng. Comm. 2015. V. 17. P. 8870. https://doi.org/10.1039/C5CE00859J
Avdeeva V.V., Kubasov A.S., Korolenko S.E. et al. // Russ. J. Inorg. Chem. 2022. V. 67. P. 1169. https://doi.org/10.1134/S0036023622080022
Il’inchik E.A., Polyanskaya T.M., Drozdova M.K. et al. // Russ. J. Gen. Chem. 2005. V. 75. P. 1545. https://doi.org/10.1007/s11176-005-0464-y
Avdeeva V.V., Kubasov A.S., Korolenko S.E. et al. // Polyhedron. 2022. V. 217. P. 115740. https://doi.org/10.1016/j.poly.2022.115740
Sirivardane U., Chu S.S.C., Hosmane N.S. et al. // Acta Crystallogr., Sect. C. 1989. V. 45. P. 333. https://doi.org/10.1107/S0108270188010716
Avdeeva V.V., Vologzhanina A.V., Kubasov A.S. et al. // Inorganics. 2022. V. 10. P. 99. https://doi.org/10.3390/inorganics10070099
Miller H.C., Miller N.E., Muetterties E.L. // J. Am. Chem. Soc. 1963. V. 85. P. 3885. https://doi.org/10.1021/ja00906a033
Spackman P.R.X., Turner M.J., McKinnon J.J. et al. // J. Appl. Crystallogr. 2021. V. 54. P. 1006. https://doi.org/10.1107/S1600576721002910
Sheldrick G.M. // Acta Crystallogr., Sect. C. 2015. V. 71. P. 3.
Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Crystallogr. 2009. V. 42. P. 339.
Soleymani-Babadi S., Beheshti A., Bahrani-Pour M. et al. // Cryst. Growth Des. 2019. V. 19. P. 4934. https://doi.org/10.1021/acs.cgd.9b00038
Barnett S.A., Blake A.J., Champness M.R. et al. // J. Chem. Soc., Dalton Trans. 2001. P. 567. https://doi.org/10.1039/b008715g
Richards P.I., Steiner A. // Inorg. Chem. 2004. V. 43. P. 2810. https://doi.org/10.1021/ic035455e