Mixed-carboxylate cadmium–europium compounds with monocarboxylic acid anions

M. A. Shmelev; Шмелев М. А.; T. D. Shatrov; Шатров Т. Д.; O. V. Zvereva; Зверева О. В.; A. A. Levina; Левина А. А.; J. K. Voronina; Воронина Ю. К.; A. A. Sidorov; Сидоров А. А.; I. L. Eremenko; Еременко И. Л.

doi:10.31857/S0132344X24120032

Mixed-carboxylate cadmium–europium compounds with monocarboxylic acid anions

Authors: Shmelev M.A.¹, Shatrov T.D.¹^,2, Zvereva O.V.¹^,3, Levina A.A.⁴, Voronina J.K.¹, Sidorov A.A.¹, Eremenko I.L.¹
Affiliations:
1. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
2. Moscow State University
3. National Research University Higher School of Economics
4. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences
Issue: Vol 50, No 12 (2024)
Pages: 833–843
Section: Articles
URL: https://rjeid.com/0132-344X/article/view/676744
DOI: https://doi.org/10.31857/S0132344X24120032
EDN: https://elibrary.ru/LMEQGM
ID: 676744

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Abstract

A series of mixed-carboxylate EuCd compounds with 1,10-phenanthroline (phen) and anions of benzoic H(Bz), pentabenzoic H(Pfb), 3,5-dinitrobenzoic H(3,5-Nbz), and 3,5-di-tert-butylbenzoic H(Dtbbz) acids is synthesized: [Eu₂Cd₂(Phen)₂(Рfb)_5,4(Bz)_4,6].2MeCN (I), [Eu₂(H₂O)₂Cd₂(Phen)₂(3,5-Nbz)_4,1(Bz)_5,9] (II) and [EuCd₂(EtOH)₄(Dtbbz)₆(Pfb)] (III). The variation of combinations of aromatic anions makes it possible to reveal the influence of diverse factors on the compositions and structures of new compounds. In the case of benzoate‒pentafluorobenzoate compound I and 3,5-dinitrobenzoate‒benzoate compound II, the aromatic substituents of the anions have nonintegral populations and occupy close positions in the structure of the complex. The combination of the more bulky 3,5-di-tert-butylbenzoate and pentafluorobenzoate anions in compound III results in the formation of a compound with integral populations of the positions of the anions. The synthesized compounds are characterized by XRD, IR spectroscopy, and C, H, N elemental analysis.

Keywords

mixed-carboxylate complexes, cadmium, europium, XRD, noncovalent interactions

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Han L.-J., Kong Y.-J., Sheng N., Jiang X.-L. // J. Fluor. Chem. 2014. V. 166. P. 122.
Bünzli J.-C.G. // Chem. Rev. 2010. V. 110. № 5. P. 2729.
Kotova O., Comby S., Lincheneau C., Gunnlaugsson T. // Chem. Sci. 2017. V. 8. P. 3419.
Maouche R., Belaid S., Benmerad B. et al. // Inorg. Chim. Acta. 2020. V. 501. P. 119309.
Belousov Y., Drozdov A.A., Taydakov I.V. et al. // Coord. Chem. Rev. 2021. V. 445. P. 214084.
Bovkunova A.A., Bazhina E.S., Evstifeev I.S. et al. // Dalton Trans. 2021. V. 50. P. 12275.
Bernot K., Daiguebonne C., Calvez G. et al. // Acc. Chem. Res. 2021. V. 54. № 2. P. 427.
Costa I.F., Blois L., Paolini T.B. et al. // Coord. Chem. Rev. 2024. V. 502. P. 215590.
Wang H., Li H., Yang L. et al. // Mol. Cryst. Liq. 2022. V. 736. P. 113.
Silva A. I. S., Lima N.B.D., Simas A.M., Gonçalves S.M. C. // ACS Omega. 2017. V. 2(10). P. 6786.
Brito-Santos G., Hernández-Rodríguez C., Gil-Hernández B. et al. // Dalton Trans. 2022. V. 51. P. 3146.
Silva A.I.S., Santos V.F.C., Lima N.B.D. et al. // RSC Adv. 2016. V. 6. P. 90934.
Melo L.L.L.S., Castro Jr. G.P., Gonçalves S.M. C. // Inorg. Chem. 2019. V. 58(5). P. 3265.
Shmelev M.A., Polunin R.A., Gogoleva N.V. et al. // Molecules. 2021. V. 26. № 14. P. 4296.
Шмелев М.А., Воронина Ю.К., Гоголева Н.В. и др. // Коорд. химия. 2022. Т. 48 № 4. С. 229 (Shmelev M.A., Voronina Yu. K., Gogoleva N.V. et al. // Russ. J. Coord. Chem. 2022. V. 48. № 4. P. 224). https://doi.org/10.1134/S1070328422040042.
Melnikov S.N., Evstifeev I.S., Nikolaveskii S.A. et al. // New J. Chem. 2021. V. 45. P. 13349.
Shmelev M.A., Voronina J.K., Evtyukhin M.A. et al. // Inorganics. 2022. V. 10. № 11. P. 194.
Voronina J.K., Yambulatov D.S., Chistyakov A.S. et al. // Crystals. 2023. V. 13. № 4. P. 678.
Шмелев М.А., Чистяков А.С., Разгоняева Г.А. и др. // Журн. структур. химии. 2024. Т. 65. № 2. С. 122814 (Shmelev M.A., Chistyakov A.S., Razgonyaeva G.A. et al. // J. Struct. Chem. 2024. V. 65. P. 362).
Kashyap C., Ullah S.S., Mazumder L.J., Kanti Guha A. // Comput. Theor. Chem. 2018. V. 1130. P. 134.
Belousov Y., Kiskin M.A., Sidoruk A.V. et al. // Aust. J. Chem. 2022. V. 75. № 9. P. 572.
Schwabedissen J., Trapp P.C., Stammler H.-G. et al. // Chem. Eur. J. 2019. V. 25. № 30. P. 7339.
Varadwaj P.R., Varadwaj A., Marques H.M., Yamashita K. // Computation 2018. V. 6(4). P. 51.
Coates G.W., Dunn A.R., Henling L. . // J. Am. Chem. Soc. 1998. V. 120. № 15. P. 3641.
Brend’amour S., Gilmer J., Bolte M. et al. // Chem. — Eur. J. 2018. V. 24. № 63. P. 16910.
Biradha K., Santra R. // Chem. Soc. Rev. 2013. V. 42. P. 950.
Jassal A.K., Sran B.S., Suffren Y. et al. // Dalton Trans. 2018. V. 47. P. 4722.
De Bettencourt-Dias A., Viswanathan S. // Dalton Trans. 2006. P. 4093.
Tsaryuka V., Kudryashova V., Gawryszewska P. et al. // Photochem. Photobiol. 2012. V. 239. P. 37.
Roy S., Bauza A., Frontera A. et al. // Inorg. Chim. Acta. 2016. V. 440. P. 38.
Шмелев М.А., Гоголева Н.В., Иванов В.К. и др. // Коорд. химия. 2022. Т. 48(9). С. 515 (Shmelev M.A., Gogoleva N.V., Ivanov V.K. et al. // Russ. J. Coord. Chem. 2022. V. 48. № 9. P. 539).
Shmelev M.A., Gogoleva N.V., Sidorov A.A. et al. // ChemistrySelect. 2020. V. 5. № 28. P. 8475.
Ларионов С.В., Кириченко В.Н., Расторгуев А.А. и др. // Коорд. химия. 1997. Т. 23. № 6. С. 432 (Larionov S.V., Kirichenko V.N., Rastorguev A.A. et al. // Russ. J. Coord. Chem. 1997. V. 23(6). P. 465).
Jassal A.K., Sharma S., Hundal G., Hundal M.S. // Cryst. Growth Des. 2015. V. 15. № 1, P. 79.
Moreno-Gómez L., Sánchez-Férez F., Calvet T. et al. // Inorg. Chim. Acta. 2020. V. 506. P. 119561.
SMART (control) and SAINT (integration). Software. Version 5.0. Madison (WI, USA): Bruker AXS Inc., 1997.
Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3.
Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Cryst. 2009. V. 42. P. 339.
Casanova D., Llunell M., Alemany P., Alvarez S. et al. // Chem. Eur. J. 2005. V. 11. P. 1479.
Shmelev M.A., Chistyakov A.S., Razgonyaeva G.A. et al. // Crystals. 2022. V. 12. № 4. P. 508.
Shmelev M.A., Kuznetsova G.N., Gogoleva N.V. et al. // Russ. Chem. Bull. 2021. V. 70. P. 830 (Шмелев М А., Кузнецова Г.Н., Гоголева Н.В. и др. // Изв. АН. Сер. хим. 2021. Т. 70. С. 830). https://doi.org/10.1007/s11172-021-3156-9
Seera R., Cherukuvada S., Guru Row T.N. // Cryst. Growth Des. 2021. V. 21. № 8. P. 4607.
Reddy L.S., Bhatt P.M., Banerjee R. et al. // Chem. Asian J. 2007. V. 2. P. 505.
Jetti R.K.–R., Boese R., Thallapally P.K., Desiraju G.R. // Cryst.Growth Des. 2003. V. 3. P. 1033.
Sharada D., Saha A., Saha B.K. // New J. Chem. 2019. V. 43. P. 7562.
Lynch D.E., Smith G., Byriel K.A., Kennard C.H.L. // Aust. J. Chem. 1994. V. 47. P. 1789.
Jin S., Wang D. // J. Mol. Struct. 2013. V. 1037. P. 242.
Jones C.L., Skelton J.M., Parker S.C. et al. // CrystEngComm. 2019. V. 21. P. 1626.
Arora K.K., Pedireddi V.R. // Tetrahedron. 2004. V. 60. P. 919.
Shmelev M.A., Kiskin M.A, Voronina J.K. et al. // Materials. 2020. V. 13. № 24, № 5689.
Shmelev M. A., Gogoleva N.V., Sidorov A.A. et al. // Inorg. Chim. Acta. 2021. V. 515. P. 120050.
Sidorov A.A., Gogoleva N.V., Bazhina E.S. et al. // Pure Appl. Chem. 2020. V. 92. № 7. P. 1093.
Shmelev M.A., Voronina Yu.K., Gogoleva N.V. et al. // Russ. Chem. Bull. 2020. V. 69. P. 1544 (Шмелев М.А., Воронина Ю.К., Гоголева Н.В. и др. // Изв. АН. Сер. хим. 2020. Т. 69, С. 1544).