Crystallochemical Role of Benzoate and Phenylacetate Ions in Structures of Coordination 3d-Metal Compounds

M. O. Karasev; Карасев М. О.; V. A. Fomina; Фомина В. А.; I. N. Karaseva; Карасева И. Н.; D. V. Pushkin; Пушкин Д. В.

doi:10.31857/S0132344X23700226

Crystallochemical Role of Benzoate and Phenylacetate Ions in Structures of Coordination 3d-Metal Compounds

Authors: Karasev M.O.¹, Fomina V.A.¹, Karaseva I.N.², Pushkin D.V.¹
Affiliations:
1. Samara National Research University, Samara, Russia
2. Samara State Technical University, Samara, Russia
Issue: Vol 49, No 4 (2023)
Pages: 246-256
Section: Articles
URL: https://ruspoj.com/0132-344X/article/view/667521
DOI: https://doi.org/10.31857/S0132344X23700226
EDN: https://elibrary.ru/FZCIBQ
ID: 667521

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Abstract

A crystal chemical analysis of the 3d-metal benzoate- and phenylacetate-containing compounds is carried out in terms of the stereoatomic crystal structure model using characteristics of the Voronoi–Dirichlet polyhedra. Coordination types of benzoate and phenylacetate anions toward the transition metals from Ti to Zn are considered. The influence of the coordination type on the characteristics of M–O bonds in the crystal structures is revealed. The electron-donating ability of benzoate and phenylacetate anions toward 3d metals is quantitatively estimated using the 18-electron rule.

Keywords

Voronoi–Dirichlet polyhedra, crystal chemical analysis, crystallochemical formula, coordination types, benzoates, phenylacetates, 18-electron rule, electron-donating ability

References

Помогайло А.Д., Джардималиева Г.И. Мономерные и полимерные карбоксилаты металлов / Науч. ред. Алдошин С.М. М.: Физматлит, 2009. 400 с.
Agarwal R.A., Gupta. N.K. // Coord. Chem. Rev. 2017. V. 332. P. 100. https://doi.org/10.1016/j.ccr.2016.11.002
Jin K., Lee B., Park. J. // Coord. Chem. Rev. 2021. V. 427. P. 213473. https://doi.org/10.1016/j.ccr.2020.213473
Cambridge Structural Database System. Version 5.32. Cambridge: Crystallographic Data Centre, 2022.
Blatov V.A., Shevchenko A.P., Serezhkin V.N. // Russ. J. Coord. Chem. 1999. V. 25. № 7. P. 453 (Блатов В.А., Шевченко А.П., Сережкин В.Н. // Коорд. химия. 1999. Т. 25. № 7. С. 483).
Сережкин В.Н., Блатов В.А., Шевченко А.П. // Коорд. химия. 1995. Т. 21. № 3. С. 163.
Сережкин В.Н., Буслаев Ю.А. // Журн. неорган. химии. 1997. Т. 42. № 7. С. 1180 (Serezhkin V.N., Byslaev Yu.A. // Russ. J. Inorg. Chem. 1997. V. 42. № 7. P. 1064).
Сережкин В.Н., Сережкина Л.Б. // Коорд. химия. 1999. Т. 25. № 3. С. 182.
Сережкин В.Н., Михайлов Ю.Н., Буслаев Ю.А. // Журн. неорган. химии. 1997. Т. 42. № 12. С. 2036 (Serezhkin V.N., Mikhailov Yu.N., Byslaev Yu.A. // Russ. J. Inorg. Chem. 1997. V. 42. № 12. P. 1871).
Serezhkin V.N., Vologzhanina A.V., Serezhkina L.B. et al. // Acta Crystallogr. B. 2009. V. 65. № 1. P. 45. https://doi.org/10.1107/S0108768108038846
Vrablova A., Cernak J., Rajnak C. et al. // Dalton Trans. 2018. V. 47. № 43. P. 15523. https://doi.org/10.1039/C8DT03610A
Abtab S.M.T., Audhya A., Kundu N. et al. // Dalton Trans. 2013. V. 42. № 5. P. 1848. https://doi.org/10.1039/C2DT30347G
Scheiper C., Wolper C., Blaser D. // Z. Naturforsch. B. 2014. V. 69. № 11/12. P. 1365. https://doi.org/10.5560/ZNB.2014-4133
Spohn M., Strahle J. // Z. Naturforsch. B. 1988. V. 43. P. 540.
Harris G.W., Albers M.O., Boeyens J.C.A., Coville N.J. // Organometallics. 1983. V. 2. № 12. P. 609. https://doi.org/10.1021/om00077a007
Van Rooyen P.H., Dillen J.L.M., Lotz S., Schindehutte M. // J. Organomet. Chem. 1984. V. 273. № 1. P. 61. https://doi.org/10.1016/0022-328X(84)80506-9
Saillard J.Y., Grandjean D. // Acta Crystallogr. B. 1976. V. 32. № 8. P. 2285. https://doi.org/10.1107/S0567740876007607
Saillard J.Y., Grandjean D., Le Beuze A., Simonneaux G. // J. Organomet. Chem. 1981. V. 204. № 2. P. 197. https://doi.org/10.1016/S0022-328X(00)84585-4
Andrianov V.G., Struchkov Yu.T., Baranetzkaya N.K. et al. // J. Organomet. Chem. 1975. V. 101. № 2. P. 209. https://doi.org/10.1016/S0022-328X(00)86404-9
Saillard J.Y., le Borgne G., Grandjean D. // J. Organomet. Chem. 1975. V. 94. № 3. P. 409. https://doi.org/10.1016/S0022-328X(00)86950-8
Braga D., Maini L., Grepioni F. // Organometallics. 2001. V. 20. № 9. P. 1875 https://doi.org/10.1021/om0010722
Atencio R., Brammer L., Fang S.Y., Pigge F.C. // New J. Chem. 1999. V. 23. № 5. P. 461. https://doi.org/10.1039/A901925A
Xu W., Jin L., Liu B.B. // Acta. Crystallogr. E. 2011. V. 67. № 10. P. m1334. https://doi.org/10.1107/S1600536811035483
Zhu H.L., Xu W., Lin J.L. et al. // J. Coord. Chem. 2012. V. 65. № 22. P. 3983. https://doi.org/10.1080/00958972.2012.730145
Benslimane M., Redjel Y.K., Merazig H., Daran J.C. // Acta. Crystallogr. E. 2013. V. 67. № 7. P. m397. https://doi.org/10.1107/S160053681301581X
Iqbal M., Ali S., Tahir M.N. // Z. Anorg. Allg. Chem. 2018. V. 644. № 3. P. 172. https://doi.org/10.1002/zaac.201700375
Murugesapandian B., Roesky P.W. // Heteroat. Chem. 2011. V. 22. № 3–4. P. 294. https://doi.org/10.1002/hc.20679
Вайнштейн Б.К., Фридкин В.М., Инденмоб В.Л. Современная кристаллография в 4-х томах. М.: Наука, 1979. Т. 1. С. 161.
Сережкина Л.Б., Сережкин В.Н. // Журн. неорган. химии. 1996. Т. 41. № 3. С. 438.
Matsushima H., Ishiwa E., Koikawa M. et al. // Chem. Lett. 1995. V. 24. № 2. P. 129.