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Russian Journal of Coordination Chemistry

, Volume 45, Issue 8, pp 573–584 | Cite as

Quantum Chemical Simulation of Hexa-, Penta-, and Tetracoordination Modes in Stereoisomers of the Co(II) and Ni(II) Bis(ligand) Complexes Based on (N,O,S(Se))-Tridentate Azomethines

  • N. N. KharabayevEmail author
Article
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Abstract

The molecular structures and relative energies of hexa-, penta-, and tetracoordinated stereoisomers of the Co(II) and Ni(II) bis(ligand) complexes based on (N,O,Y)-tridentate azomethines with the phenyl thio(seleno) ether substituent at the azomethine nitrogen atom (coordination modes of the competing stereoisomers MN2O2Y2, MN2O2Y, or MN2O2 (Y = S, Se)) are calculated using the density functional theory. Hexacoordination is predominant in the Co(II) and Ni(II) complexes (combined with tetracoordination for the Co(II) complexes), unlike pentacoordination prevailing in similar Co(II) and Ni(II) complexes based on azomethines with thio(seleno)benzimidazole fragments (with Y atoms in the thione form). The quantum chemical simulation is performed for possible stereoisomerization reactions in the CoL2 complexes to take into account the role of interconfiguration transitions in the competition of the hexa-, penta-, and tetracoordinated stereoisomers.

Keywords:

quantum chemical simulation coordination compounds stereoisomerization tridentate azomethines 

Notes

ACKNOWLEDGMENTS

N.N. Kharabaev acknowledges Academician V.I. Min-kin for fruitful consultations during this study.

FUNDING

This work was supported by the Ministry of Education and Science of the Russian Federation (design part of the state task in the sphere of scientific activities, project no. 4.844.2017/PCh).

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Copyright information

© Pleiades Publishing, Ltd. 2019

Authors and Affiliations

  1. 1.Research Institute of Physical and Organic Chemistry, Southern Federal UniversityRostov-on-DonRussia

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