Remote hydroxyl group induced structural diversities in antimony(III) chalcogenones

Mannarsamy, M. and Prabusankar, G (2022) Remote hydroxyl group induced structural diversities in antimony(III) chalcogenones. Polyhedron, 219. pp. 1-8. ISSN 0277-5387

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Abstract

The remote hydroxyl functional group induced structural diversities in benzimidazolin-2-chalcogenone complexes of antimony(III) have been investigated. The hydroxyl functionalized imidazole chalcogenone based antimony(III) halides have been synthesized and characterized by FT-IR, 1H and 13C NMR, TGA, CHNS, UV–visible, Raman and single-crystal X-ray diffraction techniques. The structural investigation reveals that the dinuclear [{(μ2-L1/L2)SbX2(μ2-X)}2]∞ (L1 = 1-(2-hydroxyethyl)-3-isopropyl-benzimidazole-2-selenone; L2 = 1-(2-hydroxyethyl)-3-isopropyl-benzimidazole-2-selenone; X = Cl or Br) core in the coordination polymer forms an Sb(III) chalcogenone corrugated coordination layer through strong intermolecular coordination, which is triggered by the hydroxyl functional group of the ligand. The central metal ion shows a distorted octahedral geometry. The Hirshfeld surface analysis was mapped using pseudo-mirrored 2D fingerprint plots to study the short interatomic distances in the crystal structure. The major short inter-atomic distances are covered by H····X and H····H in the Hirshfeld surfaces. © 2022 Elsevier Ltd

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IITH Creators:

IITH Creators	ORCiD
Prabusankar, G	UNSPECIFIED

Item Type:

Article

Additional Information:

We gratefully acknowledge the DST-SERB (EMR/2017/001211) for financial support. MM thank CSIR-SRF (No: 09/1001(0025)/2016-EMR- I) for the Ph.D. fellowship

Uncontrolled Keywords:

Antimony(III), Coordination Polymers, Imidazole Selone, Imidazole Thione, Main Group Chemistry

Subjects:

Chemistry

Divisions:

Department of Chemistry

Depositing User:

. LibTrainee 2021

Date Deposited:

25 Jun 2022 04:16

Last Modified:

27 Jun 2022 05:09