Novel complexes possessing Hg–(Cl, Br, I)⋯O=C halogen bonding and unusual Hg₂S₂(Br/I)₄ kernel. The usefulness of τ₄′ structural parameter - Publication - Bridge of Knowledge

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Novel complexes possessing Hg–(Cl, Br, I)⋯O=C halogen bonding and unusual Hg₂S₂(Br/I)₄ kernel. The usefulness of τ₄′ structural parameter

Abstract

One mononuclear and two binuclear Hg(II) complexes have been synthesized and characterized by X-ray diffraction, ATR IR and Hirshfeld surface analysis. Single-crystal X-ray diffraction showed that binuclear compounds are centrosymmetric and isostructural. All complexes form bifurcated intermolecular N–H···O hydrogen bonds that contribute to a formation of the centrosymmetric dimers. In binuclear complexes, sulfur atoms of thiourea ligands take the bridging role. These are the first examples of such compounds with mercury. In binuclear complexes of group 12 elements, halogens are usually the bridging atoms. The geometries of binuclear complexes are highly distorted with alarmingly low value of τ₄' parameter suggesting presence of additional donor that turned out to be phenyl ring (Hg···π interaction). The crystal structures are stabilized by additional noncovalent interactions, including halogen bonding which leads to the formation of chains. The differences and similarities of these complexes indicate that halogen ions have a great impact on the structures. Presented complexes comprise unique interactions between mercury-bonded halogen atoms and neighboring oxygen atoms of carbonyl groups (Hg–(Cl,Br, I)···O=C contacts).

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Category:
Articles
Type:
artykuł w czasopiśmie wyróżnionym w JCR
Published in:
POLYHEDRON no. 146, pages 35 - 41,
ISSN: 0277-5387
Language:
English
Publication year:
2018
Bibliographic description:
Rosiak D., Okuniewski A., Chojnacki J.: Novel complexes possessing Hg–(Cl, Br, I)⋯O=C halogen bonding and unusual Hg₂S₂(Br/I)₄ kernel. The usefulness of τ₄′ structural parameter// POLYHEDRON. -Vol. 146, (2018), s.35-41
DOI:
Digital Object Identifier (open in new tab) 10.1016/j.poly.2018.02.016
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