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Bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(II)

The title compound, [Ni(S(2)C(2)(C(6)H(4)-p-Cl)(2))(2)] or [Ni(C(14)H(8)Cl(2)S(2))(2)], crystallizes in the triclinic space group P [Image: see text] as pairs of mol­ecules disposed about an inversion center at the bc face of the cell. Close inter­molecular C—H⋯S (2.884 Å) and C—H⋯Ni (3.032 Å) conta...

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Autores principales: Koehne, Sydney, Mirmelli, Bailey, Mague, Joel T., Donahue, James P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462000/
https://www.ncbi.nlm.nih.gov/pubmed/36340872
http://dx.doi.org/10.1107/S2414314622001481
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author Koehne, Sydney
Mirmelli, Bailey
Mague, Joel T.
Donahue, James P.
author_facet Koehne, Sydney
Mirmelli, Bailey
Mague, Joel T.
Donahue, James P.
author_sort Koehne, Sydney
collection PubMed
description The title compound, [Ni(S(2)C(2)(C(6)H(4)-p-Cl)(2))(2)] or [Ni(C(14)H(8)Cl(2)S(2))(2)], crystallizes in the triclinic space group P [Image: see text] as pairs of mol­ecules disposed about an inversion center at the bc face of the cell. Close inter­molecular C—H⋯S (2.884 Å) and C—H⋯Ni (3.032 Å) contacts that are less than the sum of the van der Waals radii appear to induce slight bowing of the mol­ecular planes toward one another. The angles at which the four p-ClC(6)H(4)- rings join the NiS(2)C(2) chelate rings [39.37 (9)– 53.41 (6)°] are similarly influenced by these inter­molecular contacts. In the larger packing arrangement, sheets of mol­ecules extend in the direction of the ac face diagonal. [Image: see text]
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spelling pubmed-94620002022-11-04 Bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(II) Koehne, Sydney Mirmelli, Bailey Mague, Joel T. Donahue, James P. IUCrdata Data Reports The title compound, [Ni(S(2)C(2)(C(6)H(4)-p-Cl)(2))(2)] or [Ni(C(14)H(8)Cl(2)S(2))(2)], crystallizes in the triclinic space group P [Image: see text] as pairs of mol­ecules disposed about an inversion center at the bc face of the cell. Close inter­molecular C—H⋯S (2.884 Å) and C—H⋯Ni (3.032 Å) contacts that are less than the sum of the van der Waals radii appear to induce slight bowing of the mol­ecular planes toward one another. The angles at which the four p-ClC(6)H(4)- rings join the NiS(2)C(2) chelate rings [39.37 (9)– 53.41 (6)°] are similarly influenced by these inter­molecular contacts. In the larger packing arrangement, sheets of mol­ecules extend in the direction of the ac face diagonal. [Image: see text] International Union of Crystallography 2022-02-17 /pmc/articles/PMC9462000/ /pubmed/36340872 http://dx.doi.org/10.1107/S2414314622001481 Text en © Koehne et al. 2022 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Koehne, Sydney
Mirmelli, Bailey
Mague, Joel T.
Donahue, James P.
Bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(II)
title Bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(II)
title_full Bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(II)
title_fullStr Bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(II)
title_full_unstemmed Bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(II)
title_short Bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(II)
title_sort bis[1,2-bis­(4-chloro­phen­yl)­ethyl­ene-1,2-dithiol­ato(1–)]nickel(ii)
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462000/
https://www.ncbi.nlm.nih.gov/pubmed/36340872
http://dx.doi.org/10.1107/S2414314622001481
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