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1,3-Dimesitylimidazolidinium tetra­chloridogold(III) dichloro­methane solvate

The title ionic compound, (C(21)H(27)N(2))[AuCl(4)]·CH(2)Cl(2), was obtained from the reaction of 1,3-dimesitylimidazolidinium chloride with t-BuOK and a solution of AuCl(3) in tetra­hydro­furan. In the crystal structure, numerous weak C—H⋯Cl hydrogen bonds form double layers parallel to (100), whic...

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Detalles Bibliográficos
Autores principales: Hagos, Tesfamariam K., Nogai, Stefan D., Dobrzańska, Liliana, Cronje, Stephanie
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959617/
https://www.ncbi.nlm.nih.gov/pubmed/21580818
http://dx.doi.org/10.1107/S1600536808031115
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author Hagos, Tesfamariam K.
Nogai, Stefan D.
Dobrzańska, Liliana
Cronje, Stephanie
author_facet Hagos, Tesfamariam K.
Nogai, Stefan D.
Dobrzańska, Liliana
Cronje, Stephanie
author_sort Hagos, Tesfamariam K.
collection PubMed
description The title ionic compound, (C(21)H(27)N(2))[AuCl(4)]·CH(2)Cl(2), was obtained from the reaction of 1,3-dimesitylimidazolidinium chloride with t-BuOK and a solution of AuCl(3) in tetra­hydro­furan. In the crystal structure, numerous weak C—H⋯Cl hydrogen bonds form double layers parallel to (100), which are further stabilized by π–π inter­actions between mesitylene rings [centroid–centroid distance = 4.308 (4) Å], resulting in the formation of a three-dimensional supra­molecular assembly.
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spelling pubmed-29596172010-12-30 1,3-Dimesitylimidazolidinium tetra­chloridogold(III) dichloro­methane solvate Hagos, Tesfamariam K. Nogai, Stefan D. Dobrzańska, Liliana Cronje, Stephanie Acta Crystallogr Sect E Struct Rep Online Metal-Organic Papers The title ionic compound, (C(21)H(27)N(2))[AuCl(4)]·CH(2)Cl(2), was obtained from the reaction of 1,3-dimesitylimidazolidinium chloride with t-BuOK and a solution of AuCl(3) in tetra­hydro­furan. In the crystal structure, numerous weak C—H⋯Cl hydrogen bonds form double layers parallel to (100), which are further stabilized by π–π inter­actions between mesitylene rings [centroid–centroid distance = 4.308 (4) Å], resulting in the formation of a three-dimensional supra­molecular assembly. International Union of Crystallography 2008-10-04 /pmc/articles/PMC2959617/ /pubmed/21580818 http://dx.doi.org/10.1107/S1600536808031115 Text en © Hagos et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Metal-Organic Papers
Hagos, Tesfamariam K.
Nogai, Stefan D.
Dobrzańska, Liliana
Cronje, Stephanie
1,3-Dimesitylimidazolidinium tetra­chloridogold(III) dichloro­methane solvate
title 1,3-Dimesitylimidazolidinium tetra­chloridogold(III) dichloro­methane solvate
title_full 1,3-Dimesitylimidazolidinium tetra­chloridogold(III) dichloro­methane solvate
title_fullStr 1,3-Dimesitylimidazolidinium tetra­chloridogold(III) dichloro­methane solvate
title_full_unstemmed 1,3-Dimesitylimidazolidinium tetra­chloridogold(III) dichloro­methane solvate
title_short 1,3-Dimesitylimidazolidinium tetra­chloridogold(III) dichloro­methane solvate
title_sort 1,3-dimesitylimidazolidinium tetra­chloridogold(iii) dichloro­methane solvate
topic Metal-Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959617/
https://www.ncbi.nlm.nih.gov/pubmed/21580818
http://dx.doi.org/10.1107/S1600536808031115
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