The 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical

The asymmetric unit of the title compound, C(8)H(6)ClN(2)S(2), comprises two mol­ecules forming a dimer via π–π stacking inter­actions [centroid–centroid distance = 3.634 (10) Å] and intra­dimer S⋯S contacts [3.012 (4) and 3.158 (4) Å] between the two mol­ecules in a cis-antarafacial arrangement....

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Detalles Bibliográficos
Autores principales: Cole, Jacqueline M., Aherne, Christine M., Howard, Judith A. K., Banister, Arthur J., Waddell, Paul G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200813/
https://www.ncbi.nlm.nih.gov/pubmed/22059054
http://dx.doi.org/10.1107/S1600536811034751
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author Cole, Jacqueline M.
Aherne, Christine M.
Howard, Judith A. K.
Banister, Arthur J.
Waddell, Paul G.
author_facet Cole, Jacqueline M.
Aherne, Christine M.
Howard, Judith A. K.
Banister, Arthur J.
Waddell, Paul G.
author_sort Cole, Jacqueline M.
collection PubMed
description The asymmetric unit of the title compound, C(8)H(6)ClN(2)S(2), comprises two mol­ecules forming a dimer via π–π stacking inter­actions [centroid–centroid distance = 3.634 (10) Å] and intra­dimer S⋯S contacts [3.012 (4) and 3.158 (4) Å] between the two mol­ecules in a cis-antarafacial arrangement.
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spelling pubmed-32008132011-11-06 The 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical Cole, Jacqueline M. Aherne, Christine M. Howard, Judith A. K. Banister, Arthur J. Waddell, Paul G. Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(8)H(6)ClN(2)S(2), comprises two mol­ecules forming a dimer via π–π stacking inter­actions [centroid–centroid distance = 3.634 (10) Å] and intra­dimer S⋯S contacts [3.012 (4) and 3.158 (4) Å] between the two mol­ecules in a cis-antarafacial arrangement. International Union of Crystallography 2011-08-27 /pmc/articles/PMC3200813/ /pubmed/22059054 http://dx.doi.org/10.1107/S1600536811034751 Text en © Cole et al. 2011 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 Organic Papers
Cole, Jacqueline M.
Aherne, Christine M.
Howard, Judith A. K.
Banister, Arthur J.
Waddell, Paul G.
The 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical
title The 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical
title_full The 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical
title_fullStr The 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical
title_full_unstemmed The 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical
title_short The 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical
title_sort 4-(3-chloro-4-methyl­phen­yl)-1,2,3,5-dithia­diazol-3-yl radical
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200813/
https://www.ncbi.nlm.nih.gov/pubmed/22059054
http://dx.doi.org/10.1107/S1600536811034751
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