2,2′-(Sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole)

In the title compound, C(16)H(12)N(2)S(3), the two benzothia­zole groups are oriented differently with respect to the –CH(2)– groups, one being approximately staggered and one nearly eclipsed. A sulfur–π inter­action of 3.3627 (11) Å is observed between the bridging thio­ether S atom and a thia­zole...

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Detalles Bibliográficos
Autores principales: Strasser, Christoph E., de Jongh, Leigh-Anne, Raubenheimer, Helgard G., Cronje, Stephanie
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052028/
https://www.ncbi.nlm.nih.gov/pubmed/21522378
http://dx.doi.org/10.1107/S1600536811004478
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author Strasser, Christoph E.
de Jongh, Leigh-Anne
Raubenheimer, Helgard G.
Cronje, Stephanie
author_facet Strasser, Christoph E.
de Jongh, Leigh-Anne
Raubenheimer, Helgard G.
Cronje, Stephanie
author_sort Strasser, Christoph E.
collection PubMed
description In the title compound, C(16)H(12)N(2)S(3), the two benzothia­zole groups are oriented differently with respect to the –CH(2)– groups, one being approximately staggered and one nearly eclipsed. A sulfur–π inter­action of 3.3627 (11) Å is observed between the bridging thio­ether S atom and a thia­zole ring. The crystal packing is further stabilized by inter­molecular C—H⋯N and C—H⋯π inter­actions.
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spelling pubmed-30520282011-04-26 2,2′-(Sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole) Strasser, Christoph E. de Jongh, Leigh-Anne Raubenheimer, Helgard G. Cronje, Stephanie Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(12)N(2)S(3), the two benzothia­zole groups are oriented differently with respect to the –CH(2)– groups, one being approximately staggered and one nearly eclipsed. A sulfur–π inter­action of 3.3627 (11) Å is observed between the bridging thio­ether S atom and a thia­zole ring. The crystal packing is further stabilized by inter­molecular C—H⋯N and C—H⋯π inter­actions. International Union of Crystallography 2011-02-12 /pmc/articles/PMC3052028/ /pubmed/21522378 http://dx.doi.org/10.1107/S1600536811004478 Text en © Strasser 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
Strasser, Christoph E.
de Jongh, Leigh-Anne
Raubenheimer, Helgard G.
Cronje, Stephanie
2,2′-(Sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole)
title 2,2′-(Sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole)
title_full 2,2′-(Sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole)
title_fullStr 2,2′-(Sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole)
title_full_unstemmed 2,2′-(Sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole)
title_short 2,2′-(Sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole)
title_sort 2,2′-(sulfanediyldimethyl­ene)bis­(1,3-benzothia­zole)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052028/
https://www.ncbi.nlm.nih.gov/pubmed/21522378
http://dx.doi.org/10.1107/S1600536811004478
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AT dejonghleighanne 22sulfanediyldimethylenebis13benzothiazole
AT raubenheimerhelgardg 22sulfanediyldimethylenebis13benzothiazole
AT cronjestephanie 22sulfanediyldimethylenebis13benzothiazole

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