Bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide

In the title compound, C(20)H(20)N(2)S(4), the N-containing six-membered rings of the two tetra­hydro­quinoline moieties adopt half-chair conformations. Intra­molecular C—H⋯S hydrogen bonding stabilizes the mol­ecular structure. In the crystal, mol­ecules associate via weak C—H⋯π inter­actions....

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Detalles Bibliográficos
Autores principales: Srinivasan, N., Thirumaran, S., Selvanayagam, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589024/
https://www.ncbi.nlm.nih.gov/pubmed/23476260
http://dx.doi.org/10.1107/S1600536812047320
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author Srinivasan, N.
Thirumaran, S.
Selvanayagam, S.
author_facet Srinivasan, N.
Thirumaran, S.
Selvanayagam, S.
author_sort Srinivasan, N.
collection PubMed
description In the title compound, C(20)H(20)N(2)S(4), the N-containing six-membered rings of the two tetra­hydro­quinoline moieties adopt half-chair conformations. Intra­molecular C—H⋯S hydrogen bonding stabilizes the mol­ecular structure. In the crystal, mol­ecules associate via weak C—H⋯π inter­actions.
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spelling pubmed-35890242013-03-08 Bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide Srinivasan, N. Thirumaran, S. Selvanayagam, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(20)N(2)S(4), the N-containing six-membered rings of the two tetra­hydro­quinoline moieties adopt half-chair conformations. Intra­molecular C—H⋯S hydrogen bonding stabilizes the mol­ecular structure. In the crystal, mol­ecules associate via weak C—H⋯π inter­actions. International Union of Crystallography 2012-11-24 /pmc/articles/PMC3589024/ /pubmed/23476260 http://dx.doi.org/10.1107/S1600536812047320 Text en © Srinivasan et al. 2012 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
Srinivasan, N.
Thirumaran, S.
Selvanayagam, S.
Bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide
title Bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide
title_full Bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide
title_fullStr Bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide
title_full_unstemmed Bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide
title_short Bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide
title_sort bis(1,2,3,4-tetra­hydro­quinoline-1-thio­carbon­yl) disulfide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589024/
https://www.ncbi.nlm.nih.gov/pubmed/23476260
http://dx.doi.org/10.1107/S1600536812047320
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AT thirumarans bis1234tetrahydroquinoline1thiocarbonyldisulfide
AT selvanayagams bis1234tetrahydroquinoline1thiocarbonyldisulfide

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