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6,7,6′,7′-Tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate
The title compound, C(42)H(24)N(4)S(4)·2CHCl(3), a symmetrical tetrathiafulvalene (TTF) derivative, was prepared by a triethylphosphite-mediated self-coupling reaction of 6,7-diphenyl-1,3-dithia-5,8-diazacyclopenta[b]napthalen-2-one. The asymmetric unit contains two TTF molecules and four c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200811/ https://www.ncbi.nlm.nih.gov/pubmed/22064676 http://dx.doi.org/10.1107/S1600536811029540 |
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author | Bolligarla, Ramababu Durgaprasad, Gummadi Das, Samar K. |
author_facet | Bolligarla, Ramababu Durgaprasad, Gummadi Das, Samar K. |
author_sort | Bolligarla, Ramababu |
collection | PubMed |
description | The title compound, C(42)H(24)N(4)S(4)·2CHCl(3), a symmetrical tetrathiafulvalene (TTF) derivative, was prepared by a triethylphosphite-mediated self-coupling reaction of 6,7-diphenyl-1,3-dithia-5,8-diazacyclopenta[b]napthalen-2-one. The asymmetric unit contains two TTF molecules and four chloroform solvent molecules. Cl⋯Cl interactions [contact distances = 3.263 (1)–3.395 (2) Å] are present between the solvent molecules, resulting in a tape along the bc plane. The crystal packing features weak C—H⋯Cl and C—H⋯N hydrogen bonds, resulting in the formation of a two-dimensional supramolecular network. |
format | Online Article Text |
id | pubmed-3200811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32008112011-11-06 6,7,6′,7′-Tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate Bolligarla, Ramababu Durgaprasad, Gummadi Das, Samar K. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(42)H(24)N(4)S(4)·2CHCl(3), a symmetrical tetrathiafulvalene (TTF) derivative, was prepared by a triethylphosphite-mediated self-coupling reaction of 6,7-diphenyl-1,3-dithia-5,8-diazacyclopenta[b]napthalen-2-one. The asymmetric unit contains two TTF molecules and four chloroform solvent molecules. Cl⋯Cl interactions [contact distances = 3.263 (1)–3.395 (2) Å] are present between the solvent molecules, resulting in a tape along the bc plane. The crystal packing features weak C—H⋯Cl and C—H⋯N hydrogen bonds, resulting in the formation of a two-dimensional supramolecular network. International Union of Crystallography 2011-08-02 /pmc/articles/PMC3200811/ /pubmed/22064676 http://dx.doi.org/10.1107/S1600536811029540 Text en © Bolligarla 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 Bolligarla, Ramababu Durgaprasad, Gummadi Das, Samar K. 6,7,6′,7′-Tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate |
title | 6,7,6′,7′-Tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate |
title_full | 6,7,6′,7′-Tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate |
title_fullStr | 6,7,6′,7′-Tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate |
title_full_unstemmed | 6,7,6′,7′-Tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate |
title_short | 6,7,6′,7′-Tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate |
title_sort | 6,7,6′,7′-tetraphenyl-2,2′-bi[1,3-dithia-5,8-diazacyclopenta[b]naphthalenylidene] chloroform disolvate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200811/ https://www.ncbi.nlm.nih.gov/pubmed/22064676 http://dx.doi.org/10.1107/S1600536811029540 |
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