2,2′-Bithio­phene-3,3′-dicarbonitrile

The complete mol­ecule of the title compound, C(10)H(4)N(2)S(2), is generated by an inversion center situated at the mid-point of the bridging C—C bond. The bithio­phene ring system is planar [maximum deviation = 0.003 (2) Å] and the central C—C bond length is 1.450 (2) Å. There are no significant i...

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Detalles Bibliográficos
Autores principales: Novina, J. Josephine, Vasuki, G., Karthik, Durai, Thomas, K. R. Justin
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/PMC3414987/
https://www.ncbi.nlm.nih.gov/pubmed/22904974
http://dx.doi.org/10.1107/S1600536812032503
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author Novina, J. Josephine
Vasuki, G.
Karthik, Durai
Thomas, K. R. Justin
author_facet Novina, J. Josephine
Vasuki, G.
Karthik, Durai
Thomas, K. R. Justin
author_sort Novina, J. Josephine
collection PubMed
description The complete mol­ecule of the title compound, C(10)H(4)N(2)S(2), is generated by an inversion center situated at the mid-point of the bridging C—C bond. The bithio­phene ring system is planar [maximum deviation = 0.003 (2) Å] and the central C—C bond length is 1.450 (2) Å. There are no significant inter­molecular inter­actions in the crystal structure, which is stabilized by van der Waals inter­actions.
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spelling pubmed-34149872012-08-17 2,2′-Bithio­phene-3,3′-dicarbonitrile Novina, J. Josephine Vasuki, G. Karthik, Durai Thomas, K. R. Justin Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete mol­ecule of the title compound, C(10)H(4)N(2)S(2), is generated by an inversion center situated at the mid-point of the bridging C—C bond. The bithio­phene ring system is planar [maximum deviation = 0.003 (2) Å] and the central C—C bond length is 1.450 (2) Å. There are no significant inter­molecular inter­actions in the crystal structure, which is stabilized by van der Waals inter­actions. International Union of Crystallography 2012-07-25 /pmc/articles/PMC3414987/ /pubmed/22904974 http://dx.doi.org/10.1107/S1600536812032503 Text en © Novina 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
Novina, J. Josephine
Vasuki, G.
Karthik, Durai
Thomas, K. R. Justin
2,2′-Bithio­phene-3,3′-dicarbonitrile
title 2,2′-Bithio­phene-3,3′-dicarbonitrile
title_full 2,2′-Bithio­phene-3,3′-dicarbonitrile
title_fullStr 2,2′-Bithio­phene-3,3′-dicarbonitrile
title_full_unstemmed 2,2′-Bithio­phene-3,3′-dicarbonitrile
title_short 2,2′-Bithio­phene-3,3′-dicarbonitrile
title_sort 2,2′-bithio­phene-3,3′-dicarbonitrile
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414987/
https://www.ncbi.nlm.nih.gov/pubmed/22904974
http://dx.doi.org/10.1107/S1600536812032503
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