4,6-Bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine

The title compound, C(35)H(30)N(2)S(3), has been synthesized by a solvent-free reaction. The mol­ecule exhibits an E,E configuration, the benzene rings and pyrimidine rings being located on the opposite sides of the C=C bonds. The centroid–centroid separation of 3.5808 (17) Å indicates the existence...

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Detalles Bibliográficos
Autores principales: Wang, Min, Cheng, Le-Hua, Chu, Xian-Ping, Xu, Shi-You
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2007
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915314/
https://www.ncbi.nlm.nih.gov/pubmed/21200822
http://dx.doi.org/10.1107/S1600536807065063
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author Wang, Min
Cheng, Le-Hua
Chu, Xian-Ping
Xu, Shi-You
author_facet Wang, Min
Cheng, Le-Hua
Chu, Xian-Ping
Xu, Shi-You
author_sort Wang, Min
collection PubMed
description The title compound, C(35)H(30)N(2)S(3), has been synthesized by a solvent-free reaction. The mol­ecule exhibits an E,E configuration, the benzene rings and pyrimidine rings being located on the opposite sides of the C=C bonds. The centroid–centroid separation of 3.5808 (17) Å indicates the existence of π–π stacking between nearly parallel pyrimidine and benzene rings of adjacent mol­ecules.
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spelling pubmed-29153142010-12-30 4,6-Bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine Wang, Min Cheng, Le-Hua Chu, Xian-Ping Xu, Shi-You Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(35)H(30)N(2)S(3), has been synthesized by a solvent-free reaction. The mol­ecule exhibits an E,E configuration, the benzene rings and pyrimidine rings being located on the opposite sides of the C=C bonds. The centroid–centroid separation of 3.5808 (17) Å indicates the existence of π–π stacking between nearly parallel pyrimidine and benzene rings of adjacent mol­ecules. International Union of Crystallography 2007-12-12 /pmc/articles/PMC2915314/ /pubmed/21200822 http://dx.doi.org/10.1107/S1600536807065063 Text en © International Union of Crystallography 2008 http://journals.iucr.org/services/termsofuse.html This is an open-access article distributed under the terms described at http://journals.iucr.org/services/termsofuse.html.
spellingShingle Organic Papers
Wang, Min
Cheng, Le-Hua
Chu, Xian-Ping
Xu, Shi-You
4,6-Bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine
title 4,6-Bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine
title_full 4,6-Bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine
title_fullStr 4,6-Bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine
title_full_unstemmed 4,6-Bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine
title_short 4,6-Bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine
title_sort 4,6-bis[4-(benzyl­sulfan­yl)styr­yl]-2-(methyl­sulfan­yl)pyrimidine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915314/
https://www.ncbi.nlm.nih.gov/pubmed/21200822
http://dx.doi.org/10.1107/S1600536807065063
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AT chenglehua 46bis4benzylsulfanylstyryl2methylsulfanylpyrimidine
AT chuxianping 46bis4benzylsulfanylstyryl2methylsulfanylpyrimidine
AT xushiyou 46bis4benzylsulfanylstyryl2methylsulfanylpyrimidine

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