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r-1,t-3-Bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane
The title compound, C(30)H(32)N(4), was synthesized by the photodimerization of trans-4-{2-[4-(dimethylamino)phenyl]ethenyl}pyridine in benzene upon irradiation with UV light. This photodimer has a puckered cyclobutane ring with the four aryl substituents in an r-1,t-2,c-3,t conformation. The...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998431/ https://www.ncbi.nlm.nih.gov/pubmed/24765012 http://dx.doi.org/10.1107/S1600536814002311 |
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author | Zhang, Shuguang Zhuang, Junpeng |
author_facet | Zhang, Shuguang Zhuang, Junpeng |
author_sort | Zhang, Shuguang |
collection | PubMed |
description | The title compound, C(30)H(32)N(4), was synthesized by the photodimerization of trans-4-{2-[4-(dimethylamino)phenyl]ethenyl}pyridine in benzene upon irradiation with UV light. This photodimer has a puckered cyclobutane ring with the four aryl substituents in an r-1,t-2,c-3,t conformation. The puckering angle of the cyclobutane ring is 32.22 (7)°, which is the largest among reported tetraaryl-substituted cyclobutanes. In the crystal, the molecules form a hollow, one-dimensional structure extending parallel to the c axis via two different pairs of C—H⋯π interactions. |
format | Online Article Text |
id | pubmed-3998431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-39984312014-04-24 r-1,t-3-Bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane Zhang, Shuguang Zhuang, Junpeng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(30)H(32)N(4), was synthesized by the photodimerization of trans-4-{2-[4-(dimethylamino)phenyl]ethenyl}pyridine in benzene upon irradiation with UV light. This photodimer has a puckered cyclobutane ring with the four aryl substituents in an r-1,t-2,c-3,t conformation. The puckering angle of the cyclobutane ring is 32.22 (7)°, which is the largest among reported tetraaryl-substituted cyclobutanes. In the crystal, the molecules form a hollow, one-dimensional structure extending parallel to the c axis via two different pairs of C—H⋯π interactions. International Union of Crystallography 2014-02-15 /pmc/articles/PMC3998431/ /pubmed/24765012 http://dx.doi.org/10.1107/S1600536814002311 Text en © Zhang and Zhuang 2014 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 Zhang, Shuguang Zhuang, Junpeng r-1,t-3-Bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane |
title |
r-1,t-3-Bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane |
title_full |
r-1,t-3-Bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane |
title_fullStr |
r-1,t-3-Bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane |
title_full_unstemmed |
r-1,t-3-Bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane |
title_short |
r-1,t-3-Bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane |
title_sort | r-1,t-3-bis[4-(dimethylamino)phenyl]-c-2,t-4-bis(pyridin-4-yl)cyclobutane |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998431/ https://www.ncbi.nlm.nih.gov/pubmed/24765012 http://dx.doi.org/10.1107/S1600536814002311 |
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