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(E)-1-[4-(Methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one
In the title molecule, C(16)H(14)OS, the dihedral angle between the phenyl and benzene rings is 3.81 (15)°. The H atoms of the central enone group are trans. The propenone unit makes dihedral angles of 11.73 (18) and 11.62 (17)° with the benzene and phenyl rings, respectively. The crystal structure...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961704/ https://www.ncbi.nlm.nih.gov/pubmed/21202897 http://dx.doi.org/10.1107/S1600536808017200 |
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author | Thiruvalluvar, A. Subramanyam, M. Butcher, R. J. Karabasanagouda, T. Adhikari, A. V. |
author_facet | Thiruvalluvar, A. Subramanyam, M. Butcher, R. J. Karabasanagouda, T. Adhikari, A. V. |
author_sort | Thiruvalluvar, A. |
collection | PubMed |
description | In the title molecule, C(16)H(14)OS, the dihedral angle between the phenyl and benzene rings is 3.81 (15)°. The H atoms of the central enone group are trans. The propenone unit makes dihedral angles of 11.73 (18) and 11.62 (17)° with the benzene and phenyl rings, respectively. The crystal structure is stabilized by weak C—H⋯O and C—H⋯π interactions. |
format | Text |
id | pubmed-2961704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29617042010-12-30 (E)-1-[4-(Methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one Thiruvalluvar, A. Subramanyam, M. Butcher, R. J. Karabasanagouda, T. Adhikari, A. V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title molecule, C(16)H(14)OS, the dihedral angle between the phenyl and benzene rings is 3.81 (15)°. The H atoms of the central enone group are trans. The propenone unit makes dihedral angles of 11.73 (18) and 11.62 (17)° with the benzene and phenyl rings, respectively. The crystal structure is stabilized by weak C—H⋯O and C—H⋯π interactions. International Union of Crystallography 2008-06-13 /pmc/articles/PMC2961704/ /pubmed/21202897 http://dx.doi.org/10.1107/S1600536808017200 Text en © Thiruvalluvar et al. 2008 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 Thiruvalluvar, A. Subramanyam, M. Butcher, R. J. Karabasanagouda, T. Adhikari, A. V. (E)-1-[4-(Methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one |
title | (E)-1-[4-(Methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one |
title_full | (E)-1-[4-(Methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one |
title_fullStr | (E)-1-[4-(Methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one |
title_full_unstemmed | (E)-1-[4-(Methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one |
title_short | (E)-1-[4-(Methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one |
title_sort | (e)-1-[4-(methylsulfanyl)phenyl]-3-phenylprop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961704/ https://www.ncbi.nlm.nih.gov/pubmed/21202897 http://dx.doi.org/10.1107/S1600536808017200 |
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