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(E)-3-(4-Chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one
In the title compound, C(19)H(13)ClO, the benzene ring and the naphthalene system, are twisted by 12.3 (3) and 36.1 (2)°, respectively, and in opposite directions with respect to the central propenone bridge. The bond-angle pattern within the benzene ring is influence by both substituents; these inf...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971946/ https://www.ncbi.nlm.nih.gov/pubmed/21578952 http://dx.doi.org/10.1107/S1600536809050508 |
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author | Dutkiewicz, Grzegorz Samshuddin, S. Narayana, B. Yathirajan, H. S. Kubicki, Maciej |
author_facet | Dutkiewicz, Grzegorz Samshuddin, S. Narayana, B. Yathirajan, H. S. Kubicki, Maciej |
author_sort | Dutkiewicz, Grzegorz |
collection | PubMed |
description | In the title compound, C(19)H(13)ClO, the benzene ring and the naphthalene system, are twisted by 12.3 (3) and 36.1 (2)°, respectively, and in opposite directions with respect to the central propenone bridge. The bond-angle pattern within the benzene ring is influence by both substituents; these influences are almost additive. In the crystal, the molecules are linked by C—H⋯O and C—H⋯Cl interactions. |
format | Text |
id | pubmed-2971946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29719462010-12-30 (E)-3-(4-Chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one Dutkiewicz, Grzegorz Samshuddin, S. Narayana, B. Yathirajan, H. S. Kubicki, Maciej Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(13)ClO, the benzene ring and the naphthalene system, are twisted by 12.3 (3) and 36.1 (2)°, respectively, and in opposite directions with respect to the central propenone bridge. The bond-angle pattern within the benzene ring is influence by both substituents; these influences are almost additive. In the crystal, the molecules are linked by C—H⋯O and C—H⋯Cl interactions. International Union of Crystallography 2009-11-28 /pmc/articles/PMC2971946/ /pubmed/21578952 http://dx.doi.org/10.1107/S1600536809050508 Text en © Dutkiewicz et al. 2009 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 Dutkiewicz, Grzegorz Samshuddin, S. Narayana, B. Yathirajan, H. S. Kubicki, Maciej (E)-3-(4-Chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one |
title | (E)-3-(4-Chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one |
title_full | (E)-3-(4-Chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one |
title_fullStr | (E)-3-(4-Chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one |
title_full_unstemmed | (E)-3-(4-Chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one |
title_short | (E)-3-(4-Chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one |
title_sort | (e)-3-(4-chlorophenyl)-1-(1-naphthyl)prop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971946/ https://www.ncbi.nlm.nih.gov/pubmed/21578952 http://dx.doi.org/10.1107/S1600536809050508 |
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