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(E)-3-(4-Chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one
In the title chalcone derivative, C(15)H(8)Cl(4)O, the C=C double bond exists in an E configuration and the dihedral angle between the two benzene rings is 48.13 (11)°. In the crystal, molecules are arranged into columns and stacked down the a axis featuring possible weak aromatic π–π stacking inte...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051492/ https://www.ncbi.nlm.nih.gov/pubmed/21522935 http://dx.doi.org/10.1107/S1600536810053213 |
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author | Fun, Hoong-Kun Yeap, Chin Sing Prasad, D. Jagadeesh Nayak, Suresh P. Laxmana, K. |
author_facet | Fun, Hoong-Kun Yeap, Chin Sing Prasad, D. Jagadeesh Nayak, Suresh P. Laxmana, K. |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | In the title chalcone derivative, C(15)H(8)Cl(4)O, the C=C double bond exists in an E configuration and the dihedral angle between the two benzene rings is 48.13 (11)°. In the crystal, molecules are arranged into columns and stacked down the a axis featuring possible weak aromatic π–π stacking interactions [centroid–centroid separation = 3.888 (2) Å]. |
format | Text |
id | pubmed-3051492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30514922011-04-26 (E)-3-(4-Chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one Fun, Hoong-Kun Yeap, Chin Sing Prasad, D. Jagadeesh Nayak, Suresh P. Laxmana, K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title chalcone derivative, C(15)H(8)Cl(4)O, the C=C double bond exists in an E configuration and the dihedral angle between the two benzene rings is 48.13 (11)°. In the crystal, molecules are arranged into columns and stacked down the a axis featuring possible weak aromatic π–π stacking interactions [centroid–centroid separation = 3.888 (2) Å]. International Union of Crystallography 2011-01-08 /pmc/articles/PMC3051492/ /pubmed/21522935 http://dx.doi.org/10.1107/S1600536810053213 Text en © Fun et al. 2011 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 Fun, Hoong-Kun Yeap, Chin Sing Prasad, D. Jagadeesh Nayak, Suresh P. Laxmana, K. (E)-3-(4-Chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one |
title | (E)-3-(4-Chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one |
title_full | (E)-3-(4-Chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one |
title_fullStr | (E)-3-(4-Chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one |
title_full_unstemmed | (E)-3-(4-Chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one |
title_short | (E)-3-(4-Chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one |
title_sort | (e)-3-(4-chlorophenyl)-1-(2,3,4-trichlorophenyl)prop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051492/ https://www.ncbi.nlm.nih.gov/pubmed/21522935 http://dx.doi.org/10.1107/S1600536810053213 |
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