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2,3-Dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one

In the title compound [systematic name: 4-(2,3-dibromo-3-phenyl­propano­yl)-3-phenyl-1,2,3-oxadiazol-3-ylium-5-olate], C(17)H(12)Br(2)N(2)O(3), the oxadiazole ring is essentially planar, with a maximum deviation of 0.001 (3) Å. The central oxadiazole ring makes dihedral angles of 73.3 (2) and 29.0 (...

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Autores principales: Fun, Hoong-Kun, Hemamalini, Madhukar, Nithinchandra, Kalluraya, Balakrishna
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099808/
https://www.ncbi.nlm.nih.gov/pubmed/21754100
http://dx.doi.org/10.1107/S1600536811008026
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author Fun, Hoong-Kun
Hemamalini, Madhukar
Nithinchandra,
Kalluraya, Balakrishna
author_facet Fun, Hoong-Kun
Hemamalini, Madhukar
Nithinchandra,
Kalluraya, Balakrishna
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound [systematic name: 4-(2,3-dibromo-3-phenyl­propano­yl)-3-phenyl-1,2,3-oxadiazol-3-ylium-5-olate], C(17)H(12)Br(2)N(2)O(3), the oxadiazole ring is essentially planar, with a maximum deviation of 0.001 (3) Å. The central oxadiazole ring makes dihedral angles of 73.3 (2) and 29.0 (2)° with the adjacent and remote phenyl rings, respectively. In the crystal, adjacent mol­ecules are connected by C—H⋯O hydrogen bonds, forming a supra­molecular chain along the c axis. There is an intra­molecular C—H⋯O hydrogen bond, which generates an S(6) ring motif.
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spelling pubmed-30998082011-07-13 2,3-Dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one Fun, Hoong-Kun Hemamalini, Madhukar Nithinchandra, Kalluraya, Balakrishna Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound [systematic name: 4-(2,3-dibromo-3-phenyl­propano­yl)-3-phenyl-1,2,3-oxadiazol-3-ylium-5-olate], C(17)H(12)Br(2)N(2)O(3), the oxadiazole ring is essentially planar, with a maximum deviation of 0.001 (3) Å. The central oxadiazole ring makes dihedral angles of 73.3 (2) and 29.0 (2)° with the adjacent and remote phenyl rings, respectively. In the crystal, adjacent mol­ecules are connected by C—H⋯O hydrogen bonds, forming a supra­molecular chain along the c axis. There is an intra­molecular C—H⋯O hydrogen bond, which generates an S(6) ring motif. International Union of Crystallography 2011-03-09 /pmc/articles/PMC3099808/ /pubmed/21754100 http://dx.doi.org/10.1107/S1600536811008026 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
Hemamalini, Madhukar
Nithinchandra,
Kalluraya, Balakrishna
2,3-Dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one
title 2,3-Dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one
title_full 2,3-Dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one
title_fullStr 2,3-Dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one
title_full_unstemmed 2,3-Dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one
title_short 2,3-Dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one
title_sort 2,3-dibromo-3-phenyl-1-(3-phenyl­sydnon-4-yl)propan-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099808/
https://www.ncbi.nlm.nih.gov/pubmed/21754100
http://dx.doi.org/10.1107/S1600536811008026
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