(Z)-3-(9-Anthr­yl)-1-(2-thien­yl)prop-2-en-1-one

There are two crystallographically independent mol­ecules in the asymmetric unit of the title heteroaryl chalcone, C(21)H(14)OS: the dihedral angle between the thio­phene and anthracene rings is 75.07 (17)° in one mol­ecule and 76.32 (17)° in the other. The crystal structure is consolidated by short...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Suwunwong, Thitipone, Boonnak, Nawong, Chantrapromma, Suchada
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969873/
https://www.ncbi.nlm.nih.gov/pubmed/21577575
http://dx.doi.org/10.1107/S1600536809031900
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author Fun, Hoong-Kun
Suwunwong, Thitipone
Boonnak, Nawong
Chantrapromma, Suchada
author_facet Fun, Hoong-Kun
Suwunwong, Thitipone
Boonnak, Nawong
Chantrapromma, Suchada
author_sort Fun, Hoong-Kun
collection PubMed
description There are two crystallographically independent mol­ecules in the asymmetric unit of the title heteroaryl chalcone, C(21)H(14)OS: the dihedral angle between the thio­phene and anthracene rings is 75.07 (17)° in one mol­ecule and 76.32 (17)° in the other. The crystal structure is consolidated by short C⋯O [3.348 (5)–3.394 (5) Å], C⋯S [3.607 (5)–3.666 (5) Å] and S⋯O [2.926 (3) Å] contacts, as well as by C—H⋯π and π–π inter­actions [Cg⋯Cg = 3.745 (3) Å].
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spelling pubmed-29698732010-12-30 (Z)-3-(9-Anthr­yl)-1-(2-thien­yl)prop-2-en-1-one Fun, Hoong-Kun Suwunwong, Thitipone Boonnak, Nawong Chantrapromma, Suchada Acta Crystallogr Sect E Struct Rep Online Organic Papers There are two crystallographically independent mol­ecules in the asymmetric unit of the title heteroaryl chalcone, C(21)H(14)OS: the dihedral angle between the thio­phene and anthracene rings is 75.07 (17)° in one mol­ecule and 76.32 (17)° in the other. The crystal structure is consolidated by short C⋯O [3.348 (5)–3.394 (5) Å], C⋯S [3.607 (5)–3.666 (5) Å] and S⋯O [2.926 (3) Å] contacts, as well as by C—H⋯π and π–π inter­actions [Cg⋯Cg = 3.745 (3) Å]. International Union of Crystallography 2009-08-15 /pmc/articles/PMC2969873/ /pubmed/21577575 http://dx.doi.org/10.1107/S1600536809031900 Text en © Fun 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
Fun, Hoong-Kun
Suwunwong, Thitipone
Boonnak, Nawong
Chantrapromma, Suchada
(Z)-3-(9-Anthr­yl)-1-(2-thien­yl)prop-2-en-1-one
title (Z)-3-(9-Anthr­yl)-1-(2-thien­yl)prop-2-en-1-one
title_full (Z)-3-(9-Anthr­yl)-1-(2-thien­yl)prop-2-en-1-one
title_fullStr (Z)-3-(9-Anthr­yl)-1-(2-thien­yl)prop-2-en-1-one
title_full_unstemmed (Z)-3-(9-Anthr­yl)-1-(2-thien­yl)prop-2-en-1-one
title_short (Z)-3-(9-Anthr­yl)-1-(2-thien­yl)prop-2-en-1-one
title_sort (z)-3-(9-anthr­yl)-1-(2-thien­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969873/
https://www.ncbi.nlm.nih.gov/pubmed/21577575
http://dx.doi.org/10.1107/S1600536809031900
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AT chantraprommasuchada z39anthryl12thienylprop2en1one

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