Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol

Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol

The mol­ecule of the title compound, C25H24O, obtained by acid-catalysed 1,3-migration of an alcohol group, is T-shaped. The planes of the two phenyl rings are inclined to one another by 81.9 (2)°. In the crystal, mol­ecules are linked by O-H...O hydrogen bonds, forming chains along [001].

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Main Authors: Ganguly, Rakesh, Sally, Chan, Philip Wai Hong
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2015
Subjects:
DRNTU::Science::Chemistry::Crystallography
Online Access:https://hdl.handle.net/10356/107448
http://hdl.handle.net/10220/25618
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1074482023-02-28T19:47:37Z Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol Ganguly, Rakesh Sally Chan, Philip Wai Hong School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Crystallography The mol­ecule of the title compound, C25H24O, obtained by acid-catalysed 1,3-migration of an alcohol group, is T-shaped. The planes of the two phenyl rings are inclined to one another by 81.9 (2)°. In the crystal, mol­ecules are linked by O-H...O hydrogen bonds, forming chains along [001]. Published version 2015-05-20T03:24:15Z 2019-12-06T22:31:21Z 2015-05-20T03:24:15Z 2019-12-06T22:31:21Z 2015 2015 Journal Article Ganguly, R., Sally, & Chan, P. W. H. (2015). Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol. Acta crystallographica section E : crystallographic communications, 71(1). 2056-9890 https://hdl.handle.net/10356/107448 http://hdl.handle.net/10220/25618 10.1107/S205698901402742X 25705512 en Acta crystallographica section E : crystallographic communications © 2015 The Authors(published by International Union of Crystallography). This paper was published in Acta Crystallographica Section E: Crystallographic Communications and is made available as an electronic reprint (preprint) with permission of The Authors(published by International Union of Crystallography). The paper can be found at the following official DOI: [http://dx.doi.org/10.1107/S205698901402742X]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Chemistry::Crystallography
spellingShingle DRNTU::Science::Chemistry::Crystallography
Ganguly, Rakesh
Sally
Chan, Philip Wai Hong
Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol
description The mol­ecule of the title compound, C25H24O, obtained by acid-catalysed 1,3-migration of an alcohol group, is T-shaped. The planes of the two phenyl rings are inclined to one another by 81.9 (2)°. In the crystal, mol­ecules are linked by O-H...O hydrogen bonds, forming chains along [001].
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Ganguly, Rakesh
Sally
Chan, Philip Wai Hong
format Article
author Ganguly, Rakesh
Sally
Chan, Philip Wai Hong
author_sort Ganguly, Rakesh
title Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol
title_short Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol
title_full Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol
title_fullStr Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol
title_full_unstemmed Crystal structure of (Z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol
title_sort crystal structure of (z)-1-phenyl-3-styrylundeca-2-en-4,10-diyn-1-ol
publishDate 2015
url https://hdl.handle.net/10356/107448
http://hdl.handle.net/10220/25618
_version_ 1759857444385718272

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