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3,3,4,4,5,5-Hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene
The title compound, C(61)H(68)F(8)O(2)S(2), is a photochromic liquid crystal based on diarylethene as photoswitchable unit. The F atoms connected to the benzene rings are disordered over two positions; the site-occupation factors refined to 0.830 (3)/0.170 (3). The molecule adopts a photo-active a...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961548/ https://www.ncbi.nlm.nih.gov/pubmed/21202692 http://dx.doi.org/10.1107/S1600536808010635 |
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author | Frigoli, Michel Marrot, Jérôme Mehl, Georg H. Larpent, Chantal |
author_facet | Frigoli, Michel Marrot, Jérôme Mehl, Georg H. Larpent, Chantal |
author_sort | Frigoli, Michel |
collection | PubMed |
description | The title compound, C(61)H(68)F(8)O(2)S(2), is a photochromic liquid crystal based on diarylethene as photoswitchable unit. The F atoms connected to the benzene rings are disordered over two positions; the site-occupation factors refined to 0.830 (3)/0.170 (3). The molecule adopts a photo-active antiparallel conformation and the distance between the two reactive C atoms of the thiophene rings is 3.448 (3) Å. The dihedral angles between the central cyclopentene ring and the adjacent thiophene rings are 43.56 (3) and 48.58 (3)°. These structural elements exhibit a suitable geometry for photochromic behaviour in the crystalline state. |
format | Text |
id | pubmed-2961548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29615482010-12-30 3,3,4,4,5,5-Hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene Frigoli, Michel Marrot, Jérôme Mehl, Georg H. Larpent, Chantal Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(61)H(68)F(8)O(2)S(2), is a photochromic liquid crystal based on diarylethene as photoswitchable unit. The F atoms connected to the benzene rings are disordered over two positions; the site-occupation factors refined to 0.830 (3)/0.170 (3). The molecule adopts a photo-active antiparallel conformation and the distance between the two reactive C atoms of the thiophene rings is 3.448 (3) Å. The dihedral angles between the central cyclopentene ring and the adjacent thiophene rings are 43.56 (3) and 48.58 (3)°. These structural elements exhibit a suitable geometry for photochromic behaviour in the crystalline state. International Union of Crystallography 2008-05-03 /pmc/articles/PMC2961548/ /pubmed/21202692 http://dx.doi.org/10.1107/S1600536808010635 Text en © Frigoli et al. 2008 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 Frigoli, Michel Marrot, Jérôme Mehl, Georg H. Larpent, Chantal 3,3,4,4,5,5-Hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene |
title | 3,3,4,4,5,5-Hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene |
title_full | 3,3,4,4,5,5-Hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene |
title_fullStr | 3,3,4,4,5,5-Hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene |
title_full_unstemmed | 3,3,4,4,5,5-Hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene |
title_short | 3,3,4,4,5,5-Hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene |
title_sort | 3,3,4,4,5,5-hexafluoro-1,2-bis[5-(2-fluoro-4′-undecyloxybiphenyl-4-yl)-2-methyl-3-thienyl]cyclopentene |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961548/ https://www.ncbi.nlm.nih.gov/pubmed/21202692 http://dx.doi.org/10.1107/S1600536808010635 |
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