Triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate

The asymmetric unit of the title salt, C(28)H(28)O(3)P(+)·Cl(−)·H(2)O, contains a benzyl­triphenyl­phospho­nium cation, a chloride counter-ion, and a water mol­ecule of crystallization. The 3,4,5-trimeth­oxy substituents of the benzylic functionality are arranged with the 3,5-methyl groups lying app...

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Detalles Bibliográficos
Autores principales: Barkell, Alice M., Sharp, Jonathan, Simpson, Stephen J.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959282/
https://www.ncbi.nlm.nih.gov/pubmed/21201090
http://dx.doi.org/10.1107/S1600536808027712
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author Barkell, Alice M.
Sharp, Jonathan
Simpson, Stephen J.
author_facet Barkell, Alice M.
Sharp, Jonathan
Simpson, Stephen J.
author_sort Barkell, Alice M.
collection PubMed
description The asymmetric unit of the title salt, C(28)H(28)O(3)P(+)·Cl(−)·H(2)O, contains a benzyl­triphenyl­phospho­nium cation, a chloride counter-ion, and a water mol­ecule of crystallization. The 3,4,5-trimeth­oxy substituents of the benzylic functionality are arranged with the 3,5-methyl groups lying approximately in the aromatic ring plane while the 4-methyl group is out of the plane.
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spelling pubmed-29592822010-12-30 Triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate Barkell, Alice M. Sharp, Jonathan Simpson, Stephen J. Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title salt, C(28)H(28)O(3)P(+)·Cl(−)·H(2)O, contains a benzyl­triphenyl­phospho­nium cation, a chloride counter-ion, and a water mol­ecule of crystallization. The 3,4,5-trimeth­oxy substituents of the benzylic functionality are arranged with the 3,5-methyl groups lying approximately in the aromatic ring plane while the 4-methyl group is out of the plane. International Union of Crystallography 2008-09-06 /pmc/articles/PMC2959282/ /pubmed/21201090 http://dx.doi.org/10.1107/S1600536808027712 Text en © Barkell 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
Barkell, Alice M.
Sharp, Jonathan
Simpson, Stephen J.
Triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate
title Triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate
title_full Triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate
title_fullStr Triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate
title_full_unstemmed Triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate
title_short Triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate
title_sort triphenyl(3,4,5-trimethoxy­benzyl)­phospho­nium chloride monohydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959282/
https://www.ncbi.nlm.nih.gov/pubmed/21201090
http://dx.doi.org/10.1107/S1600536808027712
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AT sharpjonathan triphenyl345trimethoxybenzylphosphoniumchloridemonohydrate
AT simpsonstephenj triphenyl345trimethoxybenzylphosphoniumchloridemonohydrate

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