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(S)-Alanine–(S)-2-phen­oxy­propionic acid (1/1)

In the title co-crystal, C(3)H(7)NO(2)·C(9)H(10)O(3), the (S)-alanine mol­ecule exists in the zwitterionic form stabilized by two pairs of N(+)—H⋯O(−) hydrogen bonds and an electrostatic inter­action between the ammonium center and the carboxyl­ate anion, forming a sheet along the ab plane. The carb...

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Detalles Bibliográficos
Autores principales: Amimoto, Kiichi, Nishioka, Yuma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379311/
https://www.ncbi.nlm.nih.gov/pubmed/22719509
http://dx.doi.org/10.1107/S1600536812020727
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author Amimoto, Kiichi
Nishioka, Yuma
author_facet Amimoto, Kiichi
Nishioka, Yuma
author_sort Amimoto, Kiichi
collection PubMed
description In the title co-crystal, C(3)H(7)NO(2)·C(9)H(10)O(3), the (S)-alanine mol­ecule exists in the zwitterionic form stabilized by two pairs of N(+)—H⋯O(−) hydrogen bonds and an electrostatic inter­action between the ammonium center and the carboxyl­ate anion, forming a sheet along the ab plane. The carboxyl group of the (S)-2-phen­oxy­propionic acid mol­ecule is connected to the top and bottom of the sheet via N(+)—H⋯O=C and O—H⋯O(−) [R (2) (2)(7) graph set] hydrogen bonds, giving an (S,S)-homochiral layer, in which both methyl groups of (S)-alanine and the phenyl rings of (S)-2-phen­oxy­propionic acid are oriented in the same direction along the b axis.
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spelling pubmed-33793112012-06-20 (S)-Alanine–(S)-2-phen­oxy­propionic acid (1/1) Amimoto, Kiichi Nishioka, Yuma Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title co-crystal, C(3)H(7)NO(2)·C(9)H(10)O(3), the (S)-alanine mol­ecule exists in the zwitterionic form stabilized by two pairs of N(+)—H⋯O(−) hydrogen bonds and an electrostatic inter­action between the ammonium center and the carboxyl­ate anion, forming a sheet along the ab plane. The carboxyl group of the (S)-2-phen­oxy­propionic acid mol­ecule is connected to the top and bottom of the sheet via N(+)—H⋯O=C and O—H⋯O(−) [R (2) (2)(7) graph set] hydrogen bonds, giving an (S,S)-homochiral layer, in which both methyl groups of (S)-alanine and the phenyl rings of (S)-2-phen­oxy­propionic acid are oriented in the same direction along the b axis. International Union of Crystallography 2012-05-16 /pmc/articles/PMC3379311/ /pubmed/22719509 http://dx.doi.org/10.1107/S1600536812020727 Text en © Amimoto and Nishioka 2012 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
Amimoto, Kiichi
Nishioka, Yuma
(S)-Alanine–(S)-2-phen­oxy­propionic acid (1/1)
title (S)-Alanine–(S)-2-phen­oxy­propionic acid (1/1)
title_full (S)-Alanine–(S)-2-phen­oxy­propionic acid (1/1)
title_fullStr (S)-Alanine–(S)-2-phen­oxy­propionic acid (1/1)
title_full_unstemmed (S)-Alanine–(S)-2-phen­oxy­propionic acid (1/1)
title_short (S)-Alanine–(S)-2-phen­oxy­propionic acid (1/1)
title_sort (s)-alanine–(s)-2-phen­oxy­propionic acid (1/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379311/
https://www.ncbi.nlm.nih.gov/pubmed/22719509
http://dx.doi.org/10.1107/S1600536812020727
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