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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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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. |
format | Online Article Text |
id | pubmed-3379311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT amimotokiichi salanines2phenoxypropionicacid11 AT nishiokayuma salanines2phenoxypropionicacid11 |