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l-Tryptophan 4-nitrophenol trisolvate
The title compound, C(11)H(12)N(2)O(2)·3C(6)H(5)NO(3), comprises a zwitterionic amino acid formed by two nearly planar groups: (i) the indole ring and Cβ, and (ii) the carboxyl group, Cα, as well as the amine N atom, with r.m.s. deviations of 0.0084 and 0.0038 Å, respectively. The angle between thes...
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/PMC3297960/ https://www.ncbi.nlm.nih.gov/pubmed/22412763 http://dx.doi.org/10.1107/S1600536812007817 |
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author | Rodrigues, V. H. Costa, M. M. R. R. Belsley, M. de Matos Gomes, E. |
author_facet | Rodrigues, V. H. Costa, M. M. R. R. Belsley, M. de Matos Gomes, E. |
author_sort | Rodrigues, V. H. |
collection | PubMed |
description | The title compound, C(11)H(12)N(2)O(2)·3C(6)H(5)NO(3), comprises a zwitterionic amino acid formed by two nearly planar groups: (i) the indole ring and Cβ, and (ii) the carboxyl group, Cα, as well as the amine N atom, with r.m.s. deviations of 0.0084 and 0.0038 Å, respectively. The angle between these idealized planes is 39.47 (9)°. The amine group of the amino acid is in a syn (−sc) arrangement relative to the ring system. The overall crystal structure results from the packing of sheets parallel to the (001) planes. These sheets are formed by a pair of screw axis related parallel networks bound by hydrogen-bond and π–π stacking interactions. The intermolecular cohesion of all organic residues in each of the latter two-dimensional networks is achieved via strong hydrogen bonding, nitro–π and π–π stacking interactions. |
format | Online Article Text |
id | pubmed-3297960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32979602012-03-12 l-Tryptophan 4-nitrophenol trisolvate Rodrigues, V. H. Costa, M. M. R. R. Belsley, M. de Matos Gomes, E. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(12)N(2)O(2)·3C(6)H(5)NO(3), comprises a zwitterionic amino acid formed by two nearly planar groups: (i) the indole ring and Cβ, and (ii) the carboxyl group, Cα, as well as the amine N atom, with r.m.s. deviations of 0.0084 and 0.0038 Å, respectively. The angle between these idealized planes is 39.47 (9)°. The amine group of the amino acid is in a syn (−sc) arrangement relative to the ring system. The overall crystal structure results from the packing of sheets parallel to the (001) planes. These sheets are formed by a pair of screw axis related parallel networks bound by hydrogen-bond and π–π stacking interactions. The intermolecular cohesion of all organic residues in each of the latter two-dimensional networks is achieved via strong hydrogen bonding, nitro–π and π–π stacking interactions. International Union of Crystallography 2012-02-29 /pmc/articles/PMC3297960/ /pubmed/22412763 http://dx.doi.org/10.1107/S1600536812007817 Text en © Rodrigues et al. 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 Rodrigues, V. H. Costa, M. M. R. R. Belsley, M. de Matos Gomes, E. l-Tryptophan 4-nitrophenol trisolvate |
title |
l-Tryptophan 4-nitrophenol trisolvate |
title_full |
l-Tryptophan 4-nitrophenol trisolvate |
title_fullStr |
l-Tryptophan 4-nitrophenol trisolvate |
title_full_unstemmed |
l-Tryptophan 4-nitrophenol trisolvate |
title_short |
l-Tryptophan 4-nitrophenol trisolvate |
title_sort | l-tryptophan 4-nitrophenol trisolvate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297960/ https://www.ncbi.nlm.nih.gov/pubmed/22412763 http://dx.doi.org/10.1107/S1600536812007817 |
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