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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...

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Autores principales: Rodrigues, V. H., Costa, M. M. R. R., Belsley, M., de Matos Gomes, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
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.
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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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