L-Tryptophan 4-nitrophenol trisolvate
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/22198 |
Resumo: | The title compound, C11H12N2O2 3C6H5NO3, comprises a zwitterionic amino acid formed by two nearly planar groups: (i) the indole ring and C , and (ii) the carboxyl group, C , as well as the amine N atom, with r.m.s. deviations of 0.0084 and 0.0038 A ˚ , 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 – stacking interactions. The intermolecular cohesion of all organic residues in each of the latter two-dimensional networks is achieved via strong hydrogen bonding, nitro– and – stacking interactions. |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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7160 |
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L-Tryptophan 4-nitrophenol trisolvatedata-to-parameter ratio = 10.5mean s(C-C) = 0.003 ÅR factor = 0.035single-crystal X-ray studyT = 291 KwR factor = 0.101Science & TechnologyThe title compound, C11H12N2O2 3C6H5NO3, comprises a zwitterionic amino acid formed by two nearly planar groups: (i) the indole ring and C , and (ii) the carboxyl group, C , as well as the amine N atom, with r.m.s. deviations of 0.0084 and 0.0038 A ˚ , 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 – stacking interactions. The intermolecular cohesion of all organic residues in each of the latter two-dimensional networks is achieved via strong hydrogen bonding, nitro– and – stacking interactions.This work was supported by funds from FEDER via the COMPETE (Programa Operacional Factores de Competitividade) programme and by the Fundacao para a Ciencia e a Tecnologia (project PEst-C/FIS/UI0036/2011).WileyUniversidade do MinhoRodrigues, VitorCosta, MargaridaBelsley, M.Gomes, E. Matos20122012-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/22198eng1600-536810.1107/S1600536812007817info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:12:56Zoai:repositorium.sdum.uminho.pt:1822/22198Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:04:57.471597Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
L-Tryptophan 4-nitrophenol trisolvate |
title |
L-Tryptophan 4-nitrophenol trisolvate |
spellingShingle |
L-Tryptophan 4-nitrophenol trisolvate Rodrigues, Vitor data-to-parameter ratio = 10.5 mean s(C-C) = 0.003 Å R factor = 0.035 single-crystal X-ray study T = 291 K wR factor = 0.101 Science & Technology |
title_short |
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_sort |
L-Tryptophan 4-nitrophenol trisolvate |
author |
Rodrigues, Vitor |
author_facet |
Rodrigues, Vitor Costa, Margarida Belsley, M. Gomes, E. Matos |
author_role |
author |
author2 |
Costa, Margarida Belsley, M. Gomes, E. Matos |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Rodrigues, Vitor Costa, Margarida Belsley, M. Gomes, E. Matos |
dc.subject.por.fl_str_mv |
data-to-parameter ratio = 10.5 mean s(C-C) = 0.003 Å R factor = 0.035 single-crystal X-ray study T = 291 K wR factor = 0.101 Science & Technology |
topic |
data-to-parameter ratio = 10.5 mean s(C-C) = 0.003 Å R factor = 0.035 single-crystal X-ray study T = 291 K wR factor = 0.101 Science & Technology |
description |
The title compound, C11H12N2O2 3C6H5NO3, comprises a zwitterionic amino acid formed by two nearly planar groups: (i) the indole ring and C , and (ii) the carboxyl group, C , as well as the amine N atom, with r.m.s. deviations of 0.0084 and 0.0038 A ˚ , 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 – stacking interactions. The intermolecular cohesion of all organic residues in each of the latter two-dimensional networks is achieved via strong hydrogen bonding, nitro– and – stacking interactions. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012 2012-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/1822/22198 |
url |
http://hdl.handle.net/1822/22198 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1600-5368 10.1107/S1600536812007817 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Wiley |
publisher.none.fl_str_mv |
Wiley |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799132460454248448 |