L-Tryptophan 4-nitrophenol trisolvate

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Vitor
Data de Publicação: 2012
Outros Autores: Costa, Margarida, Belsley, M., Gomes, E. Matos
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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spelling 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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