Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.

Detalhes bibliográficos
Autor(a) principal: Teixeira, Róbson Ricardo
Data de Publicação: 2016
Outros Autores: Barbosa, Luiz Cláudio de Almeida, Antolinez, Isabel Valero, Correa, Rodrigo de Souza, Martins, Felipe Terra, Doriguetto, Antônio Carlos
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UFOP
Texto Completo: http://www.repositorio.ufop.br/handle/123456789/7069
Resumo: We have here elucidated the crystal structures of five nostoclide analogues. A common feature in all compounds is a substituent at the para-position of the benzylidene group. Compounds with either bromine (3) or hydroxyl (4) as para-substituent crystallizes with Z’ ¼ 2 as result of conformerism. It was also observed that Z' > 1 in the compound with a para-dimethylamino substituent (1). However, its four crystallographically independent molecules are conformationally similar. They are not related by crystallographic symmetry due to the offset packing of their CeH … O]C nonclassical hydrogen bonded double chains. This compound (1) has also crystallized in a chiral space group (P21) despite the lack of a stereocenter. Such enantiomorphism phenomenon is related to the presence of only one of the two mirror benzyl conformations with phenyl ring at the equatorial position opposite the lactone oxygen atom. The molecular mean plane of nostoclide analogues has been featured by high level of planarity, except in the brominated compound where two twisted conformations occurred due to rotations on the single bond axis into benzylidene group. The benzyl conformation has been the greatest difference between the two crystallographically independent molecules of the para-hydroxylated compound (4). The crystal packing of the compounds is marked by double catemer motif assembled through CeH … O] C non-classical hydrogen bonds, although CeH … p interactions do play an important role in stabilizing the crystal packing of some compounds of the series.
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spelling Teixeira, Róbson RicardoBarbosa, Luiz Cláudio de AlmeidaAntolinez, Isabel ValeroCorrea, Rodrigo de SouzaMartins, Felipe TerraDoriguetto, Antônio Carlos2016-11-07T13:20:26Z2016-11-07T13:20:26Z2016TEIXEIRA, R. R. et al. Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues. Journal of Molecular Structure, v. 1106, p. 291-299, 2016. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0022286015304014>. Acesso em: 26 set. 2016.0022-2860http://www.repositorio.ufop.br/handle/123456789/7069O periódico Journal of Molecular Structure concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 3958741415552.info:eu-repo/semantics/openAccessNostoclidesButenolidesGama-lactonesGama-alkylidenebutenolidesCrystal structureConformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleWe have here elucidated the crystal structures of five nostoclide analogues. A common feature in all compounds is a substituent at the para-position of the benzylidene group. Compounds with either bromine (3) or hydroxyl (4) as para-substituent crystallizes with Z’ ¼ 2 as result of conformerism. It was also observed that Z' > 1 in the compound with a para-dimethylamino substituent (1). However, its four crystallographically independent molecules are conformationally similar. They are not related by crystallographic symmetry due to the offset packing of their CeH … O]C nonclassical hydrogen bonded double chains. This compound (1) has also crystallized in a chiral space group (P21) despite the lack of a stereocenter. Such enantiomorphism phenomenon is related to the presence of only one of the two mirror benzyl conformations with phenyl ring at the equatorial position opposite the lactone oxygen atom. The molecular mean plane of nostoclide analogues has been featured by high level of planarity, except in the brominated compound where two twisted conformations occurred due to rotations on the single bond axis into benzylidene group. The benzyl conformation has been the greatest difference between the two crystallographically independent molecules of the para-hydroxylated compound (4). The crystal packing of the compounds is marked by double catemer motif assembled through CeH … O] C non-classical hydrogen bonds, although CeH … p interactions do play an important role in stabilizing the crystal packing of some compounds of the series.porreponame:Repositório Institucional da UFOPinstname:Universidade Federal de Ouro Preto (UFOP)instacron:UFOPLICENSElicense.txtlicense.txttext/plain; charset=utf-8924http://www.repositorio.ufop.br/bitstream/123456789/7069/2/license.txt62604f8d955274beb56c80ce1ee5dcaeMD52ORIGINALARTIGO_ConfomerismEnantiomorphismDouble.pdfARTIGO_ConfomerismEnantiomorphismDouble.pdfapplication/pdf2524312http://www.repositorio.ufop.br/bitstream/123456789/7069/1/ARTIGO_ConfomerismEnantiomorphismDouble.pdf342ec8f6cb11128190d79006d735b10aMD51123456789/70692019-10-15 10:22:22.661oai:localhost: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ório InstitucionalPUBhttp://www.repositorio.ufop.br/oai/requestrepositorio@ufop.edu.bropendoar:32332019-10-15T14:22:22Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP)false
dc.title.pt_BR.fl_str_mv Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.
title Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.
spellingShingle Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.
Teixeira, Róbson Ricardo
Nostoclides
Butenolides
Gama-lactones
Gama-alkylidenebutenolides
Crystal structure
title_short Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.
title_full Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.
title_fullStr Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.
title_full_unstemmed Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.
title_sort Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues.
author Teixeira, Róbson Ricardo
author_facet Teixeira, Róbson Ricardo
Barbosa, Luiz Cláudio de Almeida
Antolinez, Isabel Valero
Correa, Rodrigo de Souza
Martins, Felipe Terra
Doriguetto, Antônio Carlos
author_role author
author2 Barbosa, Luiz Cláudio de Almeida
Antolinez, Isabel Valero
Correa, Rodrigo de Souza
Martins, Felipe Terra
Doriguetto, Antônio Carlos
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Teixeira, Róbson Ricardo
Barbosa, Luiz Cláudio de Almeida
Antolinez, Isabel Valero
Correa, Rodrigo de Souza
Martins, Felipe Terra
Doriguetto, Antônio Carlos
dc.subject.por.fl_str_mv Nostoclides
Butenolides
Gama-lactones
Gama-alkylidenebutenolides
Crystal structure
topic Nostoclides
Butenolides
Gama-lactones
Gama-alkylidenebutenolides
Crystal structure
description We have here elucidated the crystal structures of five nostoclide analogues. A common feature in all compounds is a substituent at the para-position of the benzylidene group. Compounds with either bromine (3) or hydroxyl (4) as para-substituent crystallizes with Z’ ¼ 2 as result of conformerism. It was also observed that Z' > 1 in the compound with a para-dimethylamino substituent (1). However, its four crystallographically independent molecules are conformationally similar. They are not related by crystallographic symmetry due to the offset packing of their CeH … O]C nonclassical hydrogen bonded double chains. This compound (1) has also crystallized in a chiral space group (P21) despite the lack of a stereocenter. Such enantiomorphism phenomenon is related to the presence of only one of the two mirror benzyl conformations with phenyl ring at the equatorial position opposite the lactone oxygen atom. The molecular mean plane of nostoclide analogues has been featured by high level of planarity, except in the brominated compound where two twisted conformations occurred due to rotations on the single bond axis into benzylidene group. The benzyl conformation has been the greatest difference between the two crystallographically independent molecules of the para-hydroxylated compound (4). The crystal packing of the compounds is marked by double catemer motif assembled through CeH … O] C non-classical hydrogen bonds, although CeH … p interactions do play an important role in stabilizing the crystal packing of some compounds of the series.
publishDate 2016
dc.date.accessioned.fl_str_mv 2016-11-07T13:20:26Z
dc.date.available.fl_str_mv 2016-11-07T13:20:26Z
dc.date.issued.fl_str_mv 2016
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dc.identifier.citation.fl_str_mv TEIXEIRA, R. R. et al. Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues. Journal of Molecular Structure, v. 1106, p. 291-299, 2016. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0022286015304014>. Acesso em: 26 set. 2016.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufop.br/handle/123456789/7069
dc.identifier.issn.none.fl_str_mv 0022-2860
identifier_str_mv TEIXEIRA, R. R. et al. Conformerism, enantiomorphism and double catemer motifs in para-substituted nostoclide analogues. Journal of Molecular Structure, v. 1106, p. 291-299, 2016. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0022286015304014>. Acesso em: 26 set. 2016.
0022-2860
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