Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
DOI: | 10.1021/jp103665b |
Texto Completo: | http://hdl.handle.net/10316/18076 https://doi.org/10.1021/jp103665b |
Resumo: | Methyl 4-chloro-5-phenyl-1,3-oxazole-2-carboxylate (MCPOC) has been synthesized and isolated in cryogenic matrices (argon and xenon). FTIR spectroscopy studies on the matrix isolated compound, supported by DFT(B3LYP)/6-311++G(d,p) calculations, allow for the identification of two low-energy conformers (I and II) of the molecule, which differ from each other in the orientation of the ester group relative to the oxazole ring. In both these conformers, the ester moiety is in the s-cis configuration (O═C—O—CH3 dihedral: 0°). Conformer II is ca. 3.0 kJ mol−1 higher in energy than form I in the gas phase. Two additional higher energy conformers, III and IV, with relative energies of ca. 30 and 45 kJ mol−1, respectively, were predicted to exist by the calculations, corresponding to structures where the ester group is in an approximately s-trans arrangement. Annealing of the compound isolated in xenon at 60 K led to aggregation and simultaneous reduction of the population of I compared to that of the more polar conformer II. These results suggest the inversion of the order of stability of the two conformers in that matrix, eventually accompanied by a higher trend of conformer I to aggregate. Full assignment of the observed infrared bands to the two experimentally accessible conformers was carried out for the matrix isolated monomeric species. In addition, the infrared spectra of the neat compound in the low-temperature (10 K) amorphous and crystalline phases, as well as the infrared and Raman spectra of the crystal at room temperature were also obtained and assigned. |
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Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylateMethyl 4-chloro-5-phenyl-1,3-oxazole-2-carboxylate (MCPOC) has been synthesized and isolated in cryogenic matrices (argon and xenon). FTIR spectroscopy studies on the matrix isolated compound, supported by DFT(B3LYP)/6-311++G(d,p) calculations, allow for the identification of two low-energy conformers (I and II) of the molecule, which differ from each other in the orientation of the ester group relative to the oxazole ring. In both these conformers, the ester moiety is in the s-cis configuration (O═C—O—CH3 dihedral: 0°). Conformer II is ca. 3.0 kJ mol−1 higher in energy than form I in the gas phase. Two additional higher energy conformers, III and IV, with relative energies of ca. 30 and 45 kJ mol−1, respectively, were predicted to exist by the calculations, corresponding to structures where the ester group is in an approximately s-trans arrangement. Annealing of the compound isolated in xenon at 60 K led to aggregation and simultaneous reduction of the population of I compared to that of the more polar conformer II. These results suggest the inversion of the order of stability of the two conformers in that matrix, eventually accompanied by a higher trend of conformer I to aggregate. Full assignment of the observed infrared bands to the two experimentally accessible conformers was carried out for the matrix isolated monomeric species. In addition, the infrared spectra of the neat compound in the low-temperature (10 K) amorphous and crystalline phases, as well as the infrared and Raman spectra of the crystal at room temperature were also obtained and assigned.American Chemical Society2010-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/18076http://hdl.handle.net/10316/18076https://doi.org/10.1021/jp103665bengLopes, SusyNunes, Cláudio M.Gómez-Zavaglia, AndreaMelo, Teresa M. V. D. Pinho eFausto, Ruiinfo: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:RCAAP2021-09-03T10:28:42Zoai:estudogeral.uc.pt:10316/18076Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:46.925630Repositório 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 |
Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate |
title |
Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate |
spellingShingle |
Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate Lopes, Susy Lopes, Susy |
title_short |
Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate |
title_full |
Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate |
title_fullStr |
Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate |
title_full_unstemmed |
Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate |
title_sort |
Conformational Space and Vibrational Spectra of Methyl 4-Chloro-5-phenyl-1,3-oxazole-2-carboxylate |
author |
Lopes, Susy |
author_facet |
Lopes, Susy Lopes, Susy Nunes, Cláudio M. Gómez-Zavaglia, Andrea Melo, Teresa M. V. D. Pinho e Fausto, Rui Nunes, Cláudio M. Gómez-Zavaglia, Andrea Melo, Teresa M. V. D. Pinho e Fausto, Rui |
author_role |
author |
author2 |
Nunes, Cláudio M. Gómez-Zavaglia, Andrea Melo, Teresa M. V. D. Pinho e Fausto, Rui |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Lopes, Susy Nunes, Cláudio M. Gómez-Zavaglia, Andrea Melo, Teresa M. V. D. Pinho e Fausto, Rui |
description |
Methyl 4-chloro-5-phenyl-1,3-oxazole-2-carboxylate (MCPOC) has been synthesized and isolated in cryogenic matrices (argon and xenon). FTIR spectroscopy studies on the matrix isolated compound, supported by DFT(B3LYP)/6-311++G(d,p) calculations, allow for the identification of two low-energy conformers (I and II) of the molecule, which differ from each other in the orientation of the ester group relative to the oxazole ring. In both these conformers, the ester moiety is in the s-cis configuration (O═C—O—CH3 dihedral: 0°). Conformer II is ca. 3.0 kJ mol−1 higher in energy than form I in the gas phase. Two additional higher energy conformers, III and IV, with relative energies of ca. 30 and 45 kJ mol−1, respectively, were predicted to exist by the calculations, corresponding to structures where the ester group is in an approximately s-trans arrangement. Annealing of the compound isolated in xenon at 60 K led to aggregation and simultaneous reduction of the population of I compared to that of the more polar conformer II. These results suggest the inversion of the order of stability of the two conformers in that matrix, eventually accompanied by a higher trend of conformer I to aggregate. Full assignment of the observed infrared bands to the two experimentally accessible conformers was carried out for the matrix isolated monomeric species. In addition, the infrared spectra of the neat compound in the low-temperature (10 K) amorphous and crystalline phases, as well as the infrared and Raman spectra of the crystal at room temperature were also obtained and assigned. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-08 |
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/10316/18076 http://hdl.handle.net/10316/18076 https://doi.org/10.1021/jp103665b |
url |
http://hdl.handle.net/10316/18076 https://doi.org/10.1021/jp103665b |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
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 |
repository.mail.fl_str_mv |
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_version_ |
1822183294002790400 |
dc.identifier.doi.none.fl_str_mv |
10.1021/jp103665b |