β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x

Detalhes bibliográficos
Ano de defesa: 2008
Autor(a) principal: Campos, Patrick Teixeira lattes
Orientador(a): Martins, Marcos Antonio Pinto lattes
Banca de defesa: Bonfada, Élida lattes, Siqueira, Geonir Machado lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Química
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/10435
Resumo: The molecular study by X-ray diffraction of β-aminovinyl ketones [R3C(O)CH=C(R1)N(R4R5), onde R3 = CF3, CCl3, CHCl2; R1 = H, Me; R4 = H; R5 = benzyl, Ph, 5-methylisoxazol-3-yl; R4, R5 = -(CH2)4-, -(CH2)2O(CH2)2-], methyl 5- hydroxy-5-trihalomethyl-4,5-dihydro-1H-pyrazole-1-carboxylate [3-(R1), 4-(R2), and 5- (R3) substituted, where R1 = H, Me; R2 = H, Me; R3 = CCl3, CF3], 1-cyanoacetyl-5- trifluorometyl-5-hydroxy-4,5-dihydro-1H-pyrazole [3-(R1) and 4-(R2) substituted, where R1 = H, Ph; R1, R2 = -(CH2)4-, R2 = H] and 5-triclorometyl-5-hydroxy-4,5- dihydroisoxazole [3-(R1) substituted, where R1 = Ph, 4Br-Ph, tien-2-yl] were reported. The β-aminovinyl ketones have showed the fragment O=C-C=C-N essentially plane, as well as, the heterocyclic rings 4,5-dihydropyrazole and 4,5-dihydroisoxazole. The shorter bond lengths of b-aminovinyl ketones indicated an eletronic resonance effect in the conjugated system O=C-C=C-N. This effect also was encountered in the double bond N2=C3 of the rings 4,5-dihydropyrazole and 4,5-dihydroisoxazole and the substituent of the 3-position of this rings, when this substituent was an aromatic ring. In general, the molecules studied have its crytalline packing governed by intraand intermolecular hydrogen bond.
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spelling 2017-05-222017-05-222008-08-08CAMPOS, Patrick Teixeira. β-Enaminones, 5-hydroxy-4,5-dihydropyrazole and 5-hydroxy-4,5-dihydroisoxazole halomethyl Substituted: molecular study by x-ray Diffractometry. 2008. 187 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2008.http://repositorio.ufsm.br/handle/1/10435The molecular study by X-ray diffraction of β-aminovinyl ketones [R3C(O)CH=C(R1)N(R4R5), onde R3 = CF3, CCl3, CHCl2; R1 = H, Me; R4 = H; R5 = benzyl, Ph, 5-methylisoxazol-3-yl; R4, R5 = -(CH2)4-, -(CH2)2O(CH2)2-], methyl 5- hydroxy-5-trihalomethyl-4,5-dihydro-1H-pyrazole-1-carboxylate [3-(R1), 4-(R2), and 5- (R3) substituted, where R1 = H, Me; R2 = H, Me; R3 = CCl3, CF3], 1-cyanoacetyl-5- trifluorometyl-5-hydroxy-4,5-dihydro-1H-pyrazole [3-(R1) and 4-(R2) substituted, where R1 = H, Ph; R1, R2 = -(CH2)4-, R2 = H] and 5-triclorometyl-5-hydroxy-4,5- dihydroisoxazole [3-(R1) substituted, where R1 = Ph, 4Br-Ph, tien-2-yl] were reported. The β-aminovinyl ketones have showed the fragment O=C-C=C-N essentially plane, as well as, the heterocyclic rings 4,5-dihydropyrazole and 4,5-dihydroisoxazole. The shorter bond lengths of b-aminovinyl ketones indicated an eletronic resonance effect in the conjugated system O=C-C=C-N. This effect also was encountered in the double bond N2=C3 of the rings 4,5-dihydropyrazole and 4,5-dihydroisoxazole and the substituent of the 3-position of this rings, when this substituent was an aromatic ring. In general, the molecules studied have its crytalline packing governed by intraand intermolecular hydrogen bond.Neste trabalho foi descrito o estudo molecular por difração de raios-X de β- aminovinil cetonas [R3C(O)CH=C(R1)N(R4R5), onde R3 = CF3, CCl3, CHCl2; R1 = H, Me; R4 = H; R5 = benzila, Ph, 5-metilisoxazol-3-ila; R4, R5 = -(CH2)4-, -(CH2)2O(CH2)2- ], 1-metilcarboxilato-5-trialometil-5-hidróxi-4,5-diidropirazóis [3-(R1), 4-(R2) e 5-(R3) substituídos, onde R1 = H, Me; R2 = H, Me; R3 = CCl3, CF3], 1-cianoacetil-5- trifluormetil-5-hidróxi-4,5-diidropirazóis [3-(R1) e 4-(R2) substituídos, onde R1 = H, Ph; R1, R2 = -(CH2)4-, R2 = H] e 5-triclorometil-5-hidróxi-4,5-diidroisoxazóis [3-(R1) substituído, onde R1 = Ph, 4-BrPh, tien-2-ila]. As b-aminovinil cetonas apresentaram o fragmento O=C-C=C-N e os anéis heterocíclicos, 4,5-diidropirazol e 4,5- diidroisoxazol, essencialmente planos. Os dados relacionados aos comprimentos de ligações do sistema conjugado O=C-C=C-N indicaram um efeito de ressonância eletrônica nas β-aminovinil cetonas. Esse efeito foi encontrado também na ligação dupla N2=C3 dos anéis 4,5-diidropirazóis e 4,5-diidroisoxazóis e o substituinte da posição-3 dos mesmos, quando este fosse um anel aromático. De maneira geral, as moléculas estudadas têm seu empacotamento cristalino governado por ligações de hidrogênio intra- e intermoleculares.Coordenação de Aperfeiçoamento de Pessoal de Nível Superiorapplication/pdfporUniversidade Federal de Santa MariaPrograma de Pós-Graduação em QuímicaUFSMBRQuímicaEstrutura cristalinaEnaminonasPirazóisIsoxazóisRaios-XCrystal structureEnaminonesPyrazolesIsoxazolesX-rayCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICAβ-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-xβ-Enaminones, 5-hydroxy-4,5-dihydropyrazole and 5-hydroxy-4,5-dihydroisoxazole halomethyl Substituted: molecular study by x-ray Diffractometryinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisMartins, Marcos Antonio Pintohttp://lattes.cnpq.br/6457412713967642Bonfada, Élidahttp://lattes.cnpq.br/3766944383521830Siqueira, Geonir Machadohttp://lattes.cnpq.br/3245577879591660http://lattes.cnpq.br/9549998755426589Campos, Patrick Teixeira100600000000400500500300500c28419d9-6027-4f9c-acd2-76e8067a85d1c2c55a9e-8ad6-49d1-943c-06500fac843d121bd459-256a-44f6-9b15-f9498178583939dc23ab-ef8b-429d-9c37-d1efcde74a4cinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALPATRICKTEIXEIRACAMPOS.pdfapplication/pdf23891996http://repositorio.ufsm.br/bitstream/1/10435/1/PATRICKTEIXEIRACAMPOS.pdf03a13174eea5b9fc07bb613d56c31ca4MD51TEXTPATRICKTEIXEIRACAMPOS.pdf.txtPATRICKTEIXEIRACAMPOS.pdf.txtExtracted texttext/plain257995http://repositorio.ufsm.br/bitstream/1/10435/2/PATRICKTEIXEIRACAMPOS.pdf.txta8f705869033652cf9d0488849a076dfMD52THUMBNAILPATRICKTEIXEIRACAMPOS.pdf.jpgPATRICKTEIXEIRACAMPOS.pdf.jpgIM Thumbnailimage/jpeg5864http://repositorio.ufsm.br/bitstream/1/10435/3/PATRICKTEIXEIRACAMPOS.pdf.jpgfee25e8807e03271d8cadf9569ba436bMD531/104352023-04-20 10:09:40.019oai:repositorio.ufsm.br:1/10435Repositório Institucionalhttp://repositorio.ufsm.br/PUBhttp://repositorio.ufsm.br/oai/requestopendoar:39132023-04-20T13:09:40Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.por.fl_str_mv β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x
dc.title.alternative.eng.fl_str_mv β-Enaminones, 5-hydroxy-4,5-dihydropyrazole and 5-hydroxy-4,5-dihydroisoxazole halomethyl Substituted: molecular study by x-ray Diffractometry
title β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x
spellingShingle β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x
Campos, Patrick Teixeira
Estrutura cristalina
Enaminonas
Pirazóis
Isoxazóis
Raios-X
Crystal structure
Enaminones
Pyrazoles
Isoxazoles
X-ray
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x
title_full β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x
title_fullStr β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x
title_full_unstemmed β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x
title_sort β-Enaminonas, 5-hidróxi-4,5-diidropirazóis e 5-Hidróxi-4,5-diidroisoxazóis halometilsubstituídos: estudo molecular por difração de raios-x
author Campos, Patrick Teixeira
author_facet Campos, Patrick Teixeira
author_role author
dc.contributor.advisor1.fl_str_mv Martins, Marcos Antonio Pinto
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/6457412713967642
dc.contributor.referee1.fl_str_mv Bonfada, Élida
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/3766944383521830
dc.contributor.referee2.fl_str_mv Siqueira, Geonir Machado
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/3245577879591660
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/9549998755426589
dc.contributor.author.fl_str_mv Campos, Patrick Teixeira
contributor_str_mv Martins, Marcos Antonio Pinto
Bonfada, Élida
Siqueira, Geonir Machado
dc.subject.por.fl_str_mv Estrutura cristalina
Enaminonas
Pirazóis
Isoxazóis
Raios-X
topic Estrutura cristalina
Enaminonas
Pirazóis
Isoxazóis
Raios-X
Crystal structure
Enaminones
Pyrazoles
Isoxazoles
X-ray
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Crystal structure
Enaminones
Pyrazoles
Isoxazoles
X-ray
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description The molecular study by X-ray diffraction of β-aminovinyl ketones [R3C(O)CH=C(R1)N(R4R5), onde R3 = CF3, CCl3, CHCl2; R1 = H, Me; R4 = H; R5 = benzyl, Ph, 5-methylisoxazol-3-yl; R4, R5 = -(CH2)4-, -(CH2)2O(CH2)2-], methyl 5- hydroxy-5-trihalomethyl-4,5-dihydro-1H-pyrazole-1-carboxylate [3-(R1), 4-(R2), and 5- (R3) substituted, where R1 = H, Me; R2 = H, Me; R3 = CCl3, CF3], 1-cyanoacetyl-5- trifluorometyl-5-hydroxy-4,5-dihydro-1H-pyrazole [3-(R1) and 4-(R2) substituted, where R1 = H, Ph; R1, R2 = -(CH2)4-, R2 = H] and 5-triclorometyl-5-hydroxy-4,5- dihydroisoxazole [3-(R1) substituted, where R1 = Ph, 4Br-Ph, tien-2-yl] were reported. The β-aminovinyl ketones have showed the fragment O=C-C=C-N essentially plane, as well as, the heterocyclic rings 4,5-dihydropyrazole and 4,5-dihydroisoxazole. The shorter bond lengths of b-aminovinyl ketones indicated an eletronic resonance effect in the conjugated system O=C-C=C-N. This effect also was encountered in the double bond N2=C3 of the rings 4,5-dihydropyrazole and 4,5-dihydroisoxazole and the substituent of the 3-position of this rings, when this substituent was an aromatic ring. In general, the molecules studied have its crytalline packing governed by intraand intermolecular hydrogen bond.
publishDate 2008
dc.date.issued.fl_str_mv 2008-08-08
dc.date.accessioned.fl_str_mv 2017-05-22
dc.date.available.fl_str_mv 2017-05-22
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dc.identifier.citation.fl_str_mv CAMPOS, Patrick Teixeira. β-Enaminones, 5-hydroxy-4,5-dihydropyrazole and 5-hydroxy-4,5-dihydroisoxazole halomethyl Substituted: molecular study by x-ray Diffractometry. 2008. 187 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2008.
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/10435
identifier_str_mv CAMPOS, Patrick Teixeira. β-Enaminones, 5-hydroxy-4,5-dihydropyrazole and 5-hydroxy-4,5-dihydroisoxazole halomethyl Substituted: molecular study by x-ray Diffractometry. 2008. 187 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2008.
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dc.publisher.department.fl_str_mv Química
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