Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)

Detalhes bibliográficos
Ano de defesa: 2022
Autor(a) principal: Dozza, Bianca lattes
Orientador(a): Iglesias, Bernardo Almeida lattes
Banca de defesa: Costa, Luiz Antônio Sodré, Diógenes, Izaura Cirino Nogueira
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Química
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufsm.br/handle/1/26755
Resumo: The purpose of this work was the synthesis of the free-base corrole 5,15- bis(pentafluorophenyl)-10-{[(pyridin-4-yl)vinyl]phenyl}corrole and its metallic derivatives containing bipyridine complexes of platinum(II) and palladium(II), having as starting materials 5-(pentafluorophenyl)dipyrromethane, 4-[(pyridin-4-yl)vinyl]benzaldehyde, cisdichloro(2,2'-bipyridine)platinum(II) and cis-dichloro (2,2'-bipyridine)palladium(II). The compounds were characterized by elemental analysis (CHN%) and High-Resolution Mass Spectrometry, as well as by electron spectroscopy in the ultraviolet and visible regions, fluorescence emission spectroscopy (steady state and time-resolved) and electrochemistry (cyclic voltammetry). In order to evaluate the photobiological properties of the compounds, aggregation studies in different solvents, photostability measurements, partition coefficient calculations, as well as assays for the generation of reactive oxygen species, such as singlet oxygen and superoxide radical, were also developed. Furthermore, the interaction of the compounds with DNA was investigated experimentally via spectroscopy in the UV-Vis regions and fluorescence emission, and also by viscosimetry, using competing dyes for interaction sites in the biomolecule, such as: acridine orange, ethidium bromide, methyl green and 4',6-diamidino-2-phenylindole. All compounds studied showed good photostability. The free-base corrole H3VpyCor showed a reasonable quantum yield of fluorescence and displays hydrophobic behavior. Possibly, it interacts more effectively in the minor groove of DNA, according to high values of suppression constants (Ksv and kq), and also by theoretical molecular docking calculations. The PtVpyCor derivative showed relevant results in the generation of superoxide radicals, as well as the possibility of interacting with DNA in an intercalative form and through the minor groove. Finally, the PdVpyCor derivative presented the best result in the generation of singlet oxygen, according to values of quantum yield (ΦΔ) and photo-oxidation constant (kfo), and also exhibited the possibility of intercalation with DNA, besides to interaction with the minor groove.
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spelling 2022-11-04T16:37:39Z2022-11-04T16:37:39Z2022-09-27http://repositorio.ufsm.br/handle/1/26755The purpose of this work was the synthesis of the free-base corrole 5,15- bis(pentafluorophenyl)-10-{[(pyridin-4-yl)vinyl]phenyl}corrole and its metallic derivatives containing bipyridine complexes of platinum(II) and palladium(II), having as starting materials 5-(pentafluorophenyl)dipyrromethane, 4-[(pyridin-4-yl)vinyl]benzaldehyde, cisdichloro(2,2'-bipyridine)platinum(II) and cis-dichloro (2,2'-bipyridine)palladium(II). The compounds were characterized by elemental analysis (CHN%) and High-Resolution Mass Spectrometry, as well as by electron spectroscopy in the ultraviolet and visible regions, fluorescence emission spectroscopy (steady state and time-resolved) and electrochemistry (cyclic voltammetry). In order to evaluate the photobiological properties of the compounds, aggregation studies in different solvents, photostability measurements, partition coefficient calculations, as well as assays for the generation of reactive oxygen species, such as singlet oxygen and superoxide radical, were also developed. Furthermore, the interaction of the compounds with DNA was investigated experimentally via spectroscopy in the UV-Vis regions and fluorescence emission, and also by viscosimetry, using competing dyes for interaction sites in the biomolecule, such as: acridine orange, ethidium bromide, methyl green and 4',6-diamidino-2-phenylindole. All compounds studied showed good photostability. The free-base corrole H3VpyCor showed a reasonable quantum yield of fluorescence and displays hydrophobic behavior. Possibly, it interacts more effectively in the minor groove of DNA, according to high values of suppression constants (Ksv and kq), and also by theoretical molecular docking calculations. The PtVpyCor derivative showed relevant results in the generation of superoxide radicals, as well as the possibility of interacting with DNA in an intercalative form and through the minor groove. Finally, the PdVpyCor derivative presented the best result in the generation of singlet oxygen, according to values of quantum yield (ΦΔ) and photo-oxidation constant (kfo), and also exhibited the possibility of intercalation with DNA, besides to interaction with the minor groove.Este trabalho teve como propósito a síntese do corrol base-livre 5,15-bis(pentafluorofenil)-10- {[(piridin-4-il)vinil]fenil}corrol e seus derivados metalados contendo complexos bipiridínicos de platina(II) e paládio(II), tendo como materiais de partida 5- (pentafluorofenil)dipirrometano, 4-[(piridin-4-il)vinil]benzaldeído, cis-dicloro(2,2'- bipiridina)platina(II) e cis-dicloro(2,2'-bipiridina)paládio(II). Os compostos foram caracterizados por análise elementar (CHN%) e espectrometria de massas de alta resolução, bem como por espectroscopia eletrônica nas regiões do ultravioleta e do visível, espectroscopia de emissão de fluorescência (estado estacionário e resolvida no tempo) e eletroquímica (voltametria cíclica). Para avaliar as propriedades fotobiológicas dos compostos, também foram desenvolvidos estudos de agregação em diferentes solventes, medidas de fotoestabilidade, cálculos dos coeficientes de partição, bem como ensaios de geração de espécies reativas de oxigênio, tais como oxigênio singleto e radical superóxido. Além disso, a interação dos compostos com DNA foi investigada experimentalmente via espectroscopia de absorção eletrônica nas regiões UV-Vis e de emissão de fluorescência, e também por viscosimetria, utilizando corantes competidores por sítios de interação na biomolécula, tais como:alaranjado de acridina, brometo de etídio, verde de metila e 4',6- diamidino-2-fenilindol. Todos os compostos estudados apresentaram boa fotoestabilidade. O corrol base-livre H3VpyCor apresentou um rendimento quântico de fluorescência razoável e exibiu comportamento hidrofóbico. Possivelmente, interage de forma mais eficaz no sulco menor do DNA, conforme valores elevados das constantes de supressão (Ksv e kq), e também pelos cálculos teóricos de docking molecular. O derivado PtVpyCor mostrou resultados relevantes na geração de radicais superóxido, assim como a possibilidade de interação com o DNA de forma intercalativa e pelo sulco menor. Finalmente, o derivado PdVpyCor apresentou o melhor resultado na geração de oxigênio singleto, de acordo com valores de rendimento quântico (ΦΔ) e da constante de foto-oxidação (kfo), e ainda exibiu possibilidade de intercalação com o DNA, além de interação com o sulco menor.Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPqporUniversidade Federal de Santa MariaCentro de Ciências Naturais e ExatasPrograma de Pós-Graduação em QuímicaUFSMBrasilQuímicaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessCorróisFotofísicaInteração com DNACorrolesPhotophysicsDNA interactionsCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICASíntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)Synthesis, characterization and photobiological application of 10-{[(pyridin-4-yl)vinyl]phenyl}corrole and its Pt(II) and Pd(II) complexesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisIglesias, Bernardo Almeidahttp://lattes.cnpq.br/4402375533322977Back, Davi FernandoCosta, Luiz Antônio SodréDiógenes, Izaura Cirino Nogueirahttp://lattes.cnpq.br/0216853484149395Dozza, Bianca1006000000006006006006006006003140bdfe-ad7b-478b-8ebd-065c1627c132ac2200c9-bdfe-4dc6-a1f8-58087e8a8410f0cc6403-1f8e-4818-b26c-00ade9ca8fb15c4afbb1-17bc-43e7-90d3-62828eb855821aac493f-d2f7-483f-bd84-645ad05a880freponame:Biblioteca Digital de Teses e Dissertações do UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALDIS_PPGQUÍMICA_2022_DOZZA_BIANCA.pdfDIS_PPGQUÍMICA_2022_DOZZA_BIANCA.pdfDissertação de mestradoapplication/pdf3602311http://repositorio.ufsm.br/bitstream/1/26755/1/DIS_PPGQU%c3%8dMICA_2022_DOZZA_BIANCA.pdff62c8bc9aa58d3a07a50375401df9f8fMD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; 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dc.title.por.fl_str_mv Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)
dc.title.alternative.eng.fl_str_mv Synthesis, characterization and photobiological application of 10-{[(pyridin-4-yl)vinyl]phenyl}corrole and its Pt(II) and Pd(II) complexes
title Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)
spellingShingle Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)
Dozza, Bianca
Corróis
Fotofísica
Interação com DNA
Corroles
Photophysics
DNA interactions
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)
title_full Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)
title_fullStr Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)
title_full_unstemmed Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)
title_sort Síntese, caracterização e aplicação fotobiológica de 10-{[(piridin-4-il)vinil]fenil}corrol e seus complexos de Pt(II) e Pd(II)
author Dozza, Bianca
author_facet Dozza, Bianca
author_role author
dc.contributor.advisor1.fl_str_mv Iglesias, Bernardo Almeida
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/4402375533322977
dc.contributor.advisor-co1.fl_str_mv Back, Davi Fernando
dc.contributor.referee1.fl_str_mv Costa, Luiz Antônio Sodré
dc.contributor.referee2.fl_str_mv Diógenes, Izaura Cirino Nogueira
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/0216853484149395
dc.contributor.author.fl_str_mv Dozza, Bianca
contributor_str_mv Iglesias, Bernardo Almeida
Back, Davi Fernando
Costa, Luiz Antônio Sodré
Diógenes, Izaura Cirino Nogueira
dc.subject.por.fl_str_mv Corróis
Fotofísica
Interação com DNA
topic Corróis
Fotofísica
Interação com DNA
Corroles
Photophysics
DNA interactions
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Corroles
Photophysics
DNA interactions
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description The purpose of this work was the synthesis of the free-base corrole 5,15- bis(pentafluorophenyl)-10-{[(pyridin-4-yl)vinyl]phenyl}corrole and its metallic derivatives containing bipyridine complexes of platinum(II) and palladium(II), having as starting materials 5-(pentafluorophenyl)dipyrromethane, 4-[(pyridin-4-yl)vinyl]benzaldehyde, cisdichloro(2,2'-bipyridine)platinum(II) and cis-dichloro (2,2'-bipyridine)palladium(II). The compounds were characterized by elemental analysis (CHN%) and High-Resolution Mass Spectrometry, as well as by electron spectroscopy in the ultraviolet and visible regions, fluorescence emission spectroscopy (steady state and time-resolved) and electrochemistry (cyclic voltammetry). In order to evaluate the photobiological properties of the compounds, aggregation studies in different solvents, photostability measurements, partition coefficient calculations, as well as assays for the generation of reactive oxygen species, such as singlet oxygen and superoxide radical, were also developed. Furthermore, the interaction of the compounds with DNA was investigated experimentally via spectroscopy in the UV-Vis regions and fluorescence emission, and also by viscosimetry, using competing dyes for interaction sites in the biomolecule, such as: acridine orange, ethidium bromide, methyl green and 4',6-diamidino-2-phenylindole. All compounds studied showed good photostability. The free-base corrole H3VpyCor showed a reasonable quantum yield of fluorescence and displays hydrophobic behavior. Possibly, it interacts more effectively in the minor groove of DNA, according to high values of suppression constants (Ksv and kq), and also by theoretical molecular docking calculations. The PtVpyCor derivative showed relevant results in the generation of superoxide radicals, as well as the possibility of interacting with DNA in an intercalative form and through the minor groove. Finally, the PdVpyCor derivative presented the best result in the generation of singlet oxygen, according to values of quantum yield (ΦΔ) and photo-oxidation constant (kfo), and also exhibited the possibility of intercalation with DNA, besides to interaction with the minor groove.
publishDate 2022
dc.date.accessioned.fl_str_mv 2022-11-04T16:37:39Z
dc.date.available.fl_str_mv 2022-11-04T16:37:39Z
dc.date.issued.fl_str_mv 2022-09-27
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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url http://repositorio.ufsm.br/handle/1/26755
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dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
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rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
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dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química
dc.publisher.initials.fl_str_mv UFSM
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Química
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas
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