Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial
Autor(a) principal: | |
---|---|
Data de Publicação: | 2013 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFSCAR |
Texto Completo: | https://repositorio.ufscar.br/handle/ufscar/6254 |
Resumo: | In order to simulate the photoinduced electron-transfer steps in the photosystem II (PSII), the mononuclear complexes fac-[Mn(CO)3(phen)(L)]+, L= imidazole and substituted imidazoles were synthesized to mimic the photochemical step of the natural photosynthesis (manganese cluster). Also the binuclear complexes [Ru(BL2)2Mn(CO)3(phen)]3+, BL2 = bridge ligand (4'-(4- pyridyl)-2,2':6',2''-terpyridine e 4'-(4-pyridyl)-2,6-di(2-pirazynil)pyridine) and polynuclear complexes cis,fac-[(phen)2Ru(BL)2Mn(CO)3(L)]2 6+, BL = bridge ligand (4,4'-bipyridine e pyrazine) were synthesized to mimic the donor step (Chlorophylla P680 - manganese cluster) in natural photosynthesis. The new complexes were characterized by elemental analysis, spectroscopic (EPR, UVvis, FTIR, NMR) and electrochemical (cyclic voltammetry and spectroelectrochemistry) techniques. The complex fac- [Mn(CO)3(phen)(4meim)]+ (fac-4meim) in aqueous solution and in the absence of oxidizing agents is able to split water molecules producing molecular oxygen. The photo-redox process involves 4-electron/4H+ mechanism in a similar way of the Mn cluster in the PSII. The photoinduced electron donor properties of fac- 4meim were evaluated using methylviologen (MV2+) as an electron acceptor molecule and through the experiments using oxygen evolution sensor, Clarktype microelectrodes. The absorption spectra of the tetranuclear complexes exhibit intense absorptions in the visible region and a broad emission at 590 nm, showing a biexponential luminescent decay kinectic in according to the population of the excited emissive state ILCT and MLCT. The luminescent properties of the Ru(II) mononuclear complex were intensified in the bi- and tetranuclear complexes, probably due to a high symmetry and rigidity of the system, the complex using pirazine ligand showed different behavior. The photoinduced electron transfer reactions (ET) in the bi- and polinuclear complexes in presence of the acceptor MV2+ were possible only using TEOA as electron donor. Another problem found to the bi- and polinuclear complexes was the photodissociation and solvent interaction during photolysis. The molecular oxygen production of the complexes Ru-4,4'bpy-Mn e Ru-pyterpy-Mn, in aqueous solution during photolysis was certified. The photocatalytic properties of the complexes are interesting to the search of new compounds to be used in the artificial photosynthesis. |
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Aguiar, Inara deCarlos, Rose Mariahttp://lattes.cnpq.br/1589143355309943http://lattes.cnpq.br/841927314505256645df3113-e2fe-4810-89e7-376b6a7b3ff02016-06-02T20:34:40Z2013-04-232016-06-02T20:34:40Z2013-02-01https://repositorio.ufscar.br/handle/ufscar/6254In order to simulate the photoinduced electron-transfer steps in the photosystem II (PSII), the mononuclear complexes fac-[Mn(CO)3(phen)(L)]+, L= imidazole and substituted imidazoles were synthesized to mimic the photochemical step of the natural photosynthesis (manganese cluster). Also the binuclear complexes [Ru(BL2)2Mn(CO)3(phen)]3+, BL2 = bridge ligand (4'-(4- pyridyl)-2,2':6',2''-terpyridine e 4'-(4-pyridyl)-2,6-di(2-pirazynil)pyridine) and polynuclear complexes cis,fac-[(phen)2Ru(BL)2Mn(CO)3(L)]2 6+, BL = bridge ligand (4,4'-bipyridine e pyrazine) were synthesized to mimic the donor step (Chlorophylla P680 - manganese cluster) in natural photosynthesis. The new complexes were characterized by elemental analysis, spectroscopic (EPR, UVvis, FTIR, NMR) and electrochemical (cyclic voltammetry and spectroelectrochemistry) techniques. The complex fac- [Mn(CO)3(phen)(4meim)]+ (fac-4meim) in aqueous solution and in the absence of oxidizing agents is able to split water molecules producing molecular oxygen. The photo-redox process involves 4-electron/4H+ mechanism in a similar way of the Mn cluster in the PSII. The photoinduced electron donor properties of fac- 4meim were evaluated using methylviologen (MV2+) as an electron acceptor molecule and through the experiments using oxygen evolution sensor, Clarktype microelectrodes. The absorption spectra of the tetranuclear complexes exhibit intense absorptions in the visible region and a broad emission at 590 nm, showing a biexponential luminescent decay kinectic in according to the population of the excited emissive state ILCT and MLCT. The luminescent properties of the Ru(II) mononuclear complex were intensified in the bi- and tetranuclear complexes, probably due to a high symmetry and rigidity of the system, the complex using pirazine ligand showed different behavior. The photoinduced electron transfer reactions (ET) in the bi- and polinuclear complexes in presence of the acceptor MV2+ were possible only using TEOA as electron donor. Another problem found to the bi- and polinuclear complexes was the photodissociation and solvent interaction during photolysis. The molecular oxygen production of the complexes Ru-4,4'bpy-Mn e Ru-pyterpy-Mn, in aqueous solution during photolysis was certified. The photocatalytic properties of the complexes are interesting to the search of new compounds to be used in the artificial photosynthesis.A fim de simular as reações de transferência de elétrons fotoinduzidas, que ocorrem no fotossistema II (FSII), foram sintetizados os complexos mononucleares fac-[Mn(CO)3(phen)(L)]+ onde L= imidazol e imidazóis substituídos, para mimetizar a etapa fotoquímica da fotossíntese natural (cluster de Mn(II)) e os complexos binucleares [Ru(BL2)2Mn(CO)3(phen)]3+, BL2 = ligante ponte (4'-(4-piridil)-2,2':6',2''-terpiridina e 4'-(4-pyridil)-2,6-di(2- pirazinil)piridina) e polinucleares cis,fac-[(phen)2Ru(BL)2Mn(CO)3(L)]2 6+, BL = ligante ponte (4,4'-bipiridina e pirazina) para mimetizarem a etapa doadora da fotossíntese natural (Clorofila P680 - cluster de Mn(II)). Os novos complexos sintetizados foram caracterizados por análise elementar, técnicas espectroscópicas (RPE, UV-vis, IV, RMN, luminescência) e eletroquímicas (voltametria cíclica e espectroeletroquímica). O complexo fac- [Mn(CO)3(phen)(4meim)]+ (fac-4meim) em solução aquosa e na ausência de agentes oxidantes é capaz de clivar a molécula de água produzindo oxigênio molecular. O processo fotoredox envolve 4 elétrons/4H+ de maneira similar a etapa química do FSII. As propriedades fotocatalíticas do complexo fac-4meim foram confirmadas frente ao receptor de elétrons MV2+ e nos experimentos utilizando microeletrodos seletivos de oxigênio, do tipo Clark. Os espectros de absorção dos complexos tetranucleares exibiram intensa absorção na região do visível e apresentaram uma larga emissão em 590 nm apresentando cinética de decaimento luminescente biexponencial coerente com a população dos estados excitados emissivos de ILCT e MLCT. As propriedades luminescentes dos complexos mononucleares de Ru(II) foram intensificadas nos complexos bi- e XIV tetranucleares, provavelmente devido ao aumento de simetria e rigidez do sistema, a única excessão é observada para o complexo com o ligante pirazina. As reações de transferência de elétrons fotoinduzidas (TE) dos complexos bi- e polinucleares na presença do receptor de elétrons MV2+ foram possíveis apenas na presença do doador de elétrons TEOA. Outro problema encontrado para os sistemas bi- e polinucleares foi a fotodissociação e interação com o solvente durante a fotólise. A produção de oxigênio molecular em soluções aquosas durante a fotólise foram comprovadas para os complexos Ru-4,4'bpy-Mn e Rupyterpy- Mn. As propriedades fotocatalíticas observadas para estes compostos são interessantes na busca de compostos que mimetizem a fotossíntese natural.Financiadora de Estudos e Projetosapplication/pdfporUniversidade Federal de São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarBRTransferência de elétronsComplexos de rutênioComplexos de manganêsFotossíntese artificialFotoquímicaCélulas solaresCIENCIAS EXATAS E DA TERRA::QUIMICAReações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificialPhotoinduced electron transfer reaction of binuclear complexes: towards artificial photosynthesis.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesis-1-181ea1b7e-7dcf-438f-a839-b8cab12c5740info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINAL5023.pdfapplication/pdf6583719https://repositorio.ufscar.br/bitstream/ufscar/6254/1/5023.pdf985c4f31057497a00516797169af68e3MD51TEXT5023.pdf.txt5023.pdf.txtExtracted texttext/plain0https://repositorio.ufscar.br/bitstream/ufscar/6254/4/5023.pdf.txtd41d8cd98f00b204e9800998ecf8427eMD54THUMBNAIL5023.pdf.jpg5023.pdf.jpgIM Thumbnailimage/jpeg9431https://repositorio.ufscar.br/bitstream/ufscar/6254/5/5023.pdf.jpgee185d8308d43479b76fa4ad25049887MD55ufscar/62542023-09-18 18:30:36.011oai:repositorio.ufscar.br:ufscar/6254Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-09-18T18:30:36Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false |
dc.title.por.fl_str_mv |
Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial |
dc.title.alternative.eng.fl_str_mv |
Photoinduced electron transfer reaction of binuclear complexes: towards artificial photosynthesis. |
title |
Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial |
spellingShingle |
Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial Aguiar, Inara de Transferência de elétrons Complexos de rutênio Complexos de manganês Fotossíntese artificial Fotoquímica Células solares CIENCIAS EXATAS E DA TERRA::QUIMICA |
title_short |
Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial |
title_full |
Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial |
title_fullStr |
Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial |
title_full_unstemmed |
Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial |
title_sort |
Reações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial |
author |
Aguiar, Inara de |
author_facet |
Aguiar, Inara de |
author_role |
author |
dc.contributor.authorlattes.por.fl_str_mv |
http://lattes.cnpq.br/8419273145052566 |
dc.contributor.author.fl_str_mv |
Aguiar, Inara de |
dc.contributor.advisor1.fl_str_mv |
Carlos, Rose Maria |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/1589143355309943 |
dc.contributor.authorID.fl_str_mv |
45df3113-e2fe-4810-89e7-376b6a7b3ff0 |
contributor_str_mv |
Carlos, Rose Maria |
dc.subject.por.fl_str_mv |
Transferência de elétrons Complexos de rutênio Complexos de manganês Fotossíntese artificial Fotoquímica Células solares |
topic |
Transferência de elétrons Complexos de rutênio Complexos de manganês Fotossíntese artificial Fotoquímica Células solares CIENCIAS EXATAS E DA TERRA::QUIMICA |
dc.subject.cnpq.fl_str_mv |
CIENCIAS EXATAS E DA TERRA::QUIMICA |
description |
In order to simulate the photoinduced electron-transfer steps in the photosystem II (PSII), the mononuclear complexes fac-[Mn(CO)3(phen)(L)]+, L= imidazole and substituted imidazoles were synthesized to mimic the photochemical step of the natural photosynthesis (manganese cluster). Also the binuclear complexes [Ru(BL2)2Mn(CO)3(phen)]3+, BL2 = bridge ligand (4'-(4- pyridyl)-2,2':6',2''-terpyridine e 4'-(4-pyridyl)-2,6-di(2-pirazynil)pyridine) and polynuclear complexes cis,fac-[(phen)2Ru(BL)2Mn(CO)3(L)]2 6+, BL = bridge ligand (4,4'-bipyridine e pyrazine) were synthesized to mimic the donor step (Chlorophylla P680 - manganese cluster) in natural photosynthesis. The new complexes were characterized by elemental analysis, spectroscopic (EPR, UVvis, FTIR, NMR) and electrochemical (cyclic voltammetry and spectroelectrochemistry) techniques. The complex fac- [Mn(CO)3(phen)(4meim)]+ (fac-4meim) in aqueous solution and in the absence of oxidizing agents is able to split water molecules producing molecular oxygen. The photo-redox process involves 4-electron/4H+ mechanism in a similar way of the Mn cluster in the PSII. The photoinduced electron donor properties of fac- 4meim were evaluated using methylviologen (MV2+) as an electron acceptor molecule and through the experiments using oxygen evolution sensor, Clarktype microelectrodes. The absorption spectra of the tetranuclear complexes exhibit intense absorptions in the visible region and a broad emission at 590 nm, showing a biexponential luminescent decay kinectic in according to the population of the excited emissive state ILCT and MLCT. The luminescent properties of the Ru(II) mononuclear complex were intensified in the bi- and tetranuclear complexes, probably due to a high symmetry and rigidity of the system, the complex using pirazine ligand showed different behavior. The photoinduced electron transfer reactions (ET) in the bi- and polinuclear complexes in presence of the acceptor MV2+ were possible only using TEOA as electron donor. Another problem found to the bi- and polinuclear complexes was the photodissociation and solvent interaction during photolysis. The molecular oxygen production of the complexes Ru-4,4'bpy-Mn e Ru-pyterpy-Mn, in aqueous solution during photolysis was certified. The photocatalytic properties of the complexes are interesting to the search of new compounds to be used in the artificial photosynthesis. |
publishDate |
2013 |
dc.date.available.fl_str_mv |
2013-04-23 2016-06-02T20:34:40Z |
dc.date.issued.fl_str_mv |
2013-02-01 |
dc.date.accessioned.fl_str_mv |
2016-06-02T20:34:40Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/doctoralThesis |
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doctoralThesis |
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publishedVersion |
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https://repositorio.ufscar.br/handle/ufscar/6254 |
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https://repositorio.ufscar.br/handle/ufscar/6254 |
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por |
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openAccess |
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Universidade Federal de São Carlos |
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Programa de Pós-Graduação em Química - PPGQ |
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UFSCar |
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BR |
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Universidade Federal de São Carlos |
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