dc.contributorCarlos, Rose Maria
dc.contributorhttp://lattes.cnpq.br/1589143355309943
dc.contributorhttp://lattes.cnpq.br/8419273145052566
dc.creatorAguiar, Inara de
dc.date.accessioned2013-04-23
dc.date.accessioned2016-06-02T20:34:40Z
dc.date.available2013-04-23
dc.date.available2016-06-02T20:34:40Z
dc.date.created2013-04-23
dc.date.created2016-06-02T20:34:40Z
dc.date.issued2013-02-01
dc.identifierhttps://repositorio.ufscar.br/handle/ufscar/6254
dc.description.abstractIn 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.
dc.publisherUniversidade Federal de São Carlos
dc.publisherBR
dc.publisherUFSCar
dc.publisherPrograma de Pós-Graduação em Química - PPGQ
dc.rightsAcesso Aberto
dc.subjectTransferência de elétrons
dc.subjectComplexos de rutênio
dc.subjectComplexos de manganês
dc.subjectFotossíntese artificial
dc.subjectFotoquímica
dc.subjectCélulas solares
dc.titleReações de transferência de elétrons fotoinduzidas em complexos binucleares : em direção a fotossíntese artificial
dc.typeTesis


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