Fe Iii Porphyrin
Mostrando 1-12 de 14 artigos, teses e dissertações.
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1. Anionic Iron(III) Porphyrin Immobilized on/into Exfoliated Macroporous Layered Double Hydroxides as Catalyst for Oxidation Reactions
A oxidação de substratos orgânicos é uma importante classe de reações explorada visando a produção de insumos industriais tais como epóxidos, álcoois e cetonas. As metaloporfirinas são compostos com reconhecida atividade catalítica que mimetizam processos de oxidação que ocorrem em seres vivos. A sua imobilização em diferentes sólidos robust
J. Braz. Chem. Soc.. Publicado em: 2014-12
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2. Biomimetic oxidation studies of monensin A catalyzed by metalloporphyrins: identification of hydroxyl derivative product by electrospray tandem mass spectrometry
Monensin A is an important commercially available natural product isolated from Streptomyces cinnamonensins that shows antibiotic and anti-parasitic activities. This molecule has a significant influence in the antibiotic market, but until now there are no studies on putative metabolite formations. Bioorganic catalysts applying metalloporphyrins and mono-oxyg
Rev. bras. farmacogn.. Publicado em: 09/08/2013
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3. Iron(III) porphyrin covalently supported onto magnetic amino-functionalized nanospheres as catalyst for hydrocarbon and herbicide oxidations
Este trabalho descreve a imobilização por ligação covalente de uma ferroporfirina, cloreto de 5,10,15,20-tetraquis(pentafluorofenil)porfirinaferro(III) (FeTFPP), sobre nanoesferas de maguemita cobertas com sílica aminofuncionalizada. O material resultante (nomeadoγ-Fe2O3/SiO2-NHFeP) foi caracterizado por espectroscopia no infravermelho por refletância
J. Braz. Chem. Soc.. Publicado em: 31/07/2012
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4. Comparative study of hydrocarbon oxygenation with ironchlorins and ironporphyrins as catalysts in homogeneous and heterogeneizated systems / Estudo comparativo da oxigenação de hidrocarbonetos com ferroclorinas e ferroporfirinas como catalisadores em meio homogêneo e heterogeneizados
In this work, the cyclohexane oxidation and the (Z)-cyclooctene epoxidation with iodosylbenzene (PhIO) e H2O2 as oxidants were studied. A comparison between fluorinated FeIIIchlorins and FeIIIporphyrins, [Fe(TFPCMG)]Cl, [Fe(TFPCMGCH3)]Cl2, [Fe(TFPP)]Cl, [Fe(TF4TMAPP)](CF3SO3)5 as catalysts was made either in solution or supported in silica matrices via eletr
Publicado em: 2008
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5. Electrochemical determination of oncocalyxone A using an iron-phthalocyanine/iron-porphyrin modified glassy carbon electrode
Descreve-se, no presente trabalho, o desenvolvimento de um sensor voltamétrico altamente sensível para a oncocalixona A, utilizando-se eletrodo de carbono vítreo modificado com uma bi-camada de ftalocianina tetrassulfonada de ferro(II) (FeTSPc) e tetra-(N-metil-4-piridil)-porfirina de ferro(III) (FeT4MPyP). O eletrodo modificado apresentou alta atividade
Journal of the Brazilian Chemical Society. Publicado em: 2008
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6. Metalloporhyrins as Biomimetical MOdels of Cytochrome P450 in the Oxidation of Pesticides / Metaloporfirinas como modelos biomiméticos do citocromo P450 na oxidação de pesticidas"
In this work we investigated the ability of metalloporphyrin model systems to mimic the action of cytochrome P450 in the oxidation of a herbicide, atrazine. To this end, we employed the second generation commercially available metalloporphyrins metal (III) 5,10,15,20-tetrakis(2,6-dichlorophenyl)porphyrin chloride [M(TDCPP)Cl] and metal (III) 5,10,15,20- tetr
Publicado em: 2006
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7. Photodynamic action of mesoporphyrins on mitochondrial functions and LNCaP cell viability / Ação fotodinamica de meso-porfirinas sobre função mitocondrial e viabilidade de celulas LNCaP
The action of irradiated cationic Fe(III)TMPyP and anionic Fe(III)TPPS4 forms of mesoporphyrins on mitochondrial functions was investigated using experimental conditions that caused minimal effects on mitochondria in the dark. Treatment of mitochondria with 1 µM Fe(III)TMPyP for 2 min decreased the respiratory control by 3% in the dark and 28% after irradia
Publicado em: 2006
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8. Síntese, caracterização e atividade catalítica de novos catalisadores metaloporfirínicos suportados / Synthesis, characterization and catalytic activity of novel anchored metalloporphyrin catalysts
In this work the second generation metalloporphyrin Me(TFPP)Cl (Me = Fe and Mn) [5,10, 15, 20 ? tetrakis(pentafluorophenyl) porphyrin iron (III) or manganese (III) chloride] was covalently anchored to aminofunctionalyzed supports, through nucleophilic substituition of the para-fluorine atoms of the pentafluorophenyl meso-aryl groups, with the objective of ob
Publicado em: 2004
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9. The pH dependence of the mechanism of reaction of hydrogen peroxide with a nonaggregating, non-mu-oxo dimer-forming iron (III) porphyrin in water.
The reaction of hydrogen peroxide with 5, 10,15,20-tetrakis(2,6-dimethyl-3-sulfonatophenyl)porphinato- iron(III) hydrate [(P)FeIII(H2O)] has been investigated in water between pH 1 and pH 12. The water-soluble (P)FeIII(H2O) neither aggregates nor forms a mu-oxo dimer. The pH dependence and rate-limiting second-order rate constants (kly) for oxygen transfer f
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10. Picosecond photochemistry of a cofacial diporphyrin containing iron(III) and zinc(II): Mimicking electron transfer between cytochrome c and the primary electron donor in reaction centers of photosynthetic bacteria
Comparison of picosecond kinetic and spectroscopic data for Zn octaethylporphine and Fe(III)Cl octaethylporphine with that for Zn—Fe(III)Cl, a cofacial diporphyrin composed of a Zn porphyrin covalently bound to an Fe(III)Cl porphyrin with two chains of five atoms each, supports the assignment of a light-driven electron transfer (k > 1011s-1) within Zn—Fe
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11. PROTON MAGNETIC RESONANCE STUDIES OF PORPHYRIN IRON (III) CYANIDES*
The nuclear magnetic resonance (NMR) spectra at 220 Mc of cyanodeuteroporphyrin IX dimethyl ester iron (III), cyanoprotoporphyrin IX diethyl ester iron (III), and cyanoprotoporphyrin IX iron (III) in a mixed solvent of 80 per cent d5-pyridine and 20 per cent D2O have been measured. The resonances are assigned and, except for the ester alkoxy groups, are show
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12. Binding of meso-tetra (4-N-methylpyridyl) porphine to DNA.
The porphyrin photosensitizer, meso-Tetra (4-N-methyl-pyridyl) porphine tetraperchlorate is shown to unwind supercoiled ColEI DNA at a somewhat lower concentration than ethidium bromide. In contrast to this, the Fe(III) chelate of T4MPyP cannot unwind supercoiled DNA. It is concluded that these results corroborate our previous findings that, despite its larg