EPR and magnetic studies of a carboxylate-bridged dinuclear copper(II) compound: [cu2(flu)4(dmf)2]

We report magnetic and EPR (electron paramagnetic resonance) spectroscopy studies of [Cu2(flu)4(dmf)2] (flu = flufenamate and dmf = dimethylformamide), which has CuII ions in tetracarboxylate "paddle wheel" dinuclear units. Susceptibility measurements at 10 < T < 275 K allowed the evaluation of an antiferromagnetic intradinuclear exchange coupling J0 = -294 ± 5 cm-1 between CuII ions (Hex = "J0 S1·S2). EPR experiments at 300 K in powder and single-crystals at 9.5 and 34.4 GHz indicated g// = 2.373, g&#8869; = 2.073 and zero field splitting parameters D = (-0.334 ± 0.001) cm"1 and E ca. 0. EPR signal intensity measurements at X-band in the range 4 < T < 295 K indicated that J0 = "283 ± 5 cm"1. A higher limit |J´| < 5×10-3 cm-1 for the interdinuclear exchange coupling between neighbor units at ca.14.24 Å was estimated from the angular variation of the single crystal spectra around the magic angles. The results are discussed in terms of the structure of the dinuclear unit and the bridges connecting CuII ions and compared with values reported for similar compounds.Reportamos neste trabalho os estudos magnéticos e de RPE do composto [Cu2(flu)4(dmf)2] (flu = flufenamato e dmf = dimetilformamida), tendo os ions CuII como unidades dinucleares em forma de tetracarboxilato "paddle wheel". Medidas de susceptibilidade magnética na faixa de temperatura 10 < T < 275 K permitiram a determinação da energia de interação antiferromagnética J0 = -294 ± 5 cm-1 entre os íons CuII (Hex = "J0 S1·S2 ). Medidas de RPE (espectroscopia de ressonância paramagnética eletrônica) em temperatura ambiente com a amostra em pó e monocristal em bandas X e Q resultaram nos valores g// = 2.373, g&#8869; = 2.073 e parâmetros de campo zero D = (-0.334 ± 0.001) cm"1 e E ca. 0. Medidas com a intensidade integrada do sinal de RPE do monocristal na faixa de temperatura 40 < T < 295 K indicaram o valor de J0 = "283 ± 5 cm"1 . Um limite superior de |J´| < 5×10-3 cm-1 para o acoplamento de intercâmbio entre unidades dinucleares vizinhas a distâncias de ca. 14.24 Å foi estimado com base na variação angular do espectro ao redor do ângulo mágico. Os resultados são discutidos com base na estrutura da unidade dinuclear e das ligações que conectam os íons de CuII, comparando-os com compostos similares descritos na literatura.CNPq - PRONEX/FAPES

Electrocatalytic activity of catalase biomimetic systems

In this work, we describe the immobilization of the dinuclear compound [Cu2(apyhist)2Cl2](ClO4)2 (1) and its derived cations complexes, obtained in water solution or by deprotonation of the imidazolate moiety in the ligand leading to a cyclic tetranuclear species, in the Nafion® membrane on glass carbon electrode surface. After that, we studied the influence of the equilibrium in the electrocatalytic activity towards the reduction of H2O2 in the development of an amperometric sensor for the analytical determination of hydrogen peroxide. This strategy proved successful, and the electrochemical behaviour of the all complexes formed within the Nafion® coatings was characterized. We also provide evidence that its related cyclic tetranuclear imidazolate-bridged complex acts as a catalysts for the intramolecular, two-electron reduction of H2O2.FAPESP (08/53576-9; 09/13785-0; 08/578502-2)CNPq (474871/2010-0; 573672/2008-3)INCTBi

Modified silicas covalently bounded to 5,10,15,20-tetrakis(2-hydroxy-5-nitrophenyl)porphyrinato iron(III): synthesis, spectroscopic and EPR characterization. Catalytic studies

In this work we have studied cyclooctene epoxidation with PhIO, using a new iron porphyrin, 5,10,15,20-tetrakis(2-hydroxy-5-nitrophenyl)porphyrinato iron(III), supported on silica matrices via eletrostatic interaction and / or covalent bonds as catalyst. These catalysts were obtained and immobilized on the solid supports propyltrimethylammonium silica (SiN+); propyltrimethylammonium and propylimidazole silica [SiN+(IPG)] and chloropropylsilica (CPS) via elestrostatic interactions and covalent binding. Characterization of the supported catalysts by UV-Vis spectroscopy and EPR (Electron paramagnetic resonance) indicated the presence of a mixture of FeII and FeIII species in all of the three obtained catalysts. In the case of (Z)-cyclooctene epoxidation by PhIO the yields observed for cis-epoxycyclooctane were satisfactory for the reactions catalyzed by the three materials (ranging from 68% to 85%). Such results indicate that immobilization of metalloporphyrins onto solid supports via groups localized on the ortho positions of their mesophenyl rings can lead to efficient catalysts for epoxidation reactions. The catalyst 1-CPS is less active than 1-SiN and 1-SiN(IPG), this argues in favour of the immobilization of this metalloporphyrin onto solids via electrostatic interactions, which is easier to achieve and results in more active oxidation catalysts. Interestingly, the activity of the supported catalysts remained the same even after three successive recyclings; therefore, they are stable under the oxidizing conditions.Neste trabalho estudamos a epoxidação do cicloocteno com PhIO utilizando uma nova porfirina 5,10,15,20-tetraquis(2-hidroxi-5-nitrofenil)porfirinato de ferro(III), suportada em matrizes de sílica via interação eletrostática e / ou ligações covalentes, como catalisador. Estes catalisadores foram obtidos e imobilizados em suporte sólido (sílica propiltrimetilamônio (SiN+); sílica propiltrimetilamônio e propilimidazol [SiN+(IPG)] e cloropropilsílica (CPS)) via interações eletrostáticas e ligações covalentes. A caracterização do catalisador suportado por UV-Vis e EPR (ressonância eletrônica paramagnética) indicou a presença de uma mistura de espécies de FeII e FeIII em todos os catalisadores obtidos. No caso da epoxidação do (Z)-cicloocteno por PhIO, os rendimentos observados para o cis-epoxiciclooctano foram satisfatórios para as reações catalisadas pelos três materiais (entre 65 e 85%). Estes resultados indicam que a imobilização de metaloporfirinas em suportes sólidos via grupos localizados na posição orto de seus anéis mesofenil pode promover a catálise eficiente das reações de epoxidação. O catalisador 1-CPS é menos ativo que 1-SiN e 1-SiN(IPG), o que está em acordo com a imobilização destas metaloporfirinas em suportes sólidos via interações eletrostáticas, o que é mais fácil de ocorrer e resulta em um catalisador mais ativo. A atividade do catalisador suportado permaneceu a inalterada, mesmo após três reciclos sucessivos, mostrando que eles são estáveis sob condições oxidantes

Recycling of the high valence states of heme proteins by cysteine residues of thimet-oligopeptidase

The peptidolytic enzyme THIMET-oligopeptidase (TOP) is able to act as a reducing agent in the peroxidase cycle of myoglobin (Mb) and horseradish peroxidase (HRP). The TOP-promoted recycling of the high valence states of the peroxidases to the respective resting form was accompanied by a significant decrease in the thiol content of the peptidolytic enzyme. EPR (electron paramagnetic resonance) analysis using DBNBS spin trapping revealed that TOP also prevented the formation of tryptophanyl radical in Mb challenged by H2O2. The oxidation of TOP thiol groups by peroxidases did not promote the inactivating oligomerization observed in the oxidation promoted by the enzyme aging. These findings are discussed towards a possible occurrence of these reactions in cells.FAPESP (08/04948-0)CNPqUNIFESPUFABCCAPE

Interaction of Fe3+ meso-tetrakis (2,6-dichloro-3-sulfonatophenyl) porphyrin with cationic bilayers: magnetic switching of the porphyrin and magnetic induction at the interface

An organized multilayer was constructed by the layer-by-layer technique in which alternating layers of metalloporphyrin and dioctadecyldimethylammonium bromide bilayers were deposited onto an indium tin oxide surface electrode. The porphyrin molecules that are organized in the different layers showed a strong electroactivity with a well-defined electrochemical process. In LbL, electroactivity could be explained only by the occurrence of electron hoping. Thus, total Kohn–Sham density functional theory (KS-DFT) was performed to better understand the conditions responsible for the electroactivity of the metalloporphyrin layers intercalated by an insulating material. Total KS-DFT theory involves local density approximation energy calculations based on spin-polarized variant of KS-DFT theory. The results revealed a magnetization switching of the metalloporphyrin induced by the interaction with the surfactant bilayer accompanied by spin polarization of the porphyrin-interacting surfactant molecule. Although discrete, the surfactant magnetization had significant repercussions on the electron conductivity. Calculations also demonstrated loss of porphyrin symmetry promoted by a parent surfactant with a shorter hydrocarbon chain, ditetradecyldimethylammonium bromide. The calculation results were corroborated by experimental results obtained by the electron paramagnetic resonance and magnetic circular dichroism techniques.FAPESPCNPqCAPE

Structure and peroxidase activity of ferric Streptomyces clavuligerus orf10-encoded protein P450CLA: UV-visible, CD, MCD and EPR spectroscopic characterization

The present study reports the spectroscopic characterization by UV-visible absorption spectroscopy, magnetic circular dichroism (MCD) and electron paramagnetic resonance (EPR) of the recombinant orf10-encoded P450-camphor like protein (P450CLA)of Streptomyces clavuligerus expressed in Escherichia coli Rosetta in the native form and associated to external ligands containing the &#946;-lactam, oxazole and alkylamine-derived (alcohol) moieties of the clavulamic acid. Considering the diversity of potential applications for the enzyme, the reactivity with tert-butylhydroperoxide (tert-BuOOH) was also characterized. P450CLA presents a covalently bound heme group and exhibited the UV-visible, CD and MCD spectral features of P450CAM including the fingerprint Soret band at 450 nm generated by the ferrous CO-complex. P450CLA was converted to high valence species by tert-BuOOH and promoted homolytic scission of the O-O bond. The radical profile of the reaction was tert-butyloxyl as primary and methyl and butylperoxyl as secondary radicals. The secondary methyl and butylperoxyl radicals resulted respectively from the &#946;-scission of the alkoxyl radical and from the reaction of methyl radical with molecular oxygen

Supramolecular assembly of new heteropolymetalic molecules based on tetraiminodiphenolate macrocycle and hexacyanometallate anions: magnetostructural and spectroscopic properties

Herein we report on the synthesis, single crystal X-ray structure, spectroscopic and magnetic properties of [{Cu2(tidf)(H2O)}2(μ-CN)2Fe(CN)4]·6H2O (1), [Cu2(tidf)(H2O)2][Ni(CN)4] (2) and [Cu2(tidf)(H2O)2][Fe(CN)5NO]·H2O (3) (tidf = a Robson type macrocyclic ligand obtained on condensation of 2,6-diformyl-4-methylphenol and 1,3-diaminopropane). Complex (1) is pentanuclear; two paramagnetic dicopper(II) units are linked by a hexacyanoferrate(II) ion through two cyano-bridges. All compounds exhibit extensive, three-dimensional, supramolecular structures supported by classic hydrogen bonding between the coordinated aqua ligands, water molecules and cyano groups. Magnetism as a function of the temperature of complexes 1-3 is consistent with a strong antiferromagnetism with exchange parameters 2J estimated -783(29), -913(2), -905(1), respectively.CNPqFINEP (CT-Infra 03/2001)BBSR

Spectroscopic studies on copper(II)triphenylarsine oxide square planar complexes

Electronic and ESR spectra of the complexes [Cu(II)(tpaso)4][Cu(I)Cl2]2,[Cu(tpaso)4](NO3)2 and [Cu(tpaso)4](ClO. © 1985

A participação de alunos na correção das provas de uma disciplina de física no ensino superior

O presente artigo trata de uma experiência, com a participação de alunos da disciplina de Física III, no seu próprio processo de avaliação, no curso de Bacharelado de Física, do Instituto de Física de São Carlos/USP. Nosso objetivo é, portanto, relatar a realização desta alternativa no processo de avaliação, que foi levada a termo durante um semestre letivo, na referida disciplina e a análise dos resultados desta tentativa. Por meio da proposta de que os próprios alunos corrigissem as provas de outro aluno poderia haver a contribuição para um melhor aprendizado, além do início de uma formação pedagógica e de percepção do outro, o(a) colega, cuja prova passasse pela correção/avaliação do companheiro de sala. É, portanto, a proposta de participação ativa dos alunos, tanto durante as aulas perguntando livremente e tendo boa receptividade por parte do professor, como também na correção de provas, julgamento e atribuição de notas em classe e com a supervisão do docente

Synthesis, structure, and electronic and EPR spectra of copper(II) complexes containing the [CuBr4]2- anion and triphenylarsine oxide

The preparation and characterization of (Ph3AsOH)2[CuBr4] and [Cu(Ph3AsO)4][CuBr4] are reported (Ph3AsO = triphenylarsine oxide). Crystallographic analysis of the monoclinic crystals of (Ph3AsOH)2[CuBr4] (space group C2/c, a = 17.569 (3) Å, b = 13.090 (2) Å, c = 16.933 (2) Å, and β = 105.64 (2)°, R = 0.055 and Rw = 0.057) revealed the presence of compressed [CuBr4]2- tetrahedra of C2 symmetry with Cu-Br distances of 2.340 (1) and 2.437 (1) Å and trans-Br-Cu-Br angles of 139.2 (1) and 122.4 (1)°. The oxonium cations hydrogen bond to the bromine atoms involved in the longer Cu-Br bonds and the smaller trans-Br-Cu-Br angle. Single-crystal electronic and EPR spectra are interpreted in terms of the observed [CuBr4]2- geometry. Analysis of the electronic and EPR spectra of [Cu(Ph3AsO)4][CuBr4] led to the postulation of the presence of planar [Cu(Ph3AsO)4]2+ cations and distorted tetrahedral [CuBr4]2- anions. © 1992 American Chemical Society