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- Vanadium complexes: recent progress in oxidation catalysisPublication . Sutradhar, Manas; Martins, Luisa; Guedes Da Silva, M. Fátima C.; Pombeiro, ArmandoOxidovanadium complexes and, to a less extent, some non-oxido ones, are widely used as catalysts or catalyst precursors for various oxidative catalytic reactions by H2O2, (BuOOH)-Bu-t or O-2 under mild conditions. Oxidation reactions (oxidation of alkanes and alcohols, epoxidation of alkenes and allylic alcohols, oxidative bromination, sulfoxidation and oxidative Strecker reactions) of organic compounds are the most relevant ones and are reviewed considering the recent advances in the last five years (2010-2014). The main types of both homogeneous and supported vanadium catalysts and the most efficient catalytic systems in the different reactions are presented and compared. The proposed mechanisms of various catalytic oxidation processes are also outlined. (C) 2015 Elsevier B.V. All rights reserved.
- Diethydithiocarbamate complexes with metals used as food suplements show diferente effects in cancer cellsPublication . Sedlacek, Jindrich; Martins, Luisa; Danek, Petr; Pombeiro, Armando; Cvek, BorisDiethyldithiocarbamate (ditiocarb), a metabolite of the old anti-alcoholic drug disulfiram (Antabuse), forms proteasome-inhibiting metal complexes with copper or zinc that suppress cancer cells both in vitro and in vivo. The drug has been used in a clinical trial (NCT00742911) along with copper gluconate as a dietary supplement in patients with cancer spreading to the liver. In this study, we demonstrate the effect of synthetic complexes of disulfiram with four various metals (Mn, Fe, Cr and Cu) used as food supplements. These complexes may be spontaneously formed in the blood during the use of disulfiram with divalent metals and thus may suppress the growth of cancer in vivo. The cytotoxic effect of the compounds and the compounds' ability to inhibit the cellular proteasome were tested in the osteosarcoma cell line U2OS. After 48 h, copper and manganese complexes exhibited cytotoxic effect on the cell line, in sharp contrast to both iron and chromium complexes. (C) 2014 Faculty of Health and Social Studies, University of South Bohemia in Ceske Budejovice. Published by Elsevier Urban & Partner Sp. z o.o. All rights reserved.
- Trends in properties of para-substituted 3-(phenylhydrazo)pentane-2,4-dionesPublication . Kopylovich, Maximilian; Mahmudov, Kamran; Guedes Da Silva, M. Fátima C.; Martins, Luisa; Kuznetsov, Maxim L.; Silva, Telma F. S.; Fraústo Da Silva, João; Pombeiro, ArmandoTrends between the Hammett's sigma(p) and related normal sigma(n)(p), inductive sigma(I), resonance sigma(R), negative sigma(-)(p) and positive sigma(+)(p) polar conjugation and Taft's sigma(o)(p) substituent constants and the N-H center dot center dot center dot O distance, delta(N-H) NMR chemical shift, oxidation potential (E-p/2(ox), measured in this study by cyclic voltammetry (CV)) and thermodynamic parameters (pK, Delta G(0), Delta H-0 and Delta S-0) of the dissociation process of unsubstituted 3-(phenylhydrazo)pentane-2,4-dione (HL1) and its para-substituted chloro (HL2), carboxy (HL3), fluoro (HL4) and nitro (HL5) derivatives were recognized. The best fits were found for sigma(p) and/or sigma(-)(p) in the cases of d(N center dot center dot center dot O), delta(N-H) and E-p/2(ox), showing the importance of resonance and conjugation effects in such properties, whereas for the above thermodynamic properties the inductive effects (sigma(I)) are dominant. HL2 exists in the hydrazo form in DMSO solution and in the solid state and contains an intramolecular H-bond with the N center dot center dot center dot O distance of 2.588(3)angstrom. It was also established that the dissociation process of HL1-5 is non-spontaneous, endothermic and entropically unfavourable, and that the increase in the inductive effect (sigma(I)) of para-substitutents (-H < -Cl < -COOH < -F < -NO2) leads to the corresponding growth of the N center dot center dot center dot O distance and decrease of the pK and of the changes of Gibbs free energy, of enthalpy and of entropy for the HL1-5 acid dissociation process. The electrochemical behaviour of HL1-5 was interpreted using theoretical calculations at the DFT/HF hybrid level, namely in terms of HOMO and LUMO compositions, and of reactivities induced by anodic and cathodic electron-transfers. Copyright (C) 2010 John Wiley & Sons, Ltd.
- Heterogenisation of a c-scorpionate feII complex on carbon materials for cyclohexane oxidation with hydrogen peroxidePublication . Martins, Luisa; Almeida, M. Peixoto de; Carabineiro, S. A. C.; Figueiredo, J. L.; Pombeiro, ArmandoThe hydrotris(pyrazol-1-yl)methane iron(II) complex [FeCl2{h3-HC(pz)3}] (pz=pyrazol-1-yl) (1) was immobilized on three diferente carbon materials (activated carbon, carbon xerogel and multi-walled carbon nanotubes) with three different surface treatments (original, treated with nitric acid, and treated with nitric acid followed by sodium hydroxide) to produce active, selective and recyclable catalysts. The heterogenisation process was more efficient for carbon nanotubes treated with nitric acid and sodium hydroxide. An outstanding improved catalytic performance of complex 1 upon heterogenisation on carbon nanotubes treated with nitric acid and sodium hydroxide (turnover numbers up to 5.6_103 and overall yield of 21 %), relative to the homogeneous system, was achieved for the single-pot peroxidative oxidation of cyclohexane to the cyclohexanone and cyclohexanol mixture. The heterogenised systems allowed their easy recovery and reuse, at least for five consecutive cycles, maintaining 96% of the initial activity and concomitante rather high selectivity to cyclohexanol and cyclohexanone.
- Copper(II) and iron(III) complexes with arylhydrazone of ethyl 2-cyanoacetate or formazan ligands as catalysts for oxidation of alcoholsPublication . Martins, Nuno; Mahmudov, Kamran T.; Guedes Da Silva, M. Fátima C.; Martins, Luisa; Pombeiro, ArmandoThe aquasoluble [Cu(1 kappa N,O-2:2 kappa O-HL1)(S)](2) [S = CH3OH (1), (CH3)(2)NCHO (2)] and [Cu(kappa N-HL1)(en)(2)]center dot CH3OH center dot H2O (3) Cu-II complexes were prepared by the reaction of Cu-II nitrate hydrate with the new ligand (E/Z)-4-(2-(1-cyano-2-ethoxy-2-oxoethylidene)hydrazinyl)-3-hydroxybenzoic acid (H3L1), in the presence (for 3) or absence (for 1 and 2) of ethylenediamine (en), while the Fe-III complex [Fe(kappa N-3-HL2)(2)] (4) was isolated by treatment of iron(III) chloride hexahydrate with the new ligand (1E,1E)-N',2-di(1H-1,2,4-triazol-3-yl)diazenecarbohydrazonoyl cyanide (H3L2), and characterized by elemental analysis, IR spectroscopy and single crystal X-ray diffraction. Cooperative E,Z -> E isomerization of H3L1, induced by coordination and ionic interactions, occurs upon interaction with Cu-II in the presence of en. Complexes 1-4 act as catalyst precursors for the solvent-free microwave (MW) assisted selective oxidation of primary or secondary alcohols and diols to the corresponding aldehydes, ketones and diketones, respectively, with yields in the 5-99% range (TONs up to 4.96 x 10(2)) after 60 min of MW irradiation at 120 degrees C. The influence of temperature, time and organic radicals was studied and also the regioselective oxidation of the catalytic systems involving the primary and secondary alcohols.
- Gold nanoparticles deposited on surface modified carbon xerogels as reusable catalysts for cyclohexane C-H activation in the presence of CO and waterPublication . Ribeiro, Ana Paula da Costa; Martins, Luisa; Carabineiro, Sonia Alexandra Correia; Figueiredo, José; Pombeiro, ArmandoThe use of gold as a promotor of alkane hydrocarboxylation is reported for the first time. Cyclohexane hydrocarboxylation to cyclohexanecarboxylic acid (up to 55% yield) with CO, water, and peroxodisulfate in a water/acetonitrile medium at circa 50 °C has been achieved in the presence of gold nanoparticles deposited by a colloidal method on a carbon xerogel in its original form (CX), after oxidation with HNO3 (-ox), or after oxidation with HNO3 and subsequent treatment with NaOH (-ox-Na). Au/CX-ox-Na behaves as re-usable catalyst maintaining its initial activity and selectivity for at least seven consecutive cycles. Green metric values of atom economy or carbon efficiency also attest to the improvement brought by this novel catalytic system to the hydrocarboxylation of cyclohexane. View Full-Text
- Pyrazole or tris(pyrazolyl)ethanol oxo-vanadium(IV) complexes as homogeneous or supported catalysts for oxidation of cyclohexane under mild conditionsPublication . Silva, Telma F. S.; Mac Leod, Tatiana C. O.; Martins, Luisa; Guedes Da Silva, M. Fátima C.; Schiavon, Marco A.; Pombeiro, ArmandoThe oxovanadium(IV) complexes [VO(acac)(2)(Hpz)].HC(pz)(3) 1.HC(pz)(3) (acac= acetylacetonate, Hpz = pyrazole, pz = pyrazoly1) and [VOCl2{HOCH2C(pz)(3)}] 2 were obtained from reaction of [VO(acac)(2)] with hydrotris(1-pyrazolyl)methane or of VCl(3)with 2,2,2-tris(1-pyrazolyl)ethanol. The compounds were characterized by elemental analysis, IR, Far-IR and EPR spectroscopies, FAB or ESI mass-spectrometry and, for 1, by single crystal X-ray diffraction analysis. 1 and 2 exhibit catalytic activity for the oxidation of cyclohexane to the cyclohexanol and cyclohexanone mixture in homogeneous system (TONS up to 1100) under mild conditions (NCMe, 24h, room temperature) using benzoyl peroxide (BPO), tert-butyl hydroperoxide (TBHP), m-chloroperoxybenzoic acid (mCPBA), hydrogen peroxide or the urea-hydrogen peroxide adduct (UHP) as oxidants. 1 and 2 were also immobilized on a polydimethylsiloxane membrane (1-PDMS or 2-PDMS) and the systems acted as supported catalysts for the cyclohexane oxidation using the above oxidants (TONs up to 620). The best results were obtained with mCPBA or BP0 as oxidant. The effects of various parameters, such as the amount of catalyst, nitric acid, reaction time, type of oxidant and oxidant-to-catalyst molar ratio, were investigated, for both homogeneous and supported systems. (C) 2012 Elsevier B.V. All rights reserved.
- Water-soluble c-scorpionate complexes – catalytic and biological applicationsPublication . Martins, Luisa; Pombeiro, ArmandoRecent advances in the synthesis of water-soluble homoscorpionates of the tris(pyrazol-1-yl)methane type as well as of their water-soluble metal complexes are reviewed. Moreover, the application of these tris(pyrazol-1-yl)methane metal complexes as catalysts for the oxidative functionalization of inexpensive and abundant alkanes to value-added products and other industrially significant reactions is addressed. We also focus on the main biological (antiproliferative and antimicrobial) applications of such C-scorpionate-type complexes.
- C-scorpionate rhenium complexes and their application as catalysts in Baeyer-Villiger oxidation of ketonesPublication . Martins, Luisa; Pombeiro, ArmandoThis work concerns recent advances in the synthesis of tris(pyrazol-1-yl)-methane rhenium complexes and their application as catalysts for the industrially significant Baeyer-Villiger oxidative functionalization of ketones.
- Electrochemical properties of Robson type macrocyclic dicopper(II) complexesPublication . Alegria, Elisabete; Anbu, Sellamuthu; Martins, Luisa; Pombeiro, ArmandoThe redox properties of the 1,10-phenanthroline containing Robson type symmetrical macrocyclic dicopper(II) complex [Cu2L(H2O.phen)2](ClO4)2 1 (L = μ-11,23-dimethyl-3,7,15,19-tetraazatricyclo-[19.3.1.18 19,13,21] he p t a c o s a-1(24) , 2, 7, 9, 11, 13(26), 14, 19, 21(25), 22-decaene-25,26-diolate) and of its dicopper(II) precursor [Cu2L(H2O)2](ClO4)2 2 have been investigated by cyclic voltammetry and controlled potential electrolysis in different organic solvents. They exhibit two consecutive reversible one-electron reductions assigned to the CuIICuII ® CuICuII ® CuICuI cathodic processes. The results suggest that, in solution, phenanthroline does not coordinate to the metal in complex 1, but its H-bonding interaction with the water ligands can be preserved.