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  • Fe(III) complexes in cyclohexane oxidation: comparison of catalytic activities under different energy stimuli
    Publication . Roy Barman, Tannistha; Sutradhar, Manas; Alegria, Elisabete; Silva, M. Fátima C. Guedes Da; Pombeiro, Armando
    In this study, the mononuclear Fe(III) complex [Fe(HL)(NO3)(H2O)2]NO3 (1) derived from N0 -acetylpyrazine-2-carbohydrazide (H2L) was synthesized and characterized by several physicochemical methods, e.g., elemental analysis, infrared (IR) spectroscopy, electrospray ionization mass spectrometry (ESI-MS), and single crystal X-ray diffraction analysis. The catalytic performances of 1 and the previously reported complexes [Fe(HL)Cl2] (2) and [Fe(HL)Cl(µ-OMe)]2 (3) towards the peroxidative oxidation of cyclohexane under three different energy stimuli (microwave irradiation, ultrasound, and conventional heating) were compared. 1-3 displayed homogeneous catalytic activity, leading to the formation of cyclohexanol and cyclohexanone as final products, with a high selectivity for the alcohol (up to 95%). Complex 1 exhibited the highest catalytic activity, with a total product yield of 38% (cyclohexanol + cyclohexanone) under optimized microwave-assisted conditions.
  • Analysis of metallic nanoparticles embedded in thin film semiconductors for optoelectronic applications
    Publication . Fantoni, Alessandro; Fernandes, Miguel; Vygranenko, Yuri; Louro, Paula; Vieira, Manuela; Silva, R. P. O.; Teixeira, D.; Da Costa Ribeiro, Ana Paula; Prazeres, Duarte; Alegria, Elisabete
    This paper reports about a study of the local plasmonic resonance (LSPR) produced by metal nanoparticles embedded in a dielectric or semiconductor matrix. It is presented an analysis of the LSPR for different nanoparticle metals, shapes, and embedding media composition. Metals of interest for nanoparticle composition are Aluminum and Gold. Shapes of interest are nanospheres and nanotriangles. We study in this work the optical properties of metal nanoparticles diluted in water or embedded in amorphous silicon, ITO and ZnO as a function of size, aspect-ratio and metal type. Following the analysis based on the exact solution of the Mie theory and DDSCAT numerical simulations, it is presented a comparison with experimental measurements realized with arrays of metal nanospheres. Simulations are also compared with the LSPR produced by gold nanotriangles (Au NTs) that were chemically produced and characterized by microscope and optical measurements.
  • The influence of multiwalled carbon nanotubes and graphene oxide additives on the catalytic activity of 3d metal catalysts towards 1-phenylethanol oxidation
    Publication . Da Costa Ribeiro, Ana Paula; Fontolana, Emmanuele; Alegria, Elisabete; Kopylovich, Maximilian; Bertani, Roberta; Pombeiro, Armando
    3d metal (Cu, Fe, Co, V) containing composite catalysts for the solvent-free microwave-assisted trans-formation of 1-phenylethanol to acetophenone with tert-butyl hydroperoxide (TBHP) as oxidant wereprepared by ball milling. The influence of multiwalled carbon nanotubes (CNTs) and graphene oxide (GO)additives on the catalytic activity of the catalysts was studied. CNTs or GO were mixed by ball millingwith the metal salts (CoCl2), oxides (CuO, Fe2O3, V2O5) or binary systems (Fe2O3-CoCl2, CoCl2-V2O5, CuO-Fe2O3). For CoCl2-based catalytic systems, addition of small amounts (0.1–5%) of CNTs or GO leads tosignificant improvement in catalytic activity, e.g. 1% of the CNTs additive allows to rise yields from 28to 77%, under the same catalytic conditions. The CoCl2-5%CNTs composite is the most active among thestudied ones with 85% yield and TON of 43 after 1 h
  • Microwave-assisted peroxidative oxidation of toluene and 1-phenylethanol with monomeric keto and polymeric enol aroylhydrazone Cu(II) complexes
    Publication . Sutradhar, Manas; Alegria, Elisabete; Roy Barman, Tannistha; Scorcelletti, Francesco; Guedes Da Silva, M. Fátima C.; Fatima, C.; Pombeiro, Armando
    Cu(II) complexes in two different tautomeric forms (keto and enol) derived from the aroylhydrazone Schiff base 2-hydroxy(2-hydroxybenzylidene)benzohydrazide (H2L) have been synthesized and characterized by elemental analysis, IR spectroscopy, ESI-MS and single crystal X-ray crystallography. While the compound with the enol form of the ligand exists as the 1D polymer [Cu(kappa KNOO',2 kappa O',3 kappa O"-L)](n) (1), that with the keto form of the ligand occurs as the monomer [Cu(KNOO'-HL)CI(CH3OH)] (2). Both complexes act as good catalysts for the microwave-assisted peroxidative oxidation of toluene and 1-phenylethanol with tert-butyl hydroperoxide. Complex 2 exhibits the highest activity in both reactions, leading selectively to,a maximum product yield of 39 and 92%, respectively.
  • Ultrasound and radiation-induced catalytic oxidation of 1-phenylethanol to acetophenone with iron-containing particulate catalysts
    Publication . Soliman, Mohamed Mostafa Aboelhassan; Kopylovich, Maximilian N.; Alegria, Elisabete; Da Costa Ribeiro, Ana Paula; Ferraria, Ana Maria; Rego, Ana; Correia, Luís M. M.; Saraiva, Marta S.; Pombeiro, Armando
    Iron-containingparticulatecatalystsof0.1–1 µmsizewerepreparedbywetandball-milling procedures from common salts and characterized by FTIR, TGA, UV-Vis, PXRD, FEG-SEM, and XPS analyses. It was found that when the wet method was used, semi-spherical magnetic nanoparticles were formed, whereas the mechanochemical method resulted in the formation of nonmagnetic microscale needles and rectangles. Catalytic activity of the prepared materials in the oxidation of 1-phenylethanol to acetophenone was assessed under conventional heating, microwave (MW) irradiation, ultrasound (US), and oscillating magnetic field of high frequency (induction heating). In general, the catalysts obtained by wet methods exhibit lower activities, whereas the materials prepared by ball milling afford better acetophenone yields (up to 83%). A significant increase in yield (up to 4 times) was observed under the induction heating if compared to conventional heating. The study demonstrated that MW, US irradiations, and induction heating may have great potential as alternative ways to activate the catalytic system for alcohol oxidation. The possibility of the synthesized material to be magnetically recoverable has been also verified.
  • Efficient solvent-free friedel-crafts benzoylation and acylation of m-xylene catalyzed by N-acetylpyrazine-2-carbohydrazide-Fe(III)-chloro complexes
    Publication . Roy Barman, Tannistha; Sutradhar, Manas; Alegria, Elisabete; Guedes Da Silva, M. Fátima C.; Kuznetsov, Maxim L.; Pombeiro, Armando
    Reaction of N-acetylpyrazine-2-carbohydrazide (H2L) with anhydrous Fe(II) or Fe(III) chloride in CH3CN or in MeOH leads to the mononuclear [Fe(kNN’O-HL)Cl2] (1) or binuclear [Fe(kNN’O-HL) Cl(μ-OMe)]2 (2) Fe(III) complex, respectively. These complexes are characterized by elemental analysis, ESI-MS, IR spectroscopy, single-crystal X-ray crystallography, electrochemical techniques and DFT calculations. The theoretical calculations indicate that the three single-electron sequential reductions of 1 are centred at the metal, at the pyrazine group and at both, respectively. The catalytic activity of 1 and 2 was screened towards Friedel-Crafts benzoylation and acylation of m-xylene. The effects of reaction parameters, such as catalyst amount, reaction time and temperature, were studied and, under optimal conditions, 96% yield of 2,4-dimethylbenzophenone and 20% yield of 2,4-dimethylacetophenone were obtained, respectively. Complex 1 exhibited the highest activity in both reactions. The structural and electrochemical properties were supported by theoretical calculations and the importance of the Lewis acid character of the catalyst in the promotion of this catalytic reaction is discussed.
  • New copper(II) tetramer with arylhydrazone of barbituric acid and its catalytic activity in the oxidation of cyclic C5–C8 alkanes
    Publication . Sutradhar, Manas; Alegria, Elisabete; Roy Barman, Tannistha; Guedes Da Silva, M. Fátima C.; Mahmudov, Kamran T.; Guseynov, Firuddin I.; Pombeiro, Armando
    2-(2-(2,4,6-Trioxotetrahydropyrimidin-5(2H)-ylidene)hydrazinyl)terephthalic acid (H5L) was synthesized by azocoupling of diazonium salts of 2-aminoterephthalic acid with barbituric acid and characterized by IR, 1H and 13C NMR spectroscopies and ESI-MS analysis. In solution and solid state, H5L exists in the hydrazone form. The reaction of H5L with copper(II) nitrate hydrate in methanol affords the tetramer species [Cu2(μ2-1κNOO′:2κO′O″-H3L)2]2 (1) where carboxylate groups bridge two Cu(II) centers in a bridging chelate μ2-(O,O′,O′) fashion, giving rise to a cyclic Cu4O4 core. A rare and intense intermolecular non-covalent interaction of the type Ocarboxylic(lone pair)⋯π(pyrimidine), with O⋯centroid distance of 2.705 Å, was found in 1. In addition, medium intense N H⋯O and O H⋯O contacts expand the structure to a 3D network. Compound 1 behaves as efficient catalyst in the mild oxidation, by aqueous H2O2 in acidic MeCN/H2O media, of different cyclic C5–C8 alkanes to produce the corresponding alcohols and ketones. Overall product yields up to ca. 25% (based on alkane) were achieved.
  • Effect of 1,10-phenanthroline on DNA binding, DNA cleavage, cytotoxic and lactate dehydrogenase inhibition properties of Robson type macrocyclic dicopper(II) complex
    Publication . Anbu, Sellamuthu; Killivalavan, Asaithambi; Alegria, Elisabete; Mathan, Ganeshan; Kandaswamy, Muthusamy
    DNA targeting macrocyclic dicopper(II) complex, [Cu2L(H2O)2](phen)2(ClO4)2 (L = μ-11,23-dimethyl-3,7,15,19-tetraazatricyclo-[19.3.1.19,13,21] he p t a c o s a-1(24), 2, 7, 9, 11, 13(26), 14, 19, 21(25), 22-decaene-25,26-diol) (2), has been synthesized and characterized. This has been synthesized by reacting a Robson type macrocyclic precursor dicopper(II) complex [Cu2L(H2O)2](ClO4)2 (1) and 1,10-phenanthroline in ethanol. Solution ESR, electronic, and ESI-MS spectral studies suggest that 1,10-phenanthroline replaces coordinated water in 1, giving 2. The influence of the phenanthroline on DNA binding, cleavage, and anticancer properties of 2 have been investigated. Complex 2 displays better DNA binding and cleavage than 1. The dicopper(II) complexes 1 and 2 show cytotoxicity in human cervical HeLa cancer cells, giving IC50 values of 79.41 and 15.82 μM, respectively. Antiproliferative properties of 1 and 2 were confirmed by Trypan Blue exclusive assay and lactate dehydrogenase enzyme level in HeLa cancer cell lysate and content media.
  • Electrochemical properties of Robson type macrocyclic dicopper(II) complexes
    Publication . Alegria, Elisabete; Anbu, Sellamuthu; Martins, Luisa; Pombeiro, Armando
    The 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.
  • Catalytic oxidation of alcohols: recent advances
    Publication . Kopylovich, Maximilian; Ribeiro, Ana P.C.; Alegria, Elisabete; Martins, Nuno M. R.; Martins, Luisa; Pombeiro, Armando
    This review concerns metal-catalyzed reactions of oxidation of alcohols to the respective products, mainly ketones and aldehydes, mostly within the period of 2010–2014. Both conventional and unconventional systems, not only with usual reagents, but also with uncommon and prospective ones, are overviewed, with recently achieved developments.