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- The influence of multiwalled carbon nanotubes and graphene oxide additives on the catalytic activity of 3d metal catalysts towards 1-phenylethanol oxidationPublication . Da Costa Ribeiro, Ana Paula; Fontolana, Emmanuele; Alegria, Elisabete; Kopylovich, Maximilian; Bertani, Roberta; Pombeiro, Armando3d 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
- Ultrasound and radiation-induced catalytic oxidation of 1-phenylethanol to acetophenone with iron-containing particulate catalystsPublication . 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, ArmandoIron-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.
- 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.
- Catalytic oxidation of alcohols: recent advancesPublication . Kopylovich, Maximilian; Ribeiro, Ana P.C.; Alegria, Elisabete; Martins, Nuno M. R.; Martins, Luisa; Pombeiro, ArmandoThis 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.
- Ball milling as an effective method to prepare magnetically recoverable heterometallic catalysts for alcohol oxidationPublication . Fontolan, Emmanuele; Alegria, Elisabete; Da Costa Ribeiro, Ana Paula; Kopylovich, Maximilian; Bertani, Roberta; Pombeiro, ArmandoHeterometallic double Fe2O3–CoCl2, CoCl2–V2O5, MoO3–V2O5, and triple CuO–Fe2O3–CoCl2 3d metal dispersed systems were easily prepared by ball milling at room temperature and characterized by scanning electron microscopy (SEM), field emission gun scanning electron microscopy (FEGSEM), energydispersive X-ray spectroscopy (EDX) and transmission electron microscopy (TEM). They catalyze the microwave-assisted solvent-free heterogeneous oxidation of 1-phenylethanol to acetophenone with tert-butyl hydroperoxide (t-BuOOH) as oxidant, used as a model reaction. In most of the heterometallic systems a significant improvement in the catalytic activity was observed in comparison to homometallic ones. For the tested catalytic systems and experimental conditions, the CuO–Fe2O3–CoCl2 and Fe2O3–CoCl2 systems exhibit the highest activity with maximum 78% yield and TON 39 after 1 h. The possibility of magnetic recovery of the catalysts was demonstrated for the Fe2O3–CoCl2 (3:1) system.
- Synergistic catalytic action of vanadia-titania composites towards the microwave-assisted benzoin oxidationPublication . Ferretti, Francesco; Da Costa Ribeiro, Ana Paula; Alegria, Elisabete; Ferraria, Ana Maria; Kopylovich, Maximilian; Guedes Da Silva, M. Fátima C.; Marchetti, Fabio; Pombeiro, ArmandoIntensification of chemical processes according to the motto "faster, simpler, greener" is among the main concerns nowadays. One of the ways of intensification is the application of synergistic catalytic effects when the overall efficiency of a composite catalyst is much higher than the sum of the component activities. Here, we report on the preparation of synergistic catalytic materials by a simple and straightforward ball milling procedure. Oxidation of benzoin was selected as a model reaction to demonstrate the viability of the concept. For the V2O5-TiO2 (95 : 5) composite material, the synergistic effect is triggered by low power microwave irradiation with more than a tenfold jump in the catalytic activity in comparison to the activities of the individual components.
- Copper(II) and cobalt(II) tetrazole-saccharinate complexes as effective catalysts for oxidation of secondary alcoholsPublication . Frija, Luís; Alegria, Elisabete; Sutradhar, Manas; Cristiano, Maria De Lurdes; Ismael, Amin; Kopylovich, Maximilian; Pombeiro, ArmandoMononuclear Cu(II) and Co(II) complexes comprising 2-methyltetrazole-saccharinate bidentate N,N-chelating ligand have been synthesized for the first time and tested as homogeneous catalysts for oxidation of secondary alcohols in a solvent-free and microwave assisted protocol using aqueous tert-butyl hydroperoxide (TBHP) as oxidant. The developed catalytic system exhibits broad functional group compatibility, allowing efficient and selective conversion of a variety of secondary alcohols, including allylic ones, into the corresponding ketones. With typical 0.2 mol% content of the catalyst and under 20–50 W microwave irradiation, most reactions are complete within 10 min, presenting TONs up to 5.5 × 102 and TOFs up to 1.1 × 104 h−1. No additives and co-oxidants have been used, while TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxyl) acts as inhibitor in most cases. A plausible reaction mechanism involving the new catalytic systems is outlined.
- Complexes of copper(II) with 3-(ortho-substituted phenylhydrazo)pentane-2,4-diones: syntheses,properties and catalytic activity for cyclohexane oxidationPublication . Kopylovich, Maximilian N.; Nunes, Andreia C. C.; Mahmudov, Kamran; Haukka, Matti; Mac Leod, Tatiana C. O.; Martins, Luisa; Kuznetsov, Maxim L.; Pombeiro, ArmandoReactions of copper(II) with 3-phenylhydrazopentane-2,4-diones X-2-C6H4-NHN = C{C(= O)CH3}(2) bearing a substituent in the ortho-position [X = OH (H2L1) 1, AsO3H2 (H3L2) 2, Cl (HL3) 3, SO3H (H2L4) 4, COOCH3 (HL5) 5, COOH (H2L6) 6, NO2 (HL7) 7 or H (HL8) 8] lead to a variety of complexes including the monomeric [CuL4(H2O)(2)]center dot H2O 10, [CuL4(H2O)(2)] 11 and [Cu(HL4)(2)(H2O)(4)] 12, the dimeric [Cu-2(H2O)(2)(mu-HL2)(2)] 9 and the polymeric [Cu(mu-L-6)](n)] 13 ones, often bearing two fused six-membered metallacycles. Complexes 10-12 can interconvert, depending on pH and temperature, whereas the Cu(II) reactions with 4 in the presence of cyanoguanidine or imidazole (im) afford the monomeric compound [Cu(H2O)(4){NCNC(NH2)(2)}(2)](HL4)(2)center dot 6H(2)O 14 and the heteroligand polymer [Cu(mu-L-4)(im)](n) 15, respectively. The compounds were characterized by single crystal X-ray diffraction (complexes), electrochemical and thermogravimetric studies, as well as elemental analysis, IR, H-1 and C-13 NMR spectroscopies (diones) and ESI-MS. The effects of the substituents in 1-8 on the HOMO-LUMO gap and the relative stability of the model compounds [Cu(OH)(L-8)(H2O)]center dot H2O, [Cu(L-1)(H2O)(2)]center dot H2O and [Cu(L-4)(H2O)(2)]center dot H2O are discussed on the basis of DFT calculations that show the stabilization follows the order: two fused 6-membered > two fused 6-membered/5-membered > one 6-membered metallacycles. Complexes 9, 10, 12 and 13 act as catalyst precursors for the peroxidative oxidation (with H2O2) of cyclohexane to cyclohexanol and cyclohexanone, in MeCN/H2O (total yields of ca. 20% with TONs up to 566), under mild conditions.
- Mechanochemical preparation of Pd(II) and Pt(II) composites with carbonaceous materials and their application in the Suzuki-Miyaura reaction at several energy inputsPublication . Soliman, Mohamed Mostafa Aboelhassan; Peixoto, Andreia F.; Da Costa Ribeiro, Ana Paula; Kopylovich, Maximilian; Alegria, Elisabete; Pombeiro, ArmandoPd(II) and Pt(II) composites with activated carbon (AC), graphene oxide, and multiwalled carbon nanotubes were prepared by ball milling and used as catalysts for the Suzuki-Miyaura reaction, under several energy inputs (mechanical grinding, conventional heating, and microwave irradiation). The catalytic composites were characterized by ICP-MS, BET, XPS analyses, TEM, and SEM. The average particle size of the prepared composites was estimated to be in the range of 6-30 nm, while the loadings of Pd and Pt did not significantly affect the surface area of the AC support due to the tendency to agglomerate as observed by the TEM analysis. The Pd/AC composites exhibit high mechanochemical catalytic activity in cross-coupling of bromobenzene and phenylboronic acid with molar yields up to 80% with TON and TOF of 222 and 444 h(-1), respectively, achieved with Pd(4.7 wt%)-AC catalyst under the liquid assisted grinding for 0.5 h at ambient conditions, using cyclohexene as an additive.
- Simple solvent-free preparation of dispersed composites and their application as catalysts in oxidation and hydrocarboxylation of cyclohexanePublication . Alegria, Elisabete; Fontolan, Emmanuele; Da Costa Ribeiro, Ana Paula; Kopylovich, Maximilian; Domingos, Catarina; Ferraria, Ana Maria; Bertani, Roberta; Botelho do Rego, Ana M.; Pombeiro, ArmandoA simple and clean mechanochemical synthesis at room temperature was employed to prepare CuO-Fe2O3-CoCl2 (100 nm scale), MoO3-V2O5, CuO-CoCl2, Fe2O3-CoCl2, CuO-V2O5, Cu(CH3COO)(2)-V2O5, Cu(CH3COO)(2)-MoO3 (1-100 mm scale) 3d metal based dispersed composites with different ratios of components using simple metal salts/oxides and multiwalled carbon nanotubes (CNT) or graphene oxide (GO) additives (CoCl2-CNT, CoCl2-GO). The thus prepared composite materials were characterized by Xray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), field emission gun scanning electron microscopy (FEGSEM), energy-dispersive X-ray spectroscopy (EDX) and transmission electron microscopy (TEM). XPS analysis revealed no metal redox change upon ball milling treatment, which however promotes metal hydroxylation. The catalytic activity of the prepared composites in the heterogeneous low power microwave-assisted oxidation of cyclohexane with aq. H2O2 at 30 degrees C was notorious with yields up to 31% and selectivity up to 94% towards cyclohexanol (upon treatment with PPh3) for the CuO-CoCl2-based material. The hydro-carboxylation of cyclohexane with CO, water and K2S2O8 to produce cyclohexanecarboxylic acid bearing one more carbon atom at 60 degrees C is achieved with yields up to 17% for the reaction performed in the presence of the CuO-CoCl2 catalyst. The clean CuO-CoCl2 (1:2) catalyst preparation and the catalytic reaction (oxidation of cyclohexane) can be achieved in one-pot at low temperature, without any added organic solvent, and by using exclusively the mechanochemical energy input, with a marked 23% yield at 30 degrees C.