Search results for "Homogeneous catalysi"

showing 10 items of 74 documents

A new efficient, highly dispersed, Pd nanoparticulate silica supported catalyst synthesized from an organometallic precursor. Study of the homogeneou…

2018

[EN] A new Pd(0) catalyst supported on silica UVM-7 has been synthesized from the organometallic [Pd-2(mu-(C6H4) Pp(2))(2)(CH3CN)(4)](BF4)(2) precursor, characterized by the high dispersion, activity, and small size of the palladium nanoclusters fixed on the silica surface. The catalyst was tested for the Suzuki-Miyaura (SM) reaction of different 4-substitutedphenyl halides with phenylboronic acid. The kinetic study concurs with most of the catalytic action was carried out by Pd species originated by the partial solubilization of Pd immobilized on mesoporous silica. The Schmidt's analysis of differential selectivity (SADS) in several competitive SM reactions, together the STEM-HAADF and HRT…

UVM-7 silicaHeterogeneous homogeneous catalysischemistry.chemical_element010402 general chemistryHeterogeneous catalysisHRTEM XRD01 natural sciencesCatalysisNanoclustersCatalysisSuzuki-Miyaurachemistry.chemical_compoundPhysical and Theoretical ChemistryPhenylboronic acidHigh-resolution transmission electron microscopySTEM-HAADF010405 organic chemistryQUIMICA INORGANICAMesoporous silicaPalladium nanoparticles0104 chemical sciencesKinetic studychemistryChemical engineeringSelectivityPalladiumJournal of Catalysis
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Sulfur Dioxide Oxidation Catalyzed by Photosensitized Ytterbium Diphthalocyanine

2008

Oxidation of SO2 into SO3 was found effectively catalyzed by photosensitized ytterbium diphthalocyanine, YbPc2 (Pc = phthalocyanine ligand, C32H16N8) when performed in air-saturated dimethylformamide (DMF) solution at 20 °C. The process follows according to a multi-step complex mechanism involving chemical induction as its driving force. Excitation energy of the sandwich molecular system in YbPc2 is used to promote the reaction by creating a reactive intermediate form of the ytterbium complex hosting up to eight SO2 molecules. The conversion of SO2 proved complete.

YtterbiumUV–Vis spectroscopyChemistryReactive intermediateExcited stateschemistry.chemical_elementHomogeneous catalysisGeneral ChemistryPhotochemistryHomogeneous catalysisCatalysisCatalysischemistry.chemical_compoundSulfur dioxidePhthalocyanineDimethylformamideMoleculeYtterbium diphthalocyaninePhotosensitizationOrganometallic chemistryCatalysis Letters
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Electrocarboxylation of Benzyl Halides through Redox Catalysis on the Preparative Scale

2006

The electrocarboxylation of benzyl halides to the corresponding carboxylic acids through homogeneous charge-transfer catalysis was investigated both theoretically and experimentally to determine the influence of the operative parameters on the yield of the process and on the catalyst consumption. Theoretical considerations, based on fast kinetics of redox catalysis, were confirmed by the electrocarboxylation of 1-phenyl-1-chloroethane catalyzed by 1,3-benzenedicarboxylic acid di methyl ester performed at a carbon cathode under different operative conditions. We obtained high yields of the target carboxylic acid and experienced a low catalyst consumption by operating with optimized [RX]bulk/…

chemistry.chemical_classification010405 organic chemistryChemistryCarboxylic acidOrganic ChemistryInorganic chemistryHalideHomogeneous catalysisGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysis0104 chemical sciencesCatalysisCarboxylationYield (chemistry)benzyl halides • carbon dioxide • carboxylation • electrochemistry • homogeneous catalysisComputingMilieux_MISCELLANEOUS
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Insights into the Synthesis and the Solution Behavior ofmeso-Aryloxy- and Alkoxy-Substituted Porphyrins

2015

meso-RO-appended (R = alkyl, aryl) porphyrins bearing one or two OR substituents at the tetrapyrrolic macrocycle were synthesized in good yields from 5,15-dibromo-10,20-diphenylporphyrins 2H(Br2DPP), Ni(Br2DPP) and Zn(Br2DPP) using an SNAr reaction. By varying the solvent, the base, the temperature, and the time of the reaction, the optimum conditions were established, and the selective introduction of one or two meso-RO substituents at the periphery of the macrocycle was achieved. Moreover, monofunctionalization of Ni(Br2DPP) according to an SNAr reaction was used as a key step for the synthesis of rarely explored unsymmetrical porphyrinyl alkyl ethers. 1H NMR studies of these ethers in CD…

chemistry.chemical_classification010405 organic chemistryStereochemistryArylOrganic ChemistryHomogeneous catalysis010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundchemistryNucleophilic aromatic substitutionNucleophilic substitutionAlkoxy groupMoleculePhysical and Theoretical ChemistryAlkylDerivative (chemistry)European Journal of Organic Chemistry
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Anaerobic Palladium-Catalyzed Chemoselective Oxidation of Allylic and Benzylic Alcohols with α-Bromo Sulfoxide as a Co-Oxidant.

2007

A chemoselective palladium-catalyzed anaerobic oxidation of allylic and benzylic alcohols using an α-bromo sulfoxide as a co-oxidant is described for the first time. The catalyst system is simple and has a long life because of the allowance of phosphane ligands under the non-aerobic conditions. The advantages of the described method include no overoxidation of primary alcohols to carboxylic acids because of the mild conditions applied, the tolerance of oxygen-sensitive functionalities such as a carbon-carbon double bond, an organothio group, or a diorganoamino group and the effective preparation of α,β-unsaturated aldehydes and ketones, resulting from the oxidation of primary and secondary …

chemistry.chemical_classificationAllylic rearrangementPrimary (chemistry)Double bondChemistryorganic chemicalsOrganic Chemistrychemistry.chemical_elementHomogeneous catalysisSulfoxideGeneral MedicineSulfurCatalysisCatalysischemistry.chemical_compoundAlcohol oxidationHeck reactionOrganic chemistryPalladiumChemInform
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POSS nanostructures in catalysis

2020

Polyhedral oligomeric silsesquioxanes (POSS) are organic-inorganic hybrid molecules piquing the interest of researchers thanks to their synergistic features. The great versatility of POSS nanostructures arises from the easy tunability of peripheral organic moieties combined with the high thermal and chemical stability of the inner inorganic core. In this review, we highlight the use of POSS nanostructures as molecular precursors for the synthesis of homogeneous and heterogeneous catalysts able to promote many processes including alkene epoxidation, C-C bond formation, CO2 conversion, "click reactions", hydrogenation, and ethylene polymerisation, among others. In this scenario, POSS units fo…

chemistry.chemical_classificationChemical substanceMaterials scienceNanostructureMolecular modelIonic bondingNanotechnologySettore CHIM/06 - Chimica OrganicaPolymerhomogeneous catalysiCatalysisCatalysischemistryheterogeneous catalysiorganometallic catalysisMoleculeChemical stabilityPolyhedral oligomeric silsesquioxaneCatalysis Science & Technology
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Heterogeneously catalyzed Suzuki-Miyaura conversion of broad scope

2012

The reaction tolerates a broad range of functional groups in the coupling partners and is usually performed in solution under homogeneous conditions at T ¢ 60 uC using 2–3 mol% catalytic amounts. The catalyst is often a Pd(0) complex with triarylphosphane ligands. 2 The catalytic cycle (Scheme 2) begins with the oxidative addition of an aryl halide to a Pd(0) species formed in situ to form an arylpalladium(II) halide intermediate. 3 Chloroarenes, especially nonactivated aryl chlorides, are notoriously less reactive due to the stability of the C–Cl bond (the relative reactivity of Ar–X is correlated to the respective bond dissociation energy: Ph–Cl: 96 kcal mol 21 ,P h–Br: 81 kcal mol 21 ,P …

chemistry.chemical_classificationGeneral Chemical EngineeringAryl halideArylchemistry.chemical_elementHomogeneous catalysisGeneral ChemistryOxidative additionCatalysiscross-coupling heterogeneous catalysis palladium Suzuki–Miyaurachemistry.chemical_compoundchemistryCatalytic cycleOrganic chemistryReactivity (chemistry)Palladium
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Iron-Catalyzed C(sp2)-C(sp3) Cross-Coupling of Alkyl Grignard Reagents with Polyaromatic Tosylates

2017

chemistry.chemical_classificationGreen chemistry010405 organic chemistryIron catalyzedOrganic ChemistryHomogeneous catalysis010402 general chemistry01 natural sciences0104 chemical sciencesCoupling (electronics)chemistryReagentPolymer chemistryPhysical and Theoretical ChemistryAlkylEuropean Journal of Organic Chemistry
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Structure and reactivity of a mononuclear gold(II) complex.

2017

Mononuclear gold(II) complexes are very rare labile species. Transient gold(II) species have been suggested in homogeneous catalysis and in medical applications, but their geometric and electronic structures have remained essentially unexplored: even fundamental data, such as the ionic radius of gold(II), are unknown. Now, an unprecedentedly stable neutral gold(II) complex of a porphyrin derivative has been isolated, and its structural and spectroscopic features determined. The gold atom adopts a 2+2 coordination mode in between those of gold(III) (four-coordinate square planar) and gold(I) (two-coordinate linear), owing to a second-order Jahn–Teller distortion enabled by the relativistical…

chemistry.chemical_classificationIonic radius010405 organic chemistryGeneral Chemical EngineeringHomogeneous catalysisGeneral Chemistry010402 general chemistry01 natural sciencesPorphyrin0104 chemical sciencesDivalentNitrosobenzenechemistry.chemical_compoundCrystallographyHomologous serieschemistryReactivity (chemistry)Derivative (chemistry)Nature chemistry
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Soluble Single-Molecule Nanogels of Controlled Structure as a Matrix for Efficient Artificial Enzymes

2006

chemistry.chemical_classificationMolecular StructureNanogelsHomogeneous catalysisGeneral ChemistryMatrix (biology)Combinatorial chemistryCatalysisPolyethylene GlycolsMolecular WeightEnzymeMicroscopy Electron TransmissionchemistryPolyethyleneimineOrganic chemistryMoleculeMolecular imprintingAngewandte Chemie International Edition
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