Search results for " Catalysis"

showing 10 items of 585 documents

Cluster Preface: Heterogeneous Catalysis

2016

International audience; Jean-Cyrille Hierso is full professor of Chemistry since 2009, heading the group of ‘Organometallic Chemistry and Catalysis’ at the Institute of Molecular Chemistry at the University of Bourgogne Franche-Comté (UBFC). He has interest in the fields of organometallic chemistry, ligand design, homo- and heterogeneous catalysis, chemical physics, and material sciences. In 2011 he was awarded the National Prize for Coordination Chemistry from the French Chemical Society (SCF), and at the end of 2012 he was elected a junior Member of the French Professors Academy ‘Institut Universitaire de France’ (IUF).Yasuhiro Uozumi is a full professor at the Institute for Molecular Sci…

Green chemistryMolecular chemistry010405 organic chemistryOrganic ChemistryLibrary scienceNanotechnology010402 general chemistryHeterogeneous catalysis01 natural sciencesMolecular science[ CHIM ] Chemical Sciences0104 chemical sciencesChemical societychemistry.chemical_compoundsustainable chemistry - nanocatalysts - organocatalysts - gold - palladium - nanoparticles - peptides - polymer supports - inorganic supports - nanotubes - epoxidation - esterification - cross-coupling - C–H functionalization - oxidation - (hetero)arenes - Kinetics - supramolecular assembly - recovery - recyclingchemistryTeam leader[CHIM]Chemical SciencesOrganometallic chemistry
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Carbon dioxide conversion to dimethyl carbonate: The effect of silica as support for SnO2 and ZrO2 catalysts

2011

International audience; Abundant in nature, CO2 poses few health hazards and consequently is a promising alternative to phosgene feedstock according with the principles of Green Chemistry and Engineering. The synthesis organic carbonates from CO2 instead of phosgene is highly challenging as CO2 is much less reactive. As part of our ongoing research on the investigation of catalysts for dimethyl carbonate (DMC) synthesis from methanol and CO2, we herein report results aimed at comparing the catalytic behavior of new SnO2-based catalysts with that of ZrO2. Silica-supported SnO2 and ZrO2 exhibit turnover numbers which are an order of magnitude higher than those of the unsupported oxides. Tin-b…

Green chemistryZirconiumCarbon dioxide fixation010405 organic chemistryGeneral Chemical EngineeringSupported catalystschemistry.chemical_elementGeneral Chemistry010402 general chemistryHeterogeneous catalysis01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryTinOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistrySustainable chemistryZirconiumMethanolDimethyl carbonatePhosgeneTinComptes Rendus Chimie
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Ultra-Low Catalyst Loading as a Concept in Economical and Sustainable Modern Chemistry: The Contribution of Ferrocenylpolyphosphane Ligands

2007

The challenge of sustainability in modern chemistry will be met with new technologies and processes provided significant progress is made in several key research areas, such as the expansion of chemistry from renewable feedstock, the design of environmentally benign chemicals and solvents, the minimization of depletive resources, and the development of high-performance catalysis. In this prospect, ligand chemistry is a pivotal science that links modern-organic,-inorganic, -organometallic, and -coordination chemistry through a vast number of valuable applications, precisely associated to catalysis. We review in this article our recent work on catalysis promoted by original ferrocenyl tetra-,…

Green chemistryaminesSonogashira couplingHomogeneous catalysisvinylation catalystsultra-low010402 general chemistry01 natural sciencesCatalysisCoordination complexInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundcross-couplingferrocenylpolyphosphineOrganic chemistrycatalyzedDiphosphaneReactivity (chemistry)ComputingMilieux_MISCELLANEOUSAminationchemistry.chemical_classificationalkynylationligands010405 organic chemistryChemistryLigandSonogashira[CHIM.CATA]Chemical Sciences/CatalysisGeneral MedicinepalladiumCombinatorial chemistry0104 chemical sciencesHeckcoupling reactionChemInform
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Palladium Supported on Cross-Linked Imidazolium Network on Silica as Highly Sustainable Catalysts for the Suzuki Reaction under Flow Conditions

2013

Highly cross-linked imidazolium-based materials, obtained by radical oligomerization of bis-vinylimidazolium salts in the presence of 3-mercaptopropyl-modified silica gel, were used as supports for palladium catalysts. Thanks to the high imidazolium loading these materials were able to support a high amount of the metal (10 wt%). Such materials were characterized by several techniques (13C magic angle spinning nuclear magnetic resonance, the Brunauer-Emmett-Teller technique, X-ray photoelectron spectroscopy, and transmission electron microscopy). The palladium catalysts displayed good activity allowing the synthesis of several biphenyl compounds in high yields working with only 0.1 mol% of …

Green chemistryflow chemistryInorganic chemistrychemistry.chemical_elementCatalysisMetalchemistry.chemical_compoundSuzuki reactionMagic angle spinningsustainable chemistry; catalysis flow chemistrysustainable chemistryC C couplingSuzuki-Miyaura reactioncatalyst recyclingBiphenylcatalysisSilica gelSettore CHIM/06 - Chimica OrganicaGeneral ChemistrypalladiumSuzuki–Miyaura reactionchemistryvisual_artvisual_art.visual_art_mediumC-C couplingPalladiumAdvanced Synthesis & Catalysis
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An E-Factor Minimized Protocol for a Sustainable and Efficient Heck Reaction in Flow

2014

A highly sustainable and waste-minimized protocol for Heck coupling has been defined. Optimal conditions have been defined by exploiting a heterogeneous catalyst based on supported ionic liquid-like phases featuring high Pd loading (10 wt %) and by optimizing its efficiency in a recoverable green reaction medium (acetonitrile/water azeotrope). Pure products 4a–l and 6a–h have been isolated chromatography-free in high yields (74–99%) and with extremely low environmental factor (E-factor) values (2.3–5.0). With the application of flow technology, the selected heterogeneous base and Pd catalyst have been fully recovered and reused, and minimum palladium leaching allowed for isolation of the fi…

Green chemistrygreen chemistryRenewable Energy Sustainability and the EnvironmentChemistryGeneral Chemical Engineeringchemistry.chemical_elementcross-coupling. palladiumSettore CHIM/06 - Chimica OrganicaGeneral ChemistryFlow chemistryHeterogeneous catalysisCatalysischemistry.chemical_compoundChemical engineeringHeck reactioncontinuous flowEnvironmental ChemistryOrganic chemistryLeaching (metallurgy)C-C couplingAcetonitrilecross-coupling. palladium green chemistryPalladiumPalladiumACS Sustainable Chemistry & Engineering
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Recyclable heterogeneous palladium catalysts in pure water: sustainable developments in Suzuki, Heck, Sonogashira and Tsuji-Trost reactions

2010

This review summarizes the progress made essentially these last ten years on heterogeneous palladium catalysis in pure water. The work covers four important palladium-catalyzed transformations for carbon-carbon bond formation: Suzuki, Heck, Sonogashira and Tsuji-Trost reactions. The discussion focuses on the efficiency and reusability of the heterogeneous catalysts as well as on the experimental conditions from a sustainable chemistry point of view. The review is introduced by a discussion on mechanistic aspects inherent to heterogeneous catalysis.

Green chemistryheterogeneous palladium catalysts010405 organic chemistrywaterSonogashira couplingchemistry.chemical_elementGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryHeterogeneous catalysis01 natural sciences7. Clean energySuzuki reaction -Tsuji-Trost reaction0104 chemical sciencesCatalysisTsuji–Trost reaction[ CHIM.CATA ] Chemical Sciences/CatalysisHeck reactionchemistrySuzuki reactionHeck reactionOrganic chemistrySonogashira reactionComputingMilieux_MISCELLANEOUSPalladium
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Structural insight on organosilica electrodes for waste-free alcohol oxidations

2007

Organic modification of sol-gel catalytic glassy electrodes made of a thin layer of organosilica doped with nitroxyl radical TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) crucially enhances stability in the waste-free oxidation of alcohols to carbonyls in water. Structural comparison between analogous films made of organosilica and unmodified SiO2 shows that the origin of the pronounced stable activity of the ORMOSIL film lies in high hydrophobic and also in the pronounced low degree of hydrophilicity.

Green chemistryoxidationalcoholgreen chemistryInorganic chemistryAlcoholNitroxylGeneral ChemistryPhotochemistryHeterogeneous catalysisOrmosilCatalysisCatalysischemistry.chemical_compoundchemistryAlcohol oxidationsol-gelanodicTEMPOSol-gel
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Kinetic Aspects of Heterogeneous Catalytic Versus Photocatalytic Reactions

2019

Abstract Kinetics aspects of heterogeneous catalysis and photocatalysis are reported together with the most used models developed for both fields. The chapter describes the main mechanisms involved in the different processes and the parameters used to determine their performances. A comparison of the behaviors and kinetics features of heterogeneous catalysis and photocatalysis is presented.

Heterogeneous catalysiChemical engineeringChemistryturnover frequencyKineticsPhotocatalysisQuantum yieldkinetic modelquantum yieldHeterogeneous catalysisKinetic energyheterogeneous photocatalysiCatalysis
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Cross-Linked Polyamine from Imidazolium-Based Materials: A Simple Route to Useful Catalytic Materials

2018

Cross-linked polyamine-based materials were easily prepared by reduction of the corresponding cross-linked imidazolium-based materials with sodium borohydride in hot ethanol. Overall, the synthetic procedure is based on the polymerization of a suitable bis-vinylimidazolium salt with or without a suitable support, such as silica or silica-coated magnetic nanoparticles (γ-Fe2O3@SiO2), followed by reduction. This simple approach allows the synthesis of materials based on a network of secondary and tertiary amines. Materials were characterized by13C cross-polarization magic angle spinning NMR (13C CPMAS NMR), proton spin-lattice relaxation times in the rotating frame (T1ρH) and thermogravimet…

Heterogeneous catalysiHeterogeneous catalysisPolymersOrganic ChemistrySettore CHIM/06 - Chimica OrganicaIonic liquidPhysical and Theoretical ChemistryAminesPolymerAmineMaterials scienceIonic liquids
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Thiazolium-­‐based catalysts for the etherification of benzylic alcohols under solvent-­free conditions

2015

In this work, thiazolium and imidazolium hybrid materials (SBA-15-Thia and SBA-15-Imi) were prepared by grafting the bis-vinylthiazolium or imidazolium salts onto thiol functionalized SBA-15 mesostructured silica. The catalytic activity was tested for the etherification of 1-phenylethanol, in heterogeneous conditions. The reactions were performed under different gas phases and reaction times. The SBA-15-Thia displayed an excellent catalytic performance, also with others benzyl alcohols. This material was successfully used in seven consecutive runs. Further studies were carried out in homogenous conditions. The results obtained allow proving that oxygen play an active role in the reaction pr…

Heterogeneous catalysis supported catalysis etherification reactions thiazolium salts benzylic alcohols.
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