about
Silica-supported isolated gallium sites as highly active, selective and stable propane dehydrogenation catalystsBridging the Gap between Industrial and Well-Defined Supported Catalysts.Metathesis Activity Encoded in the Metallacyclobutane Carbon-13 NMR Chemical Shift TensorsMolecular and Silica-Supported Molybdenum Alkyne Metathesis Catalysts: Influence of Electronics and Dynamics on Activity Revealed by Kinetics, Solid-State NMR, and Chemical Shift Analysis.Contrasting the Role of Ni/Al2O3 Interfaces in Water-Gas Shift and Dry Reforming of Methane.CO2 -to-Methanol Hydrogenation on Zirconia-Supported Copper Nanoparticles: Reaction Intermediates and the Role of the Metal-Support Interface.Three-Dimensional Structure Determination of Surface Sites.Dynamic Nuclear Polarization Efficiency Increased by Very Fast Magic Angle Spinning.The Key RuV=O Intermediate of Site-Isolated Mononuclear Water Oxidation Catalyst Detected by in Situ X-ray Absorption Spectroscopy.Low-Temperature Wet Conformal Nickel Silicide Deposition for Transistor Technology through an Organometallic Approach.Cooperativity and Dynamics Increase the Performance of NiFe Dry Reforming Catalysts.Understanding the Lewis Acidity of Co(II) Sites on a Silica Surface.Active Sites in Supported Single-Site Catalysts: An NMR Perspective.Exploiting and Understanding the Selectivity of Ru-N-Heterocyclic Carbene Metathesis Catalysts for the Ethenolysis of Cyclic Olefins to α,ω-Dienes.Molecularly Tailored Nickel Precursor and Support Yield a Stable Methane Dry Reforming Catalyst with Superior Metal Utilization.Orbital Analysis of Carbon-13 Chemical Shift Tensors Reveals Patterns to Distinguish Fischer and Schrock Carbenes.Local Structures and Heterogeneity of Silica-Supported M(III) Sites Evidenced by EPR, IR, NMR, and Luminescence Spectroscopies.Silica-Supported Lanthanocene(II) - (SiO)LnCp* (Ln = Yb, Sm): Ultra High Molecular Weight Polyethylene without co-Catalyst.Site-isolated manganese carbonyl on bipyridine-functionalities of periodic mesoporous organosilicas: efficient CO2 photoreduction and detection of key reaction intermediates.Metal alkyls programmed to generate metal alkylidenes by α-H abstraction: prognosis from NMR chemical shift.BDPA-Nitroxide Biradicals Tailored for Efficient Dynamic Nuclear Polarization Enhanced Solid-State NMR at Magnetic Fields up to 21.1 TDecisive roles of perimeter sites in silica-supported Ag nanoparticles in selective hydrogenation of CO to methyl formate in the presence of methanolMolecular Structure and Confining Environment of Sn Sites in Single-Site Chabazite ZeolitesCO2 Hydrogenation to Formate with Immobilized Ru-Catalysts Based on Hybrid Organo-Silica Mesostructured MaterialsHighly Productive Propane Dehydrogenation Catalyst Using Silica-Supported Ga–Pt Nanoparticles Generated from Single-SitesC–H Activation and Proton Transfer Initiate Alkene Metathesis Activity of the Tungsten(IV)–Oxo ComplexIsolated Zr Surface Sites on Silica Promote Hydrogenation of CO2 to CH3OH in Supported Cu CatalystsLow-Coordinated Titanium(III) Alkyl-Molecular and Surface-Complexes: Detailed Structure from Advanced EPR SpectroscopyNMR chemical shift analysis decodes olefin oligo- and polymerization activity of d group 4 metal complexesElectronic Structure–Reactivity Relationship on Ruthenium Step-Edge Sites from Carbonyl 13C Chemical Shift AnalysisAn N-heterocyclic carbene ligand promotes highly selective alkyne semihydrogenation with copper nanoparticles supported on passivated silicaSilica-supported isolated molybdenum di-oxo species: formation and activation with organosilicon agent for olefin metathesisHighly Active and Stable Iridium Pyrochlores for Oxygen Evolution ReactionIrO2-TiO2: A High-Surface-Area, Active, and Stable Electrocatalyst for the Oxygen Evolution ReactionUnderstanding surface site structures and properties by first principles calculations: an experimental point of view!Promoting Terminal Olefin Metathesis with a Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene CatalystOne- and Two-Dimensional High-Resolution NMR from Flat SurfacesOxygen transfer in electrophilic epoxidation probed by 17O NMR: differentiating between oxidants and role of spectator metal oxo.Metal Alkyls with Alkylidynic Metal-Carbon Bond Character: Key Electronic Structures in Alkane Metathesis Precatalystsπ-Bond Character in Metal-Alkyl Compounds for C-H Activation: How, When, and Why?
P50
Q33693108-671CA4A6-A067-4E84-A862-1EEC6F7C074FQ39420515-AB7209F1-E575-4EA1-8BA6-FFFCCF9077DBQ41162489-F3088B54-133F-4D76-988B-7592BC24632FQ46272347-00A43BA0-79C0-4F71-972B-FC6CCF53789DQ46273355-58AC9332-69F6-45AB-913B-8BA1695FDA1BQ46429308-67F8CC11-8A72-4D1D-A6CE-31858012DA7AQ46442823-C944176B-3CDA-4312-BB4D-D16C67271BD4Q47098731-1C2E1BAA-972D-41CF-B167-72B20A2F8903Q47763880-4E9337B0-5462-463D-A37E-B98262BB4CD0Q48050001-39F3105E-E9A0-4128-8473-D8E8A9DB82DCQ48050238-37701B84-E071-4DA5-9197-EFC003D9A112Q48185585-73DDE23E-DDA2-46CE-89FB-81B46C28742DQ48209386-D6333896-053F-43DF-A6DB-0C941F9CD56FQ48216925-B1656FD6-DDCA-4F67-8813-5111AD3F8E7BQ48229826-FCD2800F-9EF8-4F3B-B02F-1C6D9A39D0B2Q48314562-CEA728C1-4B6E-4945-84DB-B97C8C383F9AQ48326705-00724B89-430A-494A-AD3F-8DA8AB134D23Q49609302-CECF3835-8B24-419C-B23D-0F5FB0AFDFFBQ51736266-598F51AC-1831-4D0C-B309-A0043212AE46Q55311986-0F8568F1-225E-4AE0-9C48-AA0B824F8E3FQ56981333-5C040404-B4B6-4A1C-93B9-ED20EA9C3EDEQ57063973-1027F4EA-B99A-4B3D-9AF9-8ED4C9500F09Q57443671-646C6F3C-9DC8-47B3-92F7-50A8EB12022EQ57622684-62FF7321-6987-40FC-91A6-F22ADEBF0A61Q57622703-4AF0F896-F49F-4607-B4A2-A95DD9F329CAQ57622713-371DA1DC-998B-4A6A-9FA6-64B3958E9904Q57622723-F71739FF-E4F0-4AAA-B56B-0395D19B119EQ57622738-93E62FFF-2E20-4953-B6A9-633139496325Q57622757-3C79E129-BCF4-491B-970F-4A7FB15DCFCFQ57622766-6BD136CA-5304-4DCF-9DB0-020E59714C28Q57622834-77B7F7AD-AF0A-46EB-A674-EF5F6F4412DEQ57622852-2B16FC8B-8DF5-426D-807F-EF42E0792EE7Q57622927-EAAA0465-829F-482E-A91A-59856A9CEAA3Q57622953-B2EEDDCC-D5B5-4976-8CFA-02CDC56C4757Q57622992-E3D4035C-3BD2-4BBC-BDE3-99BBC2D862D9Q57784099-717CF9A5-FADF-41CD-9D1B-22774F68D083Q62124792-9B22B344-8805-478D-AC13-00A1359F84E9Q64933671-2DC5AE67-6552-4C99-895F-B73F4AFE985FQ89567616-4A13E24D-1ED2-4C91-932B-F897D6DEEAE5Q90330981-425DF989-B7B0-48EC-A032-2ADE7AC8DD8C
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Christophe Copéret
@ast
Christophe Copéret
@en
Christophe Copéret
@es
Christophe Copéret
@nl
type
label
Christophe Copéret
@ast
Christophe Copéret
@en
Christophe Copéret
@es
Christophe Copéret
@nl
prefLabel
Christophe Copéret
@ast
Christophe Copéret
@en
Christophe Copéret
@es
Christophe Copéret
@nl
P106
P31
P496
0000-0001-9660-3890