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Chimia|December 9, 2023
HTE and Data Analysis for Discovery and Molecular-level Understanding of CatalystsJordan De Jesus Silva, Christophe CopéretAngewandte Chemie (International Ed. in English)|July 8, 2020
N-Heterocyclic Carbene Coordination to Surface Copper Sites in Selective Semihydrogenation Catalysts from Solid-State NMR SpectroscopyNicolas Kaeffer, Deni Mance, Christophe CopéretChemical Science|October 9, 2020
Electronegativity and location of anionic ligands drive yttrium NMR for molecular, surface and solid-state structuresLukas Lätsch, Erwin Lam, Christophe CopéretAngewandte Chemie (International Ed. in English)|September 18, 2018
Promoting Terminal Olefin Metathesis with a Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene CatalystMargherita Pucino, Mariko Inoue, Christopher P Gordon, et al.Chemical Science|December 12, 2022
Ga and Zn increase the oxygen affinity of Cu-based catalysts for the CO hydrogenation according to ab initio atomistic thermodynamicsAndreas Müller, Aleix Comas-Vives, Christophe CopéretThe Journal of Physical Chemistry Letters|November 27, 2019
Proton-Detected Multidimensional Solid-State NMR Enables Precise Characterization of Vanadium Surface Species at Natural AbundanceDeni Mance, Aleix Comas-Vives, Christophe CopéretChemistry (Weinheim an Der Bergstrasse, Germany)|June 1, 2019
Efficient CO2 Hydrogenation to Formate with Immobilized Ir-Catalysts Based on Mesoporous Silica BeadsHung-Kun Lo, Indre Thiel, Christophe CopéretChemistry (Weinheim an Der Bergstrasse, Germany)|February 14, 2003
Re-based heterogeneous catalysts for olefin metathesis prepared by surface organometallic chemistry: reactivity and selectivityMathieu Chabanas, Christophe Copéret, Jean-Marie BassetJournal of the American Chemical Society|May 21, 2010
Shutting down secondary reaction pathways: the essential role of the pyrrolyl ligand in improving silica supported d(0)-ML4 alkene metathesis catalysts from DFT calculationsXavier Solans-Monfort, Christophe Copéret, Odile EisensteinJournal of the American Chemical Society|December 20, 2016
Increased Back-Bonding Explains Step-Edge Reactivity and Particle Size Effect for CO Activation on Ru NanoparticlesLucas Foppa, Christophe Copéret, Aleix Comas-VivesPageof 35