Mononuclear ruthenium compounds bearing N-donor and N-heterocyclic carbene ligands: structure and oxidative catalysis

Keyphrases

• N-donor 100%
• Electronic Transfer 100%
• Catalytic Oxidation 100%
• Compound Bearing 100%
• N-heterocyclic Carbene Ligands 100%
• Ligand Structure 100%
• Ruthenium Compounds 100%
• Water Oxidation 66%
• Methanol 33%
• Catalytic Performance 33%
• Alkenes 33%
• Cis-trans Isomerization 33%
• Nucleophilic Attack 33%
• Carbenes 33%
• Stereospecific 33%
• Poor Stability 33%
• Methyl 33%
• Mononuclear Complexes 33%
• Solvent Molecules 33%
• Oxidation State 33%
• Electron-withdrawing Group 33%
• Transfer Process 33%
• α-methylstyrene 33%
• Ligand Oxidation 33%
• Stability Region 33%
• 2″-terpyridine 33%
• Electron Donor Groups 33%
• Tris(pyrazol-1-yl)methane 33%
• C-N Bond 33%
• Phthalazine 33%
• Ru Oxidation 33%
• 1H-imidazole 33%
• Bond Scission 33%
• Tetradentate Ligand 33%
• Alkene Epoxidation 33%

Chemistry

• N-Heterocyclic Carbene 100%
• Ruthenium 100%
• Donor 100%
• electronics 100%
• Ligand Structure 100%
• Alkene 66%
• Water Oxidation 66%
• Transfer Process 33%
• Electron Donor 33%
• Terpyridines 33%
• Tris 33%
• 1H-Imidazole 33%
• Phthalazine 33%
• Isopropyl Group 33%
• Methane 33%
• Isomerization 33%
• formation 33%
• Carbon Dioxide 33%
• Carbene 33%
• epoxidation 33%
• Disproportionation Reaction 33%

Chemical Engineering

• Olefin 100%
• Ruthenium Compound 100%
• Carbon Dioxide 50%
• Disproportionation 50%