Quinoline Pyridine(Imine) Iron Complexes as Catalysts for the 1,4-Hydrovinylation of 1,3-Dienes

Keyphrases

• Iron Complexes 100%
• 1,3-dienes 100%
• Butadiene 100%
• Quinoline 100%
• Pyridine-imine 100%
• 1,4-hydrovinylation 100%
• Ethylene 50%
• Cyclometalated 50%
• Diffraction 25%
• Chelates 25%
• Electronic Structure 25%
• Ethane 25%
• Labeling Experiment 25%
• Alkyl Complexes 25%
• Terpyridine 25%
• Antiferromagnetic Coupling 25%
• X-ray 25%
• Methyl 25%
• Molecular Structure 25%
• Data Combination 25%
• Lithium 25%
• Bimolecular 25%
• High Selectivity 25%
• Deuterium Labeling 25%
• Oxidative Addition 25%
• Reductive Elimination 25%
• Magnetometry 25%
• Radical Anions 25%
• 57Fe 25%
• Iron(III) Chloride 25%
• DFT Calculations 25%
• Transfer Hydrogenation 25%
• Dichlorides 25%
• 1,4-dienes 25%
• HexA 25%
• Hydrovinylation 25%
• Reactivity Decomposition 25%
• Catalyst Decomposition 25%
• High Spin 25%
• Synthesis, Characterization 25%
• Mssbauer Spectroscopy 25%
• Pyridine Diimine 25%
• H/D Scrambling 25%
• Ligand-to-ligand Hydrogen Transfer 25%

Chemistry

• Iron Complex 100%
• Hydrovinylation 100%
• Imine 100%
• Butadiene 100%
• Catalyst 100%
• Pyridine 100%
• Quinoline 100%
• Ethylene 50%
• X-Ray Diffraction 25%
• Ground State 25%
• Electronic State 25%
• Terpyridines 25%
• Antiferromagnetic 25%
• Molecular Structure 25%
• Hydrogenation 25%
• Oxidative Addition 25%
• Isopropyl Group 25%
• Reductive Elimination Reaction 25%
• Spectroscopy 25%
• Lithium 25%
• Magnetometry 25%
• Radical Anion 25%
• Hydrogen Transfer 25%
• Catalysis 25%
• Iron Dichloride 25%
• Ethane 25%
• chelate 25%
• Deuterium 25%
• Density Functional Theory 25%