Exploring C(sp³)–C(sp³) reductive elimination from an isolable iron metallacycle

Physics & Astronomy

• cyclobutane 100%
• ligands 63%
• elimination 61%
• butenes 54%
• butanes 51%
• electronic structure 46%
• iron 44%
• reactivity 41%
• iron compounds 32%
• quinones 28%
• anhydrides 27%
• carbon monoxide 23%
• photolysis 22%
• isomers 20%
• ethylene 20%
• selectivity 19%
• anions 19%
• solid state 15%
• oxidation 15%
• products 13%
• geometry 11%
• diffraction 11%
• spectroscopy 10%
• x rays 9%
• electrons 8%

Engineering & Materials Science

• Electronic structure 93%
• Ligands 83%
• Iron 56%
• Butane 54%
• Butenes 51%
• Iron compounds 37%
• Photolysis 36%
• Thermolysis 34%
• Isoprene 33%
• Isomers 31%
• Maleic anhydride 28%
• Negative ions 28%
• Spectroscopy 23%
• Carbon monoxide 23%
• Discrete Fourier transforms 22%
• Ethylene 21%
• Electrons 21%
• X ray diffraction 20%
• Oxidation 18%
• Geometry 12%

Chemical Compounds

• Phenanthroline 70%
• Reductive Elimination Reaction 68%
• Cyclobutane 31%
• Butane 20%
• Electronic State 19%
• Butene 17%
• Kochi Cross Coupling 16%
• 1,4-benzoquinone 12%
• Ligand 11%
• Elimination Reaction 10%
• Isoprene 10%
• Bipyridine 9%
• Diamagnetic 9%
• Thermolysis 9%
• Maleic Anhydride 9%
• Radical Anion 8%
• 1,10-phenanthroline 8%
• Substance Spectroscopy 8%
• Photolysis 7%
• Carbon Monoxide 7%
• Compound Isomer 6%
• Spectroscopy 5%
• Electron Particle 4%
• X-Ray Diffraction 4%
• Oxidation Reaction 4%
• Mixture 3%
• Reaction Yield 3%