Development of Bis(amidophenyl)amine Redox-active Ligands for Multi-electron Catalysis by Transition Metals Restricted; Files Only
Liu, Dan (Fall 2020)
Abstract
The development of transition metal catalysts for multi-electron chemical transformations have been investigated intensively in the past decades. Although significant progress has been made in applying precious metals such as rhodium, ruthenium or palladium for these transformations, the application of earth-abundant metals for catalyzing multi-electron chemical transformations are less well-studied.
In chapter 2 of this dissertation, the design, synthesis, characterization, and application of a series of dinuclear NiII complexes for catalytic oxidative dehydrogenation of hydrazones to form diazo compounds as the product will be described. Through modifications in the ligand scaffold, the effect of electronic properties, steric bulk, the presence of weak C-H bond, and the appearance of secondary H bonding donor on the catalytic reactivity of the corresponding NiII complexes were investigated. Chapter 3 reports the design, synthesis, and characterization of the novel 4-coordinated square planar NiII complexes for catalytic aziridinations. Mechanistic studies revealed that a 5-coordinated NiIII complex supported by a ligand radical likely acts as the reactive intermediate during the catalytic process. In Chapter 4, new RuII complexes are designed with easy preparation and purification. These RuII complexes are applied to catalytic C-H amination reactions.
Table of Contents
Chapter 1. Historical Development of Redox-active Ligands and Their Applications in Promoting First-row Transition Metal Catalysis 1
Introduction 1
Redox-active ligands in nature 2
Development of redox-active ligands 4
Dithiolene Ligand 4
Dioxolane Ligand 7
Amidophenolate and Diimine Ligand 9
Applications of first-row transition metal catalysts supported by redox-active ligands in catalysis 15
Metal Carbene chemistry 16
Metal Nitrene chemistry 17
Reference 22
Chapter 2. The Design, Synthesis and Characterization of Nickel Catalysts and Their Corresponding O2 Activation Reactivity 36
Abstract 36
Introduction 38
Results and discussion 40
Ligand synthesis 40
Synthesis of nickel complexes 42
Conclusion 66
Experimental section 68
General considerations 68
Ligand synthesis 70
Synthesis of nickel complexes 74
Catalytic aerobic oxidation procedure 81
Catalytic O-atom transfer reaction procedure 88
Appendix I 89
References 90
Chapter 3. Nitrene Transfer Reactions Catalyzed by a Nickel (II) Complex Incorporated with Redox-Active Ligands 98
Abstract 98
Introduction 99
Ligand synthesis 102
Synthesis of nickel complex 104
Results and discussion 105
Catalytic aziridinations and mechanistic studies 114
Conclusion 122
Experimental section 124
General considerations 124
Ligand synthesis 125
Synthesis of nickel complexes 130
Synthesis and characterization of PhINTs 135
General catalytic aziridination reaction procedure 135
Appendix I 139
Appendix II 140
Appendix III 141
Appendix IV 142
References 143
Chapter 4. The Design and Synthesis of Ruthenium Catalysts for C-H Aminations and Oxygenations 147
Abstract 147
Introduction 148
Ruthenium catalysts for sp3 C-H nitrogenations 149
Ruthenium catalysts for sp2 C-H nitrogenations 150
Ruthenium catalysts for sp3 C-H oxygenations 152
Ruthenium catalysts for sp2 C-H oxygenations 152
Ligand synthesis 155
Synthesis of ruthenium complexes 156
Results and discussion 157
C-H nitrogenation and oxygenations 178
Intramolecular sp3 C-H amination 178
Intramolecular sp2 C-H aminations 180
Intermolecular C-H aminations 182
Intramolecular sp2 C-H hydroxylation 183
Conclusion 184
Experimental section 185
General considerations 185
Ligand synthesis 186
Synthesis of ruthenium complexes 191
General procedures for catalytic reactions 198
Appendix I 200
Reference 201
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