Bruce H. Lipshutz2012-11-202025-02-172012-11-202012-11-20https://dl.ftveti.edu.et/handle/123456789/4233A personal account tracing the origins and continuing evolution of nickel-on-charcoal (Ni/C) as a practical, alternative, group 10 metal catalyst is presented. Discussed are applications to several ``name reactions'' which lead to both carbon ±carbon and carbon±nitrogen bond constructions utilizing inexpensive aryl chlorides as substrates. Reductions of chloroarenes are also catalyzed by Ni/C, a process which may be worthy of consideration in terms of environmental cleanup of PCBs and dioxins. Collaborative efforts are also mentioned aimed at probing the surface structure of Ni/C, with the goal of enhancing catalyst activity. Future directions for development of heterogeneous nickel catalysts are proposed. 1 Introduction: Nickel-on-Charcoal? Never Heard of It . . . 2 Mixing a Ni(II) Salt with Charcoal: Getting It to `Stick' and Reduction to Ni(0) 3 First Results: Negishi-Like Couplings with Functionalized Zinc Reagents 4 Is Ni/C Compatible with Grignard Reagents? Kumada- Like Couplings 5 Suzuki Couplings with Aryl Chlorides: Ni/C Takes the Challenge 6 Aminations of Aryl Chlorides: and the `Magic' Phosphine Ligand is. . . 7 Reductive Dechlorinations of Aryl Chlorides: Searching for a Mild Source of Hydride 8 What Does ªNi/Cº Really Look Like? Surface Science to the Rescue 9 Summary . . . and a Look AheadA personal account tracing the origins and continuing evolution of nickel-on-charcoal (Ni/C) as a practical, alternative, group 10 metal catalyst is presented. Discussed are applications to several ``name reactions'' which lead to both carbon ±carbon and carbon±nitrogen bond constructions utilizing inexpensive aryl chlorides as substrates. Reductions of chloroarenes are also catalyzed by Ni/C, a process which may be worthy of consideration in terms of environmental cleanup of PCBs and dioxins. Collaborative efforts are also mentioned aimed at probing the surface structure of Ni/C, with the goal of enhancing catalyst activity. Future directions for development of heterogeneous nickel catalysts are proposed. 1 Introduction: Nickel-on-Charcoal? Never Heard of It . . . 2 Mixing a Ni(II) Salt with Charcoal: Getting It to `Stick' and Reduction to Ni(0) 3 First Results: Negishi-Like Couplings with Functionalized Zinc Reagents 4 Is Ni/C Compatible with Grignard Reagents? Kumada- Like Couplings 5 Suzuki Couplings with Aryl Chlorides: Ni/C Takes the Challenge 6 Aminations of Aryl Chlorides: and the `Magic' Phosphine Ligand is. . . 7 Reductive Dechlorinations of Aryl Chlorides: Searching for a Mild Source of Hydride 8 What Does ªNi/Cº Really Look Like? Surface Science to the Rescue 9 Summary . . . and a Look Aheadenaromatic aminations; aryl chlorides; biaryls; crosscouplings; heterogeneous catalysis; nickel- on-charcoalArticle