Development of Nickel-on-Charcoal as a ``Dirt-Cheap'' Heterogeneous Catalyst: A Personal Account
Date
2012-11-20
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Abstract
A 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 Ahead
Description
A 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 Ahead
Keywords
aromatic aminations; aryl chlorides; biaryls; crosscouplings; heterogeneous catalysis; nickel- on-charcoal
