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Carbene-stabilized main group radicals and radical ions

Chemical Science · 2013 · Vol. 4(8) · pp. 3020–3020
Caleb D. MartinMichèle SoleilhavoupGuy Bertrand

Abstract

Shortly after their discovery at the end of the 80s, stable singlet carbenes have been recognized as excellent ligands for transition metal based catalysts, and as organo-catalysts in their own right. At the end of the 2000s, it has been shown that they can coordinate main group elements in their zero oxidation state, and even activate small molecules. This review covers examples in the literature dealing with the most recent application of stable singlet carbenes, namely their use to stabilize radicals and radical ions that are otherwise unstable.

N-Heterocyclic Carbenes in Organic and Inorganic ChemistryCatalytic Cross-Coupling ReactionsCyclopropane Reaction MechanismsRadicalSinglet stateCarbeneCatalysisChemistryPhotochemistryIonGroup (periodic table)MoleculeCombinatorial chemistry

Funding

  • National Science Foundation
Citations
486
FWCI
24.99
field-weighted impact
References
168
Percentile
100%
vs. same field & year
Citations per year
References
Understanding the M (NHC) (NHC = N-heterocyclic carbene) bond
Coordination Chemistry Reviews · 2008 · 731 citations
Heterocyclic Carbenes: Synthesis and Coordination Chemistry
Angewandte Chemie International Edition · 2008 · 2,739 citations
A stable crystalline carbene
Journal of the American Chemical Society · 1991 · 4,111 citations
N-Heterocyclic Carbenes: A New Concept in Organometallic Catalysis
Angewandte Chemie International Edition · 2002 · 3,759 citations
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Carbene-stabilized main group radicals and radical ions · Scinovex