articleTop 1% cited
Stable singlet carbenes as mimics for transition metal centers
Chemical Science · 2010 · Vol. 2(3) · pp. 389–399
David Martín(University of California, Riverside)Michèle Soleilhavoup(University of California, Riverside)Guy Bertrand✉(University of California, Riverside)
Abstract
This perspective summarizes recent results, which demonstrate that stable carbenes can activate small molecules (CO, H(2), NH(3) and P(4)) and stabilize highly reactive intermediates (main group elements in the zero oxidation state and paramagnetic species). These two tasks were previously exclusive for transition metal complexes.
N-Heterocyclic Carbenes in Organic and Inorganic ChemistryCatalytic Cross-Coupling ReactionsCarbon dioxide utilization in catalysisSinglet stateTransition metalParamagnetismMoleculeChemistryChemical physicsMetalPhotochemistryComputational chemistryCombinatorial chemistry
Funding
- National Science Foundation
- Civil Aviation Administration of China
Citations
656
FWCI
21.37
field-weighted impact
References
166
Percentile
100%
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Citations per year
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References
Imidazolylidenes, imidazolinylidenes and imidazolidines
Tetrahedron · 1999 · 941 citations
A stable crystalline carbene
Journal of the American Chemical Society · 1991 · 4,111 citations
Frustrated Lewis pairs: a new strategy to small molecule activation and hydrogenation catalysis
Dalton Transactions · 2009 · 566 citations
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