Stable Cyclic Carbenes and Related Species beyond Diaminocarbenes
Top Cited Papers
- 10 September 2010
- journal article
- review article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 49 (47) , 8810-8849
- https://doi.org/10.1002/anie.201000165
Abstract
The success of homogeneous catalysis can be attributed largely to the development of a diverse range of ligand frameworks that have been used to tune the behavior of various systems. Spectacular results in this area have been achieved using cyclic diaminocarbenes (NHCs) as a result of their strong σ‐donor properties. Although it is possible to cursorily tune the structure of NHCs, any diversity is still far from matching their phosphorus‐based counterparts, which is one of the great strengths of the latter. A variety of stable acyclic carbenes are known, but they are either reluctant to bind metals or they give rise to fragile metal complexes. During the last five years, new types of stable cyclic carbenes, as well as related carbon‐based ligands (which are not NHCs), and which feature even stronger σ‐donor properties have been developed. Their synthesis and characterization as well as the stability, electronic properties, coordination behavior, and catalytic activity of the ensuing complexes are discussed, and comparisons with their NHC cousins are made.Keywords
This publication has 583 references indexed in Scilit:
- Recently Reported Crystalline Isothiazole Carbenes: Myth or RealityAngewandte Chemie, 2007
- Isolation of Cyclopropenylidene–Lithium Adducts: The Weiss–Yoshida ReagentAngewandte Chemie International Edition in English, 2006
- Stable four-π-electron, four-membered heterocyclic cations and carbenesProceedings of the National Academy of Sciences, 2006
- Cationic η1/η2‐Gold(I) Complexes of Simple ArenesAngewandte Chemie, 2006
- CO Fixation to Stable Acyclic and Cyclic Alkyl Amino Carbenes: Stable Amino Ketenes with a Small HOMO–LUMO GapAngewandte Chemie International Edition in English, 2006
- Cyclopropenylidenes: From Interstellar Space to an Isolated Derivative in the LaboratoryScience, 2006
- An N‐Heterocyclic Carbene Ligand with Flexible Steric Bulk Allows Suzuki Cross‐Coupling of Sterically Hindered Aryl Chlorides at Room TemperatureAngewandte Chemie International Edition in English, 2003
- The “Wanzlick Equilibrium”Published by Wiley ,2000
- Das „Wanzlick-Gleichgewicht“Angewandte Chemie, 2000
- Darstellung, Struktur und Reaktivität von 1,3,4‐Triphenyl‐4,5‐dihydro‐1H‐1,2,4‐triazol‐5‐yliden, einem neuen stabilen CarbenAngewandte Chemie, 1995