Application of 1,2,3-triazolylidenes as versatile NHC-type ligands: synthesis, properties, and application in catalysis and beyond
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|Title:||Application of 1,2,3-triazolylidenes as versatile NHC-type ligands: synthesis, properties, and application in catalysis and beyond||Authors:||Donnelly, Kate F.
|Permanent link:||http://hdl.handle.net/10197/6828||Date:||11-Feb-2013||Abstract:||Triazolylidenes have rapidly emerged as a powerful subclass of N-heterocyclic carbene ligands for transition metals. They are readily available through regioselective [2 + 3] cycloaddition of alkynes and azides and subsequent metallation according to procedures established for related carbenes. Due to their mesoionic character, triazolylidenes are stronger donors than Arduengo-type imidazol-2-ylidenes. Spurred by these attractive attributes and despite their only recent emergence, triazolylidenes have shown major implications in catalysis. This feature article summarises the synthetic accessibility of triazolylidene metal complexes and their electronic and structural characteristics, and it compiles their applications, in particular, as catalyst precursors for various bond forming and redox reactions, as well as first approaches into photophysical and biochemical domains.||Type of material:||Journal Article||Publisher:||Royal Society of Chemistry||Journal:||Chemical Communications||Volume:||49||Issue:||12||Start page:||1145||End page:||1159||Copyright (published version):||2013 The Royal Society of Chemistry||Keywords:||N-heterocyclic carbenes; Suzuki-miyaura reaction; Palladium complexes; Coupling reactions; Water oxidation; Gold catalysis; Olefin metathesis; Iridium complexes; Pd nanoparticles; Click chemistry||DOI:||10.1039/c2cc37881g||Language:||en||Status of Item:||Peer reviewed||metadata.dc.date.available:||2015-08-20T15:59:31Z|
|Appears in Collections:||Chemistry Research Collection|
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