| Literature DB >> 30994943 |
Jana M Holthoff1, Elric Engelage1, Alexander B Kowsari1, Stefan M Huber1, Robert Weiss2.
Abstract
A common method to dissolve elemental gold involves the combination of an oxidant with a Lewis base that coordinates to the gold surface, thus lowering the metal's redox potential. Herein we report the usage of organic iodide salts, which provide both oxidative power and a coordinating ligand, to dissolve gold under formation of organo-gold complexes. The obtained products were identified as AuIII complexes, all featuring Au-C bonds, as shown by X-ray single-crystal analysis, and can be isolated in good yields. Additionally, our method provides direct access to N-heterocyclic carbene (NHC-type) complexes and avoids costly organometallic precursors. The investigated complexes show dynamic behavior in acetonitrile and in the case of the NHC(-type) complexes, the involved species could be identified as a monocarbene [AuI3 (carbene)] and biscarbene complex [AuI2 (carbene)2 ]+ .Entities:
Keywords: carbenes; gold complexes; halogen bonding; noble metal; oxidative addition; transition metal
Year: 2019 PMID: 30994943 DOI: 10.1002/chem.201901583
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236