| Literature DB >> 31095844 |
Miguel Baya1, Daniel Joven-Sancho1, Pablo J Alonso2, Jesús Orduna2, Babil Menjón1.
Abstract
A comparative study of the homoleptic [M(CF3 )4 ]- complexes of all three coinage metals (M=Cu, Ag, Au) reveals that homolytic M-C bond cleavage is favoured in every case upon excitation in the gas phase (CID-MS2 ). Homolysis also occurs in solution by photochemical excitation. Transfer of the photogenerated CF3 . radicals to both aryl and alkyl carbon atoms was also confirmed. The observed behaviour was rationalized by considering the electronic structure of the involved species, which all show ligand-field inversion. Moreover, the homolytic pathway constitutes experimental evidence for the marked covalent character of the M-C bond. The relative stability of these M-C bonds was evaluated by energy-resolved mass spectrometry (ERMS) and follows the order Cu<Ag≪Au. The qualitatively similar and rather uniform behaviour experimentally observed for all three coinage metals gives no ground to suggest variation in the metal oxidation state along the group.Entities:
Keywords: coinage metals; homolysis; ligand-field inversion; radicals; trifluoromethyl substituents
Year: 2019 PMID: 31095844 DOI: 10.1002/anie.201903496
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336