Ghidiu, Michael2012-10-042012-10-042012-05http://udspace.udel.edu/handle/19716/11540N-Heterocyclic Carbene (NHC) complexes of gold(I) and gold(III) of the form AuX(IPr) and AuXCl2(IPr) (IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene, X = halide or aryl) were prepared and investigated for photochemical activity. Where X = Cl, it was found that an energetically downhill oxidative addition could add an equivalent of Cl2 which could then be subsequently photoreductively eliminated in an energetically uphill step, representing a model energy storage-and-release scheme for chemical fuel formation. Where X = aryl (fluorinated phenyl derivatives), oxidative addition of Cl2 and subsequent reductive elimination produced the gold(I) complex AuCl(IPr) and the chlorinated aryl ligand. The reaction pathway was strongly dependent upon the electronics of the aryl ligand; more electron-rich ligands (X = phenyl) preferentially underwent thermal reductive elimination, while electron-poor ligands (X = pentafluorophenyl) could only be actuated photochemically. A gradient between these extremes was observed in intermediate ligands (X = 4-fluorophenyl, 2,4,6-trifluorophenyl, and 2,3,5,6-tetrafluorophenyl).en-USN-Heterocyclic Carbeneenergy storagearyl halogenationThesis