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Título: | Synthesis of propargyl-functionalized NHC gold complexes |
Autor: | Johnson, Alice CSIC ORCID; Gimeno, M. Concepción CSIC ORCID | Fecha de publicación: | 2017 | Editor: | American Chemical Society | Citación: | Organometallics 36(7): 1278-1286 (2017) | Resumen: | A series of propargyl functionalized N-heterocyclic carbene gold(I) complexes have been synthesized from the corresponding imidazolium salts with tetrabutylammonium acetylacetonate in the presence of a gold(I) precursor in a onepot reaction. Several complexes of different stoichiometries are described: [AuBr(NHC)], [Au(NHC)]Br and [Au(CF) (NHC)], and many of these have been characterized by Xray diffraction studies. Aurophilic interactions are present in the compounds bearing less sterically hindered carbenes, and secondary interactions such as hydrogen bonds, π-π stacking, or weak contacts of the gold center with the carbon of the propargyl unit have also been found. These complexes possess a high degree of water solubility, which makes them potentially useful for the synthesis of biologically active compounds or as gold catalysts in water. Activation of the propargyl unit in [AuBr(NHC)] complexes leads to the formation of interesting trimers with bridging bidentate C^C alkynyl-carbene ligands. | URI: | http://hdl.handle.net/10261/155870 | DOI: | 10.1021/acs.organomet.7b00012 | Identificadores: | doi: 10.1021/acs.organomet.7b00012 e-issn: 1520-6041 issn: 0276-7333 |
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