Tridentate, anionic tethered N-heterocyclic carbene of Pd(II) complexes |
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Authors: | Satoshi Sakaguchi Miaki Kawakami Kyung Soo Yoo |
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Affiliation: | a Department of Chemistry and Materials Engineering and High Technology Research Center, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka 564-8680, Japan b Loker Hydrocarbon Research Institute, Department of Chemistry, University of Southern California, Los Angeles, CA 90089, USA |
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Abstract: | ![]() The synthesis of a series of azolium salts such as azolium iodides and chlorides having both N-anionic functional group and N-alkyl group have been developed. Reaction of azolium iodides or chlorides with Ag2O gave the corresponding NHC-Ag complexes. It was found that the resulting NHC-Ag complexes derived from azolium iodides or chlorides differ in their physical properties. The azolium chlorides as well as azolium iodides were successfully converted into the NHC-Ag complexes, which subsequently reacted with PdCl2(CH3CN)2 to give the anionic amidate/NHC-Pd complexes. Thus, a variety of the NHC-Pd complexes could be obtained from benzimidazolium and imidazolium salts. |
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Keywords: | N-heterocyclic carbene Anionic tridentate ligand NHC-Ag complex NHC-Pd complex Ligand-transfer reaction |
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