Tridentate, anionic tethered N-heterocyclic carbene of Pd(II) complexes

被引:48
作者
Sakaguchi, Satoshi [1 ,2 ]
Kawakami, Miaki [1 ,2 ]
O'Neill, Justin [3 ]
Yoo, Kyung Soo [3 ]
Jung, Kyung Woon [3 ]
机构
[1] Kansai Univ, Fac Chem Mat & Bioengn, Dept Chem, Osaka 5648680, Japan
[2] Kansai Univ, Fac Chem Mat & Bioengn, Mat Engn & High Technol Res Ctr, Osaka 5648680, Japan
[3] Univ So Calif, Dept Chem, Loker Hydrocarbon Res Inst, Los Angeles, CA 90089 USA
基金
日本学术振兴会;
关键词
N-heterocyclic carbene; Anionic tridentate ligand; NHC-Ag complex; NHC-Pd complex; Ligand-transfer reaction; QUATERNARY STEREOGENIC CENTERS; CATALYZED CONJUGATE ADDITION; ASYMMETRIC CATALYSIS; STEREODIRECTING LIGANDS; PALLADIUM(II) COMPLEXES; COORDINATION CHEMISTRY; METAL-COMPLEXES; COPPER; HYDROGENATION; HYDROSILYLATION;
D O I
10.1016/j.jorganchem.2009.10.011
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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 Ag(2)O 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 PdCl(2)(CH(3)CN)(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. Published by Elsevier B.V.
引用
收藏
页码:195 / 200
页数:6
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