Simple, efficient and reusable Pd-NHC catalysts for hydroamination

被引:32
作者
Chen, Qian [1 ,2 ]
Lv, Lanlan [1 ,2 ]
Yu, Meng [1 ,2 ]
Shi, Yanhui [1 ,2 ]
Li, Yuling [1 ,2 ]
Pang, Guangsheng [3 ]
Cao, Changsheng [1 ,2 ]
机构
[1] Jiangsu Normal Univ, Sch Chem & Chem Engn, Xuzhou 221116, Jiangsu, Peoples R China
[2] Jiangsu Normal Univ, Jiangsu Key Lab Green Synthet Chem Funct Mat, Xuzhou 221116, Jiangsu, Peoples R China
[3] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
N-HETEROCYCLIC CARBENES; INTRAMOLECULAR HYDROAMINATION; INTERMOLECULAR HYDROAMINATION; MARKOVNIKOV HYDROAMINATION; UNACTIVATED ALKENES; COMPLEXES; AMINES; PALLADIUM(II); HYDROSILYLATION; DERIVATIVES;
D O I
10.1039/c3ra42990c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of chelating NHC-palladium complexes with different alkane-bridges of the type Pd[NHC-(CH2)(n)-NHC]X-2 (X = Br or Cl, n = 2-4) were synthesized, where NHC is a triazolyl-N-heterocyclic carbene donor ligand. The bromide complexes with n = 2 and 3 were characterized by X-ray crystallography. The effects of the length of the bridge and halide ligand on the catalytic reactivity in the hydroamination reaction were investigated. The best catalytic performance was observed with the propylene-bridged Pd-NHC bromide complex 2. The hydroamination of phenylacetylene or 4-methylphenylacetylene with various substituted anilines catalyzed by 2 yielded only Markovnikov addition products in good yield. Interestingly, this homogenous catalyst can be reused three times without significant loss in activity.
引用
收藏
页码:18359 / 18366
页数:8
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