Preparation of a nonleaching, recoverable and recyclable palladium-complex catalyst for Heck coupling reactions by immobilization on Au nanoparticles

被引:31
作者
Young, Jun-Nan [1 ]
Chang, Tsao-Ching [1 ]
Tsai, Shih-Chung [1 ]
Yang, Lin [1 ]
Yu, Shuchun Joyce [1 ]
机构
[1] Natl Chung Cheng Univ, Dept Chem & Biochem, Chiayi 621, Taiwan
关键词
Supported catalyst; Palladium; Heck reaction; Gold nanoparticles; Recyclable catalyst; PINCER COMPLEXES; HETEROGENEOUS CATALYSIS; HIGHLY EFFICIENT; MIZOROKI-HECK; GOLD; MECHANISM; SURFACES; MONOLAYERS; COLLOIDS; CLUSTERS;
D O I
10.1016/j.jcat.2010.04.005
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The loading of a palladium complex immobilized on the surface of Au nanoparticles (NPs) was controlled through coordination to a supported spacer ligand (SL = S(CH2)(11)NHP(O)(2-py)(2)) to yield catalyst particles of the composition (RS)(x)Au(SL)(y)(SL-PdCl2)(z) (SR = S(CH2)(7)CH3; x:y:z = (0.31-2.3):1:(0.45-3.3)) with diameters of 3.1-4.9 nm. A fraction of the supported spacer ligands (23-69%) was left uncapped to capture any soluble Pd species resulting from leaching. These surface-bound Pd(II)-complex catalysts were highly effective for Heck reactions of iodobenzene and alkylacrylates, yielding a maximum turnover frequency (TOF) of 4.87 x 10(4) h(1). Their catalytic activity was three- to tenfold higher than that of their unbound counterparts. These hybrid catalysts could be dissolved and precipitated. They could be quantitatively recovered and effectively recycled 15 times without significant loss of reactivity. The recovered Au NP-supported palladium could be also dissolved, precipitated and isolated. Various spectroscopic analyses were performed to determine a surface-structure composition of (RS)(x)Au(SL)(1)(SL-Pd-0)(0.53). (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:253 / 261
页数:9
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