Department of Chemistry, Jinan University, Guangzhou 510632, PR China.
Department of Chemistry, Jinan University, Guangzhou 510632, PR China.
J Colloid Interface Sci. 2017 Jul 1;497:134-143. doi: 10.1016/j.jcis.2017.02.066. Epub 2017 Feb 28.
A very easy sequential metathesis for the synthesis of Pd(II)-CMC@Ce(OH) organic/inorganic hybrid and its application as effective pre-catalyst for the Suzuki-Miyaura reaction have been reported. It was found that the Pd nanoparticles (Pd NPs) were formed in situ in the course of the Suzuki-Miyaura couplings when Pd(II)-CMC@Ce(OH) was used as a pre-catalyst. The activity of the Pd NPs in the reaction was enhanced synergistically by the unique redox properties (Ce/Ce) of Ce(OH) and coordination with carboxyl groups as well as free hydroxyl groups of the hybrid of CMC@Ce(OH). The results exhibit the Pd(0)-CMC@Ce(OH) is super over Pd(II)@CMC, Pd(II)@CeO, and Pd(II)@Ce(OH) catalysts in the Suzuki-Miyaura reaction. Moreover, the catalyst could be easily separated by simple filtration and reused at least seven runs without losing its activity.
已报道了一种非常简便的连续易位反应,用于合成 Pd(II)-CMC@Ce(OH)有机/无机杂化材料,并将其用作 Suzuki-Miyaura 反应的有效预催化剂。研究发现,当 Pd(II)-CMC@Ce(OH)用作预催化剂时,Pd(II)-CMC@Ce(OH)在 Suzuki-Miyaura 偶联反应过程中会原位形成 Pd 纳米颗粒(Pd NPs)。Ce(OH)独特的氧化还原特性(Ce/Ce)、与杂化材料中羧基和游离羟基的配位作用协同增强了 Pd NPs 在反应中的活性。结果表明,在 Suzuki-Miyaura 反应中,Pd(0)-CMC@Ce(OH)的活性优于 Pd(II)@CMC、Pd(II)@CeO 和 Pd(II)@Ce(OH)催化剂。此外,该催化剂可通过简单过滤轻松分离,并至少重复使用七次而不损失其活性。