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钯在介孔二氧化硅基质中的固定化:制备、表征及其在碳-碳偶联反应中的催化效能

Immobilization of palladium in mesoporous silica matrix: preparation, characterization, and its catalytic efficacy in carbon-carbon coupling reactions.

作者信息

Jana Sreyashi, Dutta Buddhadeb, Bera Rajesh, Koner Subratanath

机构信息

Department of Chemistry, Jadavpur University, Kolkata, India.

出版信息

Inorg Chem. 2008 Jun 16;47(12):5512-20. doi: 10.1021/ic8004294. Epub 2008 May 6.

DOI:10.1021/ic8004294
PMID:18459724
Abstract

Palladium(0) has been immobilized into the silica-based mesoporous material to develop catalyst Pd(0)-MCM-41, which is found to be highly active in carbon-carbon coupling reactions. [Pd(NH3)4]2+ ions have been incorporated into the mesoporous material during synthesis of MCM-41 and subsequently upon treatments with hydrazine hydrate Pd2+ ions present in mesoporous silica matrix were reduced to Pd(0) almost instantaneously. The catalyst has been characterized by small-angle X-ray diffraction, N2 sorption, and transmission electron microscopy (TEM). TEM and surface area measurements clearly demonstrate that the immobilization of Pd(0) into the mesoporous silica has a significant effect on pore structure of the catalyst. Nevertheless, after immobilization of palladium the meso-porosity of the material is retained, as evidenced in the nitrogen sorption measurement. The TEM micrograph shows that both MCM-41 and Pd(0)-MCM-41 have similar types of external surface morphology; however, Pd(0)-MCM-41 was less ordered. Pd(0)-MCM-41 showed high catalytic activity toward carbon-carbon bond formation reactions like Heck and Sonogashira coupling, as evidenced in high turn-over numbers. In contrast to many other Pd-based catalysts reported so far, Pd(0)-MCM-41 acts as a truly heterogeneous catalyst in C-C coupling reactions. Notably, the new heterogeneous catalyst is found to be efficient in the activation of arylchloride to give impressive conversion in cross coupling (15-45% for Heck and 30% for Sonogashira) reactions under mild conditions.

摘要

钯(0)已被固定在硅基介孔材料中,以开发催化剂Pd(0)-MCM-41,发现该催化剂在碳-碳偶联反应中具有高活性。在MCM-41的合成过程中,[Pd(NH₃)₄]²⁺离子已被引入介孔材料中,随后在用肼水处理时,介孔二氧化硅基质中存在的Pd²⁺离子几乎瞬间被还原为Pd(0)。该催化剂已通过小角X射线衍射、N₂吸附和透射电子显微镜(TEM)进行了表征。TEM和表面积测量清楚地表明,将Pd(0)固定到介孔二氧化硅中对催化剂的孔结构有显著影响。然而,钯固定后材料的介孔率得以保留,这在氮吸附测量中得到了证明。TEM显微照片显示,MCM-41和Pd(0)-MCM-41具有相似类型的外表面形态;然而,Pd(0)-MCM-41的有序度较低。Pd(0)-MCM-41对Heck和Sonogashira偶联等碳-碳键形成反应表现出高催化活性,高转化率证明了这一点。与迄今为止报道的许多其他钯基催化剂相比,Pd(0)-MCM-41在C-C偶联反应中作为真正的非均相催化剂起作用。值得注意的是,发现这种新型非均相催化剂在温和条件下对芳基氯的活化效率很高,在交叉偶联反应(Heck反应为15-45%,Sonogashira反应为30%)中能给出令人印象深刻的转化率。

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