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壳聚糖插层蒙脱石负载钯(0)和铜(II)催化剂的微观结构及在 Sonogashira 反应中的催化性能。

Microstructure and catalytic performances of chitosan intercalated montmorillonite supported palladium (0) and copper (II) catalysts for Sonogashira reactions.

机构信息

Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, College of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing 312000, China.

Zhejiang Key Laboratory of Alternative Technologies for Fine Chemicals Process, College of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing 312000, China.

出版信息

Int J Biol Macromol. 2018 Jul 1;113:1308-1315. doi: 10.1016/j.ijbiomac.2018.03.066. Epub 2018 Mar 14.

Abstract

In this study, an efficient heterogeneous catalytic material including Pd nanoparticles and Cu cations supported on montmorillonite/chitosan (MMT/CS) composite was prepared by solution intercalation and complexion methods. The valence states of Pd (both Pd(0) and Pd(II) coexisting) and Cu (mainly Cu(II)) of the Pd/Cu@MMT/CS catalyst were confirmed by the X-ray photoelectron spectroscopy (XPS) characterization. The d spacing was enlarged from 1.25nm (MMT) to 1.94nm (Pd/Cu@MMT/CS). Pd/Cu@MMT/CS catalyst had obviously bigger specific surface area (S) and total pore volume (V) than pure MMT. High resolution transmission electron microscopy (HR-TEM) observation of the Pd/Cu@MMT/CS catalyst showed that separated Pd nanoparticles sized below 3nm dispersed well both in the interlayer space and surface of MMT layers. The positron annihilation lifetime spectroscopy (PALS) was very sensitive to the microstructure changes caused by the formation of nano particles Pd after reduction of Pd/Cu@MMT/CS to Pd/Cu@MMT/CS. The prepared Pd/Cu@MMT/CS catalysts are highly active for the Sonogashira reactions of aromatic halides and alkynes in HO/ether solution, and can be recycled 6 times. The leaching of Cu species is much quicker than Pd species during recycling, which should be the main reason for the decrease in efficiency of the recycled Pd/Cu@MMT/CS catalysts.

摘要

在这项研究中,通过溶液插层和络合方法制备了一种包括负载在蒙脱石/壳聚糖(MMT/CS)复合材料上的钯纳米粒子和铜阳离子的高效多相催化材料。X 射线光电子能谱(XPS)表征证实了 Pd/Cu@MMT/CS 催化剂中 Pd(同时存在 Pd(0) 和 Pd(II))和 Cu(主要是 Cu(II))的价态。Pd/Cu@MMT/CS 催化剂的 d 间距从 1.25nm(MMT)扩大到 1.94nm。Pd/Cu@MMT/CS 催化剂的比表面积(S)和总孔体积(V)明显大于纯 MMT。Pd/Cu@MMT/CS 催化剂的高分辨率透射电子显微镜(HR-TEM)观察表明,尺寸小于 3nm 的分离钯纳米粒子在 MMT 层的层间空间和表面上分散良好。正电子湮没寿命谱(PALS)对 Pd/Cu@MMT/CS 还原为 Pd/Cu@MMT/CS 后形成纳米粒子 Pd 引起的微结构变化非常敏感。制备的 Pd/Cu@MMT/CS 催化剂在 HO/醚溶液中对芳基卤化物和炔烃的 Sonogashira 反应具有很高的活性,并且可以循环使用 6 次。在回收过程中,Cu 物种的浸出速度比 Pd 物种快得多,这应该是回收的 Pd/Cu@MMT/CS 催化剂效率降低的主要原因。

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