Constructing Polyphosphazene Microsphere-Supported Pd Nanocatalysts for Efficient Hydrogenation of Quinolines under Mild Conditions

Author:

Chen Xiufang1,Xiao Qingguang1,Yang Yiguo1,Dong Bo2,Zhao Zhengping3

Affiliation:

1. National & Local Joint Engineering Research Center for Textile Fiber Materials and Processing Technology, College of Material Science and Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, China

2. Key Laboratory of Bio-Based Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China

3. Zhijiang College, Zhejiang University of Technology, Hangzhou 310024, China

Abstract

The efficient hydrogenation of N-heterocycles with H2 under mild conditions remains a significant challenge. In this work, polyphosphazene (PZs) microspheres, novel organic–inorganic hybrid materials possessing unique –P=N– structural units and a diverse range of side groups, were used to serve as support for the design of a stable and efficient Pd nanocatalyst (Pd/PZs). The PZs microspheres were prepared by self-assembly induced by precipitation polymerization, and Pd nanoparticles were grown and loaded on the support by a chemical reduction process. Several characterization techniques, including XRD, FTIR, SEM, TEM, XPS, BET and TGA, were used to study the structural features of the nanocomposites. The results revealed that Pd nanoparticles were uniformly distributed on the PZs microspheres, with primary sizes ranging from 4 to 9 nm based on the abundance of functional P/N/O groups in PZs. Remarkably high catalytic activity and stability were observed for the hydrogenation of quinoline compounds using the Pd/PZs nanocatalyst under mild conditions. Rates of 98.9% quinoline conversion and 98.5% 1,2,3,4-tetrahydroquinoline selectivity could be achieved at a low H2 pressure (1.5 bar) and temperature (40 °C). A possible reaction mechanism for quinoline hydrogenation over Pd/PZs was proposed. This work presents an innovative approach utilizing a Pd-based nanocatalyst for highly efficient multifunctional hydrogenation.

Funder

Baima Lake Laboratory Joint Funds of the Zhejiang Provincial Natural Science Foundation of China

Scientific Research Foundation of Zhejiang Sci-Tech University

Fundamental Research Funds of Zhejiang Sci-Tech University

Publisher

MDPI AG

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