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Platinum-Imidazolyl Schiff Base Complexes Immobilized in Periodic Mesoporous Organosilica Frameworks as Catalysts for Hydrosilylation
Authors:Yingpeng Huo  Jiwen Hu  Yuanyuan Tu  Zhenzhu Huang  Shudong Lin  Yangfei Hu  Chao Feng
Institution:1. Guangzhou Institute of Chemistry, Chinese Academy of Sciences, Guangzhou, 510650 P.R. China

The University of Chinese Academy of Sciences, Beijing, 100039 P.R. China

Guangdong Provincial Key Laboratory of Organic Polymer Materials for Electronics, 510650 P.R. China

CAS Engineering Laboratory for Special Fine Chemicals, 510650 P.R. China

CASH GCC (Nanxiong) Research Institute of New Materials Co., Ltd, 512400 P.R. China;2. Guangzhou Institute of Chemistry, Chinese Academy of Sciences, Guangzhou, 510650 P.R. China;3. Guangzhou Institute of Chemistry, Chinese Academy of Sciences, Guangzhou, 510650 P.R. China

The University of Chinese Academy of Sciences, Beijing, 100039 P.R. China

CASH GCC (Nanxiong) Research Institute of New Materials Co., Ltd, 512400 P.R. China

Abstract:An imidazolyl Schiff base-containing periodic mesoporous organosilica (PMO) was synthesized via co-condensation reactions between a newly prepared bis (imidazolyl)imine-bridged bis silane and tetraethyl orthosilicate in the presence of cetyltrimethyl ammonium bromide as a soft template. The resultant as-synthesized PMO was then employed as a solid support for platinum catalysts. This complex was fully characterized via various techniques including FTIR, solid-state13C NMR, and 29Si-NMR spectroscopy, as well as N2 adsorption/desorption analysis, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) methods. In addition, the catalyst was proven to efficiently mediate hydrosilylation reactions between olefins and hydrosilanes, and it can be reused for at least five cycles without significant loss of activity.
Keywords:hydrosilylation reactions  imidazolyl Schiff base  periodic mesoporous organosilica  platinum catalysts
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