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苯基膦酸锆锚定的甲基三氧化铼作为环己烯环氧化反应的新型多相催化剂。

Zirconium phenylphosphonate-anchored methyltrioxorhenium as novel heterogeneous catalyst for epoxidation of cyclohexene.

作者信息

He Sha, Liu Xin, Zhao Hongyue, Zhu Yue, Zhang Fazhi

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China.

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing 100029, China.

出版信息

J Colloid Interface Sci. 2015 Jan 1;437:58-64. doi: 10.1016/j.jcis.2014.08.065. Epub 2014 Sep 10.

DOI:10.1016/j.jcis.2014.08.065
PMID:25313467
Abstract

Epoxidation of olefins to epoxides is widely recognized as an important unit process in the manufacture of fine chemicals and intermediates. Developing an environmentally benign heterogeneous catalytic system for olefin epoxidation with high activity and selectivity is still a challenge in this research field. Herein, we report our attempts to synthesize novel zirconium phenylphosphonate-anchored methyltrioxorhenium (MTO/ZrPP) heterogeneous catalysts by a conventional impregnation method and evaluate their catalytic performance for epoxidation of cyclohexene using urea-hydrogen peroxide adduct (UHP) as oxidant without the addition of base ligands. The MTO/ZrPP catalyst samples are characterized by powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR), inductively coupled plasma emission spectrometry (ICP-ES), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and solid-state (1)H magic-angle spinning nuclear magnetic resonance ((1)H MAS NMR) techniques. Meanwhile, the density functional theory (DFT) calculation is carried out to further understand the structure feature and interactions of the MTO/ZrPP catalyst. It is revealed that MTO is anchored on support surface by the favored hydrogen-bonding interaction between two oxo ligands of MTO and two H atoms from the adjacent phenyls of ZrPP. MTO/ZrPP catalyst displays excellent catalytic activity for cyclohexene epoxidation. Moreover, only cyclohexene oxide production can be obtained under the employed reaction conditions.

摘要

烯烃环氧化生成环氧化物被广泛认为是精细化学品和中间体制造中的一个重要单元过程。开发一种环境友好的、具有高活性和选择性的用于烯烃环氧化的多相催化体系仍然是该研究领域的一个挑战。在此,我们报道了通过传统浸渍法合成新型苯基膦酸锆锚定甲基三氧化铼(MTO/ZrPP)多相催化剂的尝试,并评估了它们以尿素-过氧化氢加合物(UHP)作为氧化剂、不添加碱配体时对环己烯环氧化的催化性能。通过粉末X射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)、电感耦合等离子体发射光谱(ICP-ES)、高分辨率透射电子显微镜(HRTEM)、X射线光电子能谱(XPS)和固态(1)H魔角旋转核磁共振((1)H MAS NMR)技术对MTO/ZrPP催化剂样品进行了表征。同时,进行了密度泛函理论(DFT)计算以进一步了解MTO/ZrPP催化剂的结构特征和相互作用。结果表明,MTO通过MTO的两个氧代配体与ZrPP相邻苯基上的两个H原子之间有利的氢键相互作用锚定在载体表面。MTO/ZrPP催化剂对环己烯环氧化显示出优异的催化活性。此外,在所采用的反应条件下仅能得到环氧环己烷产物。

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