Fabrication and Catalytic Property of an Ordered Terpyridine Pd(II)/Ni(II) Catalytic Monolayer for Suzuki Coupling Reactions

Wen Wang, Sa Bi, Huanhuan Li, Tiesheng Li
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Abstract

Fabrication, arrangement, and controllable composition of ordered organometallic films are critical for designing a highly active catalyst and investigating the catalytic mechanism. In this paper, an organometallic terpyridine Pd(II)/Ni(II) monolayer linked on the silicon substrate surface (denoted as Si-Tpy-Pd1/Ni1) was prepared and characterized using water contact angle, ultraviolet spectra, X-ray diffraction, scanning electron microscopy, and X-ray photoelectron microscopy. Si-Tpy-Pd1/Ni1 exhibited high catalytic activity, substrate applicability, and reusability after 5 runs. During recycling, the deactivation was induced by the aggregation of active Pd/Ni nanoparticles. The catalytic mechanism was heterogeneous and occurred on the Si-Tpy-Pd1/Ni1 monolayer surface; the mechanism was confirmed using hot filtrate, poison test, and a three-phase experiment. The real active center was Pdδ/Niδ+ and was formed in situ on the organometallic monolayer surface, which acted as a precursor with a synergistic effect between Pd and Ni. The electron density of Pd became more negative because of electron transfer from Ni to Pd, which facilitated the oxidative addition reaction.
铃木偶联反应中三元吡啶Pd(II)/Ni(II)单分子膜的制备及其催化性能
有序有机金属膜的制备、排列和可控组成是设计高活性催化剂和研究催化机理的关键。本文制备了一种连接在硅衬底表面的有机金属三元吡啶Pd(II)/Ni(II)单层(表示为Si-Tpy-Pd1/Ni1),并利用水接触角、紫外光谱、x射线衍射、扫描电镜和x射线光电子显微镜对其进行了表征。5次运行后,Si-Tpy-Pd1/Ni1表现出较高的催化活性、底物适用性和可重复使用性。在回收过程中,活性钯/镍纳米粒子聚集导致失活。催化机理是不均匀的,发生在Si-Tpy-Pd1/Ni1单层表面;通过热滤液、中毒试验和三相实验对其机理进行了验证。真正的活性中心是Pdδ - /Niδ+,在有机金属单层表面原位形成,起到Pd和Ni之间协同作用的前驱体作用。由于电子从Ni转移到Pd, Pd的电子密度变得更负,有利于氧化加成反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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