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通过在沸石咪唑酯骨架表面选择性掺杂镍制备的用于乙烯二聚的高活性多相催化剂。

Highly Active Heterogeneous Catalyst for Ethylene Dimerization Prepared by Selectively Doping Ni on the Surface of a Zeolitic Imidazolate Framework.

作者信息

Chen Cailing, Alalouni Mohammed R, Dong Xinglong, Cao Zhen, Cheng Qingpeng, Zheng Lirong, Meng Lingkun, Guan Chao, Liu Lingmei, Abou-Hamad Edy, Wang Jianjian, Shi Zhan, Huang Kuo-Wei, Cavallo Luigi, Han Yu

机构信息

Advanced Membranes and Porous Materials Center, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia.

KAUST Catalysis Center, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia.

出版信息

J Am Chem Soc. 2021 May 12;143(18):7144-7153. doi: 10.1021/jacs.1c02272. Epub 2021 Apr 28.

DOI:10.1021/jacs.1c02272
PMID:33908757
Abstract

The production of 1-butene by ethylene dimerization is an important chemical industrial process currently implemented using homogeneous catalysts. Here, we describe a highly active heterogeneous catalyst (Ni-ZIF-8) for ethylene dimerization, which consists of isolating Ni-active sites selectively located on the crystal surface of a zeolitic imidazolate framework. Ni-ZIF-8 can be easily prepared by a simple one-pot synthesis method in which site-specific anchoring of Ni is achieved spontaneously because of the incompatibility between the d electronic configuration of Ni and the three-dimensional framework of ZIF-8. The full exposure and square-planar coordination of the Ni sites accounts for the high catalytic activity of Ni-ZIF-8. It exhibits an average ethylene turnover frequency greater than 1 000 000 h (1-butene selectivity >85%) at 35 °C and 50 bar, far exceeding the activities of previously reported heterogeneous catalysts and many homogeneous catalysts under similar conditions. Moreover, compared to molecular Ni complexes used as homogeneous catalysts for ethylene dimerization, Ni-ZIF-8 has significantly higher stability and shows constant activity during 4 h of continuous reaction. Isotopic labeling experiments indicate that ethylene dimerization over Ni-ZIF-8 follows the Cossee-Arlman mechanism, and detailed characterizations combined with density functional theory calculations rationalize this observed high activity.

摘要

通过乙烯二聚生产1-丁烯是目前使用均相催化剂实现的重要化学工业过程。在此,我们描述了一种用于乙烯二聚的高活性多相催化剂(Ni-ZIF-8),它由选择性位于沸石咪唑酯骨架晶体表面的孤立Ni活性位点组成。Ni-ZIF-8可以通过简单的一锅合成法轻松制备,由于Ni的d电子构型与ZIF-8的三维骨架不兼容,Ni会自发地实现位点特异性锚定。Ni位点的完全暴露和平面正方形配位解释了Ni-ZIF-8的高催化活性。在35°C和50巴下,它表现出大于1000000 h的平均乙烯周转频率(1-丁烯选择性>85%),远远超过先前报道的多相催化剂以及许多均相催化剂在类似条件下的活性。此外,与用作乙烯二聚均相催化剂的分子Ni配合物相比,Ni-ZIF-8具有明显更高的稳定性,并且在4小时的连续反应中表现出恒定的活性。同位素标记实验表明,Ni-ZIF-8上的乙烯二聚遵循科斯see-阿尔曼机理,详细的表征结合密度泛函理论计算解释了观察到的高活性。

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