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通过无溶剂方法将ZrWO(OH)(HO)纳米棒原位植入分级功能化金属有机框架以提升催化性能。

In Situ Implanting ZrWO(OH)(HO) Nanorods into Hierarchical Functionalized Metal-Organic Framework via Solvent-Free Approach for Upgrading Catalytic Performance.

作者信息

Ye Gan, Shi Guangming, Wang Hanlu, Zeng Xingye, Wu Lei, Zhou Jun, Zhang Qiuli, Wei Jinshan, Li Zhiming, Nie Long, Wang Jin

机构信息

School of Chemistry and Chemical Engineering, Xi'an University of Architecture and Technology, Xi'an, 710055, China.

College of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, China.

出版信息

Small. 2024 Aug;20(32):e2311249. doi: 10.1002/smll.202311249. Epub 2024 Mar 14.

Abstract

Host-guest catalyst provides new opportunities for targeted applications and the development of new strategies for preparing host-guest catalysts is highly desired. Herein, an in situ solvent-free approach is developed for implanting ZrWO(OH)(HO) nanorods (ZrW-NR) in nitro-functionalized UiO-66(Zr) (UiO-66(Zr)-NO) with hierarchical porosity, and the encapsulation of ZrW-NR enables the as-prepared host-guest catalyst remarkably enhanced catalytic performance for both for oxidative desulfurization (ODS) and acetalization reactions. ZrW-NR@UiO-66(Zr)-NO can eliminate 500 ppm sulfur within 9 min at 40 °C in ODS, and can transform 5.6 mmol benzaldehyde after 3 min at room temperature in acetalization reaction. Its turnover frequencies reach 72.3 h at 40 °C for ODS which is 33.4 times higher than UiO-66(Zr)-NO, and 28140 h for acetalization which is the highest among previous reports. Density functional theory calculation result indicates that the W sites in ZrW-NR can decompose HO to W-peroxo intermediates that contribute to catalytic activity for the ODS reaction. This work opens a new solvent-free approach for preparing MOFs-based host-guest catalysts to upgrade their redox and acid performance.

摘要

主客体催化剂为靶向应用提供了新机遇,因此迫切需要开发制备主客体催化剂的新策略。在此,我们开发了一种原位无溶剂方法,用于将ZrWO(OH)(HO)纳米棒(ZrW-NR)植入具有分级孔隙率的硝基官能化UiO-66(Zr)(UiO-66(Zr)-NO)中,ZrW-NR的封装使所制备的主客体催化剂在氧化脱硫(ODS)和缩醛化反应中均具有显著增强的催化性能。ZrW-NR@UiO-66(Zr)-NO在ODS中于40℃下9分钟内可去除500 ppm硫,在缩醛化反应中于室温下3分钟后可转化5.6 mmol苯甲醛。其在ODS中40℃下的周转频率达到7².3 h⁻¹,比UiO-66(Zr)-NO高33.4倍,在缩醛化反应中的周转频率为28140 h⁻¹,是此前报道中的最高值。密度泛函理论计算结果表明,ZrW-NR中的W位点可将HO分解为有助于ODS反应催化活性的W-过氧中间体。这项工作开辟了一种新的无溶剂方法来制备基于金属有机框架的主客体催化剂,以提升其氧化还原和酸性性能。

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