利用配位取代策略避免铬离子的动力学惰性,快速合成铬基金属有机框架。

IF 4.3 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Pub Date : 2024-06-30 DOI:10.1021/acs.inorgchem.4c02464
Bolun Zhai, Yuhao Tang, Zhiwei Zhao, Feifei Zhang*, Jinping Li and Jiangfeng Yang*, 
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引用次数: 0

摘要

铬基金属有机框架(Cr-MOFs)因其坚固耐用和高孔隙率而在广泛的应用中极具吸引力。然而,铬离子的动力学惰性导致铬基金属有机框架的合成通常需要较长的反应时间,从而限制了其工业应用。在此,我们报告了一种基于配位取代的新型合成策略,该策略克服了铬离子的动力学惰性,可在较短时间内合成铬-MOFs。通过制备几种已知的铬-MOFs,如 TYUT-96Cr、MIL-100Cr、MIL-101Cr 和 MIL-53Cr,证明了这种策略的多功能性。PXRD、SEM、TEM、77 K N2 吸附和 TGA 均证明,采用这种新方法合成的 Cr-MOF 具有良好的结晶性、高孔隙率和出色的热稳定性。理论计算对合成机理进行了研究。
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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Avoiding the Kinetic Inertness of Chromium Ions Using a Coordination Substitution Strategy for the Rapid Synthesis of Chromium-Based Metal–Organic Frameworks

Chromium-based metal–organic frameworks (Cr-MOFs) are very attractive in a wide range of applications due to their robustness and high porosity. However, the kinetic inertness of chromium ions results in the synthesis of Cr-MOFs often taking prolonged reaction times, which limit their industrial applications. Herein, we report a novel synthesis strategy based on coordination substitution, which overcomes the kinetic inertness of chromium ions and can synthesize Cr-MOFs in a shorter time. The versatility of this strategy has been demonstrated by producing several known Cr-MOFs, such as TYUT-96Cr, MIL-100Cr, MIL-101Cr, and MIL-53Cr. PXRD, SEM, TEM, 77 K N2 adsorption, and TGA have proved that the Cr-MOFs synthesized using this new strategy have good crystallinity, high porosity, and excellent thermal stability. The synthesis mechanism was investigated using theoretical calculations.

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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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