通过后处理有效调节辐射掺杂金属有机框架内的有机自由基

IF 4.7 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Jia-Qi Xiong, Li-Fang Zeng, Zi-Yao Yang, Jian-Zhen Liao* and Hua Ke*, 
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引用次数: 0

摘要

本文报道了一种罕见的由配位驱动的自组装实现的具有一维开放通道的自由基掺杂金属有机框架(MOF)晶体。利用x射线单晶衍射、固态UV-vis-NIR漫反射光谱和电子顺磁共振分析来阐明其独特的结构,以及为什么许多有机自由基稳定地存在于晶格中。研究表明,该晶体具有较强的分子间共面π -π相互作用,窄的光学带隙(仅为1.47 eV),低LUMO和浅HOMO。这些特性允许固有的电荷转移,导致在环境条件下产生许多有机自由基。有趣的是,后处理可以有效地调节MOF中的有机自由基。机械研磨可迅速减少有机自由基的数量。然后,将样品浸泡在含有二苯胺、对甲基苯胺或咔唑(作为电子供体)的N,N-二甲基甲酰胺溶液中,或用这些胺类有机分子进行物理研磨,可以在一定程度上恢复被还原的自由基。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effective Regulation of Organic Radicals within a Radical-Doped Metal–Organic Framework by Post-Treatment

Effective Regulation of Organic Radicals within a Radical-Doped Metal–Organic Framework by Post-Treatment

This work reports a rare radical-doped metal–organic framework (MOF) crystal with one-dimensional open channels achieved by coordination-driven self-assembly. X-ray single-crystal diffraction, solid-state UV–vis–NIR diffuse reflectance spectroscopy, and electron paramagnetic resonance analysis were used to clarify its unique structure and why many organic radicals stably exist in the crystal lattice. The study shows that this crystal has strong intermolecular cofacial π–π interactions, a narrow optical bandgap (only 1.47 eV), a low LUMO, and a shallow HOMO. These features allow an inherent charge transfer, leading to the genetation of many organic radicals under ambient conditions. Interestingly, post-treatment can effectively adjust the organic radicals in this MOF. Mechanical grinding quickly reduces the number of organic radicals. Then, soaking the sample in an N,N-dimethylformamide solution with diphenylamine, para-methylaniline, or carbazole (as electron donors), or physically grinding with these amine organic molecules, can recover the reduced radicals to some degree.

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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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