在溶液和Zr (IV) 基金属有机框架中的特罗格基化学
Wei Gong1,2, Masoud Kazem-Rostami2, Florencia A Son2
1School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules and State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, China.
Journal of the American Chemical Society
|December 1, 2022
概括
这项研究探讨了特罗格在金属有机框架 (MOF) 中的基础化学,揭示了现场带排离和链接器衍生. 这导致具有独特拓和神经毒剂模拟解毒的催化活性的新型Zr-MOF.
科学领域:
- 材料化学
- 超分子化学
- 催化剂
背景情况:
- 特罗格基 (TB) 衍生因其独特的形结构而闻名.
- 在金属有机框架 (MOF) 固体中,带剪切的TBs的化学成分仍然在很大程度上未被探索.
- 对于MOF合成中的TB连接器的现场修改存在一个知识缺口.
研究的目的:
- 调查在现场带消除含有碳酸盐的溶液中的结核病和基于Zr的MOF.
- 探索新型Zr-MOFs的形成与受控的链接器衍生.
- 阐明MOF中的TB衍生和合成后修饰的机制.
主要方法:
- 在溶液中和MOF合成过程中结核病衍生物的现场除反应.
- 单晶X射线晶体学用于溶液产品的结构阐明.
- 具有不同拓的Zr-MOF (NU-1900和NU-407) 的合成和表征.
- 通过水诱导的现场链接形式的合成后修饰的研究.
主要成果:
- 单独转化甲二氨酸核为溶液中的N,N'-二甲基装饰的氨酸衍生物.
- 根据溶剂的选择,控制形成两个Zr-MOF (NU-1900和NU-407),分别具有8和12连接的拓.
- 在NU-1900中发现了一种新型的合成后水诱导的现场链接形式.
- 证明有缺陷的NU-1900作为神经毒剂模拟剂解毒的高效催化剂.
结论:
- 在Zr-MOF中结核链接物的衍生是以拓为导向的,受局部酸度的影响.
- 一个新的合成后修改途径扩大了MOF的功能化可能性.
- 缺陷的NU-1900具有显著的化学威胁缓解催化剂潜力.
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