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对乙酰氨基酚包含于机械互锁纳米笼中。

Paracetamol Inclusion in Mechanically Interlocked Nanocages.

作者信息

Elli Stefano, Famulari Antonino, Martí-Rujas Javier

机构信息

Dipartimento di Chimica Materiali e Ingegneria Chimica. ''Giulio Natta'', Politecnico di Milano, Via L. Mancinelli 7, 20131, Milan, Italy.

INSTM, Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali.

出版信息

Chempluschem. 2024 Oct;89(10):e202400332. doi: 10.1002/cplu.202400332. Epub 2024 Jul 30.

DOI:10.1002/cplu.202400332
PMID:38855862
Abstract

The solid-state synthesis and fast crystallization under kinetic control of poly-[n]-catenanes self-assembled of mechanically interlocked metal organic cages (MOCs) is virtually unexplored. This is in part, due to the lack of suitable crystals for single crystal X-ray diffraction (SC-XRD) analysis which limits their progress as advanced functional materials. Here we report the unprecedented inclusion of paracetamol in the cavities of amorphous materials constituted of ML, interlocked MOCs synthesized by mechanochemistry under kinetic control. Full structure determination of a low-crystallinity and low-resolution powders of the ML poly-[n]-catenane including paracetamol has been carried out combining XRD data and Density Functional Theory (DFT) calculations using a multi-step approach. Each ML cage contains six paracetamol guests which is confirmed by thermal analysis and NMR spectroscopy. The paracetamol loading has been also carried out by the instant synthesis method using a saturated paracetamol solution in which TPB and ZnI self-assemble immediately (i. e., 1-5 seconds) encapsulating ~7 paracetamol molecules in the ML nanocages under kinetic control also giving a good selectivity. Benzaldehyde has been included in the ML cages using amorphous ML polycatenanes showing that the icosahedral cages can serve as potential nanoreactors for instance to study Henry reactions in the solid-state.

摘要

机械互锁金属有机笼(MOC)自组装的聚[n] - 索烃在动力学控制下的固态合成和快速结晶实际上尚未得到探索。部分原因是缺乏适用于单晶X射线衍射(SC-XRD)分析的晶体,这限制了它们作为先进功能材料的发展。在此,我们报告了在动力学控制下通过机械化学合成的互锁MOCs构成的无定形材料的空腔中前所未有的对乙酰氨基酚包合情况。结合XRD数据和使用多步方法的密度泛函理论(DFT)计算,对包含对乙酰氨基酚的ML聚[n] - 索烃的低结晶度和低分辨率粉末进行了完整的结构测定。通过热分析和NMR光谱证实每个ML笼包含六个对乙酰氨基酚客体。对乙酰氨基酚的负载也通过即时合成方法进行,使用对乙酰氨基酚饱和溶液,其中TPB和ZnI在动力学控制下立即(即1 - 5秒)自组装,在ML纳米笼中包封约7个对乙酰氨基酚分子,也具有良好的选择性。使用无定形ML聚索烃将苯甲醛包含在ML笼中,表明二十面体笼可以作为潜在的纳米反应器,例如用于研究固态下的亨利反应。

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