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水中的超分子阴离子识别:氢键超分子框架的合成

Supramolecular anion recognition in water: synthesis of hydrogen-bonded supramolecular frameworks.

作者信息

Morshedi Mahbod, Thomas Michael, Tarzia Andrew, Doonan Christian J, White Nicholas G

机构信息

Research School of Chemistry , The Australian National University , Canberra , ACT , Australia . Email:

Department of Chemistry and Centre for Advanced Materials , The University of Adelaide , Adelaide , SA , Australia.

出版信息

Chem Sci. 2017 Apr 1;8(4):3019-3025. doi: 10.1039/c7sc00201g. Epub 2017 Feb 16.

Abstract

The interaction of tetratopic amidinium-containing receptors with terephthalate anions leads to porous framework materials assembled through charge-assisted hydrogen bonds. The frameworks form in good yield within minutes in water at room temperature, but no framework material is obtained if other anions (Cl, Br, NO, SO or isophthalate) are used in place of terephthalate. Two forms of the framework can be prepared: one with a connected pore network, and a more dense phase with discrete voids. We demonstrate that these are the kinetic and thermodynamic products, respectively. Either framework can be prepared independently and can be converted to the other form in response to stimuli. Furthermore, the frameworks can be controllably disassembled and reassembled in response to acid/base triggers suggesting that this new class of materials may have applications in the selective encapsulation and release of guests.

摘要

含四配位脒基受体与对苯二甲酸根阴离子的相互作用导致通过电荷辅助氢键组装而成的多孔骨架材料。在室温下,这些骨架材料能在几分钟内于水中以良好的产率形成,但如果使用其他阴离子(Cl、Br、NO、SO或间苯二甲酸根)代替对苯二甲酸根,则无法获得骨架材料。可以制备两种形式的骨架:一种具有连通的孔网络,另一种是具有离散空隙的更致密相。我们证明,它们分别是动力学产物和热力学产物。两种骨架都可以独立制备,并且可以响应刺激而相互转化。此外,这些骨架可以响应酸/碱触发而可控地拆卸和重新组装,这表明这类新型材料可能在客体的选择性封装和释放方面有应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f68/5380882/5ecfa064326e/c7sc00201g-f1.jpg

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