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十克规模快速合成在水中能强烈且选择性结合硫酸根的坚固有机笼状物。

Expedient Decagram-Scale Synthesis of Robust Organic Cages That Bind Sulfate Strongly and Selectively in Water.

作者信息

Foyle Émer M, Goodwin Rosemary J, Cox Cameron J T, Smith Bailee R, Colebatch Annie L, White Nicholas G

机构信息

Research School of Chemistry, Australian National University, Canberra, ACT 2601, Australia.

EaStCHEM School of Chemistry, The University of Edinburgh, Edinburgh EH9 3FJ, Scotland, U.K.

出版信息

J Am Chem Soc. 2024 Oct 2;146(39):27127-27137. doi: 10.1021/jacs.4c09930. Epub 2024 Sep 23.

Abstract

Selective anion recognition remains a key challenge in supramolecular chemistry: only a very small number of systems that can function in water are known, and these nearly always preferentially bind hydrophobic anions. In this work, we report three robust hexa-cationic cages that can be prepared on scales up to 14 g in two simple and high-yielding steps from commercially available materials. One of these cages displays unusually strong sulfate binding in water ( = 12,000 M), and demonstrates high selectivity for this anion over HPO/HPO in DMSO/buffer mixtures. These results demonstrate that relatively large, three-dimensional supramolecular hosts can be prepared in high yields and on large scales, and can be highly potent receptors.

摘要

选择性阴离子识别仍然是超分子化学中的一个关键挑战

已知只有极少数能在水中起作用的体系,而且这些体系几乎总是优先结合疏水性阴离子。在这项工作中,我们报告了三种坚固的六阳离子笼,它们可以通过两个简单且高产率的步骤,由市售材料制备,规模可达14克。其中一种笼子在水中表现出异常强的硫酸根结合能力(K = 12,000 M⁻¹),并且在DMSO/缓冲液混合物中对该阴离子相对于HPO₄²⁻/H₂PO₄⁻表现出高选择性。这些结果表明,相对较大的三维超分子主体可以高产率、大规模地制备,并且可以成为高效的受体。

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