Foyle Émer M, Goodwin Rosemary J, Cox Cameron J T, Smith Bailee R, Colebatch Annie L, White Nicholas G
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.
J Am Chem Soc. 2024 Oct 2;146(39):27127-27137. doi: 10.1021/jacs.4c09930. Epub 2024 Sep 23.
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.
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。