Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, UK.
Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, P. R. China.
Angew Chem Int Ed Engl. 2023 Jan 26;62(5):e202214785. doi: 10.1002/anie.202214785. Epub 2022 Dec 20.
The first examples of halogen bonding (XB) heteroditopic homo[2]catenanes were prepared by discrete Na template-directed assembly of oligo(ethylene glycol) units derived from XB donor-containing macrocycles and acyclic bis-azide precursors, followed by a Cu -mediated azide-alkyne cycloaddition macrocyclisation reaction. Extensive H NMR spectroscopic studies show the [2]catenane hosts exhibit positive cooperative ion-pair recognition behaviour, wherein XB-mediated halide recognition is enhanced by alkali metal cation pre-complexation. Notably, subtle changes in the catenanes' oligo(ethylene glycol) chain length dramatically alters their ion-binding affinity, stoichiometry, complexation mode, and conformational dynamics. Solution-phase and single-crystal X-ray diffraction studies provide evidence for competing host-separated and direct-contact ion-pair binding modes. We further demonstrate the [2]catenanes are capable of extracting solid alkali-metal halide salts into organic media.
首次通过离散的 Na 模板导向组装,由含卤素键(XB)给体大环和非环双叠氮前体衍生的聚(乙二醇)单元制备了卤素键异双[2]轮烷。随后,通过 Cu 介导的叠氮-炔环加成大环化反应进行。广泛的 1H NMR 光谱研究表明,[2]轮烷主体表现出正协同离子对识别行为,其中卤素键介导的卤化物识别通过碱金属阳离子预配合得到增强。值得注意的是,轮烷中聚(乙二醇)链长的细微变化极大地改变了它们的离子结合亲和力、化学计量、络合模式和构象动力学。溶液相和单晶 X 射线衍射研究为竞争的主体分离和直接接触离子对结合模式提供了证据。我们进一步证明[2]轮烷能够将固体碱金属卤化物盐萃取到有机介质中。