Sudan Sylvain, Fadaei-Tirani Farzaneh, Scopelliti Rosario, Ebbert Kristina E, Clever Guido H, Severin Kay
Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
Fakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, 44227, Dortmund, Germany.
Angew Chem Int Ed Engl. 2022 Jun 13;61(24):e202201823. doi: 10.1002/anie.202201823. Epub 2022 Apr 13.
Thirteen palladium-ligand assemblies with different structures and topologies were investigated for the ability to bind lithium ions. In one case, the addition of LiBF resulted in a profound structural rearrangement, converting a dincluclear [Pd L ] complex into a low-symmetry [Pd L ] assembly with two binding pockets for solvated LiBF ion pairs. The rearrangement could only be induced by Li , indicating highly specific host-guest interactions. A structural analysis of the [Pd L ] receptor revealed a compact structure with multiple intramolecular interactions, reminiscent of what is seen for natural and synthetic foldamers.
研究了13种具有不同结构和拓扑结构的钯-配体组装体结合锂离子的能力。在一种情况下,添加LiBF导致了深刻的结构重排,将双核[Pd L]配合物转化为具有两个用于溶剂化LiBF离子对结合口袋的低对称性[Pd L]组装体。这种重排只能由Li诱导,表明存在高度特异性的主客体相互作用。对[Pd L]受体的结构分析揭示了一种具有多个分子内相互作用的紧凑结构,这让人联想到天然和合成折叠体的结构。