Institute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, P.R. China.
J Am Chem Soc. 2021 Nov 17;143(45):19008-19017. doi: 10.1021/jacs.1c07971. Epub 2021 Nov 4.
Self-assembly of three-dimensional (3D) metallosupramolecular cages has drawn increasing attention for their potential to interconvert between different architectures due to the dynamic and reversible features of the coordination bond. These supramolecular transformations can provide unique approaches for the construction of stimuli-responsive supramolecular model systems to mimic biological transformation processes. While gold(I) clusters have attracted much interest due to their propensity to exhibit aurophilic interactions, the construction of 3D gold(I) cluster cages has remained a challenging and daunting task. Here, we proposed a "de-aurophilic" interaction strategy, which involves the prevention of aurophilic interaction formation between the basic [(μ-S)Au] units, to construct 3D gold(I) cluster cages. Through the judicious design of diphosphine ligands, an unprecedented class of gold(I) cluster cages with adaptive structures has been constructed. These gold(I) cluster cages are found to show intriguing stimuli-responsive structure transformation and interconversion. This work not only provides a strategy for the design and construction of novel 3D supramolecular cages based on cluster nodes but also offers a paradigm to study the stimuli-responsive structural interconversion between the unique structures of these gold(I) cluster cages.
三维(3D)金属超分子笼的自组装由于配位键的动态和可逆特性而引起了越来越多的关注,因为它们有可能在不同的结构之间相互转换。这些超分子转化可以为构建刺激响应超分子模型系统提供独特的方法,以模拟生物转化过程。虽然金(I)簇由于其表现出金键相互作用的倾向而引起了广泛关注,但构建 3D 金(I)簇笼仍然是一项具有挑战性和艰巨的任务。在这里,我们提出了一种“去金键相互作用”的策略,该策略涉及阻止基本[(μ-S)Au]单元之间形成金键相互作用,以构建 3D 金(I)簇笼。通过二膦配体的精心设计,构建了一类具有自适应结构的前所未有的金(I)簇笼。这些金(I)簇笼被发现表现出有趣的刺激响应结构转变和互变。这项工作不仅为基于簇节点设计和构建新型 3D 超分子笼提供了一种策略,而且为研究这些金(I)簇笼独特结构之间的刺激响应结构互变提供了范例。