Fakultät für Chemie und Chemische Biologie, TU Dortmund, Otto-Hahn-Strasse 6, 44227, Dortmund, Germany.
Angew Chem Int Ed Engl. 2017 Jul 3;56(28):8285-8289. doi: 10.1002/anie.201702573. Epub 2017 May 23.
Control over the integrative self-sorting of metallo-supramolecular assemblies opens up possibilities for introducing increased complexity and function into a single self-assembled architecture. Herein, the relationship between the geometry of three ligand components and morphology of three self-sorted heteroleptic [Pd L L' ] cages is examined. Pd-mediated assembly of two bis-monodentate pyridyl ligands with native bite angles of 75° and 120° affords a cis-[Pd L L' ] cage while the same reaction with two ligands with bite angles of 75° and 60° gives an unprecedented, self-penetrating structural motif; a trans-[Pd (anti-L) L' ] heteroleptic cage with a "doubly bridged figure eight" topology. Each heteroleptic assembly can be formed by cage-to-cage conversion of the homoleptic precursors and morphological control of [Pd L L' ] cages is achieved by selective ligand displacement transformations in a system of three ligands and at least six possible cage products.
控制金属超分子组装的整体自分类为在单个自组装结构中引入更高的复杂性和功能开辟了可能性。在此,研究了三个配体组件的几何形状与三个自分类杂化[PdL L']笼的形态之间的关系。Pd 介导的两个具有天然结合角为 75°和 120°的双单齿吡啶配体的组装得到顺式-[PdL L']笼,而相同反应中使用具有结合角为 75°和 60°的两个配体则得到了前所未有的自穿透结构基序;一种具有“双重桥接的数字八”拓扑结构的反式-[Pd(anti-L)L']杂化笼。每个杂化组装都可以通过同核前体的笼对笼转化来形成,并且通过在至少六个可能的笼产物的三个配体系统中进行选择性配体取代转化,可以实现[PdL L']笼的形态控制。