McKinlay Robert M, Cave Gareth W V, Atwood Jerry L
Department of Chemistry, University of Missouri, Columbia, MO 65211, USA.
Proc Natl Acad Sci U S A. 2005 Apr 26;102(17):5944-8. doi: 10.1073/pnas.0408113102. Epub 2005 Apr 14.
An important problem in designing any large network is the assembly of systems that are resilient to change. From a chemical point of view, an analogy can be used where one requires supramolecular assemblies to maintain their dimensionality combined with limited structural perturbation in response to variation in its intermolecular framework. The identification of hydrogen-bonded framework patterns within experimentally known supramolecular assemblies that are structurally robust to disruption and selective hydrogen substitution are envisioned to act as a supramolecular blueprint or template for metal-ion retroinsertion. Here, we report the formation of a large neutral discrete pseudo-spherical coordination capsule assembled from 6 pyrogallol[4]arene ligands and 24 Cu(II) metal ions. Amazingly, this coordination capsule is structurally analogous to its hydrogen-bonded counterpart. This result shows a robust ability of pyrogallol[4]arene molecules to self-assemble into large hexameric cage structures from either the hydrogen-bonding or metal-ligand coordination process. The identification of robust supramolecular assemblies that conserve their structure in response to interchangeability between hydrogen-bonded networks for metal coordination, or inversely, represents an important advancement in supramolecular design.
设计任何大型网络时的一个重要问题是构建具有抗变化能力的系统。从化学角度来看,可以进行这样的类比:需要超分子组装体在分子间框架发生变化时,既能保持其维度,又能使结构扰动受限。人们设想,在实验已知的超分子组装体中,识别出对破坏和选择性氢取代具有结构稳健性的氢键框架模式,可作为金属离子反向插入的超分子蓝图或模板。在此,我们报道了一种由6个连苯三酚[4]芳烃配体和24个铜(II)金属离子组装而成的大型中性离散伪球形配位胶囊的形成。令人惊讶的是,这种配位胶囊在结构上与其氢键对应物相似。这一结果表明,连苯三酚[4]芳烃分子具有强大的能力,能够通过氢键或金属-配体配位过程自组装成大型六聚体笼状结构。识别出在金属配位的氢键网络互换时仍能保持结构的稳健超分子组装体,或者反之亦然,这代表了超分子设计的一项重要进展。