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否则,不稳定结构会在立方八面体配位笼的腔内自组装。

Otherwise Unstable Structures Self-Assemble in the Cavities of Cuboctahedral Coordination Cages.

作者信息

Rizzuto Felix J, Ramsay William J, Nitschke Jonathan R

机构信息

Department of Chemistry , University of Cambridge , Cambridge CB2 1EW , United Kingdom.

出版信息

J Am Chem Soc. 2018 Sep 12;140(36):11502-11509. doi: 10.1021/jacs.8b07494. Epub 2018 Aug 30.

Abstract

We present a method for the directed self-assembly of interlocked structures and coordination complexes in a set of metal-organic hosts. New homo- and heteroleptic metal complexes-species that cannot be prepared outside-form within the cavities of cuboctahedral coordination cages. When linear bidentate guests and macrocycles are sequentially introduced to the host, a rotaxane is threaded internally; the resulting ternary host-guest complex is a new kind of molecular gyroscope. Tetradentate guests segregate the cavities of these cages into distinct spaces, promoting new stoichiometries and modes of ligand binding to metal ions. The behaviors of bound complexes were observed to alter markedly as a result of confinement: In situ oxidations and spin transitions, neither of which occur ex situ, were both observed to proceed. By providing a tailored space for new modes of coordination-driven self-assembly, the inner phases of cuboctahedral coordination cages provide a new medium for synthetic coordination chemistry.

摘要

我们提出了一种在一组金属有机主体中定向自组装互锁结构和配位络合物的方法。新型的均配和杂配金属络合物——在外部无法制备的物种——在立方八面体配位笼的腔内形成。当将线性双齿客体和大环依次引入主体时,一个轮烷在内部穿入;由此产生的三元主客体络合物是一种新型分子陀螺仪。四齿客体将这些笼的腔分隔成不同的空间,促进了新的化学计量比和配体与金属离子结合的模式。观察到受限导致结合络合物的行为发生显著变化:原位氧化和自旋转变(这两种情况在非原位时均不会发生)均被观察到能够进行。通过为配位驱动的自组装新模式提供定制空间,立方八面体配位笼的内相为合成配位化学提供了一种新介质。

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