卡宾
链烷
三键
化学
钴
超分子化学
轮烷
碳纤维
碳链
纳米技术
高分子化学
结晶学
组合化学
双键
分子
材料科学
有机化学
催化作用
复合材料
复合数
卡宾
作者
Connor W. Patrick,Yueze Gao,Prakhar Gupta,Amber L. Thompson,Anthony W. Parker,Harry L. Anderson
标识
DOI:10.1038/s41557-023-01374-z
摘要
Abstract Polyynes are chains of sp 1 carbon atoms with alternating single and triple bonds. As they become longer, they evolve towards carbyne, the 1D allotrope of carbon, and they become increasingly unstable. It has been anticipated that long polyynes could be stabilized by supramolecular encapsulation, by threading them through macrocycles to form polyrotaxanes—but, until now, polyyne polyrotaxanes with many threaded macrocycles have been synthetically inaccessible. Here we show that masked alkynes, in which the C≡C triple bond is temporarily coordinated to cobalt, can be used to synthesize polyrotaxanes, up to the C 68 [5]rotaxane with 34 contiguous triple bonds and four threaded macrocycles. This is the length regime at which the electronic properties of polyynes converge to those of carbyne. Cyclocarbons constitute a related family of molecular carbon allotropes, and cobalt-masked alkynes also provide a route to [3]catenanes and [5]catenanes built around cobalt complexes of cyclo[40]carbon and cyclo[80]carbon, respectively.
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