Active template strategy for the preparation of π-conjugated interlocked nanocarbons

Mechanically interlocked carbon nanostructures represent a relatively unexplored frontier in carbon nanoscience due to the difficulty in preparing these unusual topological materials. Here we illustrate an active-template method in which a [ n ]cycloparaphenylene precursor macrocycle is decorated with two convergent pyridine donors that coordinate to a metal ion. The metal ion catalyses alkyne–alkyne cross-coupling reactions within the central cavity of the macrocycle, and the resultant interlocked products can be converted into fully π -conjugated structures in subsequent synthetic steps. Specifically, we report the synthesis of a family of catenanes that comprise two or three mutually interpenetrating [ n ]cycloparaphenylene-derived macrocycles of various sizes. Additionally, a fully π -conjugated [3]rotaxane was synthesized by the same method. The development of synthetic methods to access mechanically interlocked carbon nanostructures of varying topology can help elucidate the implications of mechanical bonding for this emerging class of nanomaterials and allow structure–property relationships to be established. An active-template approach has been used to prepare π -conjugated interlocked nanocarbons derived from [ n ]cycloparaphenylenes. A metal ion bound within the central cavity of a precursor macrocycle first catalyses cross-coupling reactions and then the resulting mechanically interlocked intermediates are further transformed into π -conjugated species—[2] and [3]catenanes as well as a conjugated [3]rotaxane.