| Literature DB >> 29696797 |
Jie-Shun Cui1,2, Qian-Kai Ba1, Hua Ke1, Arto Valkonen3, Kari Rissanen3, Wei Jiang1.
Abstract
Rotaxane-based molecular shuttles are often operated using low-symmetry axles and changing the states of the binding stations. A molecular shuttle capable of directional shuttling of an acid-responsive cone-like macrocycle on a single-state symmetric dumbbell axle is now presented. The axle contains three binding stations: one symmetric di(quaternary ammonium) station and two nonsymmetric phenyl triazole stations arranged in opposite orientations. Upon addition of an acid, the protonated macrocycle shuttles from the di(quaternary ammonium) station to the phenyl triazole binding station closer to its butyl groups. This directional shuttling presumably originates from charge repulsion and an orientational binding preference between the cone-like cavity and the nonsymmetric phenyl triazole station. This mechanism for achieving directional shuttling by manipulating only the wheels instead of the tracks is new for artificial molecular machines.Entities:
Keywords: host-guest chemistry; macrocycles; molecular machines; rotaxanes; supramolecular chemistry
Year: 2018 PMID: 29696797 DOI: 10.1002/anie.201803349
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336