Influencing intramolecular motion with an alternating electric field

Analogues of mechanical devices that operate on the molecular level1,2,3,4,5, such as shuttles6,7,8,9,10, brakes11, ratchets12,13, turnstiles14 and unidirectional spinning motors15,16, are current targets of both synthetic chemistry and nanotechnology. These structures are designed to restrict the degrees of freedom of submolecular components such that they can only move with respect to each other in a predetermined manner, ideally under the influence of some external stimuli. Alternating-current (a.c.) electric fields are commonly used to probe electronic structure, but can also change the orientation of molecules17,18,19 (a phenomenon exploited in liquid crystal displays), or interact with large-scale molecular motions, such as the backbone fluctuations of semi-rigid polymers20,21. Here we show that modest a.c. fields can be used to monitor and influence the relative motion within certain rotaxanes22, molecules comprising a ring that rotates around a linear ‘thread’ carrying bulky ‘stoppers’ at each end. We observe strong birefringence at frequencies that correspond to the rate at which the molecular ring pirouettes about the thread, with the frequency of maximum birefringence, and by inference also the rate of ring pirouetting giving rise to it, changing as the electric field strength is varied. Computer simulations and nuclear magnetic resonance spectroscopy show the ring rotation to be the only dynamic process occurring on a timescale corresponding to the frequency of maximum birefringence, thus confirming that mechanical motion within the rotaxanes can be addressed, and to some extent controlled, by oscillating electric fields.