Chemists make bicycle-like molecular drive
Upon activation with light, the new molecular switch operates like the bottom bracket and pedals of a bicycle. They do not, however, perform a full rotation, but move back and forth, thus minizing the required amount of space for the switching.
Molecular cars have been known for some time, but scientists from the University of Amsterdam’s Van ‘t Hoff Institute for Molecular Sciences (HIMS) and the University of Murcia have now synthesized molecules that operate like the pedals of a bicycle. Fueled by light, the molecules can be used as molecular switches that pave the way for the design of functional molecular systems effective under severe spatial restrictions.
The research will be appear in the coming print issue of Angewandte Chemie International Edition (to be published 12 February).
Molecules that can be switched by light to change their structure are key building blocks for photoresponsive molecular nanotechnology. A major drawback of many currently available molecular switches is that they require a relatively large free volume to reverse between their two structural states. Prototypical examples are molecules in which isomerization of a double bond occurs, such as the rotor molecules of Nobel Laureate Ben Feringa.In many practical applications, for instance in catalysis, drug delivery or molecular computers, there simply is not enough space for such large-scale motion. Finding new chemical motifs that enable switching using only the bare minimum of volume is therefore of great relevance to this rapidly emerging field.
Recently, Prof. Jose Berna of the University of Murcia has proposed a new class of azodicarboxamide-based molecular switches. These are derived from a modification of the azo-moiety in azobenzene — one of the most widely employed components in ‘light switchable’ materials. Since the new systems are — in contrast to azobenzenes — no longer planar, it was expected they would exhibit different types of motion upon irradiation with light. Until now, however, studies of the actual motion taking place remained out of reach.
To investigate the exact mode of operation of the azodicarboxamide-based molecular switches, Dr Saeed Amirjalayer at the University of Amsterdam set out to measure their vibrational frequencies using extremely short pulses of infrared light (with a duration of less than a trillionth of a second). These frequencies are a fingerprint of the molecular structure and thus offer a direct means to establish exactly how the molecule changes its structure after being activated by light.
As it turned out these switches indeed exhibit a switching mechanism that is completely different when compared to the standard switches. Where the latter exhibit large-scale rotation around one bond, the new molecules operate like the bottom bracket and pedals of a bicycle. They do not, however, perform a full rotation, but move back and forth. Using advanced quantum chemical calculations it was established that the molecules become planar by light absorption and crank back as they return to their ground state.
The striking characteristic of the pedalo motion is that it is accompanied by minimal displacements of the atoms involved. The molecule thus stays more or less fixed in space and needs only a minimal switching volume. This offers opportunities for applications where motion at the molecular level is heavily restricted, such as in the solid state, on surfaces, or upon embedding in polymers.
Edited by Ariasun editorial board
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