Solvent
Mixing To Induce Molecular Motor Aggregation
into Bowl-Shaped Particles: Underlying Mechanism, Particle Nature,
and Application To Control Motor Behavior
posted on 2018-06-07, 00:00authored byLinda
E. Franken, Yuchen Wei, Jiawen Chen, Egbert J. Boekema, Depeng Zhao, Marc C. A. Stuart, Ben L. Feringa
Control
over dynamic functions in larger assemblies is key to many
molecular systems, ranging from responsive materials to molecular
machines. Here we report a molecular motor that forms bowl-shaped
particles in water and how confinement of the molecular motor affects
rotary motion. Studying the aggregation process in a broader context,
we provide evidence that, in the case of bowl-shaped particles, the
structures are not the product of self-assembly, but a direct result
of the mixing a good solvent and a (partial) non-solvent and highly
independent of the molecular design. Under the influence of the non-solvent,
droplets are formed, of which the exterior is hardened due to the
increase in the glass transition temperature by the external medium,
while the interior of the droplets remains plasticized by the solvent,
resulting in the formation of stable bowl-shaped particles with a
fluid interior, a glass-like exterior, and a very specific shape:
dense spheres with a hole in their side. Applying this to a bulky
first-generation molecular motor allowed us to change its isomerization
behavior. Furthermore, the motor shows in situ photo-switchable
aggregation-induced emission. Strong confinement prohibits the thermal
helix inversion step while altering the energy barriers that determine
the rotary motion, such that it introduces a reverse trans–cis isomerization upon heating. These studies
show a remarkable control of forward and backward rotary motion by
simply changing solvent ratios and extent of confinement.