Seven supramolecular nanotubes (inner
diameters, 35 nm) with different
ester groups on their inner surfaces were prepared from synthetic
amphiphiles and used as morphology regulators for three fluid-state
molecular assemblies: a phospholipid liposome and two surfactant micelles.
At temperatures above the gel-to-liquid crystalline phase transition
temperature (T
g–l) of the liposome
(diameter, 360 nm), encapsulation in the nanotubes led to morphological
transformation of the liposome into either a much smaller vesicle
(diameter, 8 nm) or a long, tubular nanofiber (inner diameter, 5 nm),
depending on the carbon number of the ester group on the nanotube
inner surface. Before encapsulation, the liposome had a typical lamellar
molecular packing with a stacking periodicity (d)
= 5.45 nm and T
g–l = 42.0 °C,
whereas the resulting vesicle had an interdigitated molecular packing
with d = 3.13 nm and T
g–l = 31.8 °C, although this unusual molecular packing was rearranged
back to the original lamellar molecular packing after release from
the nanotubes. The morphology of the tubular nanofiber (d = 5.06 nm and T
g–l = 48.7 °C)
was not changed before and after release from the nanotubes. The nanotubes
also induced rearrangement of an encapsulated surfactant micelle harboring
an environmentally responsive probe, pyrene, either to a spherical
morphology with a typical molecular packing of micelles, in which
pyrene existed in a monomeric state, or to a twisted, fibrous morphology
with a lamellar molecular packing, in which pyrene formed a J-type aggregate emitting excimer fluorescence. The micelle
with the twisted, fibrous morphology exhibited a helicity induced
by the confinement in the nanotubes with supramolecular chirality,
even though the surfactant itself was achiral.