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Fig. 2
Mesophases of the rod-coil diblock molecules by the increasing volume fraction of
coil segments
periods of these supramolecular structures are typically in a range of less
than 10 nm. This structural variation can be explained by considering the fact
that increasing coil volume fraction leads to a structure with larger interfa-
cial area, similar to the well-known conventional diblock copolymer phase
behavior [13, 34, 35].
A strategy to manipulate supramolecular structures assembled from rod
segments may be accessible by the alteration of the coil architecture (lin-
ear (
5
)versusbranched(
6
)) in the rod-coil system [36]. On the basis of
SAXS and TEM results, rod-coil molecules (
5
) with a linear PPO coil showed
a honeycomb-like lamellar rod assembly with hexagonally arrayed PPO coil
perforations, while the rod-coil molecules (
6
) with a dibranched PPO coil
self-organized into rod-bundles with a body-centered tetragonal symmetry
surrounded by a PPO coil matrix (Fig. 3). The notable feature is that a sim-
Fig. 3
3D supramolecular structural change from organized honeycombs (
5
)toorganized
bundles (
6
), dependent upon the coil architectural variation of the rod-coil molecule
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