Journal of the American Chemical Society,
Journal Year:
2019,
Volume and Issue:
142(2), P. 857 - 866
Published: Dec. 6, 2019
Controlling
the
self-assembled
nanoscale
ionic
aggregates
in
single-ion
conducting
polymers
is
a
crucial
step
toward
exceptional
transport
properties.
We
report
series
of
precisely
segmented
polyethylene-like
materials
containing
sulfonate
groups
(PES23)
with
Li+,
Na+,
Cs+,
or
NBu4+
counterions
synthesized
from
step-growth
polymerization.
At
room
temperature,
all
are
semicrystalline
well-defined
layers
separated
by
35-38
Å,
depending
on
cation.
In
situ
X-ray
scattering
measurements
reveal
that
layered
PES23Li,
PES23Na,
and
PES23Cs
transform,
upon
melting
PE
blocks,
into
Ia3d
gyroid
morphology.
The
gyroidal
PES23Li
PES23Na
further
evolve
hexagonal
symmetry
as
temperature
increases.
These
order-to-order
transitions
aggregate
morphologies
were
also
confirmed
oscillatory
shear
rheology.
ion
behavior
these
PES23
strongly
dependent
morphologies.
Specifically,
3D
interconnected
morphology
exhibits
higher
conductivity
than
isotropic
This
innovative
versatile
molecular
design
leads
to
unprecedented
percolated
provide
continuous
pathway
for
improved
transport.
Smart Molecules,
Journal Year:
2024,
Volume and Issue:
2(1)
Published: Feb. 29, 2024
Abstract
Smart
chiral
liquid
crystal
elastomers
are
a
class
of
soft
photonic
crystals
with
periodic
nanostructures.
There
two
kinds
structural
colors:
cholesteric
one‐dimensional
helical
nanostructure
and
blue‐phase
three‐dimensional
nanostructure.
The
self‐assembled
can
be
dynamically
controlled
under
external
stimulation,
the
reflected
color
adjusted
throughout
visible
light
range.
Along
development
innovative
material
systems
cutting‐edge
manufacturing
technologies,
researchers
have
proposed
diverse
strategies
to
design
synthesize
thoroughly
investigated
their
properties
potential
applications.
Here,
we
provide
systematic
review
progress
in
fabrication
smart
elastomers,
focusing
on
via
surface‐enforced
alignment,
bar
coating,
3D
printing,
anisotropic
deswelling
methods
as
well
self‐assembly
without
additional
alignment.
able
respond
quickly
stimuli
wide
range
applications
areas
such
adaptive
optics,
color‐changing
camouflage,
robotics,
information
encryption.
This
concludes
perspective
opportunities
challenges
for
future
elastomers.
Langmuir,
Journal Year:
2020,
Volume and Issue:
36(40), P. 11702 - 11731
Published: Sept. 14, 2020
Ionic
liquid
crystals
have
emerged
as
a
new
class
of
functional
soft
materials
in
the
last
two
decades,
and
they
exhibit
synergistic
characteristics
ionic
liquids
such
macroscopic
orientability,
miscibility
with
various
species,
phase
stability,
nanostructural
tunability,
polar
nanochannel
formation.
Owing
to
these
characteristics,
structures,
properties,
functions
been
hot
topic
chemistry,
finding
applications
including
host
frameworks
for
guest
binding,
separation
membranes,
ion-/proton-conducting
reaction
media,
optoelectronic
materials.
Although
several
excellent
review
articles
published
recently,
mainly
focused
on
fundamental
aspects,
specific
properties
crystals,
while
not
yet
discussed
at
one
time.
The
aim
this
feature
article
is
provide
an
overview
comprehensive
manner.
Angewandte Chemie International Edition,
Journal Year:
2017,
Volume and Issue:
56(45), P. 14085 - 14089
Published: Sept. 6, 2017
Supramolecular
self-assembly
of
24
forklike
mesogenic
ligands
and
12
transition
metal
ions
led
to
the
formation
giant
spherical
coordination
complexes
that
exhibit
liquid-crystalline
(LC)
phases.
Self-healing
LC
supramolecular
gels
were
also
obtained
through
introduction
these
nanostructured
into
dynamic
covalent
networks
formed
by
cross-linkers
bifunctional
polymers.
The
structures
PdII
with
72
rodlike
moieties
on
periphery
characterized
NMR,
diffusion-ordered
NMR
spectroscopy,
mass
spectrometry.
These
are
stable
lyotropic
behavior,
while
show
thermotropic
properties.
self-assembled
can
be
tuned
length
moieties.
Journal of the American Chemical Society,
Journal Year:
2019,
Volume and Issue:
142(2), P. 857 - 866
Published: Dec. 6, 2019
Controlling
the
self-assembled
nanoscale
ionic
aggregates
in
single-ion
conducting
polymers
is
a
crucial
step
toward
exceptional
transport
properties.
We
report
series
of
precisely
segmented
polyethylene-like
materials
containing
sulfonate
groups
(PES23)
with
Li+,
Na+,
Cs+,
or
NBu4+
counterions
synthesized
from
step-growth
polymerization.
At
room
temperature,
all
are
semicrystalline
well-defined
layers
separated
by
35-38
Å,
depending
on
cation.
In
situ
X-ray
scattering
measurements
reveal
that
layered
PES23Li,
PES23Na,
and
PES23Cs
transform,
upon
melting
PE
blocks,
into
Ia3d
gyroid
morphology.
The
gyroidal
PES23Li
PES23Na
further
evolve
hexagonal
symmetry
as
temperature
increases.
These
order-to-order
transitions
aggregate
morphologies
were
also
confirmed
oscillatory
shear
rheology.
ion
behavior
these
PES23
strongly
dependent
morphologies.
Specifically,
3D
interconnected
morphology
exhibits
higher
conductivity
than
isotropic
This
innovative
versatile
molecular
design
leads
to
unprecedented
percolated
provide
continuous
pathway
for
improved
transport.