ACS Materials Letters,
Journal Year:
2023,
Volume and Issue:
5(12), P. 3177 - 3183
Published: Oct. 31, 2023
Supramolecular
frameworks
obtained
via
self-assembly
of
proper
elementary
building
units
have
received
great
attention,
as
they
can
express
advanced
functions
uneasily
expressed
by
the
units.
Until
now,
construction
supramolecular
has
remained
a
challenging
task,
not
to
mention
photoresponsive
frameworks.
Here,
we
report
first
framework
(NUT-103)
hierarchical
zirconium
metal–organic
cages
containing
trinuclear
clusters
and
azobenzene-functionalized
ligands.
NUT-103
displays
permanent
porosity
reversible
properties.
Photoregulating
adsorption
CO2
was
realized
for
regulation
efficiency
reach
55%,
while
that
CH4
N2
is
only
7%
3%,
respectively.
Grand
Canonical
Monte
Carlo
simulations
demonstrate
photoregulation
property
attributed
variation
capacity
in
interstitial
region
adjacent
cages.
Moreover,
be
dissolved
form
discrete
recovered
simple
recrystallization.
The
similar
behavior
fresh
sample.
ACS Applied Materials & Interfaces,
Journal Year:
2023,
Volume and Issue:
15(8), P. 11004 - 11015
Published: Feb. 18, 2023
Developing
an
artificial
dynamic
nanoscale
molecular
machine
that
dissipatively
self-assembles
far
from
equilibrium
is
fundamentally
important
but
significantly
challenging.
Herein,
we
report
self-assembling
light-activated
convertible
pseudorotaxanes
(PRs)
show
tunable
fluorescence
and
enable
deformable
nano-assemblies.
A
pyridinium-conjugated
sulfonato-merocyanine
derivative
(EPMEH)
cucurbit[8]uril
(CB[8])
form
the
2EPMEH
⊂
CB[8]
[3]PR
in
a
2:1
stoichiometry,
which
phototransforms
into
transient
spiropyran
containing
1:1
EPSP
[2]PR
when
exposed
to
light.
The
thermally
relaxes
(reversibly)
dark
accompanied
by
periodic
changes
include
near-infrared
emission.
Moreover,
octahedral
spherical
nanoparticles
are
formed
through
dissipative
self-assembly
of
two
PRs,
Golgi
apparatus
dynamically
imaged
using
fluorescent
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Nov. 20, 2023
The
forthcoming
generation
of
materials,
including
artificial
muscles,
recyclable
and
healable
systems,
photochromic
heterogeneous
catalysts,
or
tailorable
supercapacitors,
relies
on
the
fundamental
concept
rapid
switching
between
two
more
discrete
forms
in
solid
state.
Herein,
we
report
a
breakthrough
"speed
limit"
molecules
example
sterically-demanding
spiropyran
derivatives
through
their
integration
within
solvent-free
confined
space,
allowing
for
engineering
photoresponsive
moiety
environment
tailoring
photoisomerization
rates.
presented
conceptual
approach
realized
construction
results
~1000
times
enhancement
even
state
compared
to
its
behavior
solution,
setting
record
field
compounds.
Moreover,
distinct
moieties
same
framework
provided
access
dynamic
range
rates
as
well
complementary
material's
optical
profile,
uncovering
previously
inaccessible
pathway
interstate
photoisomerization.
Chemical Science,
Journal Year:
2023,
Volume and Issue:
14(33), P. 8823 - 8830
Published: Jan. 1, 2023
Development
of
robust
multi-color
photoswitchable
fluorescent
probes
is
critical
for
many
optical
applications,
but
it
remains
a
challenge
to
rationally
design
these
probes.
Here,
we
report
new
Förster
resonance
energy
transfer-based
dual-color
nanoparticles
(DPF
NPs)
by
taking
advantage
the
distinct
properties
ligand-protected
gold
nanoclusters
(AuNCs).
Detailed
photophysical
studies
revealed
that
ultrasmall-sized
AuNCs
not
only
act
as
FRET
donors
due
their
intrinsic
fluorescence
properties,
also
play
significant
role
in
regulating
photochromic
and
aggregate
spiropyran
through
ligand-spiropyran
interactions.
These
DPF
NPs
exhibit
high
on/off
ratio
(∼90%)
both
green
red
emission,
good
reversibility
during
cycled
photo-stimulation.
Cell
imaging
experiments
showed
could
specifically
accumulate
lipid
droplets,
enable
living
cells.
Moreover,
labeling
mitochondria
with
green-emitting
marker,
demonstrated
can
distinguish
different
targets
based
on
dynamic
static
signals
at
sub-cellular
level
two
emission
channels
reliably.
This
study
provides
strategy
designing
modulating
dyes
nanoclusters,
which
be
generalized
development
other
photoswitch
systems
towards
advanced
applications.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(38)
Published: June 26, 2024
The
booming
demand
on
data
security
has
aroused
great
interest
for
developing
smart
materials
with
temporal
display
feature
and
dynamic
multicolor
fluorescence.
However,
it
remains
challenging
to
implement
both
features
most
responsive
molecules.
Herein,
we
construct
a
polymer
free
volume-controlled
"molecular
clock
emitter"
via
covalently
embedding
multi-stimuli
molecular
switch
(i.e.,
spiropyran)
into
network
poly(pentafluorophenyl
acrylate))
programmable
crosslink
density
volume.
By
the
aminolysis
of
pentafluorophenyl
ester
different
amount
diamine
crosslinkers,
pPFPA-co-SP
networks
controllable
densities
are
generated,
which
have
confinement
effects
rate
constant
SP/MC
isomerization,
thus
leading
time-dependent
photochromism.
In
addition,
PTF1,
fluorescent
probe
that
is
sensitive
rigidity,
introduced
further
endow
system
phototunable
full-color
emission.
Therefore,
relying
their
synergistical
responses
rigidity
network,
successfully
developed
versatile
emitter
an
"one
stone
two
birds"
manner,
shows
along
fluorescence
switching,
providing
potential
advanced
encryption
anticounterfeiting
high
level.
Chemical Science,
Journal Year:
2024,
Volume and Issue:
15(17), P. 6218 - 6228
Published: Jan. 1, 2024
Photoswitchable
fluorescent
nanoparticles
(PF
NPs)
are
an
emerging
type
of
optical
nanomaterial
with
distinct
photo-responsive
properties,
which
have
shown
promising
applications
in
diverse
fields
recently.
Advanced Materials,
Journal Year:
2023,
Volume and Issue:
35(41)
Published: July 3, 2023
Most
elastomers
undergo
strain-induced
crystallization
(SIC)
under
tension;
as
individual
chains
are
held
rigidly
in
a
fixed
position
by
an
applied
strain,
their
alignment
along
the
strain
field
results
shift
from
strain-hardening
(SH)
to
SIC.
A
similar
degree
of
stretching
is
associated
with
tension
necessary
accelerate
mechanically
coupled,
covalent
chemical
responses
mechanophores
overstretched
chains,
raising
possibility
interplay
between
macroscopic
response
SIC
and
molecular
mechanophore
activation.
Here,
thiol-yne-derived
stereoelastomers
doped
covalently
dipropiolate-derivatized
spiropyran
(SP)
(0.25-0.38
mol%)
reported.
The
material
properties
SP-containing
films
consistent
undoped
controls,
indicating
that
SP
reporter
mechanical
state
polymer.
Uniaxial
tensile
tests
reveal
correlations
mechanochromism
SIC,
which
strain-rate-dependent.
When
mechanochromic
stretched
slowly
point
activation,
tethered
remains
trapped
force-activated
state,
even
after
stress
removed.
Mechanophore
reversion
kinetics
correlate
rate,
resulting
highly
tunable
decoloration
rates.
Because
these
polymers
not
crosslinked,
they
recyclable
melt-pressing
into
new
films,
increasing
potential
range
strain-sensing,
morphology-sensing,
shape-memory
applications.