Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 18, 2025
Abstract
Thermochromic
fluorescent
materials
(TFMs)
have
garnered
great
attention
due
to
their
unique
fluorescence
transition
responsive
temperature.
However,
the
application
of
TFMs
is
limited
defects
such
as
low
thermosensitivity
and
a
high
temperature‐responsive
threshold
value.
In
this
case,
work
explores
feasible
strategy
for
designing
TFMs.
On
one
hand,
sterically
hindered
unilateral
tetraphenylethylene
(TPE)
substituent
introduced
into
pyrene
chromophore
in
meta‐
linkage
mode.
This
type
molecular
architecture
aimed
at
integration
both
aggregation‐induced
emission
(AIE)
character
isolated
π–π
dimer
stacking,
facilitating
achievement
contrast
intensity
(i.e.,
strongly
emissive
aggregation
state
versus
weakly
dispersion
state)
color
(
i.e
,
excimer
monomer).
other
an
effective
matrix
platform
featured
with
alky
chain
length‐dependent
temperature‐induced
phase
constructed
assist
fabrication
desired
patterns
through
temperature‐controlled
reversible
between
crystalline
non‐dispersion
liquated
states.
The
findings
demonstrate
that
these
studied
can
be
potentially
applied
temperature
indicators
switchable
dynamic
interior
decoration,
which
provides
new
avenue
design
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(32)
Published: June 24, 2024
Abstract
Ultralong
room‐temperature
phosphorescent
(URTP)
materials
have
attracted
wide
attention
in
anti‐counterfeiting,
optoelectronic
display,
and
bio‐imaging
due
to
their
special
optical
properties.
However,
blue
are
very
scarce
during
applications
because
of
the
need
simultaneously
populate
stabilize
high‐energy
excited
states.
In
this
work,
a
stepwise
stiffening
chromophore
strategy
is
proposed
suppress
non‐radiative
jump
by
continuously
reducing
internal
spin
chromophore,
successfully
developing
series
materials.
Phosphorescence
lifetimes
more
than
3
s
achieved,
with
longest
lifetime
reaching
5.44
lasting
70
naked
eye.
As
far
as
know,
best
result
that
has
been
reported.
By
adjusting
conjugation,
multicolor
phosphorescences
from
cyan
green
realized.
addition,
these
chromophores
exhibit
same
excellent
properties
urea
polyvinyl
alcohmance
(PVA).
Finally,
applied
luminescent
displays.
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 14, 2025
Abstract
Developing
photo‐switch
molecules
that
show
fluorescence
in
both
monomeric
and
aggregated
states,
with
light‐controllable
wavelength
is
far‐reaching
a
great
challenge.
Spiropyran
(SP)
has
received
considerable
attention
this
field.
Herein,
by
conjugating
naphthalimide
to
the
indole
moiety
of
SP,
new
spiropyran
derivative,
named
NMI‐SP
obtained.
shows
dual‐state
emission
excellent
its
attributed
intramolecular
charge
transfer
character.
Moreover,
demonstrates
obvious
photochromic
behavior,
accompanied
visible
color
change
from
yellow
green
THF
solution,
photo‐responsive
orange
red
state.
This
work
provides
insights
into
design
materials
based
on
SP
fluorophore
highlights
their
potential
applications
digital
coding
information
conversion.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 19, 2025
Abstract
Organic
room
temperature
phosphorescence
(ORTP)
polymer
materials
have
sparked
considerable
research
interests
in
recent
years,
but
their
optical
function
is
still
limited
for
multi‐mode
imaging.
Herein,
a
feasible
and
universal
approach
proposed
to
endow
ORTP
with
periodic
refractive
index
modulation
functions
by
holographic
patterning.
The
key
this
design
two‐stage
stepwise
crosslinking.
Stage‐1,
low
crosslinking
density
(≤0.75
mol
L
−1
),
phosphorescence‐silent
can
provide
greater
free
volume
monomer
diffusion
thus
facilitate
the
patterning
of
modulated
holograms
via
photopolymerization‐induced
phase
separation.
dense
at
stage‐2
turn
on
intensity
rising
144%
when
increases
from
3.77
4.12
.
enhanced
primarily
ascribed
increase
conformational
distortion
spin‐orbit
coupling
organic
phosphors
based
theoretical
calculations.
Eventually,
first
example
demonstrated
plastic
unique
capability
independently
displaying
andphosphorescent
images.
This
work
not
only
provides
novel
paradigm
impart
added
also
paves
way
development
high‐security
combat
counterfeiting.
Abstract
Conformational
flexibility
is
essential
to
the
stimuli-responsive
property
of
organic
materials,
but
achieving
reversible
molecular
transformation
still
challenging
in
functional
materials
for
high
energy
barriers
and
restriction
by
intermolecular
interactions.
Herein,
through
incorporation
various
steric
hindrances
into
phenothiazine
derivatives
with
different
positions
quantities
tune
conformations
adjustable
repulsive
forces,
folded
angles
gradually
changed
from
180°
90°
17
compounds.
When
angle
located
at
112°
moderated
effect,
dynamic
under
mechanical
force
has
been
achieved
low
mutually
regulated
motions,
resulting
both
self-recoverable
phosphorescence
properties
first
time.
It
opened
up
a
new
way
realize
self-recovery
which
can
facilitate
multi-functional
smart
avenue
other
fields
inspiration.
The Journal of Physical Chemistry Letters,
Journal Year:
2024,
Volume and Issue:
15(6), P. 1584 - 1589
Published: Feb. 2, 2024
Carbonyl-modified
solid-state
carbon
nitrogen
quantum
dots
(m-O═CNQDs)
have
emerged
as
promising
room-temperature
phosphorescent
(RTP)
materials
close
to
commercialization.
However,
high-crystallinity
m-O═CNQDs
are
insensitive
external
stimuli
such
water
and
heat
due
strong
stacking
interactions
between
layers,
restricting
their
applications
in
stimulus
responsive
fields.
Here,
a
polymer
template
space-confined
growth
strategy
is
established
for
the
large-scale
synthesis
of
polyvinylpyrrolidone-functionalized
with
ultralong
phosphorescence
(181
ms)
using
urea
PVP
precursors.
Theoretical
experimental
results
indicate
that
linked
at
rim
formed
by
situ
self-polymerization
inhibits
layers
increases
affinity
water,
which
key
increasing
sensitivity
water.
This
offers
new
path
developing
commercial
RTP
materials.
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(33), P. 13306 - 13312
Published: Jan. 1, 2024
A
family
of
light-responsive
photoluminescent
materials
with
self-healing
properties
were
obtained
and
applied
in
dynamic
multi-level
information
encryption
applications.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 26, 2024
Abstract
Phosphorescent
supramolecular
hydrogels
are
currently
a
prevalent
topic
for
their
great
promise
in
various
photonic
applications.
Herein,
an
efficient
near‐infrared
(NIR)
phosphorescence
hydrogel
is
reported
via
the
hierarchical
assembly
strategy
aqueous
solution,
which
fabricated
from
amphiphilic
bromonaphthalimide
pyridinium
derivative
(G),
exfoliated
Laponite
(LP)
nanosheets,
and
polymeric
polyacrylamide
(PAAm).
Initially,
G
spontaneously
self‐aggregates
into
spherical
nanoparticles
covered
with
positively
charged
units
emits
single
fluorescence
at
410
nm.
Driven
by
electrostatic
interactions
negatively
subsequently
function
as
cross‐linked
binders
coassemble
LP
engendered
red
room‐temperature
(RTP)
up
to
620
Benefiting
hydrogen‐bonding
interactions‐mediated
physical
cross‐linkage,
further
introduction
of
PAAm
not
only
significantly
elevates
mechanical
strength
showing
fast
self‐healing
capability,
but
also
increases
lifetime
2.49
4.20
ms,
especially
generating
even
higher
temperature
(
τ
363
K
=
2.46
ms).
Additionally,
RTP
energy
transfer
occurs
after
doping
small
amount
organic
dye
heptamethine
cyanine
(IR780)
acceptor
hydrogels,
resulting
long‐lived
NIR
emission
823
nm
high
donor/acceptor
ratio,
successfully
applied
cell
labeling
window.