FlexMat.,
Journal Year:
2025,
Volume and Issue:
unknown
Published: June 6, 2025
Abstract
Achieving
control
over
room‐temperature
phosphorescence
(RTP)
performance
through
delicate
molecular
engineering
and
intermolecular
interactions
is
of
great
significance
for
advancing
RTP
research.
In
this
study,
a
series
isomers
containing
up
to
four
compounds
were
synthesized
by
integrating
tetrahydroquinoline
substituent
at
different
positions
phenoxathiine
core.
All
exhibit
afterglow
emission
in
the
crystalline
state,
attributed
diverse
that
stabilize
triplet
excitons.
Notably,
variation
substitution
leads
distinct
interactions,
enabling
fine‐tuned
properties
strategic
engineering.
Among
them,
isomer
2,1‐PXTACR,
which
exhibits
robust
achieves
an
exceptional
duration
exceeding
5
s
average
lifetime
310
ms.
Furthermore,
specific
role
solid‐state
environment
stabilizing
excitons
systematically
elucidated
work.
The
modulation
strategy
established
herein
provides
valuable
insights
into
structure‐property
relationships
governing
materials
offers
rational
approach
developing
high‐performance
purely
organic
phosphorescent
systems.
The Journal of Physical Chemistry Letters,
Journal Year:
2025,
Volume and Issue:
16(2), P. 537 - 543
Published: Jan. 6, 2025
Organic
room-temperature
phosphorescent
(RTP)
materials
have
wide-ranging
applications
in
anticounterfeiting,
biodiagnostics,
and
optoelectronic
devices
due
to
their
unique
properties.
However,
it
remains
a
challenge
give
organic
RTP
dynamic
tunability
satisfy
the
demands
of
various
advanced
applications.
Herein,
we
propose
an
effective
strategy
precisely
modulate
performance
by
incorporating
metal–ligand
coordination
within
host–guest
doped
system.
The
phosphors
bipyridine
derivatives
with
excellent
properties
were
into
small-molecule
host
matrix.
Halide
salts
system
effectively
tuning
performance,
including
efficiency
lifetime,
through
coordination.
Notably,
leveraging
reversible
feature
coordination,
multilevel
information
encryption,
thermal
development
time-resolved
high
reversibility,
is
successfully
demonstrated.
work
demonstrates
that
could
serve
as
method
for
developing
efficient
tunable
Advanced Functional Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 5, 2025
Abstract
Photoactivated
circularly
polarized
afterglow
(CPA)
exhibits
broad
application
prospects
in
various
optoelectronic
areas
due
to
its
multidimensional
emission
characteristics,
including
wavelengths,
lifetimes,
and
chirality.
Achieving
photoactivated
CPA
with
extremely
high
dissymmetry
factor
(
g
lum
)
values
is
highly
desired
but
considerably
challenging.
This
work
reports
a
bilayer
assembly
(R/S‐CLC‐TPB)
integrating
TPB@PMMA
thin
film
the
selective
reflection
of
cholesteric
liquid
crystals.
Initially,
R/S‐CLC‐TPB
no
emission,
while
following
1
min
UV
irradiation,
it
achieves
an
noticeable
long
lifetime
125
ms
value
up
1.6.
enhancement
can
be
attributed
oxygen
consumption
properties
under
subsequently
minimizing
loss
triplet
exciton.
Furthermore,
by
employing
triplet‐singlet
Förster
resonance
energy
transfer
(TS‐FRET)
strategy
from
organic
persistent
room‐temperature
phosphorescence
donor
fluorescent
dye
acceptor,
color
successfully
modulated
green
orange.
Ultimately,
these
materials
demonstrate
promising
capabilities
for
advanced
multi‐level
information
encryption
utilizing
their
tunable
color,
create
multiple
layers
that
selectively
accessed
decoded
based
on
photoactivation
chiroptical
properties.
The Journal of Physical Chemistry C,
Journal Year:
2025,
Volume and Issue:
129(9), P. 4565 - 4574
Published: Feb. 24, 2025
Materials
having
room-temperature
phosphorescence
(RTP)
are
in
limelight
due
to
their
advantageous
long
luminescence
lifespan
for
applications
optoelectronics,
bioimaging,
and
security
purpose
devices.
Development
of
metal-
halogen-free
organics
persistent
RTP
has
been
envisaged
through
aggregation,
heavy
atom
substitution,
host–guest
interactions,
etc.
In
this
article,
we
present
experimental
evidence
the
effect
H-bonding
other
nonbonding
interactions
on
types
emission
five
carbazole
derivatives.
An
unsubstituted
showed
only
fluorescence
powder
form,
while
N-aryl-substituted
carbonyl
nitrile
groups
(Benzal-CN-Cbz,
Acph-CN-Cbz,
Bnph-CN-Cbz)
dual
consisting
form
under
ambient
conditions.
Acph-CN-Cbz
longest
excited-state
lifetime
exceeding
1.2
ms
form.
Benzal-CN-Cbz,
Bnph-CN-Cbz
is
correlated
evident
from
single-crystal
analysis.
involving
group
extensive
π–π
caused
close
packing
solid
state
associated
with
long-lived
triplet
excited
RTP.
Further,
a
up
1.5
s
at
temperature
air
was
displayed
drop-casted
PVA
films.
To
best
our
knowledge,
few
organics,
without
halogen
atoms,
available
such
lifetimes.
Analytical Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 24, 2025
The
uncontrolled
acute
inflammatory
response
triggers
dysregulation
of
the
immunoinflammatory
system,
contributing
to
development
and
progression
various
diseases
(AIDs).
Hypochlorite
(ClO–),
as
a
crucial
oxidative
mediator
in
AIDs,
accumulates
environment,
leading
direct
cytotoxicity,
secondary
injury,
tissue
dysfunction.
However,
achieving
rapid
detection,
accurate
tracking,
situ
monitoring,
real-time
imaging
ClO–
vivo
remains
significant
challenge.
To
address
these
issues,
we
developed
mitochondria-targeted
phosphorescent
probe
(RuDM),
which
introduces
ligand
containing
C═N
bond
recognition
site
precisely
identify
AIDs.
It
responds
rapidly
(6
s)
exhibits
long-lived
luminescence
(471
ns),
with
190-fold
enhancement
monitoring
ClO–.
Meanwhile,
density
functional
theory
(DFT)
indicates
that
RuCOOH
is
attributed
removal
an
electron-withdrawing
group
(diaminomaleonitrile)
from
RuDM,
leads
increase
intersystem
crossing
rate
greater
probability
radiative
transition
T1
state.
Finally,
RuDM
used
monitor
levels
exogenous
endogenous
cells
using
confocal
microscopy
evaluate
its
capability
for
detection
over
time
model.
above
results
suggest
novel
molecular
platform
detect
ClO–,
has
potential
practical
tool
research
on
pathogenesis
diseases.
Advanced Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 8, 2025
Abstract
Dynamic
organic
room‐temperature
phosphorescence
(RTP)
glasses
with
color
tunability
offer
significant
potential
for
practical
applications
due
to
their
high
transparency
and
excellent
machinability.
In
this
study,
efficient
dynamic
RTP
properties
are
used
as
triplet
donors,
combined
commercially
available
chromophores
singlet/triplet
acceptors,
successfully
fabricate
a
series
of
host‐guest
doping
color‐tunable
afterglow
responses
external
stimuli.
The
energy
transfer
mechanisms,
including
triplet‐to‐singlet
resonance
Dexter‐type
triplet‐to‐triplet
transfer,
confirmed
using
state‐of‐the‐art
femtosecond
time‐resolved
transient
absorption
spectroscopy.
These
demonstrate
transparency,
good
machinability,
responsiveness
study
highlights
in
large‐area
glass
fabrication,
data
encryption,
flexible
displays.
This
work
not
only
provides
simple
design
principle
developing
novel
materials
but
also
promotes
the
information
encryption
optoelectronics.