ACS Macro Letters,
Journal Year:
2025,
Volume and Issue:
unknown, P. 265 - 271
Published: Feb. 13, 2025
N-(o-Cyanophenyl)carbazole
can
be
dimerized
at
different
positions,
which
may
change
excited
state
behaviors.
Herein,
2,3′-dicyano-3,4′-di(carbazol-9-yl)biphenyl
(D34C)
is
designed
and
synthesized
doped
into
polymers.
However,
we
find
that
D34C
does
not
exhibit
room
temperature
phosphorescence
but
emits
fluorescence
(FL)
bright
thermally
activated
delayed
(TADF)
with
lifetimes
of
hundreds
milliseconds,
observed
in
diverse
matrices
such
as
PMMA,
MBS,
ABS,
PS,
HIPS,
SIS.
The
simple
positional
isomerization
makes
the
abundant
triplet
excitons
undergo
only
reverse
intersystem
crossing
rather
than
(RTP)
radiation,
rare
organic
Since
production
TADF
afterglow
requires
a
certain
excitation
time,
generally
indistinguishable
FL
efficiencies
are
separated
for
first
time.
This
work
provides
novel
polymers
mechanical
properties
also
will
evoke
subtle
design
conjugated
molecules
to
dramatically
photoexcitation
emission
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(28)
Published: May 17, 2024
Abstract
Organic
near‐infrared
(NIR)
room
temperature
phosphorescence
(RTP)
materials
become
a
hot
topic
in
bioimaging
and
biosensing
for
the
large
penetration
depth
high
signal‐to‐background
ratio
(SBR).
However,
it
is
challenging
to
achieve
persistent
NIR
severe
nonradiative
transitions
by
energy‐gap
law.
Herein,
universal
system
with
RTP
built
visible
(host)
(guest)
materials,
which
can
efficiently
suppress
rigid
environment
of
crystalline
host
good
matching,
further
promote
emission
additional
resonance
energy
transfer
(≈100%)
between
them.
The
ten‐folds
enhancement
lifetimes,
compared
those
guest
luminogens,
be
achieved
modulation
aggregated
structures
host–guest
systems.
This
work
provides
convenient
way
largely
prolong
lifetimes
various
promoting
their
application
afterglow
imaging
deeper
higher
SBRs.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(27)
Published: Feb. 25, 2024
Abstract
Despite
multifunctional
theranostics
hold
vast
potential
in
deep
tissue
bioimaging
and
tumor
therapy,
activatable
nanomedicine
with
integration
of
precise
diagnosis
effective
treatment
is
usually
achieved
at
the
cost
complicated
synthesis
chemistries.
Here,
a
facile
way
to
design
bioresponsive
Ag
2
S‐Ag
Janus
probes
coated
by
polyethylene
glycol
(PEG)
(denoted
as
AAP)
showed,
active
second
near‐infrared
window
(NIR‐II,
1000–1700
nm).
In
microenvironment,
part
can
yield
hydroxyl
radicals
(·OH)
consuming
H
O
for
high‐efficiency
chemodynamic
therapy
(CDT),
while
S
has
impressive
photothermal
(PTT).
The
synergistic
benefits
from
parts
further
boosted
CDT
effect
AAP
high
conversion
efficiency
up
56.8%.
Moreover,
multiple
lines
evidence
supported
that
extremely
faint
fluorescence
be
significantly
activated
overexpressed
levels
,
showing
bright
NIR‐II
emission
≈1270
nm
over
5.6
×
10
3
‐fold
increase
signal
intensity.
are
easily
imaging
tumor‐specific
identification,
effectively
ablate
tissues
inhibition
rate
96.2%.
This
study
expects
probe
will
open
new
route
achieve
window.
Accounts of Chemical Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 5, 2025
ConspectusBiomarkers
play
a
vital
role
in
the
regulation
of
life
processes,
especially
predicting
occurrence
and
development
diseases.
For
early
diagnosis
precise
treatment
diseases,
it
has
become
necessary
significant
to
detect
biomarkers
with
sensitivity,
accuracy,
simplicity,
convenience,
even
visualization.
Fluorescent-probe-based
techniques
have
been
recognized
as
one
most
powerful
tools
for
sensitive
detection
real
time
imaging
biological
samples.
However,
traditional
optical
probes,
mainly
including
visible
probes
(400–700
nm)
near-infrared
I
(NIR-I,
700–900
suffer
from
low
poor
resolution,
strong
absorption
scattering,
high
background
fluorescence,
which
hinder
effective
monitoring
biomarkers.Fortunately,
past
decade
witnessed
remarkable
evolution
application
fields
II
(NIR-II,
900–1700
driven
by
its
exceptional
characteristics
advancement
technologies.
Leveraging
superior
penetration
capabilities,
negligible
autofluorescence,
extended
fluorescence
emission
wavelengths,
NIR-II
fluorescent
significantly
enhance
signal-to-noise
ratio
(SNR)
vitro
(IVD)
temporal
resolution
vivo
imaging.
Our
team
committed
design
strategy,
controlled
synthesis,
luminous
mechanisms,
biomedical
applications
probes.
In
this
Account,
we
present
representative
works
recent
years
our
group
field
analytical
applications,
ranging
different
various
also
will
further
provide
general
overview
First,
are
fully
summarized,
tumor
marker
detection,
virus
bacteria
analysis,
cell
testing,
small-molecule
sensing.
Second,
adequately
discussed,
ROS
gas
monitoring,
pH
sensing,
receptor
some
serious
Finally,
outline
advantages
discuss
detail
challenges
well
their
future
development.
There
is
reasonable
prospect
that
technology
based
on
exhibit
great
potential
research
clinical
disease
diagnosis.
We
hope
Account
can
expand
reach
into
an
broader
spectrum
fields,
enhancing
impact
scientific
discovery
medical
practice.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(38)
Published: July 4, 2024
Noncovalent
spatial
interaction
has
become
an
intriguing
and
important
tool
for
constructing
optoelectronic
molecules.
In
this
study,
we
linearly
attached
three
conjugated
units
in
a
multi
π-stacked
manner
by
using
just
one
trident
bridge
based
on
indeno[2,1-b]fluorene.
To
achieve
structure,
improved
the
synthetic
approach
through
double
C-H
activation,
significantly
simplifying
preparation
process.
Due
to
proximity
of
C10,
C11,
C12
sites
indeno[2,1-b]fluorene,
derived
two
novel
donor|acceptor|donor
(D|A|D)
type
molecules,
2DMB
2DMFB,
which
exhibited
closely
packed
intramolecular
stacking,
enabling
efficient
through-space
charge
transfer.
This
molecular
construction
is
particularly
suitable
developing
high-performance
thermally
activated
delayed
fluorescence
materials.
With
donor(s)
acceptor(s)
constrained
separated
within
spatially
rigid
elevated
radiative
transition
rates,
high
photoluminescence
quantum
yields
were
achieved.
Organic
light-emitting
diodes
incorporating
2DMFB
demonstrated
superior
efficiency,
achieving
maximum
external
efficiencies
28.6
%
16.2
%,
respectively.
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(46)
Published: July 9, 2024
Abstract
In
recent
years,
there
is
a
growing
interest
in
developing
ultralong
organic
room‐temperature
phosphorescence
(ORTP)
with
lifetimes
the
range
of
seconds.
As
one
important
three
primary
colors,
blue
ORTP
an
indispensable
core
component
RTP
regulation
and
application,
however,
large
Stokes
shift
characteristics
pose
certain
challenges
ORTP.
Here,
new
family
phosphors
are
synthesized
realized
through
crystal
assembly
water
phase.
Remarkably,
compared
to
materials
obtained
phases,
enabled
long‐lived
up
2.3
s
quantum
yield
reached
as
high
29.27%.
addition
efficient
green
form,
such
dark
possessed
thermal
stability
flexible
tunability.
Moreover,
superiority
selected
components
demonstrated
by
comparing
them
polymer
proposed
show
great
potential
programmable
information
encryption/anti‐counterfeiting.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(33)
Published: May 7, 2024
Abstract
Near‐Infrared
(NIR)
phosphorescence
at
room
temperature
is
challenging
to
achieve
for
organic
molecules
due
negligible
spin–orbit
coupling
and
a
low
energy
gap
leading
fast
non‐radiative
transitions.
Here,
we
show
supramolecular
host–guest
strategy
harvest
the
from
low‐lying
triplet
state
of
C
64
nanographene
tetraimide
1
.
H
NMR
X‐ray
analysis
confirmed
:
2
stoichiometric
binding
Pt(II)
porphyrin
on
two
π‐surfaces
While
free
does
not
emission
in
NIR,
complex
solution
shows
NIR
77
K.
Further,
between
860–1100
nm,
(
λ
max
=900
τ
avg
=142
μs)
was
observed
solid‐state
sample
drop‐casted
preformed
solution.
Theoretical
calculations
reveal
non‐zero
isoenergetic
S
T
3
π‐stacked
[
⋅
porphyrin]
complex.
External
heavy‐atom‐induced
along
with
rigidification
protection
oxygen
promotes
both
intersystem
crossing
first
excited
singlet
into
manifold
lowest
Advanced Optical Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 2, 2024
Abstract
Donor–acceptor
(D–A)
structure
with
charge
transfer
(CT)
effect
is
widely
utilized
in
the
construction
of
organic
luminescent
materials.
The
adjustment
their
CT
and
related
property
usually
relies
on
changes
molecular
different
D
or
A
moieties,
which
will
lead
to
some
uncertainties
structure‐property
relationship.
With
aim
explore
clear
inherent
mechanism
for
D–A
molecule
effect,
it
ideal
that
regulation
intramolecular
one
same
can
be
realized.
Accordingly,
three
type
phosphorescence
luminogens
are
designed
synthesized.
Once
being
doped
into
polymer
matrixes,
disparate
effects
room
temperature
(RTP)
properties
achieved
a
single
molecule.
Subsequent
experiments
confirm
distributions
molecules
locally
excited
(LE)
state
mainly
responsible
distinct
RTP
behaviors,
exhibiting
well‐clarified
relationship
luminogens.
Furthermore,
transition
from
LE
even
realized
through
chemical
reaction,
leading
activated
practical
applications.