Revealing the excited-state mechanisms of the polymorphs of a hot exciton material
Ziqi Deng,
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Chao Huang,
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Yunfeng Luo
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et al.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Jan. 2, 2025
As
the
investigation
of
high
efficiency
thermally
activated
delayed
fluorescence
(TADF)
materials
become
more
mature,
regulating
emission
properties
for
single
organic
luminescence
molecules
has
gained
increasing
interest
recently.
Herein,
donor-acceptor
compounds
F-AQ
comprised
fluorene
and
anthraquinone
is
reported,
it
exhibits
a
polymorphism
with
muti-color
TADF
from
high-level
intersystem
crossing
(hRISC).
The
photodynamics
excited-state
transient
species
were
studied
by
femtosecond
absorption
(fs-TA)
spectroscopy.
result,
an
unambiguous
signal
through
space
charge
transfer
(TSCT)
was
observed
in
fs-TA
spectra
crystal
π-π
interaction
between
groups,
whereas
other
amorphous
solids
only
show
conventional
deactivation
pathway
hRISC-TADF.
In
this
study,
we
successfully
realize
direct
observation
morphism-dependent
TSCT
crystal,
which
provides
observations
solid-state
ultrafast
dynamics
deepens
insight
into
design
potential
mechanochromic
thermochromic
utilization
molecules.
There
hot
exciton
multi-colour
solid
states
luminescent
Here,
authors
report
on
polymorph
dependent
differences
behaviours.
Language: Английский
Single-Component Thioxanthone-Based Photoinitiator for Free-Radical Photopolymerization of Acrylates via UV-LED Irradiation
Saihe Yang,
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Pengzhong Chen,
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Haichao Fu
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et al.
Dyes and Pigments,
Journal Year:
2025,
Volume and Issue:
unknown, P. 112640 - 112640
Published: Jan. 1, 2025
Language: Английский
Pyrazino[2,3‐f][1,10]phenanthroline Derivatives for Oxygen‐Tolerant Dual Photoredox/Copper Catalyzed Atom Transfer Radical Polymerization with Ultra‐low Catalyst Dosage
Wanchao Hu,
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Bei Liu,
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Shiyi Li
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et al.
Chinese Journal of Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 20, 2025
Comprehensive
Summary
Substantial
progress
has
been
made
over
recent
years
in
visible
light‐driven
dual
photoredox/copper
catalyzed
atom
transfer
radical
polymerization
(photo‐ATRP)
through
the
design
of
photocatalysts
(PCs)
and
optimization
reaction
conditions.
However,
it
remains
challenging
to
achieve
efficient
photo‐ATRP
with
low
loadings
both
photocatalyst
copper(II).
In
this
study,
two
donor‐acceptor
organic
PCs
based
on
pyrazino[2,3‐
f
][1,10]phenanthroline
were
successfully
used
Cu(II)‐mediated
photo‐ATRP.
These
exhibit
excellent
light
absorption
capabilities
thermally
activated
delayed
fluorescence
(TADF)
properties.
Under
blue
irradiation,
facilitated
highly
oxygen‐tolerant
an
extremely
catalyst
loading
(50
ppb).
This
system
demonstrated
a
broad
applicability
various
monomers,
achieving
successful
methacrylates,
acrylates,
styrene.
Additionally,
large
scale
(250
mL)
was
achieved,
resulting
narrow
molecular
weight
polymers
high
monomer
conversions
chain‐end
fidelity.
work
provides
in‐depth
investigation
into
regulatory
process
photo‐ATRP,
offering
new
insights
intricate
mechanism
oxygen
tolerance.
Language: Английский
Through-Space Electron Effect Regulated Selective Expression of Ultralong Organic Room Temperature Phosphorescence and Photochromism
Lin Han,
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Youshi Lan,
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Xingda Zhang
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et al.
ACS Applied Materials & Interfaces,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 16, 2025
We
report
a
through-space
electron
effect
(TSEE)
between
two
phosphorescent
units
that
significantly
modulates
the
selective
expression
of
ultralong
organic
room-temperature
phosphorescence
(UORTP)
and
photochromism.
A
series
molecules
(DNapTr,
DNapBNT,
DNapFL,
DNapPy),
featuring
connected
by
nonconjugated
spacer,
were
synthesized.
Our
findings
reveal
both
TSEE
energy
gap
ΔE
(defined
as
EPU2
-
EPU1)
lowest
triplet
levels
(T1)
play
crucial
roles
in
determining
UORTP
photochromic
behavior
PMMA
films.
NMR
spectra
molecular
simulations
confirm
presence
TSEE,
with
their
strength
ranked
DNapPy
<
DNapFL
DNapBNT
TSEE.
The
DNap
unit
is
governed
where
moderate
inhibits
radical
cation
formation,
while
strong
promotes
it.
Consequently,
DNapTr,
exhibit
tunable
photochromism,
whereas
remains
nonphotochromic.
jointly
influenced
ΔE.
For
DNapTr
(ΔE
>
0),
excitons
are
trapped
via
leading
to
from
DNap.
In
slightly
<0),
directs
PU2.
≪
enables
Py.
By
leveraging
tuning
T1
PU2,
we
successfully
modulated
photochromism
UORTP.
This
study
provides
strategy
for
designing
intelligent
materials.
Language: Английский
Space-confined charge transfer turns on multicolor emission in metal-organic frameworks via pressure treatment
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: May 5, 2025
Single-component
multi-emissive
materials
with
stimuli-responsive
properties
offer
unique
advantages
in
the
field
of
multicolor-tunable
photoluminescence
(PL).
However,
precisely
modulating
emission
each
component
and
achieving
high-efficiency
present
a
formidable
challenge.
Herein,
we
demonstrate
that
space-confined
charge
transfer
(CT)
turns
on
bright
blue-green-white
initially
faintly
emissive
metal-organic
frameworks
(MOFs)
at
ambient
conditions
through
pressure
treatments.
Pressure
treatments
induce
transition
from
initial
long-range
CT
to
mode,
significantly
amplifying
radiative
transitions.
Furthermore,
CT,
which
occurs
between
mutually
perpendicular
ligands,
influences
spin-orbit
intersystem
crossing.
Precise
tuning
kinetics
via
multi-level
allows
us
modulate
fluorescence-to-phosphorescence
ratio,
target
MOFs.
Our
work
advances
development
smart
PL
unlocks
potential
for
their
application
atmospheric
environments.
Language: Английский
ONOO- regulating ICT of mitochondria-targeted photosensitizers to enhance Type-I photochemical reactions
Sensors and Actuators B Chemical,
Journal Year:
2024,
Volume and Issue:
unknown, P. 136810 - 136810
Published: Oct. 1, 2024
Language: Английский
Enhanced Circularly Polarized Luminescence Modulation Using Dichroic Conjugated Polymer in Cholesteric Liquid Crystals
Yihan Chen,
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Lulu Li,
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Kun Yao
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et al.
Advanced Optical Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 25, 2024
Abstract
Negative
dichroic
dyes
are
crucial
for
enhancing
the
brightness
of
liquid
crystal
displays
(LCDs)
and
modulating
circularly
polarized
luminescence
(CPL)
in
cholesteric
crystals
(CLCs)
through
supramolecular
co‐assembly.
However,
majority
fluorescent
molecules
exhibit
positive
dichroism,
there
is
a
limited
understanding
designing
negative
molecules.
In
this
paper,
novel
design
principle
proposed
to
construct
polymer
by
introducing
space
charge
transfer
(TSCT)
side
chain
structure
backbone.
Specifically,
two
conjugated
polymers
(P1,
P2)
synthesized
using
Suzuki
coupling
reaction
donor‐acceptor
(D‐A)
type
monomers
(V‐type
M1
I‐type
M2)
with
fluorenyl
monomer.
P1
exhibits
its
orientational
order
parameter
(S
F
)
up
S
FP1
=
–0.18.
On
contrary,
P2
dichroism
(
FP2
+
0.27).
This
variation
arises
from
differing
orientations
rigidly
functional
chains
FM1
0.07;
FM2
0.31),
which
affect
alignment
(parallel
or
perpendicular)
backbone
toward
CLCs
phenomenon
facilitates
controllable
precisely
modulates
handedness
CPL
signals,
thereby
facilitating
successful
implementation
multidimensional
information
encryption
systems
CLCs.
Language: Английский