Journal of Materials Chemistry C,
Journal Year:
2024,
Volume and Issue:
12(25), P. 9112 - 9129
Published: Jan. 1, 2024
Revealing
the
photobehaviour
of
a
new
BTD-based
HOF
shows
occurrence
intramolecular
charge-transfer
and
intermolecular
proton-transfer
photoevents
leading
to
different
emission
spectra
lifetimes
when
compared
molecular
units.
Chemical Society Reviews,
Journal Year:
2023,
Volume and Issue:
52(19), P. 6715 - 6753
Published: Jan. 1, 2023
This
review
not
only
highlights
the
progress
of
emission
and
electronic
behaviour
new
pyrene-based
luminescence
molecules
in
aggregated
state,
but
also
provides
a
perspective
for
understanding
mechanism
optoelectronic
properties
pyrenes.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: June 17, 2022
Clusteroluminogens
refer
to
some
non-conjugated
molecules
that
show
visible
light
and
unique
electronic
properties
with
through-space
interactions
due
the
formation
of
aggregates.
Although
mature
systematic
theories
molecular
photophysics
have
been
developed
study
conventional
conjugated
chromophores,
it
is
still
challenging
endow
clusteroluminogens
designed
photophysical
by
manipulating
interactions.
Herein,
three
donor-acceptor
structures
different
halide
substituents
are
synthesized.
These
compounds
multiple
emissions
even
single-molecule
white-light
emission
in
crystalline
state.
The
intensity
ratio
these
easily
manipulated
changing
atom
excitation
wavelength.
Experimental
theoretical
results
successfully
disclose
nature
emissions:
conjugation
for
short-wavelength
fluorescence,
charge
transfer
based
on
secondary
long-wavelength
room-temperature
phosphorescence.
introduction
not
only
enriches
their
varieties
but
also
inspires
establishment
novel
aggregate
clusteroluminescence.
Angewandte Chemie International Edition,
Journal Year:
2022,
Volume and Issue:
61(37)
Published: July 16, 2022
Dynamic
patterns
based
on
luminescent
materials
play
an
essential
role
in
the
digital
age.
However,
it
is
still
challenging
to
develop
highly
emissive
photofluorochromic
with
dynamic
behaviors
store
information
multiple
characteristics.
Here,
we
report
a
series
of
dihydroazulene-based
compounds
which
show
typical
aggregation-induced
emission
(AIE)
effect.
Moreover,
photo-switching
ability
dihydroazulene
units,
undergoing
light-induced
ring-opening,
enables
properties.
The
photofluorochromism
also
shows
quantitively
described
responses
time
and
temperature
via
reverse
ring-closing
process.
Ultimately,
rewritable
4D
system,
embedded
quick
response
code,
dot
matrix
microstructures,
color
fluorescence,
time/temperature-dependent
intensity
change,
established
patterns.
This
work
not
only
develops
AIE
skeleton
properties
but
provides
new
strategy
for
encryption
cybernetics.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(8)
Published: Jan. 2, 2024
The
length
and
mode
of
conjugation
directly
affect
the
molecular
electronic
structure,
which
has
been
extensively
studied
in
through-bond
(TBC)
systems.
Corresponding
research
greatly
promotes
development
TBC-based
luminophores.
However,
how
through-space
(TSC),
one
kind
weak
interaction,
influence
photophysical
properties
non-conjugated
luminophores
remains
a
relatively
unexplored
field.
Here,
we
unveil
non-linear
relationship
between
TSC
emission
characteristics
systems,
contrast
to
reported
proportional
correlation
TBC
More
specifically,
oligo(phenylene
methylene)s
(OPM[4]-OPM[7])
exhibit
stronger
prominent
blue
clusteroluminescence
(CL)
(≈440
nm)
compared
shorter
counterparts
(OPM[2]
OPM[3]).
OPM[6]
demonstrates
highest
solid-state
quantum
yield
(40
%),
emphasizing
importance
balancing
flexibility
rigidity.
Further
theoretical
calculations
confirmed
that
CL
these
was
determined
by
stable
derived
from
inner
rigid
Diphenylmethane
(DPM)
segments
within
oligomers
instead
outer
ones.
This
discovery
challenges
previous
assumptions
adds
new
dimension
understanding
TSC-based
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Jan. 7, 2025
Developing
donor-acceptor
[n]cycloparaphenylenes
(D-A
[n]CPPs)
with
multiple
emissions
from
different
emissive
states
remains
challenging
yet
crucial
for
achieving
white-light
emission
in
single-molecule.
Here,
we
report
our
explorations
into
acceptor
engineering
of
quinone-based
D-A
[10]CPPs
(Nq/Aq/Tq[10]CPPs)
via
a
post-lateral
annulation
using
Diels-Alder
reactions
oxTh[10]CPP.
X-ray
analysis
reveals
that
Nq[10]CPP
displays
side
by
packing
naphthoquione
stacking
while
Aq[10]CPP
adopts
an
intercalated
conformation
through
anthraquinone
interaction.
Fluorescence
investigations
reveal
the
display
distinctive
acceptor-dependent
dual-emission
both
locally
excited
state
and
charge
transfer
after
single-wavelength
excitation
organic
solvents,
consequently
leading
to
multicolor
emissions,
particular,
CHCl3
Aq[10]CPP.
In
THF/water
mixture,
oxTh[10]CPP
wide
range
fluorescence
including
as
increasing
fraction
water,
accompanying
formation
nanoparticles
demonstrated
Tyndall
effect
SEM.
Interestingly,
can
be
switched
white
blue
upon
redox.
Our
demonstrate
not
only
endows
two
distint
but
also
highlights
effective
post-synthetic
strategy
functionalizing
CPP
nanohoops
desirable
properties.
authors
yield
emission.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: June 24, 2023
Abstract
Proximity
effect,
which
refers
to
the
low-lying
(
n
,π*)
and
(π,π*)
states
with
close
energy
levels,
usually
plays
a
negative
role
in
luminescent
behaviors
of
heterocyclic
luminogens.
However,
no
systematic
study
attempts
reveal
manipulate
proximity
effect
on
properties.
Here,
we
report
series
methylquinoxaline
derivatives
different
electron-donating
groups,
show
photophysical
properties
aggregation-induced
emission
behaviors.
Experimental
results
theoretical
calculation
gradually
changed
levels
coupling
effects
closely
related
states,
intrinsically
regulate
these
With
intrinsic
nature
heterocycle-containing
compounds,
they
are
utilized
for
sensors
information
encryption
dynamic
responses
acid/base
stimuli.
This
work
reveals
both
positive
impacts
systems
provides
perspective
develop
functional
responsive
luminogens
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: July 30, 2024
Different
from
traditional
organic
luminescent
materials
based
on
covalent
delocalization,
clusteroluminescence
nonconjugated
luminogens
relies
noncovalent
through-space
conjugation
of
electrons.
However,
such
spatial
electron
delocalization
is
usually
weak,
resulting
in
low
efficiency
and
board
emission
peak
due
to
multiple
vibrational
energy
levels.
Herein,
several
are
constructed
by
employing
biphenyl
as
the
building
unit
reveal
structure-property
relationship
solve
current
challenges.
The
intramolecular
can
be
gradually
strengthened
introducing
units
stabilized
rigid
molecular
skeleton
intermolecular
interactions.
Surprisingly,
narrowband
with
full
width
at
half-maximum
40
nm
100%
successfully
achieved
via
an
asymmetric
conformation,
exhibiting
comparable
performance
conjugated
luminogens.
This
work
realizes
highly
efficient
highlights
essential
role
structural
conformation
manipulating
photophysical
properties
unconventional
materials.
Chemical Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
A
novel
rigid
macrocycle
with
aggregation-induced
emission
(AIE)
properties
was
facilely
synthesized
to
construct
efficient
artificial
light-harvesting
systems
for
photocatalysis
through
the
Förster
resonance
energy
transfer
process.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(25)
Published: Feb. 28, 2024
Abstract
Fluorescent
organic
nanoparticles
(NPs)
with
exceptional
brightness
hold
significant
promise
for
demanding
fluorescence
bioimaging
applications.
Although
considerable
efforts
are
invested
in
developing
novel
dyes
enhanced
performance,
augmenting
the
of
conventional
fluorophores
is
still
one
biggest
challenges
to
overcome.
This
study
presents
a
supramolecular
strategy
constructing
ultrabright
fluorescent
aqueous
media
(referred
as
“Supra‐fluorophores”)
derived
from
fluorophores.
To
achieve
this,
this
course
has
employed
cylindrical
nanoparticle
hydrophobic
microdomain,
assembled
by
cyclic
peptide‐diblock
copolymer
conjugate
water,
scaffold.
The
noncovalent
dispersion
fluorophore
moieties
within
microdomain
scaffold
effectively
mitigates
undesired
aggregation‐caused
quenching
and
resulting
NPs
high
brightness.
applicable
broad
spectrum
families,
covering
polyaromatic
hydrocarbons,
coumarins,
boron‐dipyrromethenes,
cyanines,
xanthenes,
squaraines.
demonstrate
quantum
yield
(>30%)
per
volume
(as
12
060
m
−1
cm
nm
−3
).
Moreover,
high‐performance
emission
NIR
region
constructed,
showcasing
up
20‐fold
increase
both
photostability.
Supra‐fluorophore
offers
versatile
effective
method
transforming
existing
into
environments,
applications
such
bioimaging.