Advanced Optical Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 3, 2024
Abstract
Development
of
chiral
aggregation‐induced
emission
(AIE)
materials
toward
hierarchical
self‐assembly
is
crucial
to
reveal
the
origin
and
evolution
life.
In
this
work,
a
pair
AIE
enantiomers
fabricated
by
attaching
typical
units
binaphthyl
core
via
single
bond
linkage.
The
behavior
inherited
from
introduced
unit
while
can
not
only
improve
photo‐physical
properties
but
also
provide
whole
molecules
with
chirality.
Moreover,
as
driven
dipolar
structure
chirality
AIEgens,
different
morphologies
such
spheres,
ribbons
or
fibers,
flowers,
even
bigger
structures
various
sizes
be
dynamically
monitored
assembled
time,
which
provided
favorable
evidence
study
structural
molecular
level
higher‐level
structure.
On
other
hand,
these
AIEgens
act
strong
electronic
acceptors
due
unit.
By
complexing
them
donors,
resulting
intermolecular
charge
transfer
induce
remarkable
red
emissions
tunable
much
their
individuals.
This
enabled
it
facile,
economic,
flexible
approach
develop
organic
photoelectric
materials.
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(47)
Published: Aug. 13, 2024
Abstract
Tuning
full‐color
emission
of
polymers
holds
significant
promise.
However,
preparing
unconventional
luminescence
with
color‐tunability
in
dilute
solution
and
understanding
the
relationship
between
non‐covalent
interactions
luminescent
behavior
remains
a
great
challenge.
We
report
two
emitters
(P1
P2)
incorporating
tetracoordinate
boron.
The
P1
non‐conjugated
D‐π‐A
structure,
exhibited
red
delayed
fluorescence
at
645
nm
quantum
yield
9.15
%
aggregates.
Notably,
wavelength
can
be
tuned
from
418
to
588
different
solvent.
Similarly,
P2
also
adjusted
by
manipulating
solvent
fluorophore.
Experimental
characterization
theoretical
calculations
indicate
that
B←N
bond
electronic
fluorophore
significantly
regulate
equilibrium
electrostatic
potential
(ESP)
intramolecular
O⋅⋅⋅O
P1,
thereby
modulating
its
wavelength.
Additionally,
these
showed
excellent
fluoride
ions
detection.
This
work
provides
new
insights
into
complex
effects
intermolecular
on
properties.
Luminescence,
Journal Year:
2024,
Volume and Issue:
39(9)
Published: Sept. 1, 2024
Abstract
Herein,
we
describe
the
design
and
development
of
a
new
cell‐permeable
aggregation‐induced
emission
(AIE)
active
3
‐ethoxysalicylaldimine‐based
symmetrical
azine
molecule
HDBE
.
The
synthesized
compound
underwent
comprehensive
investigation
different
spectroscopic
methods,
like
NMR,
mass
single
crystal
X‐ray
diffraction
analysis.
fluorophore
exhibited
bright
orange
colour
AIE
behaviour
in
THF–H
2
O
mixture.
drastic
enhancement
was
achieved
upon
adding
water
to
THF
solution
,
with
concentration
90%.
Along
dynamic
light
scattering
(DLS)
quantum
yield
measurements,
formation
aggregates
also
verified
by
scanning
electron
microscopy
(SEM)
transmission
(TEM)
Further,
demonstrated
excited
state
intramolecular
proton
transfer
(ESIPT)
characteristics
polarity
solvents,
which
corroborated
absorption,
lifetime
spectroscopical
investigations.
detailed
scrutiny
structure
displayed
two
strong
hydrogen
bonding
interactions,
while
solid‐state
fluorescent
spectra
showed
dual
that
corresponds
enol
keto
form
confirming
ESIPT
feature.
non‐toxic
cell‐permeable,
making
it
easy
label
as
biomarker
live
HeLa
cells
via
bioimaging.
These
studies
offer
quick
way
develop
both
ESIPT‐coupled
molecules
for
cell
bioimaging
applications.
Advanced Optical Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 3, 2024
Abstract
Development
of
chiral
aggregation‐induced
emission
(AIE)
materials
toward
hierarchical
self‐assembly
is
crucial
to
reveal
the
origin
and
evolution
life.
In
this
work,
a
pair
AIE
enantiomers
fabricated
by
attaching
typical
units
binaphthyl
core
via
single
bond
linkage.
The
behavior
inherited
from
introduced
unit
while
can
not
only
improve
photo‐physical
properties
but
also
provide
whole
molecules
with
chirality.
Moreover,
as
driven
dipolar
structure
chirality
AIEgens,
different
morphologies
such
spheres,
ribbons
or
fibers,
flowers,
even
bigger
structures
various
sizes
be
dynamically
monitored
assembled
time,
which
provided
favorable
evidence
study
structural
molecular
level
higher‐level
structure.
On
other
hand,
these
AIEgens
act
strong
electronic
acceptors
due
unit.
By
complexing
them
donors,
resulting
intermolecular
charge
transfer
induce
remarkable
red
emissions
tunable
much
their
individuals.
This
enabled
it
facile,
economic,
flexible
approach
develop
organic
photoelectric
materials.