Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 13, 2025
Abstract
Two
dimeric
tetracene
complexes,
Pt(L
tc
)
2
Cl
and
Pd(L
,
have
been
synthesized
by
coordination
of
a
pyridyl
substituted
acene‐
to
Pt(II)
Pd(II)
metal
center.
The
photophysical
properties
the
two
dimers
are
characterized
compared
with
free
ligand
L
as
well
corresponding
monomeric
complexes
(
)(
ref
)Cl
)(L
shed
light
on
processes
intramolecular
up‐
down‐conversion,
namely
triplet‐triplet
annihilation
singlet
fission,
respectively.
Both
show
high
fluorescence
quantum
yields,
while
emission
is
heavily
reduced
in
complexes.
Dimer
exhibits
efficient
fission
within
1.6
ns
form
correlated
triplet
pair
(T
1
T
),
confirming
that
coupling
mediated
through
over
remarkably
long
inter‐chromophore
distances.
Subsequently,
dissociates
into
triplets
+
yields
ca.
50%.
Moreover,
due
isoenergetic
level
excited
state
for
dimers,
some
observed
undergo
up‐conversion
return
state,
followed
upconverted
fluorescence.
On
other
hand,
photoexcitation
gives
kinetic
behavior
similar
monomer
no
but
fast
intersystem
crossing
hundreds
picoseconds.
It
noted
formation
dimer
low,
non‐radiative
decay
excitons
ground
dominates
both
cases.
all
metal–organic
subtle
intrachromophore
charge‐transfer
characteristics
polar
solvents
schemes
apolar
solvents.
Chemistry - A European Journal,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 29, 2025
Abstract
The
control
of
self‐organized
metal
complexes
presents
advantages
regarding
the
modulation
luminescence
through
dynamic
assembly,
rendering
them
promising
for
bioimaging.
Herein,
we
demonstrate
a
strategy
towards
series
amphiphilic
Pt(II)
featuring
bis‐cyclometalated
ligands
as
tetradentate
luminophores,
which
exhibit
enhanced
water
solubility
and
tuneable
self‐assembly
properties.
resulting
nanostructures
can
be
precisely
controlled
by
adjusting
concentration
solvent
composition,
yielding
switchable
from
red
(
i.
e
.,
excimer‐based)
to
green
monomer‐centred)
reversible
(dis−)assembly
aggregates.
Cytotoxicity
assays
confirmed
innocuous
nature
these
luminophores
at
concentrations
below
10
μM,
while
cellular
uptake
studies
demonstrated
effective
internalization
in
both
living
fixed
cells.
Using
photoluminescence
lifetime
imaging
micro(spectro)scopy,
determined
that
localized
preferentially
within
lysosomes
cells,
accumulating
nuclei
with
differences
photophysical
behavior
depending
on
whether
species
were
monomeric
or
excimeric
nature.
These
new
findings
provide
insights
into
systematic
design
water‐soluble
Pt(II)‐based
properties
supramolecular
interactions,
underlining
their
potential
use
diagnostics.
Advanced Optical Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 15, 2025
Abstract
Luminescent
switches
with
multiple
optical
outputs
are
essential
for
meeting
the
growing
demand
high‐security
encryption.
Herein,
symmetric
and
chiral
molecules
designed
synthesized
by
integrating
luminescent
planar
Pt(II)
moieties
into
SS
/
RR
‐trans‐1,2‐cyclohexane
diamine
scaffolds.
This
approach
enables
correlation
of
structures,
assemblies,
optical/chiroptical
properties
these
materials,
which
exhibit
spacer‐dependent
chiroptical
behavior.
The
more
rigid
foldamer
shows
unusual
switching
from
monomer
to
intramolecular
excimers
corresponding
circular
dichroism
circularly
polarized
luminescence
increasing
temperature,
differing
significantly
conventional
chromophores.
Based
on
its
reversible
sensitive
multicolor
phosphorescence
characteristics,
molecular
is
employed
create
a
stepwise
anticounterfeit
ink,
advancing
anti‐counterfeiting
technology.
ACS Applied Materials & Interfaces,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 15, 2025
Developing
room-temperature
phosphorescence
(RTP)
in
organic-inorganic
hybrid
perovskites
(OIHPs)
with
color
tunability
is
an
attractive
topic
for
investigating
how
the
coupling
between
organic
and
inorganic
components
affects
spin-orbital
effects
triplet
state
energy
transfer.
We
demonstrate
that
modulation
of
spacer
cations
OIHPs
can
effectively
realize
tunable
white-light
RTP.
By
gradually
substituting
2-phenylethylamine
(PEA)
(PEA)2PbBr4
naphthalene-type
(N-naphthyl
methylamine,
NMA),
excitons
be
extracted
from
part
transferred
to
produce
a
In
particular,
OIHP
crystal
stoichiometry
(PEA)0.8(NMA)1.2PbBr4
leads
warm-white
light
due
contribution
additional
ultraviolet
absorption,
which
was
then
exploited
fabricate
phosphorescent
LED.
A
similar
approach
also
applied
1-pyrenemethylamine
(PRMA)
cations.
controlling
content
ratio
PRMA
PEA
molecules,
colorful
emissions
were
realized
(PEA)x(PRMA)2-xPbBr4
(0
≤
x
2).
The
lifetimes
(PEA)1.4(PRMA)0.6PbBr4
are
3.18
ms
at
473
nm
3.02
618
nm,
respectively.
Our
results
provide
effective
strategy
synthesizing
multicolor
by
tuning
different
fluorophore
molecules.
Advanced Functional Materials,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 13, 2025
Abstract
Two
dimeric
tetracene
complexes,
Pt(L
tc
)
2
Cl
and
Pd(L
,
have
been
synthesized
by
coordination
of
a
pyridyl
substituted
acene‐
to
Pt(II)
Pd(II)
metal
center.
The
photophysical
properties
the
two
dimers
are
characterized
compared
with
free
ligand
L
as
well
corresponding
monomeric
complexes
(
)(
ref
)Cl
)(L
shed
light
on
processes
intramolecular
up‐
down‐conversion,
namely
triplet‐triplet
annihilation
singlet
fission,
respectively.
Both
show
high
fluorescence
quantum
yields,
while
emission
is
heavily
reduced
in
complexes.
Dimer
exhibits
efficient
fission
within
1.6
ns
form
correlated
triplet
pair
(T
1
T
),
confirming
that
coupling
mediated
through
over
remarkably
long
inter‐chromophore
distances.
Subsequently,
dissociates
into
triplets
+
yields
ca.
50%.
Moreover,
due
isoenergetic
level
excited
state
for
dimers,
some
observed
undergo
up‐conversion
return
state,
followed
upconverted
fluorescence.
On
other
hand,
photoexcitation
gives
kinetic
behavior
similar
monomer
no
but
fast
intersystem
crossing
hundreds
picoseconds.
It
noted
formation
dimer
low,
non‐radiative
decay
excitons
ground
dominates
both
cases.
all
metal–organic
subtle
intrachromophore
charge‐transfer
characteristics
polar
solvents
schemes
apolar
solvents.