ACS Sensors,
Год журнала:
2024,
Номер
9(9), С. 4608 - 4616
Опубликована: Авг. 8, 2024
Efficient
and
reliable
technologies
for
the
on-site
detection
of
illicit
drugs
are
important
in
drug-facilitated
crime
investigations.
However,
development
such
is
challenging.
Based
on
synthetic
optimization,
introducing
a
boron
ester
functional
group
to
two
furanic
indicators
endows
stimulus-responsive
properties
synergistically.
The
ring-opening
reaction
presence
amine-containing
generated
well-known
donor-acceptor
Stenhouse
adducts,
accompanied
by
strong
color
changes.
A
small-size
lightweight
laminated
sensor
was
integrated
based
outstanding
ratiometric
variations
active
indicators.
prototype
platform
fabricated
equipped
with
circuit
control,
mini
pump,
signal
processing
system.
user-friendly
efficient
screening
drugs,
including
phenethylamines,
amphetamines,
cathinones,
tryptamines
liquid
states
were
conducted.
response
linear
concentration
range
2.1-10.6
μg·mL
Abstract
This
study
presents
a
novel
boron‐difluoride
complex‐based
fluorescent
nanofilm
sensor
capable
of
detecting
sarin
vapors
in
the
environment
by
reporting
an
output
fluorescence
signal.
The
sensor's
evaluation
demonstrated
exceptionally
low
detection
limit
for
vapor,
even
presence
various
interfering
gases,
with
theoretical
and
practical
limits
0.7
1
ppb,
respectively.
featured
rapid
response
time
(less
than
2
s),
broad
linear
range
(1
ppb–1000
ppm),
superior
selectivity
vapor
over
group
analytes,
outperforming
existing
sensors.
Mechanistic
indicates
that
heightened
sensitivity
to
is
due
robust
affinity
nitrogen
atoms
within
core
BODIQ
unit
sarin.
Additionally,
tetraphenylethylene
structure
steric
hindrance
effectively
inhibits
tight
packing
derivatives,
forms
numerous
microporous
structures
self‐assembled
nanofilm,
which
are
beneficial
mass
transfer,
enhancing
efficiency
vapors.
Furthermore,
we
have
achieved
differentiation
sarin,
diethyl
chlorophosphate,
HCl
through
analysis
sensing
kinetic.
opens
new
avenues
sustainable,
low‐cost,
environment‐friendly
portable
devices,
as
well
environmental
monitoring
tracking
applications.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(29)
Опубликована: Апрель 8, 2024
Abstract
Currently,
most
photoredox
catalysis
polymerization
systems
are
limited
by
high
excitation
power,
long
time,
or
the
requirement
of
electron
donors
due
to
precise
design
efficient
photocatalysts
still
poses
a
great
challenge.
Herein,
we
propose
new
approach:
creation
having
low
ground
state
oxidation
potentials
and
excited
energy
levels,
along
with
through‐space
charge
transfer
(TSCT)
induced
intersystem
crossing
(ISC)
properties.
A
cabazole‐naphthalimide
(NI)
dyad
(NI‐1)
characterized
triplet
lifetime
(τ
T
=62
μs),
satisfactory
ISC
efficiency
(Φ
Δ
=54.3
%)
powerful
reduction
capacity
[Singlet:
E
1/2
(PC
+1
/*PC)=−1.93
eV,
Triplet:
/*PC)=−0.84
eV]
was
obtained.
An
rapid
(83
%
conversion
1
mM
monomer
in
30
s)
observed
under
conditions
without
donor,
power
(10
mW
cm
−2
)
catalyst
loading
(<50
μM).
In
contrast,
rate
lower
at
29
when
reference
(NI‐4)
used
for
photopolymerization
same
conditions,
demonstrating
advantage
TSCT
photocatalyst.
Finally,
material
as
photocatalyst
practical
lithography
first
achieving
pattern
resolutions
up
10
μm.
Advanced Optical Materials,
Год журнала:
2024,
Номер
12(23)
Опубликована: Май 21, 2024
Abstract
Emitters
with
the
combination
of
an
electron
donor
(D)
and
acceptor
(A)
have
been
widely
studied
usually
exhibited
interesting
photophysical
properties.
Hot
exciton
materials
involving
ordinary
D‐A
structure
typically
undergo
a
hybridized
local
charge
transfer
(HLCT)
process.
However,
hot
molecules
containing
more
D/A
fragments
are
much
less
explored.
In
this
study,
new
material
based
on
inorganic
boron
cluster
is
designed
synthesized,
which
possesses
V‐type
D–A–A′–D′
molecular
architecture.
The
emitter
shows
impressive
photoluminescence
quantum
yield
(PLQY)
up
to
90%
demonstrates
multiple
emissions,
excitation‐wavelength‐,
solvent‐,
temperature‐dependent
emissions.
These
characteristics
attributed
coexistence
HLCT
through‐space
process
(TSTC)
triggered
by
o
‐carborane
scaffold
in
excited
state.
Besides,
interchangeable
HLCT/TSCT/hRISC
processes
demonstrated
spectra
femtosecond
time‐resolved
transient
absorption
spectra.
findings
confirm
novel
mechanism,
simultaneously
induced
TSCT.
This
also
first
example
carborane‐based
molecule.
current
study
not
only
reports
architecture
for
but
gives
rise
insight
into
mechanism.
Advanced Science,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 17, 2025
Abstract
Preparing
multi‐color
and
multi‐stimuli‐responsive
circularly
polarized
luminescence
(CPL)
materials
understanding
the
evolution
of
chirality
through
visualized
mode
is
still
a
challenge.
Here,
an
encapsulation
engineering
approach
chiral
metal‐organic
frameworks
(MOFs)
proposed
to
confine
guest
emitters
realize
CPL.
Based
on
triplet‐triplet
energy
transfer
(TTET),
white
CPL
near‐infrared
room
temperature
phosphorescence
(NIR‐CPRTP)
can
be
obtained
by
introducing
pyrene
derivatives.
With
introduction
containing
vinylpyrene
group,
light‐
thermal‐responsive
with
signal
inversion
realized
reversible
[2+2]
cycloaddition
reaction
between
ligand
triggered
visible
light/ultraviolet
light
or
heating.
Furthermore,
excitation‐dependent
successfully
achieved
incorporation
excited
state
intramolecular
proton
(ESIPT)
molecules
into
nanopores.
Importantly,
magnification
greatly
enhanced
spatial
confinement,
accurate
host‐guest
single
crystal
structures
FLT@DCF‐12
FLT@LCF‐12
provide
understand
mechanism
transfer,
amplification
responsiveness.
White
LED
multiple
information
display
encryption
are
further
demonstrated.
This
breakthrough
provides
new
perspective
guest‐encapsulated
MOFs
contributes
construction
stimuli‐responsive
CPL‐active
materials.
Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
62(52)
Опубликована: Ноя. 15, 2023
Condensed
films
of
functional
luminophores
dominated
by
the
magnitude
and
dimensionality
intermolecular
interactions
play
important
roles
in
sensing
performance.
However,
controlling
molecular
assembly
regulating
photophysical
properties
remain
challenging.
In
this
study,
a
new
luminophore,
ortho-PBI-Au,
was
synthesized
anchoring
cyclometalated
alkynyl-gold(III)
unit
at
ortho-position
perylene
bisimide.
An
unprecedented
T-type
packing
model
driven
weak
Au-π
interaction
Au-H
bonds
observed,
laying
foundation
for
striking
luminophore.
Controlled
ortho-PBI-Au
air-water
interface,
realized
using
classical
Langmuir-Schaeffer
technique,
afforded
obtained
luminescent
with
different
structures.
With
an
optimized
film,
sensitive,
selective,
rapid
detection
hazardous
psychoactive
substance,
phenylethylamine
(PEA),
achieved.
The
limit,
response
time,
recovery
time
were
<4
ppb,
<1
s,
<5
respectively,
surpassing
performance
PEA
sensors
known
thus
far.
relationship
between
characters
systematically
examined
grey
relational
analysis
(GRA).
present
study
suggests
that
designing
novel
aggregation
definite
adlayer
structure
is
crucial
strategy
to
enhance
performance,
which
could
be
favorable
film-based
fluorescent
sensors.