Exploring the solubility and solvation thermodynamics of coumarin in a range of aqua-organic solvents
New Journal of Chemistry,
Год журнала:
2023,
Номер
47(28), С. 13547 - 13557
Опубликована: Янв. 1, 2023
This
study
presents
the
solubility
and
solvation
thermodynamics
of
coumarin
in
a
range
aqua-organic
solvent
mixtures
at
various
temperatures.
The
order
was
determined
as
follows:
DMF
>
DMSO
ACN
H
2
O.
Язык: Английский
An Asymmetric Coumarin‐Anthracene Conjugate as Efficient Fullerene‐Free Acceptor for Organic Solar Cells
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
unknown
Опубликована: Май 13, 2024
Asymmetric
wide-band
gap
fullerene-free
acceptors
(FFAs)
play
a
crucial
role
in
organic
solar
cells
(OSCs).
Here,
we
designed
and
synthesized
simple
asymmetric
coumarin-anthracene
conjugate
named
CA-CN
with
optical
band
of
2.1
eV
single-step
condensation
reaction.
Single
crystal
X-ray
structure
analysis
confirms
various
multiple
intermolecular
non-covalent
interactions.
The
molecular
orbital
energy
levels
estimated
from
cyclic
voltammetry
were
found
to
be
suitable
for
its
use
as
an
acceptor
OSCs.
Binary
OSCs
fabricated
using
PTB7-Th
the
donor
achieve
power
conversion
efficiency
(PCE)
11.13
%.
We
further
demonstrate
that
insertion
20
wt
%
third
component
ternary
:
DICTF
host
material
achieved
impressive
PCE
14.91
%,
improvement
~43
compared
binary
device
(10.38
%).
Importantly,
blend
enhances
absorption
coverage
400
800
nm
improves
morphology
active
layer.
findings
highlight
efficacy
design
approach
FFAs,
which
paves
way
developing
high-efficiency
at
low
cost.
Язык: Английский
Conjugated Backbone Optimization of All-Fused-Ring Acceptor for Efficient and Stable Organic Solar Cells
Chemical Communications,
Год журнала:
2024,
Номер
60(48), С. 6206 - 6209
Опубликована: Янв. 1, 2024
Three
all-fused-ring
acceptors
with
different
conjugated
backbones
are
designed
as
for
organic
solar
cells.
The
extensions
of
the
significantly
impact
photovoltaic
performance
and
stability
devices.
Язык: Английский
Diketopyrrolopyrrole-Coumarin Conjugates for Efficient Binary Organic Solar Cells
ACS Applied Energy Materials,
Год журнала:
2023,
Номер
6(17), С. 8857 - 8866
Опубликована: Авг. 18, 2023
Two
coumarin
(Cou)-functionalized
DPP
derivatives,
DPP-Cou
and
Cou-DPP-Cou,
have
been
designed,
synthesized,
characterized.
The
extension
of
the
molecular
backbone
by
an
additional
derivative
in
symmetrical
Cou-DPP-Cou
extends
absorption
to
∼750
nm
(Egopt
=
1.67
eV)
compared
∼700
1.78
for
asymmetric
DPP-Cou.
Thermogravimetric
analysis
showed
higher
thermal
stability
conjugates
one.
Both
materials
complementary
spectra
well-matched
Frontier
orbital
energy
levels
with
low
band
gap
fullerene-free
acceptor
Y7
used
as
a
donor
organic
solar
cells.
After
optimization
using
solvent
vapor
annealing
treatment,
cells
based
on
DPP-Cou:Y7
Cou-DPP-Cou:Y7
attained
overall
power
conversion
efficiencies
(PCE)
9.63
13.48%,
respectively.
improved
PCE
is
mainly
due
appropriate
morphology
faster
charge
extraction
lower
recombination.
Язык: Английский
Coumarin based fluorescent liquid crystal dimers: Synthesis, mesogenic, photophysical behavior, and DFT studies
Journal of Molecular Liquids,
Год журнала:
2024,
Номер
417, С. 126691 - 126691
Опубликована: Дек. 7, 2024
Язык: Английский
Expedient synthesis of 1,2,4-triazinyl substituted benzo[c]coumarins via double oxidation strategy
Chimica Techno Acta,
Год журнала:
2023,
Номер
10(2)
Опубликована: Апрель 11, 2023
Herein,
we
report
a
convenient
one-pot
synthesis
of
1,2,4-triazinyl
derivatives
benzocoumarins.
The
proposed
approach
consists
in
the
nucleophilic
addition
tetrahydrobenzo
annulated
dimethoxycoumarin
to
1,2,4-triazines
followed
by
double
oxidation
both
dihydrotriazine
and
groups
with
2,3-dichloro-5,6-dicyano-1,4-benzoquinone
(DDQ).
was
carried
out
presence
three-fold
excess
methanesulfonic
acid
DCM
at
room
temperature
take
place
between
positions
4
5
coumarin
1,2,4-triazine,
respectively.
step
achieved
3.6
equivalent
DDQ.
Selective
moiety,
without
affecting
fragment,
using
1.2
tetrachlorobenzoquinone
(TCQ).
differences
TCQ
DDQ
appear
be
related
higher
oxidative
potential
contrast
TCQ.
advantages
method
are
elimination
use
transition
metals,
availability
starting
materials,
simplicity
procedure.
provides
two-step
protocol
for
triazinyl
benzocoumarins,
precursors
preparation
push-pull
pyridinyl
chromophore.
Язык: Английский
Photocatalytic Synthesis of Coumarin Derivatives Using Visible-Light-Responsive Strawberry Dye-Sensitized Titanium Dioxide Nanoparticles
Nanomaterials,
Год журнала:
2023,
Номер
13(23), С. 3001 - 3001
Опубликована: Ноя. 22, 2023
This
study
presents
a
novel
method
for
the
photocatalytic
synthesis
of
4-aryl-6-(3-coumarinyl)
pyrimidin-2
(1H)-ones
(a
coumarin
derivative)
using
strawberry
dye-sensitized
TiO2
(SD-TiO2)
under
visible
light.
The
was
achieved
through
three-component,
one-pot
condensation
reaction
involving
3-acetyl
coumarin,
aldehydes,
and
urea,
utilizing
SD-TiO2
as
reusable
innovative
photocatalyst
at
room
temperature.
resulting
thoroughly
characterized
FT-IR,
XPS,
XRD,
SEM,
BET.
efficacy
evaluated
by
comparing
it
to
pristine
in
terms
activity,
optimal
conditions
process
were
determined.
Notably,
exhibited
maximum
yield
compound,
reaching
up
96%
just
30
min
with
catalyst
concentration
1
mg/mL.
surpasses
traditional
thermal
procedures
employing
reflux
conditions,
where
mg/mL
is
sufficient
complete
reaction.
further
1H-NMR
13C-NMR.
Moreover,
stability
confirmed
recyclability
experiments
spectroscopic
characterization,
demonstrating
its
practicality
three
consecutive
cycles.
Язык: Английский
Probing coumarin solubility and solvation energetics in diverse aqueous–organic solutions across a temperature range: A debut exploration
Journal of Molecular Liquids,
Год журнала:
2023,
Номер
395, С. 123832 - 123832
Опубликована: Дек. 24, 2023
Язык: Английский
An Asymmetric Coumarin‐Anthracene Conjugate as Efficient Fullerene‐Free Acceptor for Organic Solar Cells
Angewandte Chemie,
Год журнала:
2024,
Номер
136(40)
Опубликована: Май 13, 2024
Abstract
Asymmetric
wide‐band
gap
fullerene‐free
acceptors
(FFAs)
play
a
crucial
role
in
organic
solar
cells
(OSCs).
Here,
we
designed
and
synthesized
simple
asymmetric
coumarin‐anthracene
conjugate
named
CA‐CN
with
optical
band
of
2.1
eV
single‐step
condensation
reaction.
Single
crystal
X‐ray
structure
analysis
confirms
various
multiple
intermolecular
non‐covalent
interactions.
The
molecular
orbital
energy
levels
estimated
from
cyclic
voltammetry
were
found
to
be
suitable
for
its
use
as
an
acceptor
OSCs.
Binary
OSCs
fabricated
using
PTB7‐Th
the
donor
achieve
power
conversion
efficiency
(PCE)
11.13
%.
We
further
demonstrate
that
insertion
20
wt
%
third
component
ternary
:
DICTF
host
material
achieved
impressive
PCE
14.91
%,
improvement
~43
compared
binary
device
(10.38
%).
Importantly,
blend
enhances
absorption
coverage
400
800
nm
improves
morphology
active
layer.
findings
highlight
efficacy
design
approach
FFAs,
which
paves
way
developing
high‐efficiency
at
low
cost.
Язык: Английский
Superior End-Group Stacking Promotes Simultaneous Multiple Charge-Transfer Mechanisms in Organic Solar Cells with an All-Fused-Ring Nonfullerene Acceptor
ACS Applied Materials & Interfaces,
Год журнала:
2024,
Номер
16(27), С. 35390 - 35399
Опубликована: Июнь 26, 2024
The
all-fused-ring
acceptor
(AFRA)
is
a
success
for
nonfullerene
materials
and
has
attracted
considerable
attention
as
its
high
optical
chemical
stability
expected
to
reduce
energy
loss,
power
conversion
efficiency
(PCE)
approaching
15%
in
constructed
all-small-molecule
organic
solar
cells
(OSCs).
Herein,
the
intrinsic
role
of
structure
AFRA
F13
reason
PCE
were
revealed
by
comparison
with
those
typical
fused
acceptors
IDT-IC
Y6.
An
increased
degree
conjugation
leads
broader
red-shifted
absorption
peaks,
facilitating
enhancement
short-circuit
current.
Multiple
charge-transfer
mechanisms
are
mainly
attributed
higher
Frenkel
exciton
(FE)
state
due
multiple
transition
ways
C1-CN:F13
system.
number
atoms
contributing
(CT)
facilitated
existence
more
superior
stacking
patterns
easy
formation
CT
FE/CT
states
charge
separation
rate.
It
was
found
using
an
effective
strategy
enhance
end-group
stacking,
enhancing
borrowing
oscillator
strength
promote
complexes,
explaining
performance
this
OSC
device.
This
work
promising
guide
designing
efficient
future.
Язык: Английский