Perhaloacylation of α-Carbonyl Sulfoxonium Ylides
The Journal of Organic Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 2, 2025
A
mild
and
efficient
protocol
for
the
perhaloacylation
of
α-carbonyl
sulfoxonium
ylides
has
been
developed.
The
commercially
available
perfluoro-
perchloroacid
anhydrides
were
used
as
acylating
agents
in
catalyst-
additive-free
reactions
to
access
α-carbonyl-α'-perhaloacyl
high
yields.
reaction
offers
a
simple
method
prepare
valuable
polyfluorinated
organosulfur
molecules.
Language: Английский
Polynorbornenes Bearing Cyclic Fluoroalkyl Side Groups for Achieving High Glass Transition Temperature and Low Refractive Index
Makoto Uno,
No information about this author
Masafumi Sugiyama,
No information about this author
Takashi Okazoe
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et al.
Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 13, 2025
Language: Английский
Conjugated π-Extension of Small Molecular Nonfullerene Acceptor for Efficient Ternary Organic Solar Cells with an Efficiency of 19.10%
Cheng Luo,
No information about this author
Dongdong Xia,
No information about this author
Jie Wu
No information about this author
et al.
Energy & Fuels,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 14, 2025
In
this
study,
we
have
successfully
incorporated
a
small
molecular
acceptor,
Y-LC,
with
conjugated
π-extension
as
secondary
acceptor
in
the
PM6:BTP-eC9-based
organic
photovoltaics.
The
performance
of
device
was
significantly
promoted
from
18.45%
binary
system
PM6:BTP-eC9
to
over
19%
ternary
minimal
Y-LC
loading.
This
enhancement
can
be
attributed
alloy-like
structures
acceptors
and
optimized
active
layer
morphology,
which
leads
improved
hole
electron
mobilities,
thereby
suppressing
charge
recombination,
finally
resulting
higher
photocurrent
solar
cells.
Furthermore,
complementary
absorption
is
observed
PM6
BTP-eC9,
broaden
spectrum
photoactive
enable
more
photons
sunlight
absorbed.
Additionally,
facilitates
efficient
transfer
donor
by
forming
cascade
energy
levels
between
BTP-eC9.
These
advantages
collectively
contribute
superior
obtained
work
also
highlights
that
adoption
nonfullerene
suitable
π-extensions
minor
additive
photovoltaics
powerful
approach
for
achieving
state-of-the-art
Language: Английский
Asymmetric Alkyl Chain Engineering of Non-fullerene Acceptors for Efficient Organic Solar Cells
Cong Zhen Qiao,
No information about this author
Qian Xie,
No information about this author
Jie Fang
No information about this author
et al.
Chinese Journal of Polymer Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 8, 2025
Language: Английский
A Steric Camphane-Functionalized Fused-Ring Electron Acceptor for Efficient Ternary Non-Fullerene Organic Solar Cells
ACS Applied Energy Materials,
Journal Year:
2024,
Volume and Issue:
7(22), P. 10662 - 10669
Published: Nov. 9, 2024
Functionalization
of
Y-type
non-fullerene
acceptors
(Y-NFAs)
with
bulky
units
at
the
alkyl
chains,
terminal
IC
ends,
or
central
cores
has
been
an
efficient
route
to
boosting
efficiency
NFA-based
organic
solar
cells
(OSCs).
Single-crystal
structure
analysis
a
powerful
tool
provide
detailed
information,
such
as
bending
conjugated
backbone
and
packing
formats
molecules
in
solid,
which
can
supply
valuable
insight
into
performance
relation
direct
further
molecular
design
new
NFAs.
However,
growth
high-quality
single
crystals
NFAs
groups
is
often
challenging.
Herein,
we
designed
synthesized
NFA,
Norb-Y,
decorated
steric
camphane
unit
on
core
through
fused
quinoxaline
bridge.
Norb-Y
was
successfully
characterized
by
single-crystal
analysis,
revealing
well-fined
atomic
intermolecular
stacking
format.
Notably,
displays
better
coplanarity
small
dihedral
angle
18°
between
two
groups.
Moreover,
three
kinds
π–π
modes
corresponding
J-aggregation
were
identified,
including
end-to-end,
arm-to-arm,
tail-to-tail
modes,
all
contributed
segment
from
thiophene
end.
Meanwhile,
H-aggregation
associating
suppressed
units,
drives
assembly
C–H···F
H
bonds
instead.
This
kind
significance
for
reducing
voltage
loss
increasing
OSCs'
open
circuit
voltage,
finally
verified
PM6:BTP-eC9:Norb-Y-
D18:N3:Norb-Y-based
ternary
OSCs.
Language: Английский