Chemical Communications,
Journal Year:
2024,
Volume and Issue:
61(3), P. 508 - 511
Published: Nov. 26, 2024
Through
three-component
Knoevenagel
condensation,
the
first
vinyl-linked
PPh
3
-based
covalent-organic
frameworks
(Pd@TMBen-PPh
and
Pd@TMBen-4F-PPh
)
were
constructed
utilized
in
highly
efficient
Pd-catalyzed
carbonylation
coupling
reaction.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Jan. 8, 2025
The
conversion
of
solar
energy
into
chemical
or
high-value
chemicals
has
attracted
considerable
research
interest
in
the
context
global
crisis.
Hydrogen
peroxide
(H2O2)
is
a
versatile
and
powerful
oxidizing
agent
widely
used
synthesis
medical
disinfection.
H2O2
also
serves
as
clean
source
fuel
cells,
generating
electricity
with
zero-carbon
emissions.
Recently,
sustainable
production
from
water
oxygen
using
covalent
organic
frameworks
(COFs)
photocatalysts
attention;
however,
systematic
studies
highlighting
role
linkages
determining
photocatalytic
performance
are
scarce.
Under
these
circumstances,
herein,
we
demonstrate
that
varying
imine
hydrazone
within
framework
significantly
influences
production.
COFs
high-density
linkages,
providing
optimal
docking
sites
for
oxygen,
enhance
generation
activity
(1588
μmol
g−1
h−1
pure
air),
leading
to
highly
efficient
solar-to-chemical
conversion.
This
work
systematically
investigates
effect
linkage
density
on
enhancement
hydrogen
generation,
aim
achieving
high-performance
photocatalysis.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(36), P. 25118 - 25124
Published: Aug. 30, 2024
Covalent
organic
frameworks
(COFs)
are
a
class
of
crystalline
porous
materials
with
well-defined
π
arrays
and
ordered
channels,
which
can
be
predesigned
topology
diagram
prepared
via
polycondensation
reaction.
Over
the
past
decade,
various
types
building
units
different
functional
groups
have
been
developed.
Among
them,
aldehyde
is
one
most
widely
used
monomers
that
form
COFs
azine,
hydrazine,
imine,
squaranine,
C═C
linkages.
In
contrast,
its
closest
analogue,
i.e.,
ketone,
despite
broad
structural
diversity,
has
not
yet
investigated
for
design
synthesis
COFs.
Herein
we
report
first
examples
ketazine-linked
by
developing
ketones
as
to
enable
hydrazine
under
solvothermal
conditions.
We
observed
careful
screening
reaction
conditions
including
solvent,
catalyst,
concentration,
temperature,
time
leads
finding
optimal
polymerization
systems
produce
highly
Surprisingly,
ketazine
linkage
enables
conjugation
between
knot
linker
sites
renders
resultant
able
emit
strong
blue
fluorescence,
highlighting
electronic
features
this
new
family
Our
findings
bring
unprecedented
structures,
functions,
applications
field
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 3, 2025
Covalent
organic
frameworks
(COFs)
hold
promise
in
heterogeneous
metal
catalysis
benefiting
from
their
robust,
crystalline,
and
porous
structures.
However,
synthetic
challenges
persist
prolonged
crystallization
times,
limited
loading,
uncertain
coordination
environments.
Here,
we
present
the
rapid
versatile
metalation
of
new
acetylhydrazone-linked
COFs
(AH-COFs)
by
condensation
ketone
hydrazide
components,
featuring
full
conversion
within
30
min
under
open-air
mild
conditions.
The
obtained
AH-COFs
exhibit
exceptional
thermal
chemical
stability,
maintaining
high
crystallinity
microporosity
even
harsh
This
method
shows
versatility
Nano Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 23, 2025
Covalent-organic
frameworks
(COFs)
are
dynamic
covalent
porous
organic
materials
constructed
from
emissive
molecular
building
blocks.
However,
most
two-dimensional
(2D)
COFs
nonemissive
or
weakly
in
the
solid
state
owing
to
intramolecular
rotation
and
vibration
together
with
strong
π-π
interactions.
Herein,
we
report
a
pressure
strategy
achieve
bright
multicolor
emission
yellow
red
2D
triazine
triphenyl
imine
COF
(TTI-COF).
Intriguingly,
TTI-COF
experiences
24-fold
enhancement
under
mild
of
2.7
GPa
compared
initial
state.
Joint
experimental
theoretical
results
reveal
that
restricted
chemical
bond
vibrations
reduced
interactions
originating
offset
stacking
mode
account
for
significant
pressure-induced
enhancement.
Furthermore,
such
piezochromic
behavior
may
be
ascribed
decreased
energy
gap
enhanced
intermolecular
interaction.
Our
investigation
offers
constructive
guidelines
designing
high
photoluminescence
performance.
Advanced Optical Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 6, 2025
Abstract
In
order
to
inhibit
non‐radiative
decay
pathways
of
covalent‐organic
frameworks
(COFs),
a
strategy
is
proposed
block
intralayer
conjugation
and
interlayer
π–π
stacking
by
using
flexible
aggregation‐induced
emission
(AIE)
building
blocks
(4′,4′′′,4′′′′′,4′′′′′′′‐(1,2‐ethenediylidene)
tetrakis[1,1′‐biphenyl]‐4‐carbaldehyde
(TFBE))
connected
weakly
conjugated
linker.
By
the
TFBE
as
changing
flexibility
linker,
TFBE‐COFs
with
different
luminescence
properties
are
obtained.
Experimental
theoretical
results
show
that
these
have
high
crystallinity
large
layer
spacing,
among
which
photoluminescence
quantum
yield
hydrazone
(Hz)‐COF
TFBE‐ODH
(oxalyl
dihydrazide
(ODH))
in
solid
state
reaches
26.28%,
superior
most
COFs
reported
so
far.
The
excellent
attributed
non‐planar
geometry
TFBE,
inhibits
quenching.
Moreover,
π‐electron
delocalization‐induced
leaps
suppressed
further
enhances
TFBE‐COFs.
Hz‐COF
exhibits
sensing
performance
for
trace
tetracycline,
detection
limit
0.15
µ
m
.
addition,
white
light‐emitting
diodes
coated
manufactured
achieve
high‐quality
light
emission.
This
study
provides
new
design
application
high‐emission
COFs.