Modulating Quinoline-Linked Covalent Organic Frameworks via Fluorination for Boosting the Photocatalytic Air Reductive H2O2 Production
Qinfeng Rong,
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Xianlan Chen,
No information about this author
Qinyi Cheng
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et al.
ACS Sustainable Chemistry & Engineering,
Journal Year:
2024,
Volume and Issue:
12(35), P. 13306 - 13315
Published: Aug. 20, 2024
The
intrinsic
reversibility
and
strong
polarization
of
imine
linkages
limit
the
application
imine-based
covalent
organic
frameworks
(COFs)
in
photocatalysis.
Herein,
inspired
by
aza-Diels–Alder
cycloaddition
reaction,
two
quinoline-linked
fluorinated
COFs
(termed
TTB-TTA-Ph-F
TTB-TTA-Ph-3F)
are
developed
based
on
postsynthetic
modification
an
imine-linked
COF
(TTB-TTA).
simultaneous
reversibility-to-irreversibility
bond
transformation
fluorination
endow
resultant
with
improved
robustness,
extended
structural
conjugation,
intriguing
optoelectronic
properties.
introduced
fluorine
groups
change
local
electronic
structures
improve
charge
separation
transfer.
Benefiting
from
rational
design
skeleton,
TTB-TTA-Ph-3F
exhibits
excellent
activity,
giving
a
3496.9
μmol
g–1
h–1
photocatalytic
H2O2
production
rate
water
air
after
optimizing
modulation.
Language: Английский
Helicene Covalent Organic Frameworks for Robust Light Harvesting and Efficient Energy Transfers
Cong Yin,
No information about this author
Xingyao Ye,
No information about this author
Shanshan Tao
No information about this author
et al.
Angewandte Chemie International Edition,
Journal Year:
2024,
Volume and Issue:
63(45)
Published: July 18, 2024
Abstract
Helicenes
represent
a
class
of
fascinating
π
compounds
with
fused
yet
folded
backbones.
Despite
their
broad
structural
diversity,
harnessing
helicenes
to
develop
well‐defined
materials
is
still
formidable
challenge.
Here
we
report
the
synthesis
crystalline
porous
helicene
by
exploring
synthesize
covalent
2D
lattices
and
layered
frameworks.
Topology‐directed
polymerization
[6]helicenes
porphyrin
creates
networks
alternate
helicene‐porphyrin
alignment
along
x
y
directions
at
1.5‐nm
interval
develops
[6]helicene
frameworks
through
reversed
anti‐AA
stack
z
direction
form
segregated
columnar
arrays.
Notably,
this
configuration
enables
be
highly
red
luminescent
benchmark
quantum
yields.
The
trigger
effieicnt
intra‐framework
singlet‐to‐singlet
state
energy
transfer
from
facilitate
intermolecular
triplet‐to‐triplet
molecular
oxygen
produce
reactive
species,
harvesting
wide
range
photons
ultraviolet
near‐infrared
regions
for
light
emitting
photo‐to‐chemical
conversion.
This
study
introduces
new
family
extended
frameworks,
laying
groundwork
unprecedented
structures
functions.
Language: Английский
Challenges in photocatalysis using covalent organic frameworks
Journal of Physics Photonics,
Journal Year:
2024,
Volume and Issue:
6(3), P. 031001 - 031001
Published: June 12, 2024
Abstract
Photocatalysis
is
an
attractive,
energy-efficient
technology
for
organic
transformations,
polymer
synthesis,
and
degradation
of
environmental
pollutants.
There
a
need
new
photocatalysts
stable
in
different
media
that
can
be
tailored
specific
applications.
Covalent
frameworks
(COF)
are
crystalline,
nanoporous
materials
with
π
-conjugated
backbone
monomers,
representing
versatile
platforms
as
heterogeneous,
metal-free
photocatalysts.
The
structure
to
achieve
desired
photocatalytic
properties,
side-chains
mediate
adsorption,
the
provides
large
surface
area
molecular
adsorption.
While
these
properties
make
COFs
attractive
photocatalysts,
several
fundamental
questions
remain
regarding
mechanisms
reactant
transport
into
porous
COF
structures,
both
structural
chemical
stability
various
environments.
In
this
perspective,
we
provide
brief
overview
identify
challenges
should
addressed
future
research
seeking
employ
We
close
outlook
perspective
on
directions
Language: Английский
Helicene Covalent Organic Frameworks for Robust Light Harvesting and Efficient Energy Transfers
Cong Yin,
No information about this author
Xingyao Ye,
No information about this author
Shanshan Tao
No information about this author
et al.
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(45)
Published: July 18, 2024
Abstract
Helicenes
represent
a
class
of
fascinating
π
compounds
with
fused
yet
folded
backbones.
Despite
their
broad
structural
diversity,
harnessing
helicenes
to
develop
well‐defined
materials
is
still
formidable
challenge.
Here
we
report
the
synthesis
crystalline
porous
helicene
by
exploring
synthesize
covalent
2D
lattices
and
layered
frameworks.
Topology‐directed
polymerization
[6]helicenes
porphyrin
creates
networks
alternate
helicene‐porphyrin
alignment
along
x
y
directions
at
1.5‐nm
interval
develops
[6]helicene
frameworks
through
reversed
anti‐AA
stack
z
direction
form
segregated
columnar
arrays.
Notably,
this
configuration
enables
be
highly
red
luminescent
benchmark
quantum
yields.
The
trigger
effieicnt
intra‐framework
singlet‐to‐singlet
state
energy
transfer
from
facilitate
intermolecular
triplet‐to‐triplet
molecular
oxygen
produce
reactive
species,
harvesting
wide
range
photons
ultraviolet
near‐infrared
regions
for
light
emitting
photo‐to‐chemical
conversion.
This
study
introduces
new
family
extended
frameworks,
laying
groundwork
unprecedented
structures
functions.
Language: Английский