Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(12), С. 8668 - 8676
Опубликована: Март 18, 2024
Understanding
the
valency
and
structural
variations
of
metal
centers
during
reactions
is
important
for
mechanistic
studies
single-atom
catalysis,
which
could
be
beneficial
optimizing
designing
new
protocols.
Herein,
we
precisely
developed
a
Cu(I)-N4
site
catalyst
via
photoinduced
ligand
exchange
(PILE)
strategy.
The
low-valent
electron-rich
copper
species
catalyze
hydrophosphinylation
novel
single-electron
oxidative
addition
(OA)
pathway
under
light
irradiation,
considerably
decrease
energy
barrier
compared
with
well-known
hydrogen
atom
transfer
(HAT)
single
electron
(SET)
processes.
Cu(I)–Cu(II)–Cu(I)
catalytic
cycle,
photoreduction,
has
been
proven
by
multiple
in
situ
or
operando
techniques.
This
system
demonstrates
high
efficiency
requires
room
temperature
conditions
no
additives,
improves
turnover
frequency
(TOF)
to
1507
h–1.
In
particular,
this
unique
mechanism
broken
through
substrate
limitation
shows
broad
scope
different
electronic
effects
alkenes
alkynes.
Chemical Society Reviews,
Год журнала:
2023,
Номер
52(21), С. 7602 - 7664
Опубликована: Янв. 1, 2023
Carbon
nitrides,
with
feasibility
of
tailored
band
gap
via
suitable
nanoarchitectonics,
are
deemed
as
best
catalysts
amongst
existing
materials,
especially
for
HER,
OWS,
COR,
NRR,
water
oxidation,
pollutant
removal,
and
organocatalysis.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Окт. 20, 2023
Highly
effective
and
selective
noble
metal-free
catalysts
attract
significant
attention.
Here,
a
single-atom
iron
catalyst
is
fabricated
by
saturated
adsorption
of
trace
onto
zeolitic
imidazolate
framework-8
(ZIF-8)
followed
pyrolysis.
Its
performance
toward
catalytic
transfer
hydrogenation
furfural
comparable
to
state-of-the-art
up
four
orders
higher
than
other
Fe
catalysts.
Isotopic
labeling
experiments
demonstrate
an
intermolecular
hydride
mechanism.
First
principles
simulations,
spectroscopic
calculations
experiments,
kinetic
correlations
reveal
that
the
synthesis
creates
pyrrolic
Fe(II)-plN3
as
active
center
whose
flexibility
manifested
being
pulled
out
plane,
enabled
defects,
crucial
for
collocating
reagents
allowing
chemistry
proceed.
The
catalyzes
chemoselectively
several
substrates
possesses
unique
trait
whereby
hindered
more
acidic
hydrogen
donors.
This
work
paves
way
noble-metal
free
important
chemical
reactions.
Nano-Micro Letters,
Год журнала:
2024,
Номер
17(1)
Опубликована: Сен. 25, 2024
Abstract
Green
hydrogen
from
water
splitting
has
emerged
as
a
critical
energy
vector
with
the
potential
to
spearhead
global
transition
fossil
fuel-independent
society.
The
field
of
catalysis
been
revolutionized
by
single-atom
catalysts
(SACs),
which
exhibit
unique
and
intricate
interactions
between
atomically
dispersed
metal
atoms
their
supports.
Recently,
bimetallic
SACs
(bimSACs)
have
garnered
significant
attention
for
leveraging
synergistic
functions
two
ions
coordinated
on
appropriately
designed
BimSACs
offer
an
avenue
rich
metal–metal
metal–support
cooperativity,
potentially
addressing
current
limitations
in
effectively
furnishing
transformations
involve
synchronous
proton–electron
exchanges,
substrate
activation
reversible
redox
cycles,
simultaneous
multi-electron
transfer,
regulation
spin
states,
tuning
electronic
properties,
cyclic
states
low
energies.
This
review
aims
encapsulate
growing
advancements
bimSACs,
emphasis
pivotal
role
generation
via
splitting.
We
subsequently
delve
into
advanced
experimental
methodologies
elaborate
characterization
SACs,
elucidate
discuss
local
coordination
environment.
Overall,
we
present
comprehensive
discussion
deployment
bimSACs
both
evolution
reaction
oxygen
reaction,
half-reactions
electrolysis
process.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(27)
Опубликована: Апрель 23, 2024
Homogeneous
electrocatalysts
can
indirect
oxidate
the
high
overpotential
substrates
through
single-electron
transfer
on
electrode
surface,
enabling
efficient
operation
of
organic
electrosynthesis
catalytic
cycles.
However,
problems
this
chemistry
still
exist
such
as
dosage,
difficult
recovery,
and
low
efficiency.
Single-atom
catalysts
(SACs)
exhibit
atom
utilization
excellent
activity,
hold
great
promise
in
addressing
limitations
homogeneous
catalysts.
In
view
this,
we
have
employed
Fe-SA@NC
an
advanced
redox
mediator
to
try
change
situation.
was
synthesized
using
encapsulation-pyrolysis
method,
it
demonstrated
remarkable
performance
a
range
reported
reactions,
construction
various
C-C/C-X
bonds.
Moreover,
potential
exploring
new
synthetic
method
for
electrosynthesis.
We
develop
electro-oxidative
ring-opening
transformation
cyclopropyl
amides.
reaction
system,
showed
good
tolerance
drug
molecules
with
complex
structures,
well
flow
electrochemical
syntheses
gram-scale
transformations.
This
work
highlights
SACs
electrosynthesis,
thereby
opening
avenue
chemistry.
Advanced Functional Materials,
Год журнала:
2024,
Номер
unknown
Опубликована: Апрель 29, 2024
Abstract
This
study
introduces
a
novel
solution
to
the
design
of
structured
catalysts,
integrating
single‐piece
3D
printing
with
single‐atom
catalysis.
Structured
catalysts
are
widely
employed
in
industrial
processes,
as
they
provide
optimal
mass
and
heat
transfer,
leading
more
efficient
use
catalytic
materials.
They
conventionally
prepared
using
ceramic
or
metallic
bodies,
which
then
washcoated
impregnated
catalytically
active
layers.
However,
this
approach
may
lead
adhesion
issues
latter.
By
employing
photopolymerization
printing,
stable
catalyst
is
directly
shaped
into
stand‐alone,
material.
The
battery
characterization
methods
present
confirms
uniform
distribution
species
structural
integrity
Computational
fluid
dynamics
simulations
applied
demonstrate
enhanced
momentum
transfer
light
within
body.
materials
finally
evaluated
continuous‐flow
photocatalytic
oxidation
benzyl
alcohol
benzaldehyde,
relevant
reaction
prepare
biomass‐derived
building
blocks.
innovative
reported
herein
manufacture
circumvents
complexities
traditional
synthetic
methods,
offering
scalability
efficiency
improvements,
highlights
transformative
role
catalysis
engineering
revolutionize
catalysts’
design.
Abstract
Single‐atom
catalysts
(SACs)
are
gathering
significant
attention
in
chemistry
due
to
their
unique
properties,
offering
uniform
active
site
distribution
and
enhanced
selectivity.
However,
precise
structure
often
remains
unclear,
with
multiple
models
proposed
the
literature.
Understanding
coordination
environment
of
at
atomic
level
is
crucial
for
explaining
catalytic
activity.
Here,
a
comprehensive
study
SACs
made
carbon
nitride
(CN
x
)
containing
isolated
nickel
atoms
presented.
Using
combination
synthesis
techniques
characterization
methods
including
Fourier‐transform
infrared
spectroscopy,
X‐ray
absorption
spectroscopy
(XAS),
density
functional
theory
(DFT)
calculations,
local
centers
CN
‐supported
investigated.
These
results
challenge
conventional
structural
propose
new
architecture
that
better
aligns
current
experimental
evidence.
This
serves
as
foundational
step
toward
rational
approach
catalyst
development
can
facilitate
more
design
application
these
innovative
catalysts.
ACS Catalysis,
Год журнала:
2025,
Номер
15(3), С. 2180 - 2191
Опубликована: Янв. 22, 2025
Heterogeneous
metallaphotocatalytic
chemical
transformations
employing
a
recyclable
catalyst
are
highly
desirable
for
organic
synthesis.
However,
the
rational
design
and
controlled
preparation
of
well-defined,
site-isolated
metal/photo
bifunctional
heterogeneous
catalysts
to
achieve
this
goal
remain
significant
challenge.
In
study,
we
demonstrate
covalent
attachment
homogeneous
molecular
MnSalen
complex
(where
Salen
=
N,N′-bis(salicylidene)ethylenediamine)
onto
surface
graphitic
carbon
nitride
(CN)
via
an
amide
bond
visible-light-driven
chloro-
azido-fluoroalkylation
unactivated
alkenes.
The
linkage
between
CN
not
only
facilitates
electron
delocalization
enhances
light-harvesting
capabilities
photosensitizer
but
also
exerts
proximity
effect
that
markedly
ability
Mn
sites
capture
alkyl
radical
intermediates
during
reaction
process.
A
diverse
set
alkenes
could
be
efficiently
azido-fluoroalkylated
their
corresponding
difunctionalized
products
in
moderate
high
yields
with
good
functional
group
compatibility.
Furthermore,
practicability
protocol
is
illustrated
through
late-stage
diversification
various
bioactive
compounds
pharmaceuticals.
Notably,
integrated
photocatalyst
demonstrates
stability
can
recycled
at
least
10
times
without
loss
activity
selectivity.
Analytical Chemistry,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 30, 2025
The
traditional
biocatalytic
precipitation
(BCP)
strategy
often
required
the
participation
of
H2O2,
but
H2O2
had
problem
self-decomposition,
which
prevented
its
application
in
quantitative
analysis.
This
work
first
found
that
a
bimetallic
single-atom
catalyst
(Co/Zn–N–C
SAC)
could
effectively
activate
dissolved
O2
to
produce
reactive
oxygen
species
(ROS)
due
superior
oxidase
(OXD)-like
activity.
Experimental
investigations
demonstrated
Co/Zn–N–C
SAC
preferred
highly
active
hydroxyl
radicals
(•OH),
oxidized
3-amino-9-ethyl
carbazole
(AEC)
reddish-brown
insoluble
precipitates.
Based
on
this
property,
unique
oxygen-activated
photoelectrochemical
(PEC)
biosensor
was
developed
for
chloramphenicol
(CAP)
detection.
Cesium
platinum
bromide
nanocrystals
(Cs2PtBr6
NCs)
were
new
type
halide
perovskite
with
lead-free,
narrow
band
gaps,
and
water-oxygen
resistance.
Cs2PtBr6
NCs
showed
excellent
cathodal
PEC
performance
without
an
exogenous
coreactant
used
As
"proof-of-concept
application",
introduced
onto
surface
by
using
CAP
dual-aptamer
sandwich
strategy.
activated
ROS,
AEC
precipitates,
quenching
signal
In
summary,
overcome
restriction
enzymatic
BCP
requiring
improved
stability
accuracy
analysis,
also
broadened
range
coreactant-free
perovskite-type
biosensors.