Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(36)
Published: June 17, 2024
Abstract
Single‐atom
catalysts
have
emerged
as
cutting‐edge
hotspots
in
the
field
of
material
science
owing
to
their
excellent
catalytic
performance
brought
about
by
well‐defined
metal
single‐atom
sites
(M
SASs).
However,
huge
challenges
still
lie
achieving
rational
design
and
precise
synthesis
M
SASs.
Herein,
we
report
a
novel
strategy
based
on
hetero‐charge
coupling
effect
(HCCE)
prepare
SASs
loaded
N
S
co‐doped
porous
carbon
1
/NSC).
The
proposed
was
widely
applied
17
types
/NSC
composed
single
or
multi‐metal
with
integrated
regulation
coordination
environment
electronic
structure,
exhibiting
good
universality
flexible
adjustability.
Furthermore,
this
provided
low‐cost
method
efficiently
synthesizing
high
yields,
that
can
produce
more
than
50
g
catalyst
at
one
time,
which
is
key
large‐scale
production.
Among
various
as‐prepared
unary
be
Fe,
Co,
Ni,
V,
Cr,
Mn,
Mo,
Pd,
W,
Re,
Ir,
Pt,
Bi)
catalysts,
Fe
delivered
for
electrocatalytic
nitrate
reduction
NH
3
Faradaic
efficiency
86.6
%
yield
rate
1.50
mg
h
−1
cat.
−0.6
V
vs.
RHE.
Even
using
cathode
Zn‐nitrate
battery,
it
exhibited
open
circuit
voltage
1.756
energy
density
4.42
mW
cm
−2
cycling
stability.
Green Chemistry,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
A
Co-SAC
with
oxidase-like
active
sites
(CoN
4
)
has
been
fabricated
for
the
construction
of
quinazolines
and
quinazolinones
using
ethanol
as
C
2
-synthon.
Kinetic
studies
suggest
that
dehydrogenation
is
RDS
reaction.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(46), P. 31647 - 31655
Published: Nov. 7, 2024
Despite
their
significant
importance,
the
challenges
in
direct
and
diverse
synthesis
of
N-heterocyclic
γ-amino
acids/esters/ketones
hamper
exploration
applications.
Herein,
by
developing
a
multifunctional
heterogeneous
iridium
single-atom
catalyst
composed
silica-confined
species
boron-doped
ZrO
Macromolecules,
Journal Year:
2023,
Volume and Issue:
57(1), P. 122 - 131
Published: Dec. 20, 2023
The
establishment
of
facile,
efficient,
and
precise
synthetic
approaches
to
selectively
convert
stable
C–H
bonds
functional
polymers
has
great
significance
in
both
chemistry
material
science
especially
by
C(sp3)–H
activation.
Here,
an
efficient
dual
activation
polymerization
alkynes
activated
methylenes
catalyzed
Pd(PPh3)4/benzoic
acid
was
successfully
established
with
a
100%
atom
economy
excellent
regio-
stereoselectivity.
A
series
high-weight-average
molecular-weight
(Mw
approximately
66,500)
poly(aryl
butene)s
(PABs)
sole
E
configuration
were
generated
remarkable
yields
(approximately
99%).
PABs
exhibit
good
thermal
stability,
solubility,
film-forming
ability.
In
addition,
the
thin
PAB
films
display
high
refractive
indices
(RI)
up
1.7126
at
589
nm.
Because
this
strong
group
tolerance,
luminophores
can
be
readily
constructed
into
main
chain
empower
multicolored
luminescence
various
states.
Notably,
containing
tetraphenylethene
(TPE)
moiety
feature
unique
aggregation-induced
emission
(AIE)
peculiarities,
which
could
specifically
sensitively
detect
Fe(III)
ions
low
limit
detection
(LOD)
1.585
×
10–6
M.
Synthesis,
Journal Year:
2023,
Volume and Issue:
56(05), P. 733 - 750
Published: Oct. 17, 2023
Abstract
Direct
reductive
coupling
of
nitro
compounds
with
C-coupling
partners
is
an
atom-
and
step-economical
strategy
to
access
polyfunctional
advanced
amines.
Due
the
extremely
complex
process
involved
in
reduction
high
reactivity
N,O-intermediates,
few
reliable
methodologies
have
been
reported
for
since
initial
studies.
To
address
this
significant
challenge,
numerous
endeavors
devoted
important
area
over
past
hundred
years.
In
short
review,
we
summarize
recent
advances
domain
discuss
mechanisms
these
appealing
transformations.
1
Introduction
2
Reductive
Coupling
Nitro
Compounds
Organometallic
Reagents
3
Arylboronic
Acids
4
Alkenes
5
Alkyl/Aryl
Halides
6
Alcohols
Their
Derivatives
7
Conclusion
Angewandte Chemie,
Journal Year:
2024,
Volume and Issue:
136(36)
Published: June 17, 2024
Abstract
Single‐atom
catalysts
have
emerged
as
cutting‐edge
hotspots
in
the
field
of
material
science
owing
to
their
excellent
catalytic
performance
brought
about
by
well‐defined
metal
single‐atom
sites
(M
SASs).
However,
huge
challenges
still
lie
achieving
rational
design
and
precise
synthesis
M
SASs.
Herein,
we
report
a
novel
strategy
based
on
hetero‐charge
coupling
effect
(HCCE)
prepare
SASs
loaded
N
S
co‐doped
porous
carbon
1
/NSC).
The
proposed
was
widely
applied
17
types
/NSC
composed
single
or
multi‐metal
with
integrated
regulation
coordination
environment
electronic
structure,
exhibiting
good
universality
flexible
adjustability.
Furthermore,
this
provided
low‐cost
method
efficiently
synthesizing
high
yields,
that
can
produce
more
than
50
g
catalyst
at
one
time,
which
is
key
large‐scale
production.
Among
various
as‐prepared
unary
be
Fe,
Co,
Ni,
V,
Cr,
Mn,
Mo,
Pd,
W,
Re,
Ir,
Pt,
Bi)
catalysts,
Fe
delivered
for
electrocatalytic
nitrate
reduction
NH
3
Faradaic
efficiency
86.6
%
yield
rate
1.50
mg
h
−1
cat.
−0.6
V
vs.
RHE.
Even
using
cathode
Zn‐nitrate
battery,
it
exhibited
open
circuit
voltage
1.756
energy
density
4.42
mW
cm
−2
cycling
stability.