RSC Advances,
Год журнала:
2024,
Номер
14(40), С. 29184 - 29188
Опубликована: Янв. 1, 2024
An
efficient
Suzuki–Miyuara
reaction
was
developed
on
unprotected
ortho
-bromoanilines
providing
good
to
excellent
yields
a
wide
variety
of
substrates.
The
robustness
the
showcased
gram
scale.
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(10), С. 6476 - 6480
Опубликована: Март 4, 2024
We
report
the
design
and
development
of
a
transition-metal-free
cross-coupling
reaction
phenols
primary
amines
using
simple
readily
available
multifunctional
reagent.
The
reactions
work
by
induced
proximity
electronic
activation
both
nucleophile
electrophile
for
net
dehydrative
C-N
coupling
reactions.
Notably,
do
not
involve
use
transition
metal
bond
formation,
preactivation
phenol
electrophile,
or
exclusion
air
moisture.
mild
conditions
tolerate
broad
range
functional
groups
allow
this
to
be
applied
late-stage
functionalization
complex
substrates
with
wide
scope
partners.
Green Chemistry,
Год журнала:
2024,
Номер
26(18), С. 9619 - 9651
Опубликована: Янв. 1, 2024
This
review
focuses
on
advances
in
covalent
organic
framework
(COF)
photocatalysts
for
cross-coupling
reactions,
which
provide
a
greener
catalytic
route
transformations.
Catalysis Communications,
Год журнала:
2024,
Номер
187, С. 106862 - 106862
Опубликована: Фев. 1, 2024
Novel
palladium
based
magnetic
nanocatalyst
was
synthesized
by
the
co-precipitation
method
and
coated
with
silica
tea
extract
as
stabilizing
agent.
Palladation
onto
prepared
nanocomposite
done
to
get
ION-SiO2/TE-Pd(0)
catalyst.
Our
study
is
one
of
limited
number
studies
reported
for
catalytic
denitrogenative
coupling
arylbromide
arylhydrazine.
This
led
construction
important
substituted
biaryls
bearing
various
substituents
82–92%
yields.
The
characterized
using
structural
morphological
characterization
techniques.
It
also
observed
that
only
2
mol%
catalyst
sufficient
catalysis
reusable
upto
six
cycles.
Abstract
Palladium-
and
nickel-catalyzed
cross-couplings
are
powerful
methods
for
constructing
C–C
C–N
bonds,
particularly
through
Suzuki–Miyaura
Buchwald–Hartwig
reactions.
Although
aryl
iodides,
bromides,
triflates
the
most
commonly
used
substrates,
chlorides
less
frequently
utilized
due
to
their
lower
reactivity.
However,
they
appealing
because
readily
available
inexpensive.
This
short
review
highlights
recent
developments
on
of
chlorides,
using
both
homogeneous
heterogeneous
catalysis
with
palladium
nickel.
1
Introduction
2
Cross-Couplings
2.1
Homogeneous
Palladium
Catalysis
2.2
Heterogeneous
2.3
Nickel
2.4
3
Amination
Reactions
3.1
3.2
3.3
3.4
4
Conclusion
Catalysts,
Год журнала:
2025,
Номер
15(2), С. 133 - 133
Опубликована: Янв. 30, 2025
Declining
natural
resources
make
the
recovery
of
metals
from
waste
solutions
a
promising
alternative.
Moreover,
processing
into
finished
product
has
its
economic
justification
and
benefits.
Thus,
aim
this
research
was
developing
Waste
for
Product
strategy,
indicating
possibility
with
low
content
platinum-group
catalyst
synthesis.
The
results
obtained
confirmed
that
diluted
synthetic
containing
trace
amount
valuable
metal
ions
(Pd,
Pt)
can
be
used
process
Catalysts
produced
in
form
palladium
platinum
nanoparticles
were
successfully
deposited
on
Ni
foam
due
to
galvanic
displacement
mechanism.
Synthesized
catalysts
characterized
using
UV-Vis
spectrophotometry,
SEM/EDS,
XRD
techniques.
Electro-
catalytic
properties
tested
hydrogen/oxygen
evolution
reactions
methyl
orange
degradation,
respectively.
electrocatalytic
tests
indicated
modification
nickel
surface
by
consisting
noble
as
Pd
Pt
significantly
increase
activity
hydrogen
oxygen
comparison
non-treated
samples.
Catalytic
performed
degradation
shorten
time
several
hours
15
min.
most
favorable
following
order
Pd1.0Pt0@Ni
>
Pd0Pt1.0@Ni
Pd0.5Pt0.5@Ni
no
catalyst,
best
performance
pure
surface.
Catalysis Science & Technology,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 1, 2025
DFT
calculations
fully
rationalize
the
mechanistic
details
and
origins
of
chemoselectivity
for
nickel-catalyzed
arylation
amino
alcohols
with
aryl
electrophiles.