Photoelectrochemical Fe/Ni cocatalyzed C−C functionalization of alcohols
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Июнь 19, 2024
Abstract
The
simultaneous
activation
of
reactants
on
the
anode
and
cathode
via
paired
electrocatalysis
has
not
been
extensively
demonstrated.
This
report
presents
a
oxidative
reductive
catalysis
based
earth-abundant
iron/nickel
cocatalyzed
C–C
functionalization
ubiquitous
alcohols.
A
variety
alcohols
(i.e.,
primary,
secondary,
tertiary,
or
unstrained
cyclic
alcohols)
can
be
activated
at
very
low
oxidation
potential
(~0.30
V
vs.
Ag/AgCl)
photoelectrocatalysis
coupled
with
versatile
electrophiles.
reactivity
yields
wide
range
structurally
diverse
molecules
broad
functional
group
compatibility
(more
than
50
examples).
Язык: Английский
Ultrafast Photophysics of Ni(I)–Bipyridine Halide Complexes: Spanning the Marcus Normal and Inverted Regimes
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(22), С. 15506 - 15514
Опубликована: Май 22, 2024
Owing
to
their
light-harvesting
properties,
nickel–bipyridine
(bpy)
complexes
have
found
wide
use
in
metallaphotoredox
cross-coupling
reactions.
Key
these
transformations
are
Ni(I)–bpy
halide
intermediates
that
absorb
a
significant
fraction
of
light
at
relevant
reaction
irradiation
wavelengths.
Herein,
we
report
ultrafast
transient
absorption
(TA)
spectroscopy
on
library
eight
complexes,
the
first
such
characterization
any
Ni(I)
species.
The
TA
data
reveal
formation
and
decay
Ni(I)-to-bpy
metal-to-ligand
charge
transfer
(MLCT)
excited
states
(10–30
ps)
whose
relaxation
dynamics
well
described
by
vibronic
Marcus
theory,
spanning
normal
inverted
regions
as
result
simple
changes
bpy
substituents.
While
lifetimes
relatively
long
for
MLCT
first-row
transition
metal
duration
precludes
excited-state
bimolecular
reactivity
photoredox
We
also
present
one-step
method
generate
an
isolable,
solid-state
species,
which
decouples
light-initiated
from
dark,
thermal
cycles
catalysis.
Язык: Английский
Kinetics and Mechanism of PPh3/Ni-Catalyzed, Zn-Mediated, Aryl Chloride Homocoupling: Antagonistic Effects of ZnCl2/Cl–
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(43), С. 29913 - 29927
Опубликована: Окт. 18, 2024
The
Ni/PPh
Язык: Английский
Pyridine vs. Thiazole in Cyclometalated N^C^N Ni(II) Complexes
Inorganics,
Год журнала:
2025,
Номер
13(2), С. 41 - 41
Опубликована: Фев. 1, 2025
Six
N^C^N
cyclometalated
Ni(II)
complexes
[Ni(N^C^N)Cl]
or
[Ni(N^C^N’)Br]
with
symmetric
non-symmetric
N^C^N’
ligands
in
which
the
peripheral
N-groups
were
varied
pyridine
(Py),
4-thiazole
(4Tz),
2-thiazole
(2Tz),
and
2-benzothiazole
(2Btz)
complementing
previously
reported
di(2-pyridyl)phenide
[Ni(Py(Ph)Py)X]
X
=
Cl
Br.
The
synthesized
from
NiBr2
N^CH^N’
protoligands
through
base-assisted
nickelation,
while
received
N^C(Cl)^N
[Ni(COD)2]
(COD
1,5-cyclooctadiene).
Introduction
of
4Tz
on
both
sides
shifted
electrochemical
gap
ΔEexp
Eox–Ered
long
wavelength
UV-vis
absorption
maxima
to
higher
energies,
2Tz
leads
a
shift
lower
energies.
When
introducing
only
one
as
groups,
remaining
PhPy
moiety
dominates
electronic
properties
electrochemistry
photophysics
are
very
similar
Py(Ph)Py
derivatives.
In
contrast
this,
introduction
2Btz
shifts
values
regardless
two
groups
character
frontier
molecular
orbitals
complexes,
DFT
calculations
show.
Long-wavelength
absorptions
vary
416
443
nm,
their
energies
correlate
well
first
reduction
potentials.
Negishi-type
C–C
cross-coupling
reactions
gave
total
yields
ranging
1
60%
44%.
reactivities
roughly
Facilitated
(E
around
–2
higher)
goes
generally
along
improved
performance,
making
thiazole-containing
interesting
candidates
for
such
catalysis.
Язык: Английский
Protecting Group-Free Photocatalyzed O-Arylation of Quinic Acid
Tetrahedron Green Chem,
Год журнала:
2025,
Номер
unknown, С. 100070 - 100070
Опубликована: Фев. 1, 2025
Язык: Английский
Nickel catalyzed C-N coupling of haloarenes with B2N4 reagents
Nature Communications,
Год журнала:
2025,
Номер
16(1)
Опубликована: Апрель 3, 2025
Язык: Английский
Regiodivergent Radical-Relay Alkene Dicarbofunctionalization
Journal of the American Chemical Society,
Год журнала:
2024,
Номер
146(42), С. 28624 - 28629
Опубликована: Окт. 10, 2024
Herein,
we
report
a
regiodivergent
1,n-dicarbofunctionalization
of
unactivated
olefins
enabled
by
Ni-catalyzed
radical
relay
that
forges
both
C(
Язык: Английский
Enantio- and Regioselective Ni-Catalyzed Radical Relay 1,4-Arylalkylation of 1,3-Enynes to Access Chiral Tetrasubstituted Allenes
ACS Catalysis,
Год журнала:
2024,
Номер
14(18), С. 13940 - 13946
Опубликована: Сен. 5, 2024
Язык: Английский
Ni-Catalyzed Kumada–Corriu Cross-Coupling Reactions of Tertiary Grignard Reagents and Bromostyrenes
Organic Letters,
Год журнала:
2024,
Номер
26(28), С. 6047 - 6052
Опубликована: Июль 9, 2024
The
development
of
protocols
for
the
construction
congested
quaternary
centers
is
highly
sought-after.
Herein,
we
report
a
method
cross-coupling
C(sp
Язык: Английский