ACS Catalysis,
Год журнала:
2024,
Номер
14(9), С. 6897 - 6914
Опубликована: Апрель 19, 2024
A
family
of
4,4′-tBu2-2,2′-bipyridine
(tBubpy)
ligands
with
substituents
in
either
the
6-position,
4,4′-tBu2-6-Me-bpy
(tBubpyMe),
or
6
and
6′-positions,
4,4′-tBu2-6,6′-R2-bpy
(tBubpyR2;
R
=
Me,
iPr,
sBu,
Ph,
Mes),
was
synthesized.
These
were
used
to
prepare
Ni
complexes
0,
I,
II
oxidation
states.
We
observed
that
6′-positions
tBubpy
ligand
impact
properties
complexes.
For
example,
bulkier
6,6′-positions
better
stabilized
(tBubpyR2)NiICl
species
resulted
a
cleaner
reduction
from
(tBubpyR2)NiIICl2.
However,
hindered
prevented
coordination
tBubpyR2
Ni0(cod)2.
In
addition,
by
using
type
(tBubpyMe)NiCl2
(tBubpyR2)NiCl2
as
precatalysts
for
different
XEC
reactions,
we
demonstrated
6,6′-substituents
lead
major
differences
catalytic
performance.
Specifically,
while
(tBubpyMe)NiIICl2
is
one
most
active
catalysts
reported
date
can
facilitate
reactions
at
room
temperature,
lower
turnover
frequencies
containing
ligands.
detailed
study
on
intermediates
(tBubpy)Ni(Ar)I
(tBubpyMe2)Ni(Ar)I
revealed
several
factors
likely
contributed
activity.
whereas
are
low
spin
relatively
stable,
high-spin
less
stable.
Furthermore,
captures
primary
benzylic
alkyl
radicals
more
slowly
than
(tBubpy)Ni(Ar)I,
consistent
activity
former
catalysis.
Our
findings
will
assist
design
tailor-made
Ni-catalyzed
transformations.
Chemical Reviews,
Год журнала:
2021,
Номер
122(2), С. 1485 - 1542
Опубликована: Ноя. 18, 2021
The
merger
of
photoredox
catalysis
with
transition
metal
catalysis,
termed
metallaphotoredox
has
become
a
mainstay
in
synthetic
methodology
over
the
past
decade.
Metallaphotoredox
combined
unparalleled
capacity
for
bond
formation
broad
utility
photoinduced
electron-
and
energy-transfer
processes.
Photocatalytic
substrate
activation
allowed
engagement
simple
starting
materials
metal-mediated
bond-forming
Moreover,
electron
or
energy
transfer
directly
key
organometallic
intermediates
provided
novel
modes
entirely
complementary
to
traditional
catalytic
platforms.
This
Review
details
contextualizes
advancements
molecule
construction
brought
forth
by
metallaphotocatalysis.
Chemical Society Reviews,
Год журнала:
2021,
Номер
50(13), С. 7587 - 7680
Опубликована: Янв. 1, 2021
Organic
compounds
that
show
Thermally
Activated
Delayed
Fluorescence
(TADF)
have
become
wildly
popular
as
next
generation
emitters
in
organic
light-emitting
diodes
(OLEDs),
but
since
2016,
received
significant
and
increasing
attention
photocatalysts.
Chemical Reviews,
Год журнала:
2021,
Номер
122(2), С. 2429 - 2486
Опубликована: Окт. 6, 2021
Alkoxy
radicals
are
highly
reactive
species
that
have
long
been
recognized
as
versatile
intermediates
in
organic
synthesis.
However,
their
development
has
impeded
due
to
a
lack
of
convenient
methods
for
generation.
Thanks
advances
photoredox
catalysis,
enabling
facile
access
alkoxy
from
bench-stable
precursors
and
free
alcohols
under
mild
conditions,
research
interest
this
field
renewed.
This
review
comprehensively
summarizes
the
recent
progress
radical-mediated
transformations
visible
light
irradiation.
Elementary
steps
radical
generation
either
or
central
reaction
development;
thus,
each
section
is
categorized
discussed
accordingly.
Throughout
review,
we
focused
on
different
mechanisms
well
impact
synthetic
utilizations.
Notably,
catalytic
abundant
still
early
stage,
providing
intriguing
opportunities
exploit
diverse
paradigms.
Journal of the American Chemical Society,
Год журнала:
2022,
Номер
144(14), С. 6185 - 6192
Опубликована: Март 30, 2022
Alcohols
and
carboxylic
acids
are
among
the
most
commercially
abundant,
synthetically
versatile,
operationally
convenient
functional
groups
in
organic
chemistry.
Under
visible
light
photoredox
catalysis,
these
native
synthetic
handles
readily
undergo
radical
activation,
resulting
open-shell
intermediates
can
subsequently
participate
transition
metal
catalysis.
In
this
report,
we
describe
C(sp3)–C(sp3)
cross-coupling
of
alcohols
through
dual
combination
N-heterocyclic
carbene
(NHC)-mediated
deoxygenation
hypervalent
iodine-mediated
decarboxylation.
This
mild
practical
Ni-catalyzed
radical-coupling
protocol
was
employed
to
prepare
a
wide
array
alkyl–alkyl
cross-coupled
products,
including
highly
congested
quaternary
carbon
centers
from
corresponding
tertiary
or
acids.
We
demonstrate
applications
methodology
alcohol
C1-alkylation
formal
homologation,
as
well
late-stage
functionalization
drugs,
natural
biomolecules.
Journal of the American Chemical Society,
Год журнала:
2022,
Номер
144(2), С. 1045 - 1055
Опубликована: Янв. 5, 2022
Ni/photoredox
catalysis
has
emerged
as
a
powerful
platform
for
C(sp2)–C(sp3)
bond
formation.
While
many
of
these
methods
typically
employ
aryl
bromides
the
C(sp2)
coupling
partner,
variety
aliphatic
radical
sources
have
been
investigated.
In
principle,
reactions
enable
access
to
same
product
scaffolds,
but
it
can
be
hard
discern
which
method
because
nonstandardized
sets
are
used
in
scope
evaluation.
Herein,
we
report
Ni/photoredox-catalyzed
(deutero)methylation
and
alkylation
halides
where
benzaldehyde
di(alkyl)
acetals
serve
alcohol-derived
sources.
Reaction
development,
mechanistic
studies,
late-stage
derivatization
biologically
relevant
chloride,
fenofibrate,
presented.
Then,
describe
integration
data
science
techniques,
including
DFT
featurization,
dimensionality
reduction,
hierarchical
clustering,
delineate
diverse
succinct
collection
that
is
representative
chemical
space
substrate
class.
By
superimposing
examples
from
published
on
this
space,
identify
areas
sparse
coverage
high
versus
low
average
yields,
enabling
comparisons
between
prior
art
new
method.
Additionally,
demonstrate
systematically
selected
quantify
population-wide
reactivity
trends
reveal
possible
functional
group
incompatibility
with
supervised
machine
learning.
Chemical Science,
Год журнала:
2021,
Номер
12(15), С. 5450 - 5457
Опубликована: Янв. 1, 2021
This
works
demonstrates
the
implementation
of
an
electron
donor–acceptor
(EDA)
complex
platform
toward
Ni-catalyzed
C(sp3)–C(sp2)
bond
formation,
circumventing
need
for
exogenous
photocatalysts,
additives,
and
stoichiometric
metal
reductants.
Chemical Society Reviews,
Год журнала:
2021,
Номер
50(16), С. 8903 - 8953
Опубликована: Янв. 1, 2021
The
formation
of
C–aryl
bonds
has
been
the
focus
intensive
research
over
last
decades
for
construction
complex
molecules
from
simple,
readily
available
feedstocks.
Journal of the American Chemical Society,
Год журнала:
2021,
Номер
143(13), С. 4896 - 4902
Опубликована: Март 23, 2021
Under
mild
reaction
conditions
with
inexpensive
cerium
and
nickel
catalysts,
easily
accessible
free
alcohols
can
now
be
utilized
as
operationally
simple
robust
carbon
pronucleophiles
in
selective
C(sp3)–C(sp2)
cross-couplings.
Facilitated
by
automated
high-throughput
experimentation,
sterically
encumbered
benzoate
ligands
have
been
identified
for
complexes,
enabling
the
synergistic
cooperation
of
catalysis
emerging
metallaphotoredox
catalysis.
A
broad
range
aromatic
halides
facilely
employed
this
transformation,
representing
a
new
paradigm
bond
construction
between
aryl
extrusion
formaldehyde.
Moreover,
mechanistic
investigations
conducted,
leading
to
identification
tribenzoate
cerium(III)
complex
viable
intermediate.
Chemical Reviews,
Год журнала:
2023,
Номер
123(22), С. 12313 - 12370
Опубликована: Ноя. 9, 2023
Late-stage
functionalization
(LSF)
introduces
functional
group
or
structural
modification
at
the
final
stage
of
synthesis
natural
products,
drugs,
and
complex
compounds.
It
is
anticipated
that
late-stage
would
improve
drug
discovery's
effectiveness
efficiency
hasten
creation
various
chemical
libraries.
Consequently,
products
a
productive
technique
to
produce
product
derivatives,
which
significantly
impacts
biology
development.
Carbon-carbon
bonds
make
up
fundamental
framework
organic
molecules.
Compared
with
carbon-carbon
bond
construction,
activation
can
directly
enable
molecular
editing
(deletion,
insertion,
atoms
groups
atoms)
provide
more
efficient
accurate
synthetic
strategy.
However,
selective
unstrained
still
one
most
challenging
projects
in
synthesis.
This
review
encompasses
strategies
employed
recent
years
for
cleavage
by
explicitly
focusing
on
their
applicability
functionalization.
expands
current
discourse
reactions
providing
comprehensive
overview
types
bonds.
includes
C-C(sp),
C-C(sp2),
C-C(sp3)
single
bonds;
double
triple
bonds,
focus
catalysis
transition
metals
organocatalysts.
Additionally,
specific
topics,
such
as
ring-opening
processes
involving
three-,
four-,
five-,
six-membered
rings,
are
discussed,
exemplar
applications
these
techniques
showcased
context
bioactive
molecules
discovery.
aims
shed
light
advancements
field
propose
potential
avenues
future
research
realm
Chemical Reviews,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 12, 2024
Since
the
seminal
report
by
Adachi
and
co-workers
in
2012,
there
has
been
a
veritable
explosion
of
interest
design
thermally
activated
delayed
fluorescence
(TADF)
compounds,
particularly
as
emitters
for
organic
light-emitting
diodes
(OLEDs).
With
rapid
advancements
innovation
materials
design,
efficiencies
TADF
OLEDs
each
primary
color
points
well
white
devices
now
rival
those
state-of-the-art
phosphorescent
emitters.
Beyond
electroluminescent
devices,
compounds
have
also
found
increasing
utility
applications
numerous
related
fields,
from
photocatalysis,
to
sensing,
imaging
beyond.
Following
our
previous
review
2017
(