Abstract
This
review
delves
into
the
innovative
field
of
interfacial
photoelectrochemical
(iPEC)
and
(PEC)
catalysis,
dynamic
synthesis
methodologies
that
seamlessly
integrates
electrochemical
photoredox
catalysis
for
efficient
environmentally
friendly
reactions.
Utilizing
minute
quantities
photocatalysts,
visible
light
becomes
a
powerful
tool,
generating
transient
excited
states
to
catalyze
spectrum
reactions
through
single‐electron
oxidation
or
reduction
events.
The
categorizes
recent
advancements,
highlighting
applications
in
organic
synthesis,
late‐stage
modifications,
distinctive
features
methodology.
Despite
being
its
early
stages,
this
synergistic
approach
holds
great
promise
propelling
forward,
with
potential
large‐scale
diverse
functionalizations,
including
asymmetric
bioconjugation
strategies
biomolecule
modifications.
Frontiers in Chemistry,
Год журнала:
2024,
Номер
12
Опубликована: Фев. 19, 2024
This
comprehensive
review,
covering
2021-2023,
explores
the
multifaceted
chemical
and
pharmacological
potential
of
coumarins,
emphasizing
their
significance
as
versatile
natural
derivatives
in
medicinal
chemistry.
The
synthesis
functionalization
coumarins
have
advanced
with
innovative
strategies.
enabled
incorporation
diverse
functional
fragments
or
construction
supplementary
cyclic
architectures,
thereby
biological
physico-chemical
properties
compounds
obtained
were
enhanced.
unique
structure
coumarine
facilitates
binding
to
various
targets
through
hydrophobic
interactions
pi-stacking,
hydrogen
bonding,
dipole-dipole
interactions.
Therefore,
this
important
scaffold
exhibits
promising
applications
uncountable
fields
chemistry
(e.g.,
neurodegenerative
diseases,
cancer,
inflammation).
Accounts of Chemical Research,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 13, 2025
ConspectusMolecular
photoelectrocatalysis,
which
combines
the
merits
of
photocatalysis
and
organic
electrosynthesis,
including
their
green
attributes
capacity
to
offer
novel
reactivity
selectivity,
represents
an
emerging
field
in
chemistry
that
addresses
growing
demands
for
environmental
sustainability
synthetic
efficiency.
This
synergistic
approach
permits
access
a
wider
range
redox
potentials,
facilitates
transformations
under
gentler
electrode
decreases
use
external
harsh
reagents.
Despite
these
potential
advantages,
this
area
did
not
receive
significant
attention
until
2019,
when
we
others
reported
first
examples
modern
molecular
photoelectrocatalysis.
These
studies
showcased
immense
hybrid
strategy,
only
inherits
strengths
its
parent
fields
but
also
unlocks
unprecedented
enabling
challenging
mild
conditions
while
minimizing
reliance
on
stoichiometric
oxidants
or
reductants.In
Account,
present
our
efforts
develop
photoelectrocatalytic
strategies
leverage
homogeneous
catalysts
facilitate
diverse
radical
reactions.
By
integrating
electrocatalysis
with
key
photoinduced
processes
such
as
single
electron
transfer
(SET),
ligand-to-metal
charge
(LMCT),
hydrogen
atom
(HAT),
have
established
methods
transform
substrates
organotrifluoroborates,
arenes,
carboxylic
acids,
alkanes
into
reactive
intermediates.
intermediates
subsequently
engage
heteroarene
C-H
functionalization
Importantly,
photoelectrochemical
catalysts,
generated
bulk
solution
readily
participate
efficient
reactions
without
undergoing
further
overoxidation
carbocations,
common
challenge
conventional
electrochemical
systems.By
integration
photoelectrocatalysis
asymmetric
catalysis,
developed
catalysis
(PEAC),
proves
be
enantioselective
synthesis
chiral
nitriles.
involves
two
relay
catalytic
cycles:
initial
process
engenders
benzylic
radicals
from
precursors
alkyl
aryl
alkenes,
C-radicals
are
then
subjected
cyanation
subsequent
copper-electrocatalytic
cycle.Within
realm
oxidative
transformations,
anode
serves
crucial
component
recycling
generating
photocatalyst,
cathode
promotes
proton
reduction.
dual
functionality
enables
via
H
Chinese Journal of Chemistry,
Год журнала:
2023,
Номер
41(22), С. 2963 - 2968
Опубликована: Июнь 24, 2023
Comprehensive
Summary
A
photoelectrochemical
approach
for
the
C—H
silylation
of
heteroarenes
through
dehydrogenation
cross‐coupling
with
H
2
evolution
has
been
developed.
The
depends
on
hydrogen
atom
transfer
(HAT)
from
silanes
to
Cl‐radical
generated
light‐induced
homolytic
cleavage
Cl
,
in
which
was
produced
by
electrochemical
oxidation
chloride.
large
number
silylated
heterocyclic
molecules
are
rapidly
constructed
satisfactory
yields
without
relying
oxidants
and
metal
reagents.
Organic Letters,
Год журнала:
2023,
Номер
25(18), С. 3314 - 3318
Опубликована: Май 1, 2023
We
disclose
herein
an
efficient
photochemical
formal
[3+2+1]
annulation
strategy
for
the
transformation
of
diazocarbonyl
compounds
into
various
fluorinated
nitrogen-containing
heterocycles.
This
is
characterized
by
reacting
fluoroalkyl
radicals
with
α-diazoketones,
which
are
used
as
infrequent
denitrogenated
synthons
under
visible
light.
Moreover,
a
wide
range
N-heterocycles
containing
precious
CF3
and
perfluoroalkylated
groups
constructed
in
moderate
to
good
yields.
Notably,
this
may
provide
fruitful
path
synthesis
complex
organofluorides
via
diazo/fluorine/radical
chemistry.
Organic & Biomolecular Chemistry,
Год журнала:
2023,
Номер
21(15), С. 3101 - 3104
Опубликована: Янв. 1, 2023
Herein,
a
Cu(II)-catalyzed
facile
construction
of
synthetically
valuable
spiro
compounds
from
β-naphthols
in
air
is
reported,
which
N,N-dimethylaminoethanol
(DMEA)
serves
as
an
efficient
and
unique
C1
synthon.
This
transformation
proceeds
through
ortho-quinone
methide
(o-QM)
formation/Michael
addition/dearomatization
sequence,
affording
various
spiro(naphthalenenaphtho)furan-2-ones
moderate
to
excellent
yields.
Green Chemistry,
Год журнала:
2024,
Номер
26(7), С. 4199 - 4208
Опубликована: Янв. 1, 2024
A
new
photoelectrocatalytic
mode
permits
the
synthesis
of
polycyclic
pyrimidin-4-ones
through
dehydrogenative
cyclization
malonates
with
unactivated
alkenes.
Organic Chemistry Frontiers,
Год журнала:
2024,
Номер
11(14), С. 4024 - 4040
Опубликована: Янв. 1, 2024
This
review
provides
a
comprehensive
overview
of
metal
catalysis
in
photo-electrochemical
systems,
discussing
reaction
mechanisms
and
offering
prospects
for
this
triadic
catalytic
mode.
Chemical Reviews,
Год журнала:
2024,
Номер
124(21), С. 12264 - 12304
Опубликована: Окт. 23, 2024
Electrocatalysis
and
photocatalysis
have
been
the
focus
of
extensive
research
efforts
in
organic
synthesis
recent
decades,
these
powerful
strategies
provided
a
wealth
new
methods
to
construct
complex
molecules.
Despite
intense
efforts,
only
recently
has
there
significant
on
combined
use
two
modalities.
Nevertheless,
past
five
years
witnessed
rapidly
growing
interest
area
electrophotocatalysis.
This
hybrid
strategy
capitalizes
enormous
benefits
using
photons
as
reagents
while
also
employing
an
electric
potential
convenient
tunable
source
or
sink
electrons.
Research
this
topic
led
number
for
C-H
functionalization,
reductive
cross-coupling,
olefin
addition
among
others.
field
seen
broad
range
catalyst
types,
including
both
metal
organocatalysts.
Of
particular
note
work
with
open-shell
photocatalysts,
which
tend
comparatively
large
redox
potentials.
Electrochemistry
provides
means
generate
such
species,
making
electrophotocatalysis
particularly
amenable
intriguing
class
catalyst.
review
surveys
applied
synthesis,
organized
broadly
into
oxidative,
reductive,
neutral
transformations.