Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
62(44)
Опубликована: Авг. 16, 2023
Abstract
Electron‐deficient
acridones
and
in
situ
generated
acridinium
salts
are
reported
as
potent,
closed‐shell
photooxidants
that
undergo
surprising
mechanisms.
When
bridging
acyclic
triarylamine
catalysts
with
a
carbonyl
group
(acridones),
this
completely
diverts
their
behavior
away
from
open‐shell,
radical
cationic,
‘beyond
diffusion’
photocatalysis
to
closed‐shell,
neutral,
diffusion‐controlled
photocatalysis.
Brønsted
acid
activation
of
dramatically
increases
excited
state
oxidation
power
(by
+0.8
V).
Upon
reduction
protonated
acridones,
they
transform
electron‐deficient
even
more
potent
(*
E
1/2
=+2.56–3.05
V
vs
SCE).
These
oxidize
arenes
where
conventional
salt
have
thusfar
been
limited
electron‐rich
arenes.
Surprisingly,
upon
photoexcitation
these
appear
two
electron
reductive
quenching
form
acridinide
anions,
spectroscopically‐detected
forms.
This
new
behaviour
is
partly
enabled
by
catalyst
preassembly
the
arene,
contrasts
SET
salts.
Critically,
study
illustrates
how
redox
active
chromophoric
molecules
initially
considered
photocatalysts
can
during
reaction
catalytically
species
different
spectroscopic
properties.
Chemical Society Reviews,
Год журнала:
2021,
Номер
50(14), С. 7941 - 8002
Опубликована: Янв. 1, 2021
Electrochemistry
has
recently
gained
increased
attention
as
a
versatile
strategy
for
achieving
challenging
transformations
at
the
forefront
of
synthetic
organic
chemistry.
Electrochemistry's
unique
ability
to
generate
highly
reactive
radical
and
ion
intermediates
in
controlled
fashion
under
mild
conditions
inspired
development
number
new
electrochemical
methodologies
preparation
valuable
chemical
motifs.
Particularly,
recent
developments
electrosynthesis
have
featured
an
use
redox-active
electrocatalysts
further
enhance
control
over
selective
formation
downstream
reactivity
these
intermediates.
Furthermore,
electrocatalytic
mediators
enable
proceed
manner
that
is
mechanistically
distinct
from
purely
methods,
allowing
subversion
kinetic
thermodynamic
obstacles
encountered
conventional
synthesis.
This
review
highlights
key
innovations
within
past
decade
area
electrocatalysis,
with
emphasis
on
mechanisms
catalyst
design
principles
underpinning
advancements.
A
host
oxidative
reductive
are
discussed
grouped
according
classification
transformation
nature
electrocatalyst.
Chemical Reviews,
Год журнала:
2021,
Номер
122(2), С. 2752 - 2906
Опубликована: Авг. 10, 2021
Photoinduced
chemical
transformations
have
received
in
recent
years
a
tremendous
amount
of
attention,
providing
plethora
opportunities
to
synthetic
organic
chemists.
However,
performing
photochemical
transformation
can
be
quite
challenge
because
various
issues
related
the
delivery
photons.
These
challenges
barred
widespread
adoption
steps
industry.
past
decade,
several
technological
innovations
led
more
reproducible,
selective,
and
scalable
photoinduced
reactions.
Herein,
we
provide
comprehensive
overview
these
exciting
advances,
including
flow
chemistry,
high-throughput
experimentation,
reactor
design
scale-up,
combination
photo-
electro-chemistry.
Chemical Reviews,
Год журнала:
2021,
Номер
122(2), С. 2487 - 2649
Опубликована: Ноя. 9, 2021
Redox
processes
are
at
the
heart
of
synthetic
methods
that
rely
on
either
electrochemistry
or
photoredox
catalysis,
but
how
do
and
catalysis
compare?
Both
approaches
provide
access
to
high
energy
intermediates
(e.g.,
radicals)
enable
bond
formations
not
constrained
by
rules
ionic
2
electron
(e)
mechanisms.
Instead,
they
1e
mechanisms
capable
bypassing
electronic
steric
limitations
protecting
group
requirements,
thus
enabling
chemists
disconnect
molecules
in
new
different
ways.
However,
while
providing
similar
intermediates,
differ
several
physical
chemistry
principles.
Understanding
those
differences
can
be
key
designing
transformations
forging
disconnections.
This
review
aims
highlight
these
similarities
between
comparing
their
underlying
principles
describing
impact
electrochemical
photochemical
methods.
Chemical Reviews,
Год журнала:
2023,
Номер
123(8), С. 4237 - 4352
Опубликована: Янв. 24, 2023
The
emergence
of
modern
photocatalysis,
characterized
by
mildness
and
selectivity,
has
significantly
spurred
innovative
late-stage
C–H
functionalization
approaches
that
make
use
low
energy
photons
as
a
controllable
source.
Compared
to
traditional
strategies,
photocatalysis
paves
the
way
toward
complementary
and/or
previously
unattainable
regio-
chemoselectivities.
Merging
compelling
benefits
with
workflow
offers
potentially
unmatched
arsenal
tackle
drug
development
campaigns
beyond.
This
Review
highlights
photocatalytic
strategies
small-molecule
drugs,
agrochemicals,
natural
products,
classified
according
targeted
bond
newly
formed
one.
Emphasis
is
devoted
identifying,
describing,
comparing
main
mechanistic
scenarios.
draws
critical
comparison
between
established
ionic
chemistry
photocatalyzed
radical-based
manifolds.
aims
establish
current
state-of-the-art
illustrate
key
unsolved
challenges
be
addressed
in
future.
authors
aim
introduce
general
readership
functionalization,
specialist
practitioners
evaluation
methodologies,
potential
for
improvement,
future
uncharted
directions.
Advanced Functional Materials,
Год журнала:
2023,
Номер
33(14)
Опубликована: Янв. 29, 2023
Abstract
Metamaterial
absorbers
have
been
widely
studied
and
continuously
concerned
owing
to
their
excellent
resonance
features
of
ultra‐thin
thickness,
light‐weight,
high
absorbance.
Their
applications,
however,
are
typically
restricted
by
the
intrinsic
dispersion
materials
strong
resonant
patterned
arrays
(mainly
referring
narrow
absorption
bandwidth).
It
is,
therefore
essential
reassert
principles
building
broadband
metamaterial
(BMAs).
Herein,
research
progress
BMAs
from
principles,
design
strategies,
tunable
properties
functional
applications
comprehensively
deeply
summarized.
Physical
behind
briefly
discussed,
typical
strategies
in
realizing
further
emphasized,
such
as
top‐down
lithography,
bottom‐up
self‐assembly,
emerging
3D
printing
technology.
Diversified
active
components
choices,
including
optical
response,
temperature
electrical
magnetic
mechanical
multi‐parameter
responses,
reviewed
achieving
dynamically
tuned
absorption.
Following
this,
achievements
various
interdisciplinary
for
energy‐harvesting,
photodetectors,
radar‐IR
dual
stealth,
bolometers,
noise
absorbing,
imaging,
fabric
wearable
Finally,
challenges
perspectives
future
development
discussed.
Journal of the American Chemical Society,
Год журнала:
2022,
Номер
144(6), С. 2399 - 2414
Опубликована: Янв. 27, 2022
Late-stage
functionalization
of
C-H
bonds
(C-H
LSF)
can
provide
a
straightforward
approach
to
the
efficient
synthesis
functionalized
complex
molecules.
However,
LSF
is
challenging
because
bond
must
be
in
presence
various
other
functional
groups.
In
this
Perspective,
we
evaluate
aromatic
on
basis
four
criteria─reactivity,
chemoselectivity,
site-selectivity,
and
substrate
scope─and
our
own
views
current
challenges
as
well
promising
strategies
areas
growth
going
forward.
Journal of the American Chemical Society,
Год журнала:
2022,
Номер
144(28), С. 12567 - 12583
Опубликована: Июль 11, 2022
Visible-light
photocatalysis
and
electrocatalysis
are
two
powerful
strategies
for
the
promotion
of
chemical
reactions
that
have
received
tremendous
attention
in
recent
years.
In
contrast,
processes
combine
these
modalities,
an
area
termed
electrophotocatalysis,
until
recently
remained
quite
rare.
However,
over
past
several
years
a
number
reports
this
shown
potential
combining
power
light
electrical
energy
to
realize
new
catalytic
transformations.
Electrophotocatalysis
offers
ability
perform
photoredox
without
need
large
quantities
stoichiometric
or
superstoichiometric
oxidants
reductants
by
making
use
electrochemical
as
electron
source
sink.
addition,
electrophotocatalysis
is
readily
amenable
generation
open-shell
photocatalysts,
which
tend
exceptionally
strong
redox
potentials.
way,
potent
yet
selective
been
realized
under
relatively
mild
conditions.
This
Perspective
highlights
advances
provides
some
possible
avenues
future
work
growing
area.
Angewandte Chemie International Edition,
Год журнала:
2021,
Номер
61(12)
Опубликована: Сен. 3, 2021
Synthetic
photoelectrochemistry
(PEC)
is
receiving
increasing
attention
as
a
new
frontier
for
the
generation
and
handling
of
reactive
intermediates.
PEC
permits
selective
single-electron
transfer
(SET)
reactions
in
much
greener
way
broadens
redox
window
possible
transformations.
Herein,
most
recent
contributions
are
reviewed,
demonstrating
exciting
opportunities,
namely,
combination
with
other
reactivity
paradigms
(hydrogen-atom
transfer,
radical
polar
crossover,
energy
sensitization),
scalability
up
to
multigram
scale,
novel
selectivities
SET
super-oxidations/reductions
importance
precomplexation
temporally
enable
excited
ion
catalysis.
Chemical Reviews,
Год журнала:
2023,
Номер
123(19), С. 11269 - 11335
Опубликована: Сен. 26, 2023
Late-stage
functionalization
(LSF)
constitutes
a
powerful
strategy
for
the
assembly
or
diversification
of
novel
molecular
entities
with
improved
physicochemical
biological
activities.
LSF
can
thus
greatly
accelerate
development
medicinally
relevant
compounds,
crop
protecting
agents,
and
functional
materials.
Electrochemical
synthesis
has
emerged
as
an
environmentally
friendly
platform
transformation
organic
compounds.
Over
past
decade,
electrochemical
late-stage
(eLSF)
gained
major
momentum,
which
is
summarized
herein
up
to
February
2023.
Journal of the American Chemical Society,
Год журнала:
2022,
Номер
144(44), С. 20201 - 20206
Опубликована: Окт. 31, 2022
The
development
of
efficient
and
sustainable
methods
for
decarboxylative
transformations
is
great
importance
due
to
the
ease
availability
nontoxicity
carboxylic
acids.
Despite
tremendous
efforts
in
this
area,
it
remains
challenging
develop
enantioselective
direct
from
Herein
we
disclose
a
photoelectrocatalytic
method
cyanation.
photoelectrochemical
reactions
convert
acids
enantioenriched
nitriles
by
employing
cerium/copper
relay
catalysis
with
cerium
salt
catalytic
decarboxylation
chiral
copper
complex
stereoselective
C-CN
formation.