Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
62(39)
Опубликована: Июнь 30, 2023
Organomagnesium
halides
(Grignard
reagents)
are
essential
carbanionic
building
blocks
widely
used
in
carbon-carbon
and
carbon-heteroatom
bond-forming
reactions
with
various
electrophiles.
In
the
Barbier
variant
of
Grignard
synthesis,
generation
air-
moisture-sensitive
reagents
occurs
concurrently
their
reaction
an
electrophile.
Although
operationally
simpler,
classic
approach
suffers
from
low
yields
due
to
multiple
side
reactions,
thereby
limiting
scope
its
application.
Here,
we
report
a
mechanochemical
adaptation
Mg-mediated
reaction,
which
overcomes
these
limitations
facilitates
coupling
versatile
organic
(e.g.,
allylic,
vinylic,
aromatic,
aliphatic)
diverse
range
electrophilic
substrates
aromatic
aldehydes,
ketones,
esters,
amides,
O-benzoyl
hydroxylamine,
chlorosilane,
borate
ester)
assemble
C-C,
C-N,
C-Si,
C-B
bonds.
The
has
advantage
being
essentially
solvent-free,
simple,
immune
air,
surprisingly
tolerant
water
some
weak
Brønsted
acids.
Notably,
solid
ammonium
chloride
was
found
improve
ketones.
Mechanistic
studies
have
clarified
role
mechanochemistry
process,
indicating
transient
organometallics
facilitated
by
improved
mass
transfer
activation
surface
magnesium
metal.
Synthesis,
Год журнала:
2023,
Номер
55(16), С. 2439 - 2459
Опубликована: Май 3, 2023
Abstract
Although
known
for
millennia,
it
is
only
recently
that
mechanochemistry
has
received
serious
attention
by
chemists.
Indeed,
during
the
past
15
years
an
extraordinary
number
of
reports
concerning
solid-state
chemical
transformations
through
grinding
and
milling
techniques
have
been
recorded.
This
short
review
discusses
circumstances
led
this
renaissance,
highlighting
present
intense
interest
in
so-called
green
chemistry,
enabling
capacity
to
handle
insoluble
substrates,
identification
profound
influence
additives
can
on
mechanochemically
activated
reactions.
The
core
account
focuses
salient
developments
synthetic
organic
especially
amino
acid
peptide
mechanosynthesis,
successful
employment
mechanochemical
activation
combination
with
asymmetric
organocatalysis,
promising
enzymatic
whole
cell
biocatalysis,
remarkable
achievement
multicomponent
selective
reactions
via
complex,
multistep
reaction
pathways,
mechanosynthesis
representative
heterocycles.
final
section
comments
some
pending
tasks
area,
such
as
scaling-up
processes
be
practical
use
industry,
requirement
easier
more
efficient
control
parameters
monitoring
devices,
consequently
careful
analysis
additional
procedures
a
proper
understanding
phenomena.
1
Introduction
2
Brief
History
Mechanochemistry
3
Milling
Equipment
Reaction
Parameters
4
Attributes
That
Propelled
Its
Present
Renaissance
4.1
Enormous
Attention
Being
Presently
Paid
Sustainable
Chemistry
4.2
Reduced
Energy
Consumption
4.3
Additive-Based
4.4
Handling
Insoluble
Reactants
4.5
‘Impossible’
Reactions
Are
Successful
4.6
Air-
Water-Sensitive
Reagents
Ball
5
Salient
Developments
Mechanochemical
Activation
Synthetic
Organic
5.1
Amino
Acid
Peptide
Mechanosynthesis
5.2
Asymmetric
Synthesis
Organocatalysis
under
Ball-Milling
Conditions
5.3
Mechanoenzymology
5.4
Multicomponent
Activated
5.5
Heterocycles
Modification
6
Future
Directions
6.1
Scaling-Up
Protocols
6.2
Temperature-Controlled
6.3
Understanding
Transformations
6.4
Emerging
Techniques
7
Conclusions
Angewandte Chemie International Edition,
Год журнала:
2023,
Номер
62(21)
Опубликована: Март 22, 2023
Birch
reduction
has
been
widely
used
in
organic
synthesis
for
over
half
a
century
as
powerful
method
to
dearomatize
arenes
into
1,4-cyclohexadiene
derivatives.
However,
the
conventional
reaction
using
liquid
ammonia
requires
laborious
procedures
ensure
inert
conditions
and
low
temperatures.
Although
several
ammonia-free
modifications
have
reported,
development
of
an
operationally
simple,
efficient,
scalable
protocol
remains
challenge.
Herein,
we
report
lithium-based
air
without
special
operating
ball-milling
technique.
This
is
characterized
by
its
operational
simplicity
extremely
short
time
(within
1
min),
probably
owing
situ
mechanical
activation
lithium
metal,
broad
substrate
scope,
no
requirement
dry
bulk
solvents.
The
potential
our
flash
also
demonstrated
efficient
bioactive
target
molecules
gram-scale
synthesis.
Advanced Materials,
Год журнала:
2024,
Номер
36(14)
Опубликована: Янв. 4, 2024
Abstract
After
application
in
electric
vehicles,
spent
LiFePO
4
(LFP)
batteries
are
typically
decommissioned.
Traditional
recycling
methods
face
economic
and
environmental
constraints.
Therefore,
direct
regeneration
has
emerged
as
a
promising
alternative.
However,
irreversible
phase
changes
can
significantly
hinder
the
efficiency
of
process
owing
to
structural
degradation.
Moreover,
improper
storage
treatment
practices
lead
metamorphism,
further
complicating
process.
In
this
study,
sustainable
recovery
method
is
proposed
for
electrochemical
repair
LFP
batteries.
A
ligand‐chain
Zn‐complex
(ZnDEA)
utilized
regulator,
with
its
─NH─
group
alternatingly
facilitating
binding
preferential
transition
metal
ions
(Fe
3+
during
charging
Zn
2+
discharging).
This
dynamic
coordination
ability
helps
modulate
volume
within
recovered
framework.
Consequently,
framework
store
more
Li‐ions,
enhance
reversibility
between
FePO
(FP),
modify
initial
Coulombic
efficiency,
reduce
polarization
voltage
differences.
The
cells
exhibit
excellent
capacity
retention
96.30%
after
1500
cycles
at
2
C.
ligand
chain
mechanism
promotes
evolution
facilitate
ion
migration,
providing
valuable
insights
into
targeted
compensation
environmentally
friendly
practical
applications.
Chemical Science,
Год журнала:
2023,
Номер
14(27), С. 7475 - 7481
Опубликована: Янв. 1, 2023
We
demonstrate
the
use
of
a
metal
surface
to
directly
catalyse
copper-catalysed
alkyne-azide
click-coupling
(CuAAC)
reactions
under
conditions
Resonant
Acoustic
Mixing
(RAM)
-
recently
introduced
and
scalable
mechanochemical
methodology
that
uniquely
eliminates
need
for
bulk
solvent,
as
well
milling
media.
By
using
simple
copper
coil
catalyst,
this
work
shows
direct
mechanocatalysis
can
occur
in
an
impact-free
environment,
relying
solely
on
high-speed
mixing
reagents
against
surface,
without
specially
designed
containers
introducing
experimental
setup
enables
real-time
Raman
spectroscopy
monitoring
RAM
processes,
we
0th-order
reaction
kinetics
several
selected
CuAAC
reactions,
supporting
surface-based
catalysis.
The
herein
presented
RAM-based
is
simple,
effective
one-pot,
two-step
synthesis
triazoles
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Янв. 26, 2024
We
disclose
herein
a
strategy
for
the
rapid
synthesis
of
versatile
organoselenium
compounds
under
mild
conditions.
In
this
work,
magnesium-based
selenium
nucleophiles
are
formed
in
situ
from
easily
available
organic
halides,
magnesium
metal,
and
elemental
via
mechanical
stimulation.
This
process
occurs
liquid-assisted
grinding
(LAG)
conditions,
requires
no
complicated
pre-activation
procedures,
operates
broadly
across
diverse
range
aryl,
heteroaryl,
alkyl
substrates.
symmetrical
diselenides
efficiently
obtained
after
work-up
air,
while
one-pot
nucleophilic
addition
reactions
with
various
electrophiles
allow
comprehensive
unsymmetrical
monoselenides
high
functional
group
tolerance.
Notably,
method
is
applied
to
regioselective
selenylation
diiodoarenes
polyaromatic
aryl
halides
that
difficult
operate
solution
approaches.
Besides
selenium,
sulfur
tellurium
also
competent
process,
which
showcases
potential
methodology
facile
organochalcogen
compounds.
Chemical Science,
Год журнала:
2024,
Номер
15(12), С. 4452 - 4457
Опубликована: Янв. 1, 2024
In
this
study,
a
mechanochemical
protocol
for
highly
efficient
and
ammonia-free
sodium-based
Birch
reduction
was
developed,
leveraging
the
use
of
cheap
easy-to-handle
sodium
lumps
d
-(+)-glucose
as
proton
source.
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
63(28)
Опубликована: Апрель 30, 2024
Abstract
The
development
of
green
and
efficient
deuteration
methods
is
great
significance
for
various
fields
such
as
organic
synthesis,
analytical
chemistry,
medicinal
chemistry.
Herein,
we
have
developed
a
dehalogenative
strategy
using
piezoelectric
materials
catalysts
in
solid‐phase
system
under
ball‐milling
conditions.
This
non‐spontaneous
reaction
induced
by
mechanical
force.
D
2
O
can
serve
both
deuterium
source
an
electron
donor
the
transformation,
eliminating
need
additional
stoichiometric
exogenous
reductants.
A
series
(hetero)aryl
iodides
be
transformed
into
deuterated
products
with
high
incorporation.
method
not
only
effectively
overcomes
existing
synthetic
challenges
but
also
used
labelling
drug
molecules
derivatives.
Bioactivity
experiments
molecule
suggest
that
D‐ipriflavone
enhances
inhibitory
effects
on
osteoclast
differentiation
BMDMs
vitro
.
ACS Organic & Inorganic Au,
Год журнала:
2024,
Номер
4(5), С. 432 - 470
Опубликована: Авг. 7, 2024
In
recent
years,
mechanochemistry
has
become
an
innovative
and
sustainable
alternative
to
traditional
solvent-based
synthesis.
Mechanochemistry
rapidly
expanded
across
a
wide
range
of
chemistry
fields,
including
diverse
organic
compounds
active
pharmaceutical
ingredients,
coordination
compounds,
organometallic
complexes,
main
group
frameworks,
technologically
relevant
materials.
This
Review
aims
highlight
advancements
accomplishments
in
mechanochemistry,
underscoring
its
potential
as
viable
eco-friendly
conventional
solution-based
methods
the
field
synthetic
chemistry.
Chemical Science,
Год журнала:
2022,
Номер
14(3), С. 499 - 505
Опубликована: Ноя. 28, 2022
The
direct
synthesis
of
organomanganese
reagents
from
organic
halides
and
manganese
metal
remains
a
challenge.
Current
solution-based
approaches
require
the
preparation
activated
(Rieke
manganese)
or
use
multiple
additives
to
promote
insertion
into
carbon-halogen
bond.
Here,
we
show
that
mechanochemical
ball-milling
protocol
facilitates
generation
various
arylmanganese
nucleophiles
aryl
commercially
available,
unactivated
without
need
for
complicated
pre-activation
processes
additives.
These
manganese-based
carbon
can
be
used
directly
one-pot
addition
reactions
with
electrophiles
palladium-catalyzed
cross-coupling
under
bulk-solvent-free
conditions.
Importantly,
all
experimental
operations
conducted
atmospheric