Lantern‐Like Diplatinum(III)‐Catalyzed Redox‐Free Borylation or Silylation of Alkynes
Chuntao Wang,
No information about this author
Xianyang Long,
No information about this author
Tongxiang Cao
No information about this author
et al.
Chinese Journal of Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 31, 2025
Comprehensive
Summary
Binuclear
platinum(III)
complexes
were
known
for
their
high
index
of
antitumor
activity
and
a
lower
associated
nephrotoxicity.
However,
the
chemistry
reactivity
binuclear
compounds
have
not
yet
been
explored
to
same
extent
as
those
platinum(II)
platinum(IV)
species.
Here,
we
reported
first
platinum‐catalyzed
hydrosilylation,
monoborylation
diboration
reaction
alkynes
with
excellent
selectivity
yield.
Moreover,
mechanistic
investigation
by
control
experiments,
kinetic
isotope
effect
(KIE)
study,
Hammett
plots,
NMR
spectra,
UV−vis
X‐ray
photoelectron
spectroscopy
(XPS)
analysis
reveal
that
Pt(III)
2
‐catalyzed
reactions
pass
through
σ‐bond
metathesis
process
rather
than
two‐electron
redox
processes
mononuclear
platinum
catalysis.
there
are
two
different
rate‐determining
steps,
in
which
migratory
insertion
step
dominates
rate
electron
deficient
substates
rich
counterparts,
respectively.
Language: Английский
Lighting up metal nanoclusters by the H2O-dictated electron relaxation dynamics
Yuan Zhong,
No information about this author
Xue Wang,
No information about this author
Zhou Huang
No information about this author
et al.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: March 7, 2025
Abstract
The
modulation
of
traps
has
found
attractive
attention
to
optimize
the
performance
luminescent
materials,
while
understanding
trap-involved
photoluminescence
management
metal
nanoclusters
greatly
lags
behind,
thus
extensively
impeding
their
increasing
acceptance
as
promising
chromophores.
Here,
we
report
an
efficient
passivation
structural
oxygen
vacancies
in
AuAg
by
leveraging
H
2
O
molecules,
achieving
a
sensitive
color
tuning
from
536
480
nm
and
remarkably
boosting
quantum
yield
5.3%
(trap-state
emission)
91.6%
(native-state
emission).
In
detail,
favored
electron
transfer
relevant
contributes
weak
trap-state
emission,
which
is
capable
being
restrained
molecules
taking
Au-O
Ag-O
bonds.
This
scenario
allows
dominated
native-state
emission
with
faster
radiative
rate.
parallel,
can
rigidify
landscape
on
hydrogen
bonding,
enabling
suppression
electron-optical
phonon
coupling
decelerated
non-radiative
presented
study
deepens
tailoring
properties
manipulating
surface
trap
chemistry
relaxation
dynamics,
would
shed
new
light
customizable
performance.
Language: Английский
Employing Copper-Based Nanomaterials to Combat Multi-Drug-Resistant Bacteria
Yujie Zhai,
No information about this author
Zhiqing Liang,
No information about this author
Xijun Liu
No information about this author
et al.
Microorganisms,
Journal Year:
2025,
Volume and Issue:
13(4), P. 708 - 708
Published: March 21, 2025
The
rise
of
multi-drug-resistant
(MDR)
bacteria
poses
a
severe
global
threat
to
public
health,
necessitating
the
development
innovative
therapeutic
strategies
overcome
these
challenges.
Copper-based
nanomaterials
have
emerged
as
promising
agents
due
their
intrinsic
antibacterial
properties,
cost-effectiveness,
and
adaptability
for
multifunctional
approaches.
These
materials
exhibit
exceptional
potential
in
advanced
therapies,
including
chemodynamic
therapy
(CDT),
photothermal
(PTT),
photodynamic
(PDT).
Their
unique
physicochemical
such
controlled
ion
release,
reactive
oxygen
species
(ROS)
generation,
tunable
catalytic
activity,
enable
them
target
MDR
effectively
while
minimizing
off-target
effects.
This
paper
systematically
reviews
mechanisms
through
which
Cu-based
enhance
efficiency
emphasizes
specific
performance
field.
Key
factors
influencing
properties—such
electronic
interactions,
characteristics,
size
effects,
ligand
single-atom
doping,
geometric
configurations—are
analyzed
depth.
By
uncovering
copper-based
nanomaterials,
this
work
aims
inspire
approaches
that
improve
patient
outcomes,
reduce
burden
bacterial
infections,
health
initiatives.
Language: Английский
Electrochemical synthesis of allenyl silanes and allenyl boronic esters
Tingting Feng,
No information about this author
Tony Biremond,
No information about this author
Philippe Jubault
No information about this author
et al.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: May 17, 2025
Allenyl
silanes
and
boronates
are
pivotal
building
blocks
in
organic
synthesis.
Nevertheless,
their
synthesis
requires
the
manipulation
of
transition
metal
or
highly
reactive
species.
Hence,
development
more
sustainable
protocol
is
sought
after.
Here
we
show
electrochemical
allenyl
boronic
esters.
This
catalyst-free
method
proceeds
under
mild
reaction
conditions.
The
for
shows
an
excellent
efficiency
a
good
functional
group
tolerance.
isolated
yields
(28
examples,
45-95%
yields)
without
use
catalyst
A
similar
developed
boronates,
which
obtained
low
to
moderate
(13
5-55%
yields).
Finally,
mechanism
based
on
oxidative
generation
silyl
boryl
radicals
suggested
access
these
classes
allenes.
Language: Английский