Synthesis,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 28, 2024
Abstract
The
partial
reduction
of
nitroarenes
with
hydroxides
in
alcoholic
media
is
a
venerable
yet
very
direct
approach
to
the
synthesis
symmetrical
azoxyarenes.
Herein,
first
application
this
method
nitropyridines
disclosed,
presenting
its
adaptation
these
challenging
but
important
substrates.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 16, 2025
The
work
establishes
the
salt
of
a
tetra-cationic
distibane,
[L2Sb2][CF3SO3]4
=
[1]2[OTf]4
(CF3SO3
OTf),
stabilized
by
bis(α-iminopyridine)
ligand
L,
defying
Coulombic
repulsion.
synthetic
approach
involved
dehydrocoupling
reaction
when
mixture
L
and
Sb(OTf)3
in
1:1
ratio
was
treated
with
Et3SiH/LiBEt3H
as
hydride
source.
Compound
also
achieved
from
[LSbCl][OTf]2
precursor
using
Et3SiH.
Dissolution
polar
solvents
unveiled
formation
persistent
L-stabilized
dicationic
Sb(II)
radical
monomer
[1][OTf]2,
while
addition
Me3SiOTf
regenerated
dimer
[1]2[OTf]4.
homolytic
cleavage
Sb–Sb
bond
[1]24+
has
manifested
exchange
reactions
between
Ph2Ch2
(Ch
S,
Se),
giving
[LSb(SPh)][OTf]2
[2][OTf]2
[LSb(SePh)][OTf]2
[3][OTf]2,
respectively,
acetonitrile.
Reaction
p-benzoquinone
gave
[L2Sb2(C6H4O2)][OTf]4
[4][OTf]4.
An
interesting
oxygen
atom
insertion
occurred
2,2,6,6-tetramethylpiperidine-1-oxyl
(TEMPO)
to
give
[L2Sb2O][
OTf]4
[5][OTf]4.
oxo-bridged
compound
[5][OTf]4
obtained
exposure
open
air.
strong
Mn–Mn
[Mn2(CO)10]
could
be
cleaved
reacting
presence
pyridine
form
[LSbMn(CO)5][
OTf]2
[6][OTf]2.
On
other
hand,
[Co2(CO)8]
oxidative
product
[L2Sb2Co(CO)3][OTf]3
[7][OTf]3.
compounds
were
characterized
both
solid
solution
states.
Computational
studies
comprehensive
understanding
experimental
findings.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(35), P. 24515 - 24525
Published: July 30, 2024
Manganese
complexes
stand
out
as
promising
candidates
for
photocatalyst
design,
attributed
to
their
eco-
and
biocompatibility,
versatile
valence
states,
capability
facilitating
multiple
electronic
excitations.
However,
several
intrinsic
constraints,
such
inadequate
visible
light
response
short
excited-state
lifetimes,
hinder
effective
photoinduced
electron
transfer
impede
photoredox
activation
of
substrates.
To
overcome
this
obstacle,
we
have
developed
a
class
manganese
featuring
boron-incorporated
Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
13(27)
Published: June 1, 2024
Abstract
Despite
advancements
in
breast
cancer
treatment,
bone
metastases
remain
a
significant
concern
for
advanced
patients.
Current
theranostics
strategies
face
challenges
integrating
tumor
and
formation.
Herein,
this
work
develops
an
activatable
targeted
nanomedicine
AuMnCO@BSA‐N
3
(AMCBN)
to
enable
novel
collaborative
integration
of
second
near‐infrared
(NIR‐II)
fluorescence
imaging
guided
precise
osteogenic
microenvironment
remolding.
This
strategy
employs
chemical
coordination
between
noble
metal
complex
carbonyl
(MnCO),
with
surface
modification
azide
groups
enhance
affinity
through
passive
active
targeting.
The
initiated
respondent
behavior
AMCBN
by
accelerate
the
degradation
coordinated
MnCO,
resulting
rapid
release
multifunctional
agents
efficient
chemodynamic
therapy
(CDT)/gas
synergistic
therapy.
Meanwhile,
exceptional
bone‐binding
properties
controlled
Mn
2+
ions
carbon
monoxide
(CO)
microenvironment,
thereby
facilitating
expression
osteogenesis‐related
proteins
establishing
synchronous
process
tumor‐bone
repair.
Organic Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 30, 2025
A
straightforward
and
efficient
method
for
the
synthesis
of
multisubstituted
indoles
has
been
developed
through
a
dual
gold/silver-catalyzed
aminoalkynylation
2-alkynylanilines
using
hypervalent
iodine(III)
reagents
under
open-air
conditions.
This
approach
features
in
situ
generation
alkynyl
Au(III)
species,
which
facilitates
with
excellent
functional
group
tolerance
high
yields.
Mechanistic
studies
reveal
that
gold(III)
intermediate
plays
crucial
role
reaction
pathway.
Moreover,
protocol
is
scalable
to
gram
quantities
offers
potential
further
transformation
into
diverse
functionalized
compounds.