Construction of a Dual-Functionalized Acid–Base Nanocatalyst via HEPES Buffer Functionalized on Fe3O4 as a Reusable Catalyst for Annulation Reactions
Langmuir,
Journal Year:
2024,
Volume and Issue:
40(26), P. 13397 - 13411
Published: June 20, 2024
Herein,
we
present
a
highly
efficient
dual-functionalized
acid–base
nanocatalyst,
denoted
as
Fe3O4@GLYMO-HEPES,
featuring
sulfuric
acid
and
tertiary
amines
its
dual
functional
components.
This
catalyst
is
synthesized
through
the
immobilization
of
4-(2-hydroxyethyl)-1-piperazineethanesulfonic
(HEPES)
source
these
functionalities
onto
magnetite
(Fe3O4)
using
3-glycidoxypropyltriethoxysilane
(GLYMO)
linker.
Characterization
studies
confirm
integrity
Fe3O4
core,
with
GLYMO-HEPES
coating
exhibiting
no
phase
changes.
Furthermore,
Fe3O4@GLYMO-HEPES
nanoparticles
demonstrate
uniform
size
distribution
without
aggregation.
Notably,
exhibits
remarkable
stability
up
to
200
°C
possesses
saturation
magnetization
value
31.5
emu/g,
facilitating
easy
recovery
via
magnetic
separation.
These
findings
underscore
potential
versatile
recyclable
nanocatalyst
for
various
applications.
Its
catalytic
ability
was
evaluated
in
synthesis
pyrano[2,3-c]pyrazoles
2-amino-3-cyano-4H-chromenes
tandem
Knorr–Knoevenagel–Michael–Thorpe–Ziegler-type
heterocyclization
mechanism,
different
aldehydes.
A
wide
range
fused
heterocycles
having
good
excellent
yields.
The
process
cost-effective,
safe,
sustainable,
scalable,
can
be
reused
five
times.
prepared
found
stable
heterogeneous
showed
recyclability.
Language: Английский
Reconstruction of surface defects in Bi2MoO6 induced by amorphous ZnO for ultra-fast photocatalytic purification of Cr(VI)
Lili Yao,
No information about this author
Cheng-zhao Jin,
No information about this author
Xinan Yang
No information about this author
et al.
Journal of environmental chemical engineering,
Journal Year:
2025,
Volume and Issue:
13(3), P. 116553 - 116553
Published: April 11, 2025
Language: Английский
Pd-Catalyzed Transfer Hydrogenation of Alkenes Using Tetrahydroxydiboron as the Sole Hydrogen Donor
Benjamin J. Stokes,
No information about this author
Mahshid Yaghoubi,
No information about this author
Isabella C. Reyes
No information about this author
et al.
SynOpen,
Journal Year:
2024,
Volume and Issue:
08(03), P. 169 - 172
Published: July 16, 2024
Abstract
Tetrahydroxydiboron-mediated
catalytic
transfer
hydrogenations
have
typically
involved
co-additives
that,
like
tetrahydroxydiboron
itself,
are
H
atom
donors.
Herein
we
report
an
alkene
hydrogenation
method
with
as
the
sole
source
of
atoms.
The
reaction
uses
Pd(OAc)2
a
convenient
putative
colloid
pre-catalyst,
and
cyclic
monoethers
competent
solvents.
Highly
efficient
deuteration
is
demonstrated
using
tetradeuteroxydiboron.
Language: Английский
Non-classical effective methods for reduction of heteroaromatic compounds
Russian Chemical Reviews,
Journal Year:
2024,
Volume and Issue:
93(11), P. RCR5149 - RCR5149
Published: Oct. 30, 2024
The
review
summarizes
the
known
data
on
various
methods
for
saturation
and
dearomatization
of
heterocyclic
moieties,
forming
diverse
aromatic
compounds.
Since
classical
hydrogenation
substrates
with
molecular
hydrogen
has
a
number
fundamental
drawbacks
that
hinder
both
its
use
at
laboratory
level
widespread
implementation
in
industrial
production,
main
attention
is
paid
to
non-classical
described
literature
over
last
20–25years.
ammonia-free
Birch
reduction,
transfer
hydrogenation,
reduction
by
Hantzsch
esters
some
other
reactions
involving
compounds
are
summarized
systematized.
It
shown
such
or
heterocycles
can
cases
be
more
efficient
than
procedures.<br>
bibliography
includes
173
references.
Language: Английский