Organic & Biomolecular Chemistry,
Journal Year:
2023,
Volume and Issue:
22(4), P. 725 - 730
Published: Dec. 18, 2023
The
selective
formation
of
3,4-dihydroisoquinolines
was
achieved
by
incapacitating
their
further
oxidation
through
an
in
situ
protonation
with
external
Brønsted
acid.
Advanced Materials,
Journal Year:
2024,
Volume and Issue:
36(37)
Published: Feb. 20, 2024
Abstract
Liquid
organic
hydrogen
carriers
(LOHCs)
have
gained
significant
attention
for
large‐scale
storage
due
to
their
remarkable
gravimetric
capacity
(HSC)
and
compatibility
with
existing
oil
gas
transportation
networks
long‐distance
transport.
However,
the
practical
application
of
reversible
LOHC
systems
has
been
constrained
by
intrinsic
thermodynamic
properties
performances
associated
catalysts
in
(de)hydrogenation
cycles.
To
overcome
these
challenges,
thermodynamically
favored
carriers,
high‐performance
catalysts,
catalytic
procedures
need
be
developed.
Here,
advances
recent
years
summarized,
primarily
centered
on
regular
catalyzed
homogeneous
heterogeneous
including
dehydrogenative
aromatization
cycloalkanes
arenes
N
‐heterocyclics
‐heteroarenes,
as
well
reverse
hydrogenation
processes.
Furthermore,
development
metal
complexes
coupling,
a
new
family
based
alcohols
is
described
that
can
release
H
2
under
relatively
mild
conditions.
Finally,
views
next
steps
challenges
field
technology
are
provided,
emphasizing
resources
low‐cost
technologies,
scenarios.
Processes,
Journal Year:
2022,
Volume and Issue:
11(1), P. 56 - 56
Published: Dec. 26, 2022
Transitioning
to
energy-saving
and
renewable
energy
sources
is
impossible
without
accelerated
development
of
hydrogen
technologies.
This
review
summarizes
the
state-of-the-art
recent
advances
various
production
processes,
including
but
not
limited
thermochemical
electrolytic
processes.
Their
opportunities
limitations,
operating
conditions,
catalysts
are
discussed.
Nowadays,
most
still
produced
by
steam
reforming
methane,
its
partial
oxidation,
or
coal
gasification.
Considerable
attention
also
paid
natural
gas
pyrolysis.
However,
using
these
technologies
has
a
lot
impurities
needs
additional
purification.
A
series
for
purification,
filtration
through
palladium
alloy
membranes,
membrane
catalysis,
allowing
purification
in
one
stage,
The
main
way
produce
carbon-free
water
electrolysis
low-cost
from
nuclear
sources.
Both
conventional
novel
methods
storage
transportation,
which
an
important
part
economy,
reviewed.
Biohydrogen
Finally,
prospects
further
work
this
field
provided.
will
be
useful
researchers
manufacturers
working
field.
Journal of Materials Chemistry A,
Journal Year:
2023,
Volume and Issue:
11(34), P. 18236 - 18246
Published: Jan. 1, 2023
By
utilizing
an
organic
linker
containing
two
photoactive
groups,
Zr-MOF
with
multiple
photofunctionalities,
such
as
photochromism,
photo-induced
structural
transformation,
and
photo-catalysis,
has
been
explored.
The Journal of Organic Chemistry,
Journal Year:
2024,
Volume and Issue:
89(8), P. 5250 - 5265
Published: March 30, 2024
The
synthesis,
characterization,
and
catalytic
application
of
a
new
phosphine-free,
well-defined,
water-soluble,
air-stable
Mn(II)-catalyst
[Mn(L)(H2O)2Cl](Cl)
([1]Cl)
featuring
1,10-phenanthroline
based
tridentate
pincer
ligand,
2-(1H-pyrazol-1-yl)-1,10-phenanthroline
(L),
in
dehydrogenative
functionalization
alcohols
to
various
N-heterocycles
such
as
quinazolin-4(3H)-ones,
quinolines,
quinoxalines
are
reported
here.
A
wide
array
multisubstituted
quinazolin-4(3H)-ones
were
prepared
water
under
air
following
two
pathways
via
the
coupling
with
2-aminobenzamides
2-aminobenzonitriles,
respectively.
2-Aminobenzyl
alcohol
ketones
bearing
active
methylene
group
used
partners
for
synthesizing
quinoline
derivatives,
quinoxaline
derivatives
by
vicinal
diols
1,2-diamines.
In
all
cases,
reaction
proceeded
smoothly
using
our
[1]Cl
air,
affording
desired
satisfactory
yields
starting
from
cheap
readily
accessible
precursors.
Gram-scale
synthesis
compounds
indicates
industrial
relevance
synthetic
strategy.
Control
experiments
performed
understand
unveil
plausible
mechanism.
The
transition
metal
catalyzed
dehydrogenation
of
alcohols
to
carboxylate
salts
and
H2
is
an
attractive
tool
due
their
potential
use
as
LOHCs
(Liquid
Organic
Hydrogen
Carriers).
Still,
most
current
methods
encompass
harsh
conditions
two
steps
synthesis.
Herein,
we
describe
efficient
ruthenium(II)
hydrogen
production
from
benzylic
the
corresponding
benzyl
carboxylates
assisted
by
visible
light.
Our
photocatalytic
system
comprises
a
standalone
N-heterocyclic
carbene
based
piano
stool
ruthenium
complex
playing
dual
role,
harvesting
visible-light
enabling
generation
under
mild
in
aqueous
media.
Inorganic Chemistry,
Journal Year:
2023,
Volume and Issue:
62(49), P. 20228 - 20235
Published: Nov. 21, 2023
N-heteroarenes
are
a
family
of
organics
with
significant
chemical
and
pharmaceutical
applications.
They
generally
prepared
by
the
catalytic
oxidative
dehydrogenation
(ODH)
partially
saturated
N-heterocycles.
In
this
work,
we
prepare
demonstrate
ODH
applications
two
polyoxovanadate-based
metal–organic
frameworks
general
formula
{[MII(bibp)1.5][VV2O6]}·H2O
(M
=
Ni
1,
Co
2;
bibp
4,4′-bis(imidazol-1-ylmethyl)biphenyl).
based
on
nonprecious
metals,
need
no
additives
or
organic
solvents
typically
required
for
ODH,
utilize
molecular
O2
as
oxidant,
thus
possessing
all
traits
desirable
practical
catalysis.
Catalyst
1
shows
tolerance
range
substrates
different
electronic
steric
features,
including
2,3-dihydro-1H-indole
tetrahydroquinolines
substituted
various
functional
groups.
Mechanistic
studies
supported
primarily
evidence
from
electron
paramagnetic
resonance
X-ray
photoelectron
spectra
suggest
that
VV
sites
in
catalytically
responsible,
first
enabling
formation
substrate-based
radical
species
single
transfer
event
while
being
converted
into
its
mixed-valence
form,
followed
production
superoxide
anion
(O2•–)
upon
contact
O2.
The
reaction
mixture
containing
O2•–
initially
formed
then
undergoes
series
steps,
hydrogen
abstraction
hydroperoxyl
radical,
tautomerization
dehydrogenated
intermediate,
finally
repeating
cycle
aforementioned
to
achieve
high-yield
conversion
corresponding
N-heteroarenes.