Advances in CO2 activation by frustrated Lewis pairs: from stoichiometric to catalytic reactions
Md. Nasim Khan,
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Yara van Ingen,
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Tribani Boruah
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et al.
Chemical Science,
Journal Year:
2023,
Volume and Issue:
14(47), P. 13661 - 13695
Published: Jan. 1, 2023
Frustrated
Lewis
pair
systems
have
been
explored
efficiently
in
homogeneous
and
heterogeneous
conditions
for
the
activation
reduction
of
CO
2
to
various
useful
products
stoichiometric
as
well
catalytic
reactions.
Language: Английский
Development of Modular Nitrenium Bipolar Electrolytes for Possible Applications in Symmetric Redox Flow Batteries
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(28), P. 19474 - 19488
Published: July 4, 2024
Amid
the
escalating
integration
of
renewable
energy
sources,
demand
for
grid
storage
solutions,
including
non-aqueous
organic
redox
flow
batteries
(oRFBs),
has
become
ever
more
pronounced.
oRFBs
face
a
primary
challenge
irreversible
capacity
loss
attributed
to
crossover
redox-active
materials
between
half-cells.
A
possible
solution
involves
utilization
bipolar
electrolytes
that
act
as
both
catholyte
and
anolyte.
Identifying
such
molecules
poses
several
challenges
it
requires
delicate
balance
stability
oxidation
states
density,
which
is
influenced
by
separation
two
events.
We
report
development
diaminotriazolium
core
capable
producing
electronically
distinct
persistent
radical
species
with
typically
extreme
reduction
potentials
(
Language: Английский
Stabilizing 4π Electron Pyrrolyl Cations by Inducing Aromaticity
Chemical Communications,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
The
pyrrolyl
cation
is
a
4π
electron
ring
system
which
anti-aromatic
and
unstable.
Language: Английский
Nitrenium ions as new versatile reagents for electrophilic amination
Chemical Science,
Journal Year:
2023,
Volume and Issue:
14(43), P. 12034 - 12040
Published: Jan. 1, 2023
Bench-stable
N-heterocyclic
nitrenium
ions
were
used
for
the
efficient
electrophilic
amination
of
organometallic
nucleophiles.
The
previously
unexplored
N
-alkyl/aryl
triazane
intermediates
reduced
to
produce
a
diverse
scope
primary
amines.
Language: Английский