Thermostable Polyhalogen-Substituted α-Diimine Nickel Precatalysts Towards High Performance Polyethylene Elastomer
Journal of Molecular Structure,
Год журнала:
2025,
Номер
1334, С. 141892 - 141892
Опубликована: Март 1, 2025
Язык: Английский
Synergistic Effects of Methoxy and Benzhydryl Substituents in Α-Diimine Nickel Catalysts for Homo- and Copolymerization of 1-Hexene and Norbornene
Опубликована: Янв. 1, 2025
Язык: Английский
Synergistic effects of methoxy and Benzhydryl substituents in α-Diimine nickel catalysts for Homo- and copolymerization of 1-Hexene and norbornene
European Polymer Journal,
Год журнала:
2025,
Номер
unknown, С. 113908 - 113908
Опубликована: Апрель 1, 2025
Язык: Английский
Tactfully regulating the ESIPT mechanism in the Cyanine-n probe molecules by electron withdrawing substitutions
Journal of Photochemistry and Photobiology A Chemistry,
Год журнала:
2025,
Номер
unknown, С. 116425 - 116425
Опубликована: Апрель 1, 2025
Язык: Английский
Fluoro-enriched α-diimine nickel precatalysts for enhanced thermostability in synthesis of polyethylene elastomer
European Polymer Journal,
Год журнала:
2025,
Номер
unknown, С. 114004 - 114004
Опубликована: Май 1, 2025
Язык: Английский
Recent advances in nickel Catalysis for thermoplastic polyethylene elastomers: Synthesis strategies, properties, and future perspectives
Coordination Chemistry Reviews,
Год журнала:
2025,
Номер
541, С. 216833 - 216833
Опубликована: Май 31, 2025
Язык: Английский
Iminopyridine‐Nickel Precatalysts for Low Molecular Weight Branched Macro‐Olefin: Dominant β‐Elimination following Isomerization
ChemCatChem,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 28, 2024
Abstract
The
chain‐walking
mechanism,
coupled
with
β
‐elimination
reactions,
establishes
nickel
complexes
as
a
unique
class
of
catalysts
in
olefin
polymerization,
giving
access
to
variety
polyethylene
products
from
only
ethylene
monomer.
In
this
study,
set
8‐(2,6‐bis(aryl)‐3,4,5‐trifluorophenyl)imino‐5,6,7‐trihydroquinoline‐nickel
bromide
[aryl
=
Ph
2
CH
for
Ni
H
,
(4‐FPh)
F
(4‐ClPh)
Cl
(4‐MePh)
Me
(4‐
t
BuPh)
Bu
]
was
designed,
prepared,
and
investigated
polymerization.
Upon
activation
MAO,
these
precatalysts
exhibited
high
catalytic
activity
(as
3.1
×
10
6
g
mol
−1
h
)
produced
tunable
chain
walking
(branching
degree
58–90/1000C),
transfer
(polymer
M
w
0.7–2.8
kg
),
termination
reactions
(vinylene/vinyl
83.4%–93.6%).
Electron‐donating
groups
at
benzhydryl
aniline
showed
positive
influence
on
the
rate
monomer
insertion
propagation,
resulting
polymer
molecular
weights.
Change
reaction
temperature
resulted
varied
physical
states
sticky
wax
thick
oil.
Most
importantly,
is
predominant
route
produces
ratio
internal
double
bonds
(─CH═CH─/CH
═CH─
up
93.6%).
These
macromers
are
important
post‐modification
processes.
Язык: Английский