HALONICKEL 2,4-DI-t-BUTYL-6-(QUINOLIN-8-YLIMINOMETHYL)PHENOLATES: SYNTHESIS, CHARACTERIZATION AND ETHYLENE REACTIVITY
Special Issue: In Honor of the 80th Birthday of Professor Fosong Wang (Part I)|Updated:2023-01-03
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HALONICKEL 2,4-DI-t-BUTYL-6-(QUINOLIN-8-YLIMINOMETHYL)PHENOLATES: SYNTHESIS, CHARACTERIZATION AND ETHYLENE REACTIVITY
Chinese Journal of Polymer ScienceVol. 31, Issue 5, Pages: 769-777(2013)
Affiliations:
a.College of Materials Science and Engineering, Beijing Institute of Petrochemical Technology, Beijing 102617, China
b.Key Laboratory of Engineering Plastics and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
c.Department of Chemistry, University of Hull, Hull HU6 7RX, UK
Qi-song Shi, Xiang Hao, Carl Redshaw, et al. HALONICKEL 2,4-DI-t-BUTYL-6-(QUINOLIN-8-YLIMINOMETHYL)PHENOLATES: SYNTHESIS, CHARACTERIZATION AND ETHYLENE REACTIVITY[J]. Chinese Journal of Polymer Science, 2013, 31(5): 769-777. DOI: 10.1007/s10118-013-1266-z.
DOI:
Qi-song Shi, Xiang Hao, Carl Redshaw, et al. HALONICKEL 2,4-DI-t-BUTYL-6-(QUINOLIN-8-YLIMINOMETHYL)PHENOLATES: SYNTHESIS, CHARACTERIZATION AND ETHYLENE REACTIVITY[J]. Chinese Journal of Polymer Science, 2013, 31(5): 769-777. DOI: 10.1007/s10118-013-1266-z.DOI:
HALONICKEL 2,4-DI-t-BUTYL-6-(QUINOLIN-8-YLIMINOMETHYL)PHENOLATES: SYNTHESIS, CHARACTERIZATION AND ETHYLENE REACTIVITY
-butyl-6-(quinolin-8-yliminomethyl) phenolate ligands was synthesized and characterized by IR spectroscopy and elemental analysis. Molecular structures of C1 (R = H
X = Br) and C2 (R = H
X = Cl) were further confirmed by single-crystal X-ray crystallographic studies
and revealed a distorted square planar geometry at nickel. Upon activation with diethylaluminum chloride (Et
2
AlCl)
all nickel pre-catalysts displayed good catalytic activity [up to 9.3 × 10
5
g mol
−1
(Ni) h
−1
] for ethylene oligomerization with major dimerization. In the presence of methylaluminoxane (MAO)
the nickel complex C1 was capable of ethylene polymerization under 3 MPa
and produced polyethylene products with narrow polydispersity (1.16−1.73) and molecular weights in the range of 2.6−4.95 kg/mol.
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Iminopyridine Manganese and Nickel Complexes: Synthesis, Characterization and Behavior in the Polymerization of 1,3-Butadiene
Nickel(II) α-Diimine Catalysts with Carboxyl Groups for Ethylene Oligomerization and Polymerization
High Pressure Synthesis for Gold-backboned Polymer
All Polyethylene Compositions Based on Ultrahigh Molecular Weight Polyethylene Synthesized over Binary Catalyst including Zirconocenes of Various Designs
Optically Active Helical Poly(phenyl isocyanide)s Bearing Achiral Benzanilide Pendants: from Controlled Synthesis to Enantioseparation Application
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