2023
DOI: 10.1039/d3py00450c
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Facile access to diverse polyethylenesvianeutral salicylaldiminato nickel catalysts

Abstract: A new family of neutral salicylaldiminato nickel(II) catalysts (Ni1-Ni5) with various well-designed substituents ortho to the phenoxy moiety is developed, which shows moderate to high catalytic activity for ethylene polymerization...

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Cited by 8 publications
(3 citation statements)
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“…The trinuclear nickel­(II) precursor Ni 3 – Br was prepared via the reaction of tribenzyl bromide (1 equiv) with Ni­(COD) 2 (3 equiv) in the presence of excess PMe 3 (Figure ). In addition, we further chose the salicylaldimine compound as the ligand because the related salicylaldiminato nickel­(II) catalysts enabled the synthesis of UHMWPE through a living polymerization fashion reported by us recently. Treating Ni 3 – Br (1 equiv) with the ligand sodium salt (3 equiv) resulted in the formation of the trinuclear nickel­(II) catalyst Ni 3 (Figure ). Similarly, the tetranuclear nickel­(II) precursors Ni 4 * – Br and Ni 4 – Br were also prepared.…”
Section: Resultsmentioning
confidence: 99%
“…The trinuclear nickel­(II) precursor Ni 3 – Br was prepared via the reaction of tribenzyl bromide (1 equiv) with Ni­(COD) 2 (3 equiv) in the presence of excess PMe 3 (Figure ). In addition, we further chose the salicylaldimine compound as the ligand because the related salicylaldiminato nickel­(II) catalysts enabled the synthesis of UHMWPE through a living polymerization fashion reported by us recently. Treating Ni 3 – Br (1 equiv) with the ligand sodium salt (3 equiv) resulted in the formation of the trinuclear nickel­(II) catalyst Ni 3 (Figure ). Similarly, the tetranuclear nickel­(II) precursors Ni 4 * – Br and Ni 4 – Br were also prepared.…”
Section: Resultsmentioning
confidence: 99%
“…Nevertheless, despite their good performance in copolymerization processes, the high cost and relatively low activity of Pd catalysts severely restrict their practical utility. In contrast, nickel catalysts are more appealing for industrial applications due to their greater economy, larger earth abundance, and higher catalytic activity in ethylene homopolymerization [ 35 , 36 , 37 ].…”
Section: Introductionmentioning
confidence: 99%
“…1–7 Among these, nickel catalysts are considered to have more potential for industrialization due to their greater economic and environmental advantages compared to palladium. 8–11 Therefore, a series of nickel catalysts with different ligand structures are constantly emerging; 12–17 for example, representative nickel catalysts such as α-diimine nickel catalysts, 18–20 α-imino-ketone nickel catalysts 21 and salicylaldehyde imine nickel catalysts 22–24 have been widely studied.…”
Section: Introductionmentioning
confidence: 99%