Publikation: Role of Electron-Withdrawing Remote Substituents in Neutral Nickel(II) Polymerization Catalysts
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The novel neutral κ2-N,O-salicylaldiminato Ni(II) complex, [κ2-N,O-{2,6-(3′,5′-R2C6H3)2C6H3-N═C(H)-(3,5-I2-2-O-C6H2)}NiCH3(pyridine)] (1a-pyr, R = NO2), with four nitro substituents on the N-terphenyl motif is a catalyst precursor for ethylene polymerization to yield linear higher molecular weight polyethylene (e.g., Mn 2.1 × 105 g mol–1 and only 2 methyl branches per 1000 carbon atoms). A comparison with other known catalyst precursors at various polymerization conditions shows that the catalytic properties in terms of linearity and molecular weight are similar to the fluorinated catalyst precursor with R = CF3, showing that the latter is not singular, but rather suppression of chain transfer and branch formation by β-hydride elimination can also be brought about by nonfluorinated electron-withdrawing remote substituents.
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OSICHOW, Anna, Inigo GÖTTKER-SCHNETMANN, Stefan MECKING, 2013. Role of Electron-Withdrawing Remote Substituents in Neutral Nickel(II) Polymerization Catalysts. In: Organometallics. 2013, 32(18), pp. 5239-5242. ISSN 0276-7333. eISSN 1520-6041. Available under: doi: 10.1021/om400757fBibTex
@article{Osichow2013Elect-26594,
year={2013},
doi={10.1021/om400757f},
title={Role of Electron-Withdrawing Remote Substituents in Neutral Nickel(II) Polymerization Catalysts},
number={18},
volume={32},
issn={0276-7333},
journal={Organometallics},
pages={5239--5242},
author={Osichow, Anna and Göttker-Schnetmann, Inigo and Mecking, Stefan}
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<dcterms:abstract xml:lang="eng">The novel neutral κ<sup>2</sup>-N,O-salicylaldiminato Ni(II) complex, [κ<sup>2</sup>-N,O-{2,6-(3′,5′-R<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)<sub>2</sub>C<sub>6</sub>H<sub>3</sub>-N═C(H)-(3,5-I<sub>2</sub>-2-O-C<sub>6</sub>H<sub>2</sub>)}NiCH<sub>3</sub>(pyridine)] (1a-pyr, R = NO<sub>2</sub>), with four nitro substituents on the N-terphenyl motif is a catalyst precursor for ethylene polymerization to yield linear higher molecular weight polyethylene (e.g., Mn 2.1 × 10<sup>5</sup> g mol<sup>–1</sup> and only 2 methyl branches per 1000 carbon atoms). A comparison with other known catalyst precursors at various polymerization conditions shows that the catalytic properties in terms of linearity and molecular weight are similar to the fluorinated catalyst precursor with R = CF<sub>3</sub>, showing that the latter is not singular, but rather suppression of chain transfer and branch formation by β-hydride elimination can also be brought about by nonfluorinated electron-withdrawing remote substituents.</dcterms:abstract>
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