Publikation: Solid-Supported Single-Component Pd(II) Catalysts for Polar Monomer Insertion Copolymerization
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Heterogenized representatives of neutral phosphine sulfonato Pd(II) complexes for polar monomer insertion polymerization were prepared by two different approaches. [{κ2-(P,O)-(2-anisyl)2PC6H4SO2O}Pd(Me)L] (L = pyr, dmso, or Cl) complexes were physisorbed on inorganic substrates, namely, clay or silica. In addition, new phosphine sulfonato complexes bearing hydroxyl linker groups at the nonchelating P-aryl moiety were prepared. These complexes were covalently tethered to cross-linked polystyrene. All immobilized palladium complexes are active in ethylene polymerization and
ethylene/MA copolymerization without any additional cocatalyst. In addition, separation from the polymer solution formed and reutilization for another polymerization were demonstrated for polystyrene-bound complexes.
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WUCHER, Philipp, Judith Barbara SCHWADERER, Stefan MECKING, 2014. Solid-Supported Single-Component Pd(II) Catalysts for Polar Monomer Insertion Copolymerization. In: ACS Catalysis. 2014, 4(8), pp. 2672-2679. ISSN 2155-5435. eISSN 2155-5435. Available under: doi: 10.1021/cs5005954BibTex
@article{Wucher2014Solid-28481,
year={2014},
doi={10.1021/cs5005954},
title={Solid-Supported Single-Component Pd(II) Catalysts for Polar Monomer Insertion Copolymerization},
number={8},
volume={4},
issn={2155-5435},
journal={ACS Catalysis},
pages={2672--2679},
author={Wucher, Philipp and Schwaderer, Judith Barbara and Mecking, Stefan}
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<dcterms:abstract xml:lang="eng">Heterogenized representatives of neutral phosphine sulfonato Pd(II) complexes for polar monomer insertion polymerization were prepared by two different approaches. [{κ<sup>2</sup>-(P,O)-(2-anisyl)<sub>2</sub>PC<sub>6</sub>H<sub>4</sub>SO<sub>2</sub>O}Pd(Me)L] (L = pyr, dmso, or Cl) complexes were physisorbed on inorganic substrates, namely, clay or silica. In addition, new phosphine sulfonato complexes bearing hydroxyl linker groups at the nonchelating P-aryl moiety were prepared. These complexes were covalently tethered to cross-linked polystyrene. All immobilized palladium complexes are active in ethylene polymerization and<br />ethylene/MA copolymerization without any additional cocatalyst. In addition, separation from the polymer solution formed and reutilization for another polymerization were demonstrated for polystyrene-bound complexes.</dcterms:abstract>
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