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Highly isotactic polypropene prepared with rac-dimethylsilyl-bis (2-methyl-4-t-butyl-cyclopentadienyl) zirconiumdichloride : an NMR investigation of the polymer microstructure

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Brintzinger_241545.pdf
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1993

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Rieger, Bernhard
Reinmuth, Annette

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Journal of Molecular Catalysis. 1993, 82(1), pp. 67-73. ISSN 0304-5102. eISSN 1873-314X. Available under: doi: 10.1016/0304-5102(93)80071-2

Zusammenfassung

Isotactic polypropene was prepared using rac-dimethyl-silylbis(2-methyl-4-t-butyl-cyclopentadienyl) zirconiumdichloride (1) and methylalumoxane (MAO) at temperatures between 0 and 80°C and with Al/Zr ratios of 300 and 1500. The polymers, prepared at temperatures below 30°C had melting points of 162°C and above. The chain ends were determined by means of distortionless enhancement by polarization transfer (DEPT)-NMR spectroscopy. The pentad intensities were corrected according to the chemical shifts of the end groups. The intensity distributions are shown to arise from enantiomorphic site control of the chiral catalyst species.

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540 Chemie

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Chiral zirconocenes, isotactic polypropene, stereospecific olefin polymerization

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ISO 690RIEGER, Bernhard, Annette REINMUTH, Werner RÖLL, Hans-Herbert BRINTZINGER, 1993. Highly isotactic polypropene prepared with rac-dimethylsilyl-bis (2-methyl-4-t-butyl-cyclopentadienyl) zirconiumdichloride : an NMR investigation of the polymer microstructure. In: Journal of Molecular Catalysis. 1993, 82(1), pp. 67-73. ISSN 0304-5102. eISSN 1873-314X. Available under: doi: 10.1016/0304-5102(93)80071-2
BibTex
@article{Rieger1993Highl-24154,
  year={1993},
  doi={10.1016/0304-5102(93)80071-2},
  title={Highly isotactic polypropene prepared with rac-dimethylsilyl-bis (2-methyl-4-t-butyl-cyclopentadienyl) zirconiumdichloride : an NMR investigation of the polymer microstructure},
  number={1},
  volume={82},
  issn={0304-5102},
  journal={Journal of Molecular Catalysis},
  pages={67--73},
  author={Rieger, Bernhard and Reinmuth, Annette and Röll, Werner and Brintzinger, Hans-Herbert}
}
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