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    Isotactic Polymerization of Propene With Heterogeneous Catalytic-systems - A Partial Tentative Rationalization of the Behavior of Some 3rd Components

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    The stereoregulating effects of Me benzoate (I) [93-58-3] in TiCl4-MgCl2-Et3Al Ziegler catalysts for polymn. of C3H6 [115-07-1] could be attributed to slow ligand exchangers for the nonstereospecific sites and to the deactivation of the nonstereospecific sites in the presence of I. The carbon atoms of I (as a fourth component in the catalyst) were incorporated into the polymer via alkylation of I by the Ti-C bond of the active catalytic sites. The polymn. kinetics was discussed

    Trigonal bipyramidal platinum complexes as models for ziegler-natta catalytic sites

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    Five-coordinated η2-adducts of (+)-(S)-3-methyl-1-pentene (SMP) and (R,S)-3-methyl-1-pentene (RSMP) of the type [PtCl2(η2-olefin)(α-di-hydrazone)] were prepared. In solution the more stable adducts are those which have the olefin presenting to Pt the face of opposite configuration to that of the chiral substituent. In the solid state the same situation is found by X-ray analysis for the adduct of SMP, while 1H NMR studies point to the conclusion that the same configuration as the chiral substituent is preferred in the solid adduct of RSMP. These observations are compared with those in previous reports on coordination of SMP on square planar Pt and stereoselective polymerization. © 1983
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