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Zirconocenes ring-functionalized

Reduction of 2-methoxyethyl- and 2-methylthioethyl-functionalized zirconocene dichlorides with Mg/Hg in THF leads to the products of the O-Me and S-Me bond cleavage.647 For example, the reduction of (G5Me4GH2CH2EMe)(G5Me5)ZrCl2 (E = O, S) with Mg/Hg in THF gives the chelating (ring-metallated) complex... [Pg.919]

As an alternative approach, polycarbosilanes 2.31 bearing pendant zirconocene moieties have also been prepared by ring-opening polymerization of the spirocyc-lic monomer 2.30 (Eq. 2.13) [62], In this case, the materials were structurally characterized, but the soluble fraction was of low molecular weight (M < ca. 3000) and the high molecular weight fraction was insoluble in organic solvents. In the presence of activators, both fractions functioned as ethene polymerization catalysts with moderate activity [62]. [Pg.53]


See other pages where Zirconocenes ring-functionalized is mentioned: [Pg.874]    [Pg.131]    [Pg.261]    [Pg.88]    [Pg.115]    [Pg.345]    [Pg.5]    [Pg.128]    [Pg.231]    [Pg.28]    [Pg.73]    [Pg.762]    [Pg.876]    [Pg.877]    [Pg.920]    [Pg.930]    [Pg.951]    [Pg.959]    [Pg.88]    [Pg.115]    [Pg.28]    [Pg.23]    [Pg.786]    [Pg.829]    [Pg.114]    [Pg.135]    [Pg.134]    [Pg.606]    [Pg.261]   
See also in sourсe #XX -- [ Pg.4 ]




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Zirconocene

Zirconocenes

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