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is achieved using a Diels-Alder reaction of cyclopentadiene functions. This approach provides polymer supported zirconocene with a homogeneous distribution of active sites. The zirconocene-containing supported catalyst forms spherical beads and is active when combined with MAO at promoting PE formation. The polymerization activity was 5 30% that of the homogeneous catalyst, producing 5 to 66 105 g PE/Zr h. The molecular weight of the PE prepared was 6 106, and the molecular weight distribution ratio was 2.9 3.4. Rietmuller and coworkers38 recently reported locating zirconocene-containing groups on hyperbranched polysilanes for the purpose of producing stereoregular polymers. The polycarbosilane dendrite is hydroborated at the terminal vinyl groups and then the zirconocene moiety is attached. PP was produced using this dendrite in toluene at a propylene pressure of 5 bar yielding PP in moderate yields with [mmmm] values about 35%. The proposed zirconocene site is pictured in structure 7.

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advantageously is expanded on the basis of Legendre polynomials P , (dc Gennes, 1974; Luckhurst, 1993). Due to the symmetry of the phase uneven terms vanish, and the first essential contribution comes from the second-order term P . It is baaed on the projection of the preferred molecular axis on the director and consequently related to the momentary angle IY formed by these two directions. Averaging over all the molecules of the sample yields a specification of the degree of order in terms of the Maier-Saupe order parumetei- S (4.6-1) where the angular brackets and the upper bar, respectively, indicate averaging. This quantity is defined to adopt values between unity characterizing perfect alignment and zero indicating random orientation (Maier and Saupe, 1958, 1959 and 1960). Typical values of S for nematic liquid crystals are in the range from 0.3 to 0.8. It should be noted that the distribution over a sphere, i.e. in space rather than over a plane, has to be considered. Referring to a globe, the angle d states just the latitude, the length of the related parallel and thus the relevant weight within the distribution increases with sin 6. Consequently equal probability of all possible orientations leads to < sin2t9 >= 213 so that the order parameter S vanish for an isotropic sample. Larger values of < sin2,t9 > would lead to a negative value of the order parameter S , however, this indicates primarily an inappropriate assignment of the molecular axes or the director.

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+ NADH + H+ -+ glycerol + NAD'

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