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21644487498
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note
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2 was then added, at room temperature, with the aid of a syringe pump. After completion, no EDA was observed by GC. The volume was reduced to 1 mL, and then methanol was added (70 mL). The resulting solid was filtered off and washed with methanol (2 × 40 mL). Further filtration and drying under vacuum gave the functionalized polymers in 85-90% isolated yields.
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25
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21644463086
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note
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(b) Poly(ethylene-1-octene): 0.2 g was dissolved in a mixture of toluene (5 mL) and dichloromethane (5 mL). Following the above procedure, white solids were isolated in 85-90%.
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26
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21644473797
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note
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(c)Polypropylene was functionalized following the above procedure for polybutene.
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27
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21644480545
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note
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3).
-
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28
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21644459004
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note
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Molecular weight determination of polymers was carried out on a PL GPC-220 instrument equipped with a mixed B column set in trichlorobenzene at 160°C. Data are referenced vs narrow polyethylene standards. The atactic low-molecular-weight polypropylene samples were analyzed on a PL GPC-50 instrument at room temperature in THF, employing refractive index and UV-vis detection. Data are referenced to polystyrene standards.
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29
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21644464902
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note
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The increased apparent molecular weight of the functionalized product in entry 9 stands out. Changes in hydrodynamic behavior by functionalization (cf. discussion of poly(2-butene) functionalization) probably can account for the observed effect only partially, comparing these data with that of all other polymers.
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