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85034480646
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note
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3O); 1.25,1.14,1.02, 0.65, each abroad singlet, 12H (TEMPO methyls); 1.6-1.2, m, 6H (TEMPO methylenes). See Table 1 for reaction times, temperatures, and yields for the alkoxyamines synthesized by this method.
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28
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85034464692
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note
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2 and stored at -5 °C under argon prior to use. In a typical polymerization, a long dry glass tube was charged with initiator (0.045 mmol), styrene (1 mL, 8.7 mmol), and a magnetic stir bar. The glass tube was degassed via three freeze-pump-thaw cycles, and sealed by flame. The glass tube was immersed in an oil bath thermostated at 125 °C. After 12 h, the glass tube was removed and broken. The sample was dissolved in THF, and the conversion (GC) and molecular weight and polydispersity (SEC) were measured.
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0347022734
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Gnanou, Y.6
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