Abstract
[(1,5-Cyclooctadiene)(CH3)Pd(Cl)], when reacted in situ with 1 equiv of a monodentate phosphine ligand and 1 equiv of the complex Na+[3,5-(CF3)2C6H3]4B- was found to catalyze the vinyl addition polymerization of norbornene derivatives, including those with pendant oxygen functionalities. For norbornene, a polymerization rate of 1000 tons norbornene/mol Pd·h was observed at 25 °C. For several norbornene derivatives, the molecular weight of the polymer was found to decrease with increasing amounts of added 2-propanol. Mechanistic data confirm a vinyl insertion mechanism for these polymerizations. The polymerization rate was found to decrease dramatically for norbornene derivatives with pendant oxygen functionalities. The effect of coordinating solvents and the uptake of endo vs exo isomers for functionalized norbornenes was tested. Experiments show that (a) the endo isomer reacts more slowly than the exo isomer and (b) both isomers react much more slowly compared to norbornene derivatives lacking coordinati...
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