Abstract: | The reactivity of 1-phenylbutadiene (1-PBD) in cationic polymerization and the monomer structure were investigated. 1-PBD polymerized at ?78°C in several solvents initiated by cationic catalysts such as stannic chloride and tungsten hexachloride. The polymerizations proceeded predominantly via 3,4-type propagation mode, and gave low molecular weight polymers. More than one double bond of 1-PBD was consumed during the polymerizations, probably due to transfer and cyclization reactions. 1-PBD was several times as reactive as styrene and trans-1,3-pentadiene in copolymerizations. The Hammett plots of reactivities of ring-substituted 1-PBD in cationic polymerization gave the p-value of -1.20, which is 0.6 times that of styrene. The 1H and 13C NMR chemical shifts of ring-substituted 1-PBD were measured and discussed in relation to the reaction mechanism. |