The cationic copolymerization of 1,3-pentadiene (PD) with isoprene (IF
) initiated by AlCl3 was carried out in toluene. The microstructure of
the copolymer chain was characterized by IR and H-1 NMR. IP is incorp
orated in the copolymer chain mainly in cyclic segments. The PD-IP cop
olymer has a much higher cyclic content than the PD homopolymer, which
shows that the cyclization reaction during PD polymerization is enhan
ced by the addition of IP. In addition, the reactivity ratios for IP(M
(1)) and PD(M(2)) determined by the Kelen-Tudos method from low-conver
sion data are r(1) - 1.22 and r(2) = 1.09.