LIFETIME OF LIVING POLYMERS IN CATIONIC POLYMERIZATION .2. LIVING POLYMERIZATION OF ISOBUTYL VINYL ETHER INITIATED BY THE HYDROGEN IODIDE ZINC HALIDE-SYSTEMS

In the living cationic polymerization of isobutyl vinyl ether (IBVE) initiated by the hydrogen iodide/zinc halide (HI/ZnX2; X = I, Br, Cl) systems, the concentration ([P*]) of the living propagating species was determined by quenching with sodiomalonic ester (1). The quenching reaction was shown to be clean, instantaneous, and quantitative to give poly (IBVE) with a terminal malonate group from which [P*] was obtained by 1H‐NMR spectroscopy. In the polymerizations in toluene below +25°C, [P*] was constant and equal to the initial concentration ([HI]0) of hydrogen iodide, independent of the type and concentrations of ZnX2 as well as monomer conversion. At 0 and +25°C, however, the living species started decaying immediately after the complete consumption of monomer. In contrast, such a decay process was absent at −15°C even in the absence of monomer until about an hour (depending on the conditions) after the end of polymerization. The deactivation reaction was first order in [P*], and the lifetime (half‐life) of the living species was longer at lower temperature and at lower ZnX2 concentration. On the basis of these [P*] and lifetime measurements, the HI/ZnX2 systems were also compared with the HI/I2 counterpart. Copyright © 1990 John Wiley & Sons, Inc.