Kinetics of the Photopolymerization of Vinyl Monomers by Bis(Isopropylxanthogen) Disulfide. Design of Block Copolymers

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Abstract
Bis(isopropylxanthogen) disulfide (BX) has been used as a photoinitiator with various vinyl monomers at 30°C. The kinetics of polymerization of styrene (St) and methyl methacrylate (MMA) at 30°C were studied for various concentrations of monomer and initiator. The observed deviations in polymerization rate from simple kinetic theory could be explained in terms of primary radical termination. The fraction of primary radical terminating chains was obtained as a function of various concentrations. The ratio of the rate constants for chain initiation and chain termination by a primary radical was determined to be 3.34 ± 107 for St and 2.60 ± 107 for MMA. The number-average degree of polymerization (DP n) of polymers obtained by photopolym-erization with BX was found to increase linearly with conversion. However, the DP n extrapolated to zero conversion was in good agreement with that calculated on the basis of the kinetic scheme. It was found that BX had interesting properties for the design of block copolymers, i.e., BX acts as a terminator and a chain transfer agent as well as an initiator in these polymerizations. The polymers obtained with BX contained two reactive isopropyl xanthate groups bonded at their chain ends, which could also act as macrophotoinitiators.

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