Living carbocationic copolymerizations. I. Synthesis and characterization of isobutylene/p‐methylstyrene copolymers

Abstract

AbstractThe isobutylene (IB)–p‐methylstyrene (pMeSt) monomer pair readily produces by living copolymerization nearly random copolymers with up to M̄n ≈ 50,000 g mol−1 and M̄w/M̄n ≈ 1·4. The livingness of the copolymerization process and the compositional homogeneity of the copolymers have been demonstrated by the following four diagnostic plots: (A) M̄n (number‐average molecular weight) and corresponding N (number of moles of copolymer formed) vs Wp (weight of copolymer formed) for the diagnosis of chaintransfer; (B) −ln (1 – C) (C = conversion of monomers) vs time for the diagnosis of termination; (C) copolymer composition vs molecular weight; and (D) cumulative copolymer composition vs conversion for the diagnosis of true homogeneous copolymers. The theory for the use of the −ln(1 – C) vs time plot for the quantitation of irreversible termination in copolymerization has been developed. The exact conditions (i.e. nature of reagents, reagent concentrations, temperature, etc.) which lead to desirable products in terms of conversion, molecular weight, molecular weight distribution (MWD) and copolymer composition, were developed systematically by analyzing the results of a large number of experiments. The following combination of chemicals was found to lead to living copolymerization, and uniform high molecular weight, narrow MWD copolymers: IB–pMeSt 97 : 3 mol/mol with 5‐tert‐butyl‐1,3‐dicumyl methyl ether (5‐tBu‐1,3‐DiCumOMe) initiator, TiCl4 coinitiator, ethyl chloride (EtCl) solvent, triethylamine (TEA) electron pair donor (ED) and 2,6‐di‐tert‐butylpyridine (DtBP) proton trap at −52, −65 and −85°C.