Stereospecific Living Cationic Polymerization of -Vinylcarbazole through the Design of ZnCl-Derived Counteranions.

Highly stereospecific living polymerization of -vinylcarbazole (NVC) successfully proceeded via a cationic mechanism as a result of the elaborate design of counteranions using an initiating system consisting of CFSOH, BuNX (X = Cl, Br, I), and a Lewis acid catalyst. The use of ZnCl and an appropriate amount of BuNCl quantitatively generated highly isotactic polymers ( = 94%) with narrow molecular weight distributions (/ ∼ 1.3) and molecular weights proportional to monomer conversion. In this system, a ZnCl species, which was formed as a counteranion of the propagating carbocation, most likely contributed to the stereoregulation of the polymers because the value drastically varied depending on the polymerization conditions, such as the Lewis acid catalyst and amount of added salt. Isotactic poly(-vinylcarbazole) (PVK) showed different properties than atactic PVK based on fluorescence and differential scanning calorimetry (DSC) analysis.