Abstract
This article deals with (1) synthesis and anionic polymerization of a six-membered cyclic carbonate having styrene moiety, (2) anionic depolymerization of the obtained polymer, (3) radical cross-linking of the obtained polymer, and (4) anionic de-cross-linking of the cross-linked polymer. The monomer 5-ethyl-5-[(p-vinylphenyl) methoxymethyl]-1,3-dioxan-2-one (St6CC) underwent anionic polymerization with potassium tert-butoxide (t-BuOK) as an initiator in THF to afford the corresponding polycarbonate [poly(St6CC)]. It was confirmed that this polymerization was equilibrium polymerization by the relationships between the polymerization temperature and monomer conversion. Poly(St6CC) underwent anionic depolymerization with t-BuOK (5 mol % vs polymer repeating unit) as a catalyst in THF (0.1 M) at 20 °C for 24 h to recover St6CC in 60% yield. Treatment of poly(St6CC) with a radical initiator afforded the cross-linked polymer. Employment of styrene as the comonomer satisfactorily afforded the corresponding cros...
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