Reverse atom transfer radical polymerization of dimethyl itaconate initiated by a new azo initiator: AIBME.

Reverse atom transfer radical polymerization (RATRP) was used to synthesize poly(dimethyl itaconate) (PDMI) using an AIBME/CuBr 2 /dNbpy system. The number average molecular weight ( M n ) of PDMI was as high as M n = 15 000 g mol -1 , the monomer conversion rate reached up to 70%, and the dispersity remained low ( Đ = 1.06-1.38). The first-order kinetics of PDMI are discussed in detail. The AIBME initiator had a higher initiation efficiency than the AIBN initiator. As the ratio of initiator (AIBME) to catalyst (CuBr 2 ) decreased, the M n and Đ of PDMI decreased. At 60 °C and 80 °C, the M n of PDMI was much higher than the theoretical number average ( M n,th ), and the Đ of PDMI broadened with the conversion rate. At 100 °C, the Đ of PDMI remained low, and the M n of PDMI was closer to the M n,th . As the ratio of monomer (DMI) to initiator (AIBME) increased, the M n of PDMI changed little over time. These phenomena could be explained by the influence of the initiator and catalyst on polymerization kinetics.