Abstract
AbstractGraft copolymers of well‐defined structure and composition were prepared by radical copolymerization of acrylamide and poly(dodecyl acrylate) macromonomers. The macromonomers were prepared by telomerization of dodecyl acrylate in the presence of 2‐mercaptoethanol as a transfer agent, followed by reaction with acryloyl chloride. Poly(dodecyl acrylate) macromonomers with Mn = 1100, 1100, 2200 and 4600 were synthesized. The kinetics of the radical telomerization of dodecyl acrylate with 2‐mercaptoethanol and AIBN was studied at 66°C in THF. Under these conditions we obtained the transfer constant CT = 0,9. The graft copolymerization of acrylamide with the poly(dodecyl acrylate) macromonomer was carried out in the presence of the transfer agent C6F13C2H4SH. If C0 = [AIBN]/[Acrylamide] = 0,01 and R0 = [C6F13C2H4SH]/[Acrylamide] = 0,01, for acrylamide a DPn = 160 was obtained in all cases, for the macromonomer of Mn = 1100 a DPn = 2,5, and for the macromonomer of Mn > 1100 a DPn = 1.
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