Poly(A-PTHF) can not be obtained from the conventional free radical polymerization
or atom transfer radical polymerization or reversible addition-fragmentation chain transfer polymerization of A-PTHF
due to low conversion and low degree of polymerization of poly (A-PTHF).Thus
the homo-polymerization of A-PTHF macromonomer was performed under 60Co γ-irradiation with EPDTB(1-(ethoxycarbonyl)prop-1-yl dithiobenzoate) as initiator.After precipitated from methanol
pure poly(A-PTHF) was obtained.The block copolymerization of St was performed using Poly(A-PTHF) as the transfer agent and DCP(dicumy peroxide) as the initiator.Both of the homo-polymerization and the following copolymerization are controllable.The evidences are the linear relationship between In([M]0/[M]) and polymerization time
the linear evolution of Mn with conversion and the narrower polydispersities.The molecular structures of the poly(A-PTHF) and the block copolymer PSt-b-P(A-PTHF) were characterized by 1H-NMR as well as gel permeation chromatography(GPC).The polymerization mechanism of the homo-polymerization of(A-PTHF) and the copolymerization of poly(A-PTHF)with St were discussed respectively.
PREPARATION OF MONODISPERSE POLYSTYRENE-g-POLY(ETHYLENE OXIDE) MICROSPHERES BY MICROWAVE DISPERSION POLYMERIZATION
SYNTHESIS OF HYDROPHILIC POLY(METHYLACRYLIC ACID) GRAFTEDPOLYACRYLAMIDE MICROSPHERES
SYNTHESIS OF MACROMONOMER OF PST CAPPED WITH THIENYL GROUP AND STUDY OF ITS OXIDATION COUPLING POLYMERIZATION
SYNTHESIS OF A WELL-DEFINED POLY(p-VINYL BENZOIC ACID) AND ITS DIBLOCK COPOLYMER WITH STYRENE
RADICAL REVERSE ADDITION-FRAGMENTATION CHAIN TRANSFER POLYMERIZATION OF MALEIC ANHYDRIDE WITH STYRENE AND A NOVEL FUNCTIONAL BLOCK COPOLYMER PREPARED THEREFROM