The radical co- and terpolymerization of 4-[(alpha,beta,beta-trifluorovinyl)oxy]bromo benzene (TFVOBB) with 1,1-difluoroethylene (or vinylidene fluoride, VDF, or VF2,), hexafluoropropene (HFP), perfluoromethyl vinyl ether (PMVE), and chlorotrifluroroethylene (CTFE) is presented. Although TFVOBB could be thermocyclodimerized, it could not homopolymerize under radical initiation. TFVOBB could be copolymerized in solution under a radical initiator with VDF or CTFE comonomers, while its copolymerization with HFP or PMVE were unsuccessful. The terpolymerization of TFVOBB with VDF and HFP, or VDF and PMVE, or VDF and CTFE also led to original fluorinated terpolymers bearing bromoaromatic side-groups. The conditions of co- and terpolymerization were optimized in terms of the nature of the radical initiators, and of the nature of solvents (fluorinated or nonhalogenated). Various monomer concentrations in the co- and terpolymers were assessed by F-19 and H-1-NMR spectroscopy. The thermal and physico chemical properties were also studied. (C) 2004 Wiley Periodicals, Inc.