NMR spectroscopy in the optimization and evaluation of RAFT agents

The selection of a suitable mediating agent in Reversible Addition-Fragmentation Chain Transfer (RAFT) mediated polymerization is crucial to the degree of control that can be achieved. An overview of work from the Stellenbosch group is presented in which the use of NMR spectroscopy as a tool for evaluating RAFT-agents is highlighted. The occurrence of selective initialization, i.e. the selective conversion of a RAFT-agent into its single monomer adduct is discussed for various classes of monomers, as well as for copolymerization. One of the general rules for living polymerization is that chains should start growing early in the polymerization reaction. Selective initialization is claimed to be the extreme case where all chains have begun growing after the conversion of only one monomer equivalent per RAFT-agent

Initialization behavior for high target molecular weight polymers using various dithiobenzoates

In the reversible addition-fragmentation chain transfer (RAFT) mediated polymerization of methyl acrylate, a selective reaction is observed in the early stages of the polymerization. This initialization process was earlier observed in in situ 1H NMR spectroscopy experiments where extremely low target molar masses were chosen (around DP = 5). Here, for the first time, the presence of the initialization process is identified as the cause of an induction period under typical conditions of a RAFT-mediated polymerization. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 2500-2509, 200

Investigation into the initialization behaviour of RAFT-mediated styrene-maleic anhydride copolymerizations

The living radical alternating copolymerization of styrene and maleic anhydride mediated by the reversible addition–fragmentation chain transfer (RAFT) polymerization process has been studied at short chain lengths using two different dithiobenzoate RAFT agents. The results indicate specificity of addition of the RAFT-agent leaving groups for either styrene or maleic anhydride. The addition rate of the monomers and the fact that monomers are added individually favour the penultimate unit model of polymer propagatio

Investigation into the initialization behaviour of RAFT-mediated styrene-maleic anhydride copolymerizations

The living radical alternating copolymerization of styrene and maleic anhydride mediated by the reversible addition–fragmentation chain transfer (RAFT) polymerization process has been studied at short chain lengths using two different dithiobenzoate RAFT agents. The results indicate specificity of addition of the RAFT-agent leaving groups for either styrene or maleic anhydride. The addition rate of the monomers and the fact that monomers are added individually favour the penultimate unit model of polymer propagatio

Investigation into the initialization behaviour of RAFT-mediated styrene-maleic anhydride copolymerizations

The living radical alternating copolymerization of styrene and maleic anhydride mediated by the reversible addition–fragmentation chain transfer (RAFT) polymerization process has been studied at short chain lengths using two different dithiobenzoate RAFT agents. The results indicate specificity of addition of the RAFT-agent leaving groups for either styrene or maleic anhydride. The addition rate of the monomers and the fact that monomers are added individually favour the penultimate unit model of polymer propagatio

RAFT for the Control of Monomer Sequence Distribution – Single Unit Monomer Insertion (SUMI) into Dithiobenzoate RAFT Agents

In this paper we explore RAFT (reversible addition-fragmentation chain transfer) single unit monomer insertion (SUMI) into dithiobenzoates. Styrene and N-isopropylacrylamide (NIPAm) were successfully inserted into 2-cyanopropan-2-yl dithiobenzoate. Attempted SUMI of methyl methacylate (MMA) provided an oligomeric insertion product due to the low transfer constant of the dithiobenzoate in MMA polymerization. A very low yield with maleic anhydride (MAH) reflects the low reactivity of MAH towards 2-cyanopropan-2-yl radicals. We also examined insertion of MAH, styrene and NIPAm into the styrene SUMI product. Insertion of MAH was rapid and efficient. SUMI with styrene and NIPAm was slower, which is attributed both to the low monomer concentrations used and the poor leaving group ability of the propagating species. The reaction with NIPAm is additionally complicated by initiator-derived by-products