Sieving Polymer Synthesis by Reversible Addition Fragmentation Chain Transfer Polymerization — ASN Events

Sieving Polymer Synthesis by Reversible Addition Fragmentation Chain Transfer Polymerization (#272)

Yi Heng Nai 1 , Roderick Jones 2 , Michael Breadmore
  1. ACROSS, Hobart, TAS, Australia
  2. Centre for Synthesis & Chemical Biology (CSCB), UCD School of Chemistry & Chemical Biology, University College Dublin, Dublin, Ireland

Replaceable sieving polymers are the fundamental component for high resolution nucleic acids separation in CE. The choice of polymer and its physical properties play significant roles in influencing separation performance. Recently, reversible addition fragmentation chain transfer (RAFT) polymerization has been shown to be a versatile polymerization technique capable of yielding well defined polymers previously unattainable by conventional free radical polymerization.  In this study, a high molecular weight PDMA at 765, 000 gmol-1 with a PDI of 1.55 was successfully synthesized with the use of chain transfer agent – 2-propionic acidyl butyl trithiocarbonate (PABTC) in a multi-step sequential RAFT polymerization approach. This study represents the first demonstration of RAFT polymerization for synthesizing polymers with the molecular weight range suitable for high resolution DNA separation in sieving electrophoresis. Adjustment of pH in the reaction was found to be crucial for the successful RAFT polymerization of high molecular weight polymer as the buffered condition minimizes the effect of hydrolysis and aminolysis commonly associated with trithiocarbonate chain transfer agents. The separation efficiency of PABTC-PDMA was found to have marginally superior separation performance compared to a commercial PDMA formulation, POP™-CAP, of similar molecular weight range.