“…These include hydrophobic monomers such as ethylene, 14 styrene (Sty), [14][15][16][17][18][19] acrylonitrile (AN), 19,20 vinyl acetate (VAc), [21][22][23] and methyl methacrylate (MMA) 20,24,25 as well as hydrophilic monomers such as poly(ethylene glycol) methyl ether methacrylate (PEGMA), 26,27 N,N-dimethylaminoethyl methacrylate (DMAEMA), [28][29][30] N-isopropylacrylamide (NIPAM), 31,32 and N-vinylpyrrolidone (NVP). 33,34 However, with the exception of less activated monomers (LAMs) such as VAc, the reactivity ratios for these copolymerizations indicate that final polymer compositions are more gradient-like or blocky, not statistical. 17,25,29,35 Control of polymerizations incorporating CKAs has also been attempted through reversible-deactivation radical polymerization (RDRP) techniques such as Nitroxide-Mediated Polymerization (NMP), 19,36 Atom Transfer Radical Polymerization (ATRP), [37][38][39] and Reversible Addition-Fragmentation Chain-Transfer Polymerization/Macromolecular Design by Interchange of Xanthates (RAFT/MADIX) 40 but there are only a handful of examples where these techniques have been used to control copolymerizations with MDO.…”