N-Hydroxyethyl acrylamide as a functional eROP initiator for the preparation of nanoparticles under "greener" reaction conditions. Issue 42 (17th October 2022)

• Record Type: Journal Article
• Authors: Lentz, Joachim C.; Cavanagh, Robert; Moloney, Cara; Falcone Pin, Bruno; Kortsen, Kristoffer; Fowler, Harriet R.; Jacob, Philippa L.; Krumins, Eduards; Clark, Charlotte; Machado, Fabricio; Breitkreuz, Nicholas; Cale, Ben; Goddard, Amy R.; Hirst, Jonathan D.; Taresco, Vincenzo; Howdle, Steven M.
• Is Part Of: Polymer chemistry. Volume 13:Issue 42(2022)
• Page Start: 6032
• Page End: 6045
• Publication Date: 2022-10-17
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/d2py00849a
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : N -Hydroxyethyl acrylamide was used as a functional initiator to produce hybrid macromonomers via the enzymatic ring-opening polymerisation of ε-caprolactone and δ-valerolactone. Abstract : N -Hydroxyethyl acrylamide was used as a functional initiator for the enzymatic ring-opening polymerisation of ε-caprolactone and δ-valerolactone. N -Hydroxyethyl acrylamide was found not to undergo self-reaction in the presence of Lipase B from Candida antarctica under the reaction conditions employed. By contrast, this is a major problem for 2-hydroxyethyl methacrylate and 2-hydroxyethyl acrylate which both show significant transesterification issues leading to unwanted branching and cross-linking. Surprisingly, N -hydroxyethyl acrylamide did not react fully during enzymatic ring-opening polymerisation. Computational docking studies helped us understand that the initiated polymer chains have a higher affinity for the enzyme active site than the initiator alone, leading to polymer propagation proceeding at a faster rate than polymer initiation leading to incomplete initiator consumption. Hydroxyl end group fidelity was confirmed by organocatalytic chain extension with lactide. N -Hydroxyethyl acrylamide initiated polycaprolactones were free-radical copolymerised with PEGMA to produce a small set of amphiphilic copolymers. The amphiphilic polymers were shown to self-assemble into nanoparticles, and to display low cytotoxicity in 2D in vitro experiments. To increase the green credentials of the synthetic strategies, all reactions were carried out in 2-methyl tetrahydrofuran, a solvent derived from renewable resources and an alternative for the more traditionally used fossil-based solvents tetrahydrofuran, dichloromethane, and toluene.