Jang, Yoon-JungSangroniz, LeireHillmyer, Marc2022-06-212022-06-212022-06-21https://hdl.handle.net/11299/228061These files contain data along with associated output from instrumentation supporting all results in the referenced paper. The folders contain each series of data in a subfolder including ChemDraw, NMR, DSC, SEC, IR, TGA, WAXD, Tensile testing, OTR, WVTR, and TOC data for all Figures and Tables. The readme file further describes the individual files.The development of promising sustainable gas barrier materials, such as polyglycolide, poly(L-lactide), and poly(ethylene 2,5-furandicarboxylate) is an important alternative strategy to traditional plastics used for packaging where low gas permeability is beneficial. However, high degrees of crystallinity in these materials can lead to undesirably low material toughness. We report poly(ester-amide)s derived from glycolide and diamines exhibiting both high toughness and desirable gas barrier properties. These sustainable poly(ester-amide)s were synthesized from glycolide-derived diamidodiols and diacids. To understand structure-property relationships of poly(ester-amide)s, polymers with different numbers of methylene groups were compared with respect to thermal, mechanical, and gas barrier properties. As the number of methylene groups between ester groups increased, the melting temperature decreased and oxygen permeability increased in the even numbered methylene group series. We also found that they are readily degradable under neutral, acidic, and basic hydrolytic conditions. These high performance poly(ester-amide)s are promising sustainable alternatives to conventional gas barrier materials.CC0 1.0 Universalhttp://creativecommons.org/publicdomain/zero/1.0/Gas barrier materialsPoly(ester-amide)sTough gas barrier materialsSustainable polymersDuctile polymersGlycolideDatasethttps://doi.org/10.13020/2qz9-nj73