Anderson, Ryan AFine, Rachel FRapagnani, Rachel MTonks, Ian A2024-05-302024-05-302024-05-30https://hdl.handle.net/11299/263592Each type of data is collected in a single main folder (e.g., NMR, SEC dRI, etc.) and then separated into corresponding folders.These files contain primary data along with associated output from instrumentation supporting all results reported in Anderson et. al. Ring-Opening Copolymerizations of a CO2-derived δ-Valerolactone with ε-Caprolactone and L-Lactide. This work has expanded the synthetic polymer chemistry of the CO2-derived lactone EtVP through ring-opening co-polymerizations with ε-CL and LLA. Polymer properties and microstructures could be tuned through concurrent and se-quential copolymerization strategies, which led to the formation of either block, gradient, or random copolymers. ε-CL block copolymers resulted in semi-crystalline polymers regardless of the molar ratio employed. For LLA, copolymers remained amorphous, and mechanical testing showed improved elasticity relative to PLLA. Furthermore, ε-CL and LLA copolymers could be chemically recycled back to monomer utilizing Sn(Oct)2. While this work lays the foundation for EtVP-based copolymers, investigation into triblocks and other end-of-life options may further improve the potential ap-plications of these CO2-based (co)polymers.CC BY-NC-ND 4.0carbon dioxidepolyestercopolymerizationring-opening polymerizationSupporting Data for Ring-Opening Copolymerizations of a CO2-derived δ-Valerolactone with ε-Caprolactone and L-LactideDatasethttps://doi.org/10.13020/cnxb-m954