Hosford, Brandon MRamos, WilliamLamb, Jessica R2024-08-152024-08-152024-08-15https://hdl.handle.net/11299/264955A full description can be found in the README.txt file. The files below include raw data used in the corresponding manuscript including: nuclear magnetic resonance (NMR) data, size exclusion chromatography (SEC) data, thermal gravimetric analysis (TGA) data, differential scanning calorimetry (DSC) data, mass spectroscopy (MS) data. The ChemDraw schemes are included as .jpg file. All raw data was converted to .xlsx or .txt files for simplicity and can be opened using a spreadsheet editor such as Microsoft Excel. The .fid file for NMR data can be opened in any NMR analysis software (e.g. MestReNova).An ongoing challenge in polymer chemistry is accessing diverse block copolymers from multiple polymerization mechanisms and monomer classes. One strategy to accomplish this goal without intermediate compatibilization steps is the use of universal mediators. Thiocarbonyl thio (TCT) functional groups are well-known mediators to combine radical with either cationic or anionic polymerization, but a sequential cationic-anionic universal mediator system has never been reported. Herein, we report a TCT universal mediator that can sequentially perform photocontrolled cationic polymerization and thioacyl anionic group transfer polymerization to access poly(ethyl vinyl ether)-block-poly(thiirane) polymers for the first time. Thermal analyses of these block copolymers provide evidence of microphase separation. The success of this system, along with the established compatibility of radical polymerization, enabled us to further chain extend the cationic-anionic diblock using radical polymerization of N-isopropylacrylamide. The resulting terpolymer represents the first example of a triblock made from three different monomer classes incorporated via three different mechanisms without any end-group modification steps. The development of this simple, sequential synthesis using a universal mediator approach opens up new possibilities by providing facile access to diverse block copolymers of vinyl ethers, thiiranes, and acrylamides.Attribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/polymerscationicanionicradicalpolymerizationthiiranevinyl etheruniversal mediatorthiocarbonyl thioblock copolymersDatasethttps://doi.org/10.13020/jqbp-3e81