Stimuli‐responsive block–random copolymers are very useful “smart” materials as their switching behavior can be tuned by simply adjusting the composition of the random copolymer block. Because of that, we synthesized double thermoresponsive poly(N‐acryloylpyrrolidine)‐block‐poly(N‐acryloylpiperidine‐co‐N‐acryloylpyrrolidine) (PAPy‐b‐P(APi‐co‐APy)) copolymers via reversible addition fragmentation chain transfer (RAFT) polymerization and investigated their temperature‐induced self‐assembly in aqueous solution. By varying the APi/APy ratio in the random copolymer block, its phase transition temperature (PTT1) can indeed be precisely adjusted while the temperature‐induced collapse upon heating leads to a fully reversible well‐defined micellization. By making the two blocks compositionally similar to more than 60%, the polymers' mechanistic thermoresponsiveness can furthermore be changed from block‐like to rather gradient‐like behavior. This means the micellization onset at PTT1 and the corona collapse at the PTT of the more hydrophilic pure PAPy block (PTT2) overlap resulting in one single broad transition. This work thus contributes to the detailed understanding of design, synthesis and mechanistic behavior of tailored “on‐demand” switchable materials. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 399–411

Within the group of stimuli-responsive, "smart" materials, upper critical solution temperature (UCST) polymers remain sparsely investigated. Thus, this work focusses on a vastly ignored UCST polymer: polymethacrylamide (PMAAm). A cost-efficient photoiniferter reversible addition-fragmentation chain transfer (RAFT) polymerization yielding narrowly dispersed (Đ < 1.1) PMAAm is presented. This PMAAm exhibits highly thermoreversible UCST-type phase transitions (PT) in water/ethanol mixtures (ethanol content: 17-35 wt%) which are investigated via temperature dependent dynamic light scattering (DLS). Apart from the ethanol content, the PT temperature is affected by polymer mass fraction and chain length and varies between 10-80 C depending on the three mentioned parameters. Lastly, PMAAm's propensity towards amide hydrolysis and concomitant PT-suppression is investigated. Below temperatures of 40 C, PMAAm solutions show no sign of amide hydrolysis for at least three days, however, if heated to 70 C, the thermoresponsiveness gradually degrades within hours.

Despite the great potential of design of experiments (DoE) for efficiency and plannability in academic research, it remains a method predominantly used in industrial processes. From our perspective though, DoE additionally provides greater information gain than conventional experimentation approaches, even for more complex systems such as chemical reactions. Hence, this work presents a comprehensive DoE investigation on thermally initiated reversible addition–fragmentation chain transfer (RAFT) polymerization of methacrylamide (MAAm). To facilitate the adaptation of DoE for virtually every other polymerization, this work provides a step-by-step application guide emphasizing the biggest challenges along the way. Optimization of the RAFT system was achieved via response surface methodology utilizing a face-centered central composite design (FC-CCD). Highly accurate prediction models for the responses of monomer conversion, theoretical and apparent number averaged molecular weights, and dispersity are presented. The obtained equations not only facilitate thorough understanding of the observed system but also allow selection of synthetic targets for each individual response by prediction of the respective optimal factor settings. This work successfully demonstrates the great capability of DoE in academic research and aims to encourage fellow scientists to incorporate the technique into their repertoire of experimental strategies.