Reversible deactivation radical polymerization (RDRP) has revolutionized modern polymer chemistry over the past two decades, thus laying the groundwork for the synthesis of complex macromolecules and enabling the preparation of previously inaccessible materials. Reversible addition-fragmentation chain transfer (RAFT) polymerization has emerged as one of the most promising techniques because of its functional group tolerance, applicability to a wide range of vinyl monomers, and its nondemanding experimental conditions. However, despite the promise and clearly demonstrated utility of RAFT, limitations of the method sometimes still exist, including the occasional need for extended polymerization times, limited access to high molecular weight polymers, low "livingness" due to unavoidable radical termination events, etc. This Perspective focuses on recent advances that have been specifically designed to address many of these perceived limitations to reinforce the promise of RAFT for the synthesis of complex and well-defined polymers under facile conditions.

2017-08-30T02:06:43

Hydrophobicity inherently affects a solutes behavior in water, yet how polymer chain hydrophobicity impacts aggregate morphology during solution self-assembly and reorganization is largely overlooked. As polymer and nanoparticle syntheses are easily achieved, the resultant nanoparticle architectures are usually attributed to chain topology and overall degree of polymerization, bypassing how the chains may interact with water during/after self-assembly to elicit morphology changes. Herein, we demonstrate how block copolymer hydrophobicity allows control over aggregate morphology in water and leads to remarkable control over the length of polymeric nanoparticle worms. Polymerization-induced self-assembly facilitated nanoparticle synthesis through simultaneous polymerization, self-assembly, and chain reorganization during a block copolymer chain extension from a hydrophilic poly­( N , N -dimethyl­acrylamide) macro-chain-transfer agent with diacetone acrylamide and N , N -dimethyl­acrylamide. Slight variations in the monomer feed ratio dictated the block copolymer chain composition and were proposed to alter aggregate thermodynamics. Micelles, worms, and vesicles were synthesized, and the highest level of control over worm elongation attained during a polymerization is reported, simply due to the polymer chain hydrophobicity.

We report mechanistic investigations into aqueous visible-light reversible addition−fragmentation chain transfer (RAFT) polymerizations of acrylamides using eosin Y as a photoinduced electron-transfer (PET) catalyst. The photoinduced polymerization was found to be dependent upon the irradiation wavelength and reagents, where either reduction or oxidation of the PET catalyst leads to inherently different initiation and reversible-termination steps. Using blue light, multiple mechanisms of initiation are observed, depending on the presence or absence of a sacrificial reducing agent. Using green light, both an oxidative and a reductive PET initiation mechanism can be pursued. Investigations into the role of PET catalyst, wavelength, and reducing agent demonstrated that precise polymers with predictable molecular weights are best realized under an oxidative PET-RAFT mechanism. Therefore, this study provides fundamental insight into visible-light RAFT photopolymerizations and the role of eosin Y as a photoredox catalyst.

Complex coacervates can form through the electrostatic complexation of oppositely charged polymers. The material properties of the resulting coacervates can change based on the polymer chemistry and the complex interplay between electrostatic interactions and water structure, controlled by salt. We examined the effect of varying the polymer backbone chemistry using methacryloyl- and acryloyl-based complex coacervates over a range of polymer chain lengths and salt conditions. We simultaneously quantified the coacervate phase behavior and the linear viscoelasticity of the resulting coacervates to understand the interplay between polymer chain length, backbone chemistry, polymer concentration, and salt concentration. Time-salt superposition analysis was used to facilitate a broader characterization and comparison of the stress relaxation behavior between different coacervate samples. Samples with mismatched polymer chain lengths highlighted the ways in which the shortest polymer chain can dominate the resulting coacervate properties. A comparison between coacervates formed from methacryloyl vs acryloyl polymers demonstrated that the presence of a backbone methyl group affects the phase behavior, and thus the rheology in such a way that coacervates formed from methacryloyl polymers have a similar phase behavior to those of acryloyl polymers with ∼10× longer polymer chains.