Abstract
Coacervates have emerged as promising systems for achieving dynamic compartmentalization. Particularly, synthetic polymeric complex coacervates represent a well-established class. However, their stability is often compromised at high ionic strength due to charge screening effects. In contrast, simple coacervates, which arise from the phase separation of a single polymer species, exhibit structural stability at high ionic strength. Meanwhile, the development of synthetic simple coacervates remains limited and poorly understood. In this study, we present a universal strategy for creating thermoresponsive simple coacervates from synthetic copolymers comprising lower critical solution temperature (LCST)-type monomers and hydrophilic monomers. Unlike conventional complex coacervates, the resulting simple coacervates maintain their integrity at high salt concentrations. This approach provides a robust and tunable platform for designing synthetic simple coacervate systems. With the growing interest in coacervates for applications in artificial cells and compartmentalized reaction systems, our findings provide a foundational framework for expanding their functional utility.
Supplementary materials
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Supporting Information
Description
The data are available free of charge. Synthetic procedure for all copolymers. 1H-NMR spectroscopy results and GPC traces of the synthesized copolymers. Representative DLS profile of poly(NIPAAm-co-DMAAm). Representative optical microscopic images of the copolymers in aqueous media (PDF).
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Title
Supporting Movie S1
Description
Representative video demonstrating poly(NIPAAm-co-DMAAm) coacervate coalescence (MP4).
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