Ultrasmall Single-Chain Nanoparticles Derived from Amphiphilic Alternating Copolymers

The collapse or folding of an individual polymer chain into a nanoscale particle gives rise to single-chain nanoparticles (SCNPs), which share a soft nature with biological protein particles. The precise control of their properties, including morphology, internal structure, size, and deformability, are a long-standing and challenging pursuit. Herein, a new strategy based on amphiphilic alternating copolymers for producing SCNPs with ultrasmall size and uniform structure is presented. SCNPs are obtained by folding the designed alternating copolymer in N,N-dimethylformamide (DMF) and fixing it through a photocatalyzed cycloaddition reaction of anthracene units. Molecular dynamics simulation confirms the solvophilic outer corona and solvophobic inner core structure of SCNPs. Furthermore, by adjusting the length of PEG units, precise control over the mean size of SCNPs is achieved within the range of 2.8 to 3.9 nm. These findings highlight a new synthetic strategy that enables enhanced control over morphology and internal structure while achieving ultrasmall and uniform size for SCNPs. In this study, a novel approach based on amphiphilic alternating copolymers for the synthesis of small-sized and compact single-chain nanoparticles (SCNPs) structures is proposed. Precise control over the average size of SCNPs is achieved within the range of 2.8 to 3.9 nm. These findings underscore a new synthetic strategy that enables enhanced manipulation of morphology and internal architecture. image