Polymer characterization articles from across Nature Portfolio

The surface properties of the star polymer coating were evaluated with their resistance to protein adsorption and surface zeta (ζ)-potential to clarify the mechanism for inhibition of cell adhesion. The surface of the star polymer coating with a high density of poly(2-hydroxyethyl methacrylate) formed an electrically neutral diffuse brush structure in water and showed high resistance to protein adsorption. Considering the data obtained in the study, the surface ζ-potential and antibiofouling properties were correlated by controlling the molecular architecture of the coating material.

Soft interfaces formed by polymer materials are important interfaces for biological systems (biointerfaces). Controlled radical polymerization (CRP) is highly suited for designing biointerfaces composed of polymer chains because it enables precise control of the polymer architecture at the nanoscale. This focus review describes the design of functional soft interfaces based on investigations of the structure-property relationships of CRPs. In particular, polymer brush surfaces showing autonomous property changes, comb-type copolymer-driven 2D/3D transformations of lipid bilayers, and molecular interactions in bactericidal cationic polymer brushes are depicted.

Polyorganophosphazenes are macromolecules that selfassemble with antigenic proteins to enable biological functionality. Here, direct imaging by cryogenic electron microscopy reveals the coil structure of their individual chains and compact stiffened coils of their complexes with proteins.

The mechanisms of adhesion between polymers and inorganic materials are not fully understood. Here, authors demonstrate the clear evidence that the surface chemistry impacts the crosslinked structures of resins near the interfaces, resulting in different fracture behaviours and adhesive strengths.

Acid triggers the formation of radicals by Flory autoinitiation of acrylic monomers and enhances polymerization rates.

The combination of addressable synthetic macromolecules with proteins of precise structure and function often leads to materials with unique properties, as is now shown by the efficient multi-site initiation of polymer growth inside the cavity of a virus capsid.

Two-dimensional polymers can serve to organize chemical functionality periodically over large areas, but their rational synthesis has remained limited. Now, a free-standing, single-layer polymer sheet has been prepared and isolated through a two-step procedure — a photochemical reaction within a layered organic crystal followed by exfoliation.

Turning on chemical reactivity using light enables on-demand trapping of noxious gases inside a porous coordination polymer.