4.8 Article

Polymer Grafting to Polydopamine Free Radicals for Universal Surface Functionalization

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 144, Issue 15, Pages 6992-7000

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c02073

Keywords

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Funding

  1. Australian Research Council (ARC) [ARC IC170100020, FL200100124]
  2. ARC [FT170100094]
  3. ARC Centre of Excellence in Exciton Science [CE170100026]
  4. China Scholarship Council
  5. Australian Research Council [FL200100124] Funding Source: Australian Research Council

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Modifying surfaces using free radical polymerization allows the incorporation of diverse physicochemical properties of vinyl polymers onto new materials. By utilizing the surface attachment of polydopamine (PDA), a range of different surfaces were primed for free radical polymer attachment. The strategy resulted in covalent polymer attachment on both porous and nonporous substrates, imparting new properties to the functionalized materials.
Modifying surfaces using free radical polymerization (FRP) offers a means to incorporate the diverse physicochemical properties of vinyl polymers onto new materials. Here, we harness the universal surface attachment of polydopamine (PDA) to prime a range of different surfaces for free radical polymer attachment, including glass, cotton, paper, sponge, and stainless steel. We show that the intrinsic free radical species present in PDA can serve as an anchor point for subsequent attachment of propagating vinyl polymer macroradicals through radical-radical coupling. Leveraging a straightforward, twofold soak-wash protocol, FRP over the PDA-functionalized surfaces results in covalent polymer attachment on both porous and nonporous substrates, imparting new properties to the functionalized materials, including enhanced hydrophobicity, fluorescence, or temperature responsiveness. Our strategy is then extended to covalently incorporate PDA nanoparticles into organo-/hydrogels via radical cross-linking, yielding tunable PDA-polymer composite networks. The propensity of PDA free radicals to quench FRP is studied using in situ H-1 nuclear magnetic resonance and electron paramagnetic resonance spectroscopy, revealing a surface area-dependent macroradical scavenging mechanism that underpins PDA-polymer conjugation. By combining the arbitrary surface attachment of PDA with the broad physicochemical properties of vinyl polymers, our strategy provides a straightforward route for imparting unlimited new functionality to practically any surface.

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