Langmuir · 2018 · 16 citations · 53 references
Natural SciencesChemistryMaterials ScienceNanomaterialsNanotechnologySurface ScienceInorganic NanoparticlesPhotochemistrySelf-assembled MaterialsSelf-assembled NanostructuresSelf-assemblySelf-assembly Of NanomaterialsAmphiphilic Self-assemblyGold NanostructuresGold Surface FunctionalizationHydrogen Bonding InteractionsPh DependencePhotochemical FunctionalizationReversible Self-assemblyStimuli-responsive Self-assembly
Herein, an interesting light-induced self-assembly behavior from non-photoresponsive gold nanoparticles (Au NPs) was reported. Specifically, a pH-responsive amphiphile SPBwas developed that contained a particular phenylboronic acid moiety and showed excellent surface activity at the neutral and basic conditions, thereby stabilizing Au NPs well. Accordingly, the SPB-functionalized Au NPs showed strong pH dependence that there presented the pH-induced reversible self-assembly behavior. Furthermore, the introduction of a small amount of commercially available photoacid generator named diphenyliodonium nitrate (DIN) into the system could endow it with apparent light-switchable self-assembly behavior. The pH- and light-induced self-assembly behaviors of SPB-functionalized Au NPs in the absence and presence of DIN, respectively, were systematically studied by various techniques including UV-vis spectrum, transmission electron microscope, nuclear magnetic resonance, and Fourier transform infrared spectroscopy, which evidently confirmed that the stimuli-responsive self-assembly was controlled by the hydrogen-bonding interactions between phenylboronic acid moieties. Attributing to the light-induced obvious color change from bright-red to deep purple, the system was applied in particle imprinting successfully.
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