Journal of the American Chemical Society · 2016 · 238 citations · 47 references
Natural SciencesChemical EngineeringChemistryCatalysisNanomaterialsNanotechnologyInorganic NanoparticlesNanocatalysisNanomaterials SynthesisNanoparticle DesignNanoparticle SynthesisSurface Functionalization Of NanomaterialsClick ChemistryCross-linkingIn Situ Chemical ReductionLow-toxicity MaterialsLow-toxicity ReagentsMetal NanoparticlesMetal-organic Supramolecular AssembliesSupramolecular Synthons
We show that copper-containing metal-organic nanoparticles (MONPs) are readily synthesized via Cu(II)-mediated intramolecular cross-linking of aspartate-containing polyolefins in water. In situ reduction with sodium ascorbate yields Cu(I)-containing MONPs that serve as highly efficient supramolecular catalysts for alkyne-azide "click chemistry" reactions, yielding the desired 1,4-adducts at low parts per million catalyst levels. The nanoparticles have low toxicity and low metal loadings, making them convenient, green catalysts for alkyne-azide "click" reactions in water. The Cu-MONPs enter cells and perform efficient, biocompatible click chemistry, thus acting as intracellular nanoscale molecular synthesizers.
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