AI Article Synopsis

  • A novel copper sulfate-based catalyst was created using a self-assembly process with a specific amphiphilic polymer, which enhances its effectiveness for click chemistry reactions.
  • The catalyst features a unique structure with globular particles and layered composites, enabling it to facilitate a wide range of chemical reactions, like the Huisgen 1,3-dipolar cycloaddition.
  • This solid-phase catalyst is highly efficient, demonstrating impressive catalytic turnover and can be reused multiple times without losing effectiveness, consistently producing the desired triazole compounds.

Article Abstract

Self-assembly of copper sulfate and a poly(imidazole-acrylamide) amphiphile provided a highly active, reusable, globular, solid-phase catalyst for click chemistry. The self-assembled polymeric Cu catalyst was readily prepared from poly(N-isopropylacrylamide-co-N-vinylimidazole) and CuSO(4) via coordinative convolution. The surface of the catalyst was covered with globular particles tens of nanometers in diameter, and those sheetlike composites were layered to build an aggregated structure. Moreover, the imidazole units in the polymeric ligand coordinate to CuSO(4) to give a self-assembled, layered, polymeric copper complex. The insoluble amphiphilic polymeric imidazole Cu catalyst with even 4.5-45 mol ppm drove the Huisgen 1,3-dipolar cycloaddition of a variety of alkynes and organic azides, including the three-component cyclization of a variety of alkynes, organic halides, and sodium azide. The catalytic turnover number and frequency were up to 209000 and 6740 h(-1), respectively. The catalyst was readily reused without loss of catalytic activity to give the corresponding triazoles quantitatively.

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Source
http://dx.doi.org/10.1021/ja3036543DOI Listing

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