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Surfactant‐Assisted Suzuki–Miyaura Coupling Reaction of Unreactive Chlorobenzene over Hydrotalcite‐Supported Palladium Catalyst

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A hydrotalcite-supported palladium chloride (PdCl2/HT) catalyst has been developed for the Suzuki–Miyaura coupling (SMC) reaction. As-prepared PdCl2/HT effectively catalyzed the SMC reaction of bromobenzene under air to afford >99 % biphenyl… Click to show full abstract

A hydrotalcite-supported palladium chloride (PdCl2/HT) catalyst has been developed for the Suzuki–Miyaura coupling (SMC) reaction. As-prepared PdCl2/HT effectively catalyzed the SMC reaction of bromobenzene under air to afford >99 % biphenyl yields and the catalyst could be reused without any significant loss in catalytic activity. The moderate activity (69 % biphenyl yields) of the PdCl2/HT catalyst for chlorobenzene was improved, resulting in biphenyl yields of up to 96 % using a surfactant as an additive. Among various surfactants employed, Triton X-100 (TX-100) enhanced the catalytic performances of PdCl2/HT the most. The X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS) of bare and surfactant-treated PdCl2/HT catalysts depicted the ligation of the Pd species by TX-100 influenced the electronic structure of the Pd species, leading to efficient catalysis.

Keywords: supported palladium; reaction; spectroscopy; suzuki miyaura; catalyst; hydrotalcite supported

Journal Title: Asian Journal of Organic Chemistry
Year Published: 2017

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