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Highly efficient and recyclable water-soluble fullerene-supported PdCl2 nanocatalyst in Suzuki–Miyaura cross-coupling reaction

机译:铃木-宫浦交叉偶联反应中高效可回收的水溶性富勒烯负载型PdCl2纳米催化剂

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摘要

A water-soluble fullerene-supported PdCl _(2) nanocatalyst [C _(60) -TEG _(S) /PdCl _(2) ] was prepared by coordination of water-soluble fullerene nanoparticles with palladium chloride. In pure water, the catalytic activity of nanocatalyst [C _(60) -TEG _(S) /PdCl _(2) ] for Suzuki–Miyaura cross-coupling reaction was investigated under different reaction conditions. The results showed that biphenyl compounds could be synthesized in high yields at room temperature using 0.01 mol% of [C _(60) -TEG _(S) /PdCl _(2) ] as the catalyst and K _(2) CO _(3) as the base with the reaction time of 4 h. The catalyst was recycled five times, and the yield clearly did not decrease.
机译:通过将水溶性富勒烯纳米粒子与氯化钯配位制备了水溶性富勒烯负载的PdCl _(2)纳米催化剂[C _(60)-TEG _(S)/ PdCl _(2)]。在纯净水中,研究了在不同反应条件下纳米催化剂[C _(60)-TEG _(S)/ PdCl _(2)]对Suzuki-Miyaura交叉偶联反应的催化活性。结果表明,使用0.01 mol%的[C _(60)-TEG _(S)/ PdCl _(2)]作为催化剂和K _(2)CO _可以在室温下高收率合成联苯化合物。 (3)以碱为反应时间为4 h。将该催化剂循环五次,产率显然没有降低。

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