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Palladium supported on an ion exchange resin for the Suzuki©\Miyaura reaction A B S T R A C T A basic anion exchange resin, Amberlite IRA©\900, was loaded with Pd(C3H5)(C5H5) by an easy metal©\organic chemical vapor deposition (MOCVD) approach to give Pd@IRA©\900 catalyst after reduction at room temperature. Ultraviolet©\Visible spectroscopy results showed a red shift of the absorption peak of Pd2+after the Pd precursor was loaded on the resin, indicating that a chemical reaction occurred between the precursor and the support. Pd nanoparticles with 2.6nm of average size were well dispersed on the support.The Pd@IRA©\900 catalyst showed high activity for different kinds of aryl halides in Suzuki©\Miyaura coupling reactions under mild and aerobic conditions. Excellent recyclability of Pd@IRA©\900 catalyst was also observed in the Suzuki©\Miyaura coupling reaction of iodobenzene and phenylboronic acid.A bifunctional catalyst Pd@IRA©\900(OH) was synthesized by pretreating the ion exchange resin support with NaOH before Pd loading, which successfully catalyzed the Suzuki©\Miyaura reaction of iodobenzene and phenylboronic acid without base under aerobic conditions. |
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