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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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