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Atomically dispersed palladium catalyses Suzuki–Miyaura reactions under phosphine-free conditions

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Single-atom catalysts have emerged as a new frontier in catalysis science. However, their applications are still limited to small molecule activations in the gas phase, the classic organic transformations catalyzed… Click to show full abstract

Single-atom catalysts have emerged as a new frontier in catalysis science. However, their applications are still limited to small molecule activations in the gas phase, the classic organic transformations catalyzed by single-atom catalysts are still rare. Here, we report the use of a single-atom Pd catalyst for the classic Suzuki–Miyaura carbon–carbon coupling reaction under phosphine-free and open-air conditions at room temperature. The single-atom Pd catalyst is prepared through anchoring Pd on bimetal oxides (Pd-ZnO-ZrO 2 ). The significant synergetic effect of ZnO and ZrO 2 is observed. The catalyst exhibits high activity and tolerance of a wide scope of substrates. Characterization demonstrates that Pd single atoms are coordinated with two oxygen atoms in Pd-ZnO-ZrO 2  catalyst. The catalyst can be fabricated on a multi-gram scale using a simple in situ co-precipitation method, which endows this catalytic system with great potential in practical applications. Single-atom heterogeneous catalysts are widely studied, but few examples are known which promote carbon–carbon bond formation. Here single palladium atoms supported by crystalline ZnO-ZrO 2 catalyse Suzuki–Miyaura couplings.

Keywords: zno zro; suzuki miyaura; single atom; catalyst; phosphine free

Journal Title: Communications Chemistry
Year Published: 2020

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