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通过蛋白质限域构建钯和铜拥挤单原子以促进Sonogashira反应

Constructing Pd and Cu Crowding Single Atoms by Protein Confinement to Promote Sonogashira Reaction.

作者信息

Zhao Qinying, Zhao Xudong, Liu Zhiyi, Ge Yi, Ruan Jiaxiong, Cai Hongyi, Zhang Shasha, Ye Chenliang, Xiong Yu, Chen Wei, Meng Ge, Liu Zhiliang, Zhang Jian

机构信息

Key Laboratory of Carbon Materials of Zhejiang Province, Key Lab of Biohealth Materials and Chemistry of Wenzhou, College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang, 325035, China.

College of Material Sciences and Chemical Engineering, Harbin Engineering University, Harbin, Heilongjiang, 150001, China.

出版信息

Adv Mater. 2024 Sep;36(36):e2402971. doi: 10.1002/adma.202402971. Epub 2024 Jul 16.

Abstract

For multicenter-catalyzed reactions, it is important to accurately construct heterogeneous catalysts containing multiple active centers with high activity and low cost, which is more challenging compared to homogeneous catalysts because of the low activity and spatial confinement of active centers in the loaded state. Herein, a convenient protein confinement strategy is reported to locate Pd and Cu single atoms in crowding state on carbon coated alumina for promoting Sonogashira reaction, the most powerful method for constructing the acetylenic moiety in molecules. The single-atomic Pd and Cu centers take advantage in not only the maximized atomic utilization for low cost, but also the much-enhanced performance by facilitating the activation of aryl halides and alkynes. Their locally crowded dispersion brings them closer to each other, which facilitates the transmetallation process of acetylide intermediates between them. Thus, the Sonogashira reaction is drove smoothly by the obtained catalyst with a turnover frequency value of 313 h, much more efficiently than that by commercial Pd/C and CuI catalyst, conventional Pd and Cu nanocatalysts, and mixed Pd and Cu single-atom catalyst. The obtained catalyst also exhibits the outstanding durability in the recycling test.

摘要

对于多中心催化反应而言,精确构建具有高活性和低成本的含多个活性中心的非均相催化剂至关重要,与均相催化剂相比,这更具挑战性,因为负载状态下活性中心的活性较低且存在空间限制。在此,报道了一种简便的蛋白质限域策略,可将处于拥挤状态的钯和铜单原子定位在碳包覆氧化铝上,以促进Sonogashira反应,这是构建分子中炔基部分最有效的方法。单原子钯和铜中心不仅因低成本而具有最大化的原子利用率,还通过促进芳基卤化物和炔烃的活化而使性能大幅提高。它们局部拥挤的分散状态使它们彼此更靠近,这有利于它们之间乙炔化物中间体的转金属化过程。因此,所制备的催化剂能顺利驱动Sonogashira反应,其周转频率值为313 h,比商业钯/碳和碘化亚铜催化剂、传统钯和铜纳米催化剂以及混合钯和铜单原子催化剂更高效。所获得的催化剂在循环测试中也表现出出色的耐久性。

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