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DOI码：10.1021/acs.nanolett.4c00163

发表刊物：Nano Letters

摘要：Tuning electronic characteristics of metal–ligand bonds based on reaction pathways to achieve efficient catalytic processes has been widely studied and proven to be feasible in homogeneous catalysis, but it is scarcely investigated in heterogeneous catalysis. Herein, we demonstrate the regulation of the electronic configuration of Ir–O bonds in an Ir single-atom catalyst according to the borane activation mechanism. Ir–O bonds in Ir1/Ni(OH)x are found to be more electron-poor than those in Ir1/NiOx. Despite the mild solvent-free conditions and ambient temperature, Ir1/Ni(OH)x exhibits outstanding performance for the hydroboration of alkenes, furnishing the desired alkylboronic esters with a turnover frequency value of ≤3060 h–1 and 99% anti-Markovnikov selectivity, which is significantly better than that of Ir1/NiOx (42 h–1). It is further proven that the more electron-poor Ir–O bonds as active centers are more oxidative and so benefit the activation of the H–B bond in the reductive pinacolborane.

论文类型：期刊论文

学科门类：理学

文献类型：J

卷号：24

页面范围：5165-5173

是否译文：否

发表时间：2024-05-01

收录刊物：SCI

发布期刊链接：https://pubs.acs.org/doi/10.1021/acs.nanolett.4c00163