Recyclable Porous Organic Polymer-Supported Single-Atom Ruthenium Catalyst for Strong Si–F Bond Activation: Catalytic Si–F/Si–H and Si–F/Si–O Cross-Coupling Reactions

IF 5 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2025-04-01 DOI:10.1021/acs.orglett.5c00851
Shanshan Xu, Zhenning Sun, Juanjuan Zheng, Ruxin Jin, Ping Li, Feng Xie, Chenggang Ci, Bin Li
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Abstract

Developing efficient methods for strong Si–F σ-bond activation is very important in organosilicon chemistry. We report the preparation of a novel porous organic polymer (POP)-supported single-atom Ru catalyst (POPs-Ru SACs) that was successfully applied in catalytic strong Si–F/Si–H and Si–F/Si–O cross-coupling reactions. Various disiloxanes with functional group tolerance were produced under mild conditions. Furthermore, the POPs-Ru SACs catalyst exhibited excellent recyclability for Si–F and Si–H cross-coupling reactions. Density functional theory calculations were performed to verify the mechanism of POPs-Ru SACs-catalyzed Si–F/Si–H cross-coupling reactions.

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用于强 Si-F 键活化的可回收多孔有机聚合物支撑单原子钌催化剂:催化 Si-F/Si-H 和 Si-F/Si-O 交叉偶联反应
在有机硅化学中,开发有效的强Si-F - σ键活化方法是非常重要的。本文报道了一种新型多孔有机聚合物(POP)负载单原子Ru催化剂(POP -Ru SACs)的制备,并成功应用于催化强Si-F / Si-H和Si-F / Si-O交叉偶联反应。在温和条件下,制备了多种具有官能团耐受性的二硅氧烷。此外,pop - ru SACs催化剂在Si-F和Si-H交叉偶联反应中表现出良好的可回收性。通过密度泛函理论计算验证了pop - ru sacs催化Si-F / Si-H交叉偶联反应的机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Organic Letters
Organic Letters 化学-有机化学
CiteScore
9.30
自引率
11.50%
发文量
1607
审稿时长
1.5 months
期刊介绍: Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.
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