硫醇衍生物与芳基卤化物的可见光驱动无催化剂 C-S 交叉偶联。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-10-18 DOI:10.1039/d4ob01415d
Zhiqiang Liu, Yansong Hu, Shutao Wang, Yating Ding, Zhengze Zhang, Yi-Feng Qiu, Zhao Liu, Junqiang Lei
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引用次数: 0

摘要

据报道,在烷基硫醇衍生物和(杂)芳基卤化物之间存在一种温和、可扩展和高产的可见光促进的 C-S 交叉偶联,无需金属、配体或光催化剂,与传统的 C-S 键形成策略相比具有优势。实验和计算机理研究支持电子供体-受体(EDA)复合物的形成,该复合物在没有光氧化催化剂的情况下经历可见光诱导的电荷转移来启动 C-S 键的形成。
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Visible-light-driven catalyst-free C-S cross-coupling of thiol derivatives and aryl halides.

A mild, scalable, and high-yielding visible-light-promoted C-S cross-coupling between alkyl thiol derivatives and (hetero)aryl halides without the need for metals, ligands, or photocatalysts is reported, offering advantages over traditional C-S bond forming strategies. The formation of an electron donor-acceptor (EDA) complex is supported by experimental and computational mechanistic studies, which undergoes visible-light-induced charge transfer to initiate C-S bond formation in the absence of a photoredox catalyst.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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