硫醚合成中高效C─S偶联的铜单原子催化剂。

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Dr. Theodore A. Gazis, Shilpa Palit, Dr. Luis A. Cipriano, Nicolò Allasia, Dr. Sean M. Collins, Prof. Dr. Quentin M. Ramasse, Dr. Ik Seon Kwon, Prof. Dr. Martin Sterrer, Dr. Giovanni Di Liberto, Prof. Dr. Gianvito Vilé
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引用次数: 0

摘要

碳杂原子交叉偶联反应已成为合成化学中不可缺少的工具。然而,碳-硫(C─S)键的形成仍然非常不发达,而碳-硫(C─S)键是生产用于制药、农药和先进材料的硫醚所必需的。工业上的C─S偶联方法仍然依赖于昂贵的均相催化剂,这些催化剂的可回收性很差,而且容易受到硫致失活的影响。在这项工作中,我们报告了一种铜单原子催化剂,其中Cu位点原子分散在介孔石墨氮化碳上,在温和条件下和克尺度上实现了高效,选择性和可回收的C─S交叉偶联反应。该催化剂具有优异的抗硫醇中毒性能,并能在多次催化循环中保持较高的性能。先进的表征技术,包括像差校正电子显微镜、x射线吸收光谱和单原子敏感电子能量损失光谱,证实了Cu位点的原子色散和稳定的配位环境。结合密度泛函理论模拟和自由基清除实验,我们的机制研究支持一个协调的氧化加成途径,不包括自由基中间体。这些结果为非均相C─S耦合提供了关键见解,并展示了单原子催化剂在解决硫化学长期挑战方面的能力,为精细化学和药物合成的更环保、更可扩展的工艺铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Copper Single-Atom Catalyst for Efficient C─S Coupling in Thioether Synthesis

Copper Single-Atom Catalyst for Efficient C─S Coupling in Thioether Synthesis

Carbon-heteroatom cross-coupling reactions have become indispensable tools in synthetic chemistry. However, the formation of carbon–sulfur (C─S) bonds, which are essential for producing thioethers used in pharmaceuticals, agrochemicals, and advanced materials, remains significantly underdeveloped. Industrial C─S coupling methods still rely on expensive, homogeneous catalysts that suffer from poor recyclability and are susceptible to sulfur-induced deactivation. In this work, we report a copper single-atom catalyst, where Cu sites are atomically dispersed on mesoporous graphitic carbon nitride, to enable efficient, selective, and recyclable C─S cross-coupling reactions under mild conditions and on a gram scale. The catalyst exhibits excellent resistance to thiol poisoning and maintains high performance over multiple catalytic cycles. Advanced characterization techniques, including aberration-corrected electron microscopy, X-ray absorption spectroscopy, and single-atom-sensitive electron energy loss spectroscopy, confirm the atomic dispersion and stable coordination environment of Cu sites. Combined with density functional theory simulations and radical scavenging experiments, our mechanistic investigations support a concerted oxidative addition pathway, which excludes radical intermediates. These results provide key insights into heterogeneous C─S coupling and demonstrate the power of single-atom catalysts in addressing long-standing challenges in sulfur chemistry, paving the way toward greener and more scalable processes for fine chemical and pharmaceutical synthesis.

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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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