催化作用
硫醚
硫黄
杂原子
化学
二苯并噻吩
铜
碳纤维
多相催化
组合化学
纳米技术
光化学
材料科学
有机化学
复合材料
复合数
戒指(化学)
作者
Theodore A. Gazis,Santi R. Palit,Luis A. Cipriano,Nicolò Allasia,Sean M. Collins,Quentin M. Ramasse,Ik Seon Kwon,Martin Sterrer,Giovanni Di Liberto,Gianvito Vilé
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-08-06
卷期号:64 (38): e202510632-e202510632
被引量:4
标识
DOI:10.1002/anie.202510632
摘要
Abstract 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI