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Wavelength-Selective C–C and C–N Bond Formation via Defect-Engineered ZnIn2S4
ACS Catalysis ( IF 11.3 ) Pub Date : 2024-07-19 , DOI: 10.1021/acscatal.4c02199
Xiaohui Leng 1, 2 , Xin Zhou 2 , Lu Ma 3 , Yonghua Du 3 , Ouwen Peng 2 , Zhongxin Chen 2 , Jinhui Pan 1, 2 , Ming-Yu Qi 4 , Jian-Hui Zheng 4 , Yi-Jun Xu 4 , Kian Ping Loh 1, 2
Affiliation  

Visible light induced oxidative C–C and C–N coupling provides a milder alternative to the current synthetic strategies. However, the photochemical C–C coupling of benzylamine and chromoselective C–C/C–N conversion are not widely reported. Herein, we demonstrate that the introduction of indium vacancies in ZnIn2S4 improves the catalytic activity for C–C coupling of benzylamine and imparts a strong chromoselectivity for C–C or C–N coupled products. A high C–C selectivity of ∼80% is achieved with a benzylamine conversion of ∼80%. Mechanistic studies unveil the switchable reaction routes between kinetically favored C–C coupling and thermodynamically favored C–N coupling under specific illumination conditions.

中文翻译:


通过缺陷工程 ZnIn2S4 形成波长选择性 C-C 和 C-N 键



可见光诱导的氧化 C-C 和 C-N 偶联为当前的合成策略提供了一种更温和的替代方案。然而,苄胺的光化学C-C偶联和选择性C-C/C-N转化尚未得到广泛报道。在此,我们证明在 ZnIn 2 S 4 中引入铟空位提高了苄胺 C-C 偶联的催化活性,并赋予 C-C 或 C- 很强的颜色选择性。 N 耦合产品。苯甲胺转化率约为 80%,C-C 选择性高达 80%。机理研究揭示了特定光照条件下动力学上有利的 C-C 耦合和热力学上有利的 C-N 耦合之间的可切换反应路线。
更新日期:2024-07-22
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