Ghasimi Saman, Bretschneider Simon A, Huang Wei, Landfester Katharina, Zhang Kai A I
Max Planck Institute for Polymer Research Ackermannweg 10 Mainz 55128 Germany.
Adv Sci (Weinh). 2017 May 22;4(8):1700101. doi: 10.1002/advs.201700101. eCollection 2017 Aug.
The Stille coupling reaction is a versatile method to mainly form aromatic C-C bonds. However, up to now, the use of palladium catalysts is necessary. Here, a palladium-free and photocatalytic Stille-type coupling reaction of aryl iodides and aryl stannanes catalyzing a conjugated microporous polymer-based phototcatalyst under visible light irradiation at room temperature is reported. The novel coupling reaction mechanism occurs between the photogenerated aryl radical under oxidative destannylation of the aryl stannane, and the electron-activated aryl iodide, resulting into the aromatic C-C bond formation reaction. The visible light-promoted Stille-type coupling reaction using the polymer-based pure organic photocatalyst offers a simple, sustainable, and more economic synthetic pathway toward palladium-free aromatic C-C bond formation.
施蒂勒偶联反应是一种主要用于形成芳族碳-碳键的通用方法。然而,到目前为止,钯催化剂的使用是必不可少的。在此,报道了一种在室温可见光照射下,基于共轭微孔聚合物的光催化剂催化芳基碘化物和芳基锡烷的无钯光催化施蒂勒型偶联反应。这种新型偶联反应机理发生在芳基锡烷氧化脱锡过程中产生的光生芳基自由基与电子活化的芳基碘化物之间,从而导致芳族碳-碳键的形成反应。使用基于聚合物的纯有机光催化剂的可见光促进施蒂勒型偶联反应为无钯芳族碳-碳键的形成提供了一种简单、可持续且更经济的合成途径。