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Nondirecting Group sp3 C−H Activation for Synthesis of Bibenzyls via Homo‐coupling as Catalyzed by Reduced Graphene Oxide Supported PtPd@Pt Porous Nanospheres
Advanced Synthesis & Catalysis ( IF 4.4 ) Pub Date : 2018-01-02 , DOI: 10.1002/adsc.201701389
Zheng-Jun Wang 1 , Jing-Jing Lv 2 , Rong-Nan Yi 1 , Min Xiao 1 , Jiu-Ju Feng 2 , Zhi-Wu Liang 1 , Ai-Jun Wang 2 , Xinhua Xu 1
Affiliation  

The use of heterogeneous bimetallic Pd‐based nanocatalyst for directing the inactivated sp3 C−H coupling has been scarcely explored. This work reported the formation of symmetrical C−C bonds from the inactivated sp3 C−H bonds catalyzed by employing reduced graphene oxide supported PtPd@Pt porous nanospheres. The reaction of sp3 C−H activation proceeded under mild conditions without any solvent, ligand or directing group. It is a higher atom‐, step‐ and cost‐effectiveness strategy for developing heterogeneous catalysts in the synthesis of bibenzyls with various functional groups (e. g. aryl, alkyl, methoxyl, halogen, ester, and pyridyl).

中文翻译:

还原性氧化石墨烯负载的PtPd @ Pt多孔纳米球催化的非偶合基团sp3 C–H活化,通过均相偶合合成联苄。

很少探索使用非均相双金属钯基纳米催化剂指导失活的sp 3 C-H偶联。这项工作报道了通过使用还原性氧化石墨烯负载的PtPd @ Pt多孔纳米球催化的灭活的sp 3 C-H键形成对称的C-C键。sp 3 C H活化反应在温和条件下进行,没有任何溶剂,配体或指导基团。在合成具有各种官能团(例如芳基,烷基,甲氧基,卤素,酯和吡啶基)的联苄中,开发多相催化剂是一种更高的原子,步骤和成本效益策略。
更新日期:2018-01-02
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