M Vageesh, Joshi Harsh, A S Anupriya, Dey Raju
Department of Chemistry, National Institute of Technology Calicut, 673601, Kozhikode, Kerala, India.
Chem Asian J. 2025 Jan 2;20(1):e202400989. doi: 10.1002/asia.202400989. Epub 2024 Nov 12.
Herein, we report an inexpensive first-row transition metal Ni heterogeneous catalytic system for the C -mono alkylation of fluorene using alcohols as alkylating agents via borrowing hydrogen strategy. The catalytic protocol displayed versatility with high yields of the desired products using various types of primary alcohols, including aryl/hetero aryl methanols, and aliphatic alcohols as alkylating agents. The catalyst Ni NPs@N-C was synthesized via high-temperature pyrolysis strategy, using ZIF-8 as the sacrificial template. The Ni NPs@N-C catalyst was characterized by XPS, HR-TEM, HAADF-STEM, XRD and ICP-MS. The catalyst is stable even in the air at room temperature, displayed excellent activity and could be recycled 5 times without appreciable loss of its activity.
在此,我们报道了一种廉价的第一行过渡金属镍多相催化体系,该体系通过借氢策略,以醇类作为烷基化试剂,用于芴的C-单烷基化反应。该催化方案具有通用性,使用各种类型的伯醇(包括芳基/杂芳基甲醇和脂肪醇)作为烷基化试剂时,均可高产率地得到所需产物。催化剂Ni NPs@N-C通过高温热解策略合成,以ZIF-8作为牺牲模板。通过XPS、高分辨透射电子显微镜(HR-TEM)、高角度环形暗场扫描透射电子显微镜(HAADF-STEM)、X射线衍射(XRD)和电感耦合等离子体质谱(ICP-MS)对Ni NPs@N-C催化剂进行了表征。该催化剂即使在室温空气中也很稳定,表现出优异的活性,并且可以循环使用5次而其活性没有明显损失。