Wu Zhilei, Lan Xingwang, Zhang Yaxin, Li Meng, Bai Guoyi
Key Laboratory of Chemical Biology of Hebei Province, Key Laboratory of Analytical Science and Technology of Hebei Province, College of Chemistry and Environmental Science, Hebei University, Baoding, 071002, P. R. China.
Dalton Trans. 2019 Aug 7;48(29):11063-11069. doi: 10.1039/c9dt01859j. Epub 2019 Jun 28.
Two metal-organic frameworks (MOFs), namely, [DyCuI(NA)(DMF)] (1) and [GdCuI(IN)(DMF)]·5DMF (2) (HNA = nicotinic acid, HIN = isonicotinic acid), constructed based on lanthanide ions and copper iodide clusters ([CuI] and [CuI]) were successfully synthesized and characterized. Compound 1 has a three-dimensional framework and compound 2 displays a two-dimensional plane with sql topology, respectively. Both of them exhibit high thermostability and solvent stabilities. Additionally, catalytic explorations reveal that 1 displays higher catalytic activity than 2 for the carboxylic cyclization of propargyl alcohols. More importantly, 1 also exhibits excellent catalytic performance in the carboxylation reactions of CO and terminal propargylic alcohols with various substituents. To the best of our knowledge, this is the first example of non-noble metal based MOF catalysts for the carboxylative cyclization of propargyl alcohols with CO under atmospheric pressure and at room temperature, which provides a highly promising approach for MOFs in the catalytic conversion of CO to valuable chemicals.
成功合成并表征了两种基于镧系离子和碘化铜簇([CuI]和[CuI])构建的金属有机框架(MOF),即[DyCuI(NA)(DMF)](1)和[GdCuI(IN)(DMF)]·5DMF(2)(HNA = 烟酸,HIN = 异烟酸)。化合物1具有三维框架结构,化合物2呈现具有sql拓扑结构的二维平面。它们都表现出高的热稳定性和溶剂稳定性。此外,催化研究表明,在炔丙醇的羧基环化反应中,1比2表现出更高的催化活性。更重要的是,1在CO与具有各种取代基的末端炔丙醇的羧化反应中也表现出优异的催化性能。据我们所知,这是在常压和室温下用于炔丙醇与CO羧基环化反应的非贵金属基MOF催化剂的首个实例,这为MOF在将CO催化转化为有价值化学品方面提供了一种极具前景的方法。