Self-Supporting Metal-Organic Layers as Single-Site Solid Catalysts

被引:350
作者
Cao, Lingyun [1 ]
Lin, Zekai [2 ]
Peng, Fei [3 ]
Wang, Weiwei [1 ]
Huang, Ruiyun [1 ]
Wang, Cheng [1 ]
Yan, Jiawei [1 ]
Liang, Jie [3 ]
Zhang, Zhiming [1 ]
Zhang, Teng [2 ]
Long, Lasheng [1 ]
Sun, Junliang [3 ,4 ]
Lin, Wenbin [1 ,2 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, iCHEM, PCOSS, Xiamen 361005, Peoples R China
[2] Univ Chicago, Dept Chem, 5735 S Ellis Ave, Chicago, IL 60637 USA
[3] Stockholm Univ, Berzelii Ctr EXCELLENT Porous Mat, Dept Mat & Environm Chem, S-10691 Stockholm, Sweden
[4] Peking Univ, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
基金
美国国家科学基金会;
关键词
alkenes; hafnium; heterogeneous catalysis; hydrosilylation; metal-organic layers; FRAMEWORK; 2D; NANOSHEETS; SHEETS;
D O I
10.1002/anie.201512054
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-organic layers (MOLs) represent an emerging class of tunable and functionalizable two-dimensional materials. In this work, the scalable solvothermal synthesis of self-supporting MOLs composed of [Hf6O4(OH)(4)(HCO2)(6)] secondary building units (SBUs) and benzene-1,3,5-tribenzoate (BTB) bridging ligands is reported. The MOL structures were directly imaged by TEM and AFM, and doped with 4-(4-benzoate)-(2,2,2-terpyridine)-5,5-dicarboxylate (TPY) before being coordinated with iron centers to afford highly active and reusable single-site solid catalysts for the hydrosilylation of terminal olefins. MOL-based heterogeneous catalysts are free from the diffusional constraints placed on all known porous solid catalysts, including metal-organic frameworks. This work uncovers an entirely new strategy for designing single-site solid catalysts and opens the door to a new class of two-dimensional coordination materials with molecular functionalities.
引用
收藏
页码:4962 / 4966
页数:5
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