Ruthenium-p-cymene Complex Side-Wall Covalently Bonded to Carbon Nanotubes as Efficient Hybrid Transfer Hydrogenation Catalyst

被引:5
作者
Blanco, Matias [1 ]
Cembellin, Sara [2 ]
Agnoli, Stefano [3 ]
Aleman, Jose [1 ,4 ]
机构
[1] Univ Autonoma Madrid, Dept Organ Chem, C Francisco Tomas & Valiente 7, Madrid 28049, Spain
[2] Univ Complutense Madrid, Organ Chem Dept, Fac Chem, Ave Complutense S-N, Madrid 28040, Spain
[3] Univ Padua, Dept Chem Sci, Interuniv Reatt Chim & Catalisi CIRCC, Via Marzolo 1, I-35131 Padua, Italy
[4] Univ Autonoma Madrid, Inst Adv Res Chem Sci IAdChem, C Francisco Tomas & Valiente 7, Madrid 28049, Spain
基金
欧洲研究理事会;
关键词
Carbon Nanotubes; Ruthenium complexes; Functionalization; Transfer Hydrogenation; Catalysis; ASYMMETRIC TRANSFER HYDROGENATION; N-HETEROCYCLIC CARBENES; C-H; GRAPHENE; KETONES; IRIDIUM; LIGANDS; RH; ALDEHYDES; RU;
D O I
10.1002/cctc.202101442
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A half-sandwich ruthenium-p-cymene organometallic complex has been immobilized at Single Walled Carbon Nanotubes (SWNT) sidewalls through a stepwise covalent chemistry protocol. The introduction of amino groups by means of diazonium-chemistry protocols leads the grafting at the outer walls of the nanotubes. This hybrid material is active in the transfer hydrogenation of ketones to yield alcohols, using as hydrogen source 2-propanol. SWNT-NH2-Ru presents a broad scope, performing the reaction under aerobic conditions and can be recycled over 9 consecutive reaction runs without losing activity or leaching ruthenium out. Comparison of the activity with related homogeneous catalysts reveals an improved performance due to the covalent bond between the metal and the material, achieving turnover frequencies as high as 192774 h(-1).
引用
收藏
页码:5156 / 5165
页数:10
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