Enhancing the hydrogen transfer catalytic activity of hybrid carbon nanotube-based NHC-iridium catalysts by increasing the oxidation degree of the nanosupport

被引:18
作者
Blanco, Matias [1 ]
Alvarez, Patricia [1 ]
Blanco, Clara [1 ]
Victoria Jimenez, M. [2 ]
Perez-Torrente, Jesus J. [2 ]
Oro, Luis A. [2 ]
Blasco, Javier [3 ]
Cuartero, Vera [4 ]
Menendez, Rosa [1 ]
机构
[1] CSIC, Inst Nacl Carbon INCAR, POB 73, Oviedo 33080, Spain
[2] Univ Zaragoza, ISQCH CSIC, Dept Inorgan Chem, E-50009 Zaragoza, Spain
[3] Univ Zaragoza, CSIC, ICMA, Dept Fis Mat Condensada, E-50009 Zaragoza, Spain
[4] ESRF European Synchrotron, 71 Ave Martyrs, Grenoble, France
关键词
N-HETEROCYCLIC CARBENES; ABSORPTION FINE-STRUCTURE; GRAPHENE OXIDE; CHEMICAL OXIDATION; COMPLEXES; SPECTROSCOPY; IMMOBILIZATION; REACTIVITY; STRATEGY; LIGANDS;
D O I
10.1039/c5cy01998b
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
CVD-grown multiwalled carbon nanotubes were purified by applying four different treatments with increasing oxidation severity. The growing severity of the treatment results in progressive oxygen functionalization of the surface along with introduction of an increasing quantity of defects on the carbon nanotube walls. Iridium-N-heterocyclic carbene complexes were covalently anchored to those oxidized surfaces through their surface carboxylic acids via acetyl linkers. The carbon nanotube-based iridium-NHC hybrid materials developed are active in the hydrogen-transfer reduction of cyclohexanone to cyclohexanol with 2-propanol/KOH as hydrogen source but with rather different activity. The catalytic activity of the hybrid catalysts is strongly influenced by the type and amount of oxygenated functionalization resulting from the treatment applied to the support, being the most active and the most oxidized material.
引用
收藏
页码:5504 / 5514
页数:11
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