Vanadium Catalyst on Isostructural Transition Metal, Lanthanide, and Actinide Based Metal-Organic Frameworks for Alcohol Oxidation

Wang, X; Zhang, X; Li, P; Otake, KI; Cui, Y; Lyu, J; Krzyaniak, MD; Zhang, Y; Li, Z; Liu, J; Buru, CT; Islamoglu, T; Wasielewski, MR; Li, Z; Farha, OK

HERO ID

6308162

Reference Type

Journal Article

Year

2019

Language

English

PMID

31083934

HERO ID 6308162
In Press No
Year 2019
Title Vanadium Catalyst on Isostructural Transition Metal, Lanthanide, and Actinide Based Metal-Organic Frameworks for Alcohol Oxidation
Authors Wang, X; Zhang, X; Li, P; Otake, KI; Cui, Y; Lyu, J; Krzyaniak, MD; Zhang, Y; Li, Z; Liu, J; Buru, CT; Islamoglu, T; Wasielewski, MR; Li, Z; Farha, OK
Journal Journal of the American Chemical Society
Volume 141
Issue 20
Page Numbers 8306-8314
Abstract The understanding of the catalyst-support interactions has been an important challenge in heterogeneous catalysis since the supports can play a vital role in controlling the properties of the active species and hence their catalytic performance. Herein, a series of isostructural mesoporous metal-organic frameworks (MOFs) based on transition metals, lanthanides, and actinides (Zr, Hf, Ce, Th) were investigated as supports for a vanadium catalyst. The vanadium species was coordinated to the oxo groups of the MOF node in a single-ion fashion, as determined by single-crystal X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy, and diffuse reflectance UV-vis spectroscopy. The support effects of these isostructural MOFs were then probed using the aerobic oxidation of 4-methoxybenzyl alcohol as a model reaction. The turnover frequency was found to be correlated with the electronegativity and oxidation state of the metal cations on the supporting MOF nodes, highlighting an important consideration when designing catalyst supports.
Doi 10.1021/jacs.9b02603
Pmid 31083934
Wosid WOS:000469292300039
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English