期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 38, 页码 12642-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja8042849
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资金
- Deutsche Forschungsgemeinschaft
The direct experimental evidence shows that ethylbenzene disproportionation is a transition state shape selective reaction on zeolites: a bimolecular reaction mechanism via diphenylethane-mediated pathway on large-pore zeolites X and Y (ca. 0.74 nm) and a monomolecular reaction mechanism on medium-pore zeolites ZSM-5 (ca. 0.56 nm) via the ethoxy-mediated intermolecular ethyl group transfer. The lifetime of bulky diphenylethane species was prolonged by a fine-tune of FAU-zeolites, which makes this transition state detectable by C-13 MAS NMR spectroscopy. Due to tunable catalytic properties and pore shapes, zeolites are promising catalysts toward emulating the efficiency and selectivity in desired reactions.
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