催化作用
化学
沸石
路易斯酸
金属有机骨架
普林斯反应
选择性
异构化
布朗斯特德-洛瑞酸碱理论
分子筛
甲醛
硅酸铝
羟醛缩合
化学工程
无机化学
有机化学
吸附
工程类
作者
Maksym Opanasenko,Amarajothi Dhakshinamoorthy,Young Kyu Hwang,Jong‐San Chang,Hermenegildo Garcı́a,Jiřı́ Čejka
出处
期刊:Chemsuschem
[Wiley]
日期:2013-04-16
卷期号:6 (5): 865-871
被引量:79
标识
DOI:10.1002/cssc.201300032
摘要
Abstract The catalytic performance of a set of metal–organic frameworks [CuBTC, FeBTC, MIL‐100(Fe), MIL‐100(Cr), ZIF‐8, MIL‐53(Al)] was investigated in the Prins condensation of β‐pinene with formaldehyde and compared with the catalytic behavior of conventional aluminosilicate zeolites BEA and FAU and titanosilicate zeolite MFI (TS‐1). The activity of the investigated metal–organic frameworks (MOFs) increased with the increasing concentration of accessible Lewis acid sites in the order ZIF‐8<MIL‐53(Al)<FeBTC<MIL‐100(Cr)<MIL‐100(Fe). Unwanted β‐pinene‐like isomerization takes place on the strong Brønsted acid sites of zeolites BEA and FAU, which showed significantly lower selectivity to the target nopol than the MOFs. Its high activity, the preservation of its structure and active sites, and the possibility to use it in at least three catalytic cycles without loss of activity make MIL‐100 (Fe) the best performing catalyst of the series for the Prins condensation of β‐pinene and paraformaldehyde. Our report exemplifies the advantages of MOFs over zeolites as solid catalysts in liquid‐phase reactions for the production of fine chemicals.
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