J. Heyrovský Institute of Physical Chemistry, Academy of Sciences of Czech Republic, v.v.i. Dolejškova 3, 182 23 Prague 8, Czech Republic.
ChemSusChem. 2013 May;6(5):865-71. doi: 10.1002/cssc.201300032. Epub 2013 Apr 16.
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.
研究了一组金属有机骨架[CuBTC、FeBTC、MIL-100(Fe)、MIL-100(Cr)、ZIF-8、MIL-53(Al)]在β-蒎烯与甲醛的Prins 缩合反应中的催化性能,并与传统的铝硅酸盐沸石 BEA 和 FAU 以及钛硅酸盐沸石 MFI(TS-1)的催化行为进行了比较。所研究的金属有机骨架(MOFs)的活性随着可及路易斯酸位浓度的增加而增加,顺序为 ZIF-8<MIL-53(Al)<FeBTC<MIL-100(Cr)<MIL-100(Fe)。β-蒎烯类似的异构化发生在沸石 BEA 和 FAU 的强布朗斯台德酸位上,它们对目标 nopol 的选择性明显低于 MOFs。其高活性、结构和活性位的保持,以及在不损失活性的情况下至少在三个催化循环中使用的可能性,使 MIL-100(Fe)成为β-蒎烯和多聚甲醛 Prins 缩合反应中性能最好的催化剂。我们的报告例证了 MOFs 作为液相反应中固体催化剂在精细化学品生产中的优势超过沸石。