One-step room-temperature synthesis of [Al]MCM-41 materials for the catalytic conversion of phenylglyoxal to ethylmandelate

Zichun Wang, Yijiao Jiang, Rafal Rachwalik, Zhongwen Liu, Jeffrey Shi, Michael Hunger*, Jun Huang

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

36 Citations (Scopus)

Abstract

Mesoporous [Al]MCM-41 materials with nSi/nAl ratios of 15 to 50 suitable for the direct catalytic conversion of phenylglyoxal to ethylmandelate have been successfully synthesized at room temperature within 1 h. The surface areas and pore sizes of the obtained [Al]MCM-41 materials are in the ranges of 1005-1246 m2 g-1 and 3.44-3.99 nm, respectively, for the different nSi/nAl ratios. For all [Al]MCM-41 catalysts, most of the Al species were tetrahedrally coordinated with Si in the next coordination sphere of atoms. 1H and 13C magic-angle spinning NMR spectroscopic investigations indicated that the acid strength of the SiOH groups on these [Al]MCM-41 catalysts and the density of these surface sites are enhanced with increasing Al content in the synthesis gels. These surface sites with enhanced acid strength were found to be catalytically active sites for phenylglyoxal conversion. The [Al]MCM-41 material with nSi/nAl=15 showed the highest phenylglyoxal conversion (93.4 %) and selectivity to ethylmandelate (96.9 %), whereas the [Al]MCM-41 material with nSi/nAl=50 reached the highest turnover frequency (TOF=99.3 h-1). This is a much better catalytic performance than that of a dealuminated zeolite Y (TOF=1.7 h-1) used as a reference catalyst, which is explained by lower reactant transport limitations in mesoporous materials than that in the microporous zeolite. Mesopores flex their catalytic muscles: Mesoporous [Al]MCM-41 materials with nSi/nAl ratios of 15 to 50 suitable for the direct catalytic conversion of phenylglyoxal to ethylmandelate were successfully synthesized at room temperature within 1 h.

Original languageEnglish
Pages (from-to)3889-3896
Number of pages8
JournalChemCatChem
Volume5
Issue number12
DOIs
Publication statusPublished - Dec 2013
Externally publishedYes

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