Inorganic Chemistry, Vol.51, No.12, 6953-6961, 2012
Strategic Design and Refinement of Lewis Acid-Base Catalysis by Rare-Earth-Metal-Containing Polyoxometalates
Efficient polyoxometalate (POM)-based Lewis acid base catalysts of the rare-earth-metal-containing POMs (TBA(6)RE-POM, RE = Y3+, Nd3+, Eu3+, Gd3+, Tb3+, or Dy3+) were designed and synthesized by reactions of TBA(4)H(4)[gamma-SiW10O36] (TBA = tetra-n-butylammonium) with RE(acac)3 (acac = acetylacetonato). TBA(6)RE-POM consisted of two silicotungstate units pillared by two rare-earth-metal cations. Nucleophilic oxygen-enriched surfaces of negatively charged POMs and the incorporated rare-earth-metal cations could work as Lewis bases and Lewis acids, respectively. Consequently, cyanosilylation of carbonyl compounds with trimethylsilyl cyanide ((TMS)CN) was efficiently promoted in the presence of the rare-earth-metal-containing POMs via the simultaneous activation of coupling partners on the same POM molecules. POMs with larger metal cations showed higher catalytic activities for cyanosilylation because of the higher activation ability of C=O bonds (higher Lewis acidities) and sterically less hindered Lewis acid sites. Among the POM catalysts examined, the neodymium-containing POM showed remarkable catalytic performance for cyanosilylation of various kinds of structurally diverse ketones and aldehydes, giving the corresponding cyanohydrin trimethylsilyl ethers in high yields (13 substrates, 94 99%). In particular, the turnover frequency (714 000 h(-1)) and the turnover number (23 800) for the cyanosilylation of n-hexanal were of the highest level among those of previously reported catalysts.