摘要

Styrene oxidation with iodosylbenzene catalyzed by a Mn-porphyrin/Au-cluster binary system was investigated from several aspects to disclose the mechanism of unique and prominent positive effects of Au clusters. In the catalytic system utilizing a fixed amount of Mn(TPP)Cl (TPP = tetraphenylporphinato) and a varying amount of dodecanethiolate-capped Au cluster (Au: SC12, 1), the reaction rate was increased sigmoidally with the increase of the charged amount of 1. From these profiles together with the results of absorption spectral studies, a possible mechanism involving two cluster molecules is proposed. Comparative studies utilizing Mn(TPP) Cl and Mn(TMP)Cl (TMP = tetramesitylporphinato) showed that the latter is superior in terms of the robustness towards oxidative degradation and catalytic activity. Furthermore, at a certain condition, a characteristic induction period was observed only for the reaction with conformationally rigid and sterically hindered Mn(TMP) Cl. Analogous Au clusters protected by non-thiolate ligands such as triphenylphosphine and poly(N-vinyl-2-pyrrolidone) also promoted the catalytic oxidation by Mn(TMP) Cl. Based on these observations, we discuss the critical paths and factors that govern the catalytic activity of the present binary catalyst system.

  • 出版日期2008

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