Fukuzumi Shunichi, Kobayashi Takeshi, Suenobu Tomoyoshi
Department of Material and Life Science, Graduate School of Engineering, Osaka University, SORST (Japan) Science and Technology Agency (JST), 2-1 Yamada-oka, Suita, Osaka 565-0871, Japan.
ChemSusChem. 2008;1(10):827-34. doi: 10.1002/cssc.200800147.
Formic acid (HCOOH) decomposes efficiently to afford H2 and CO2 selectively in the presence of a catalytic amount of a water-soluble rhodium aqua complex, [Rh(III)(Cp*)(bpy)(H2O)]2+ (Cp*=pentamethylcyclopentadienyl, bpy=2,2'-bipyridine) in aqueous solution at 298 K. No CO was produced in this catalytic decomposition of HCOOH. The decomposition rate reached a maximum value at pH 3.8. No deterioration of the catalyst was observed during the catalytic decomposition of HCOOH, and the catalytic activity remained the same for the repeated addition of HCOOH. The rhodium-hydride complex was detected as the catalytic active species that undergoes efficient H/D exchange with water. When the catalytic decomposition of HCOOH was performed in D2O, D2 was produced selectively. Such an efficient H/D exchange and the observation of a deuterium kinetic isotope effect in the catalytic decomposition of DCOOH in H2O provide valuable mechanistic insight into this efficient and selective decomposition process.
在298K的水溶液中,在催化量的水溶性铑水合配合物[Rh(III)(Cp*)(bpy)(H2O)]2+(Cp* = 五甲基环戊二烯基,bpy = 2,2'-联吡啶)存在下,甲酸(HCOOH)能有效分解,选择性地生成H2和CO2。在该甲酸催化分解过程中未产生CO。分解速率在pH 3.8时达到最大值。在甲酸催化分解过程中未观察到催化剂的降解,并且对于重复添加甲酸,催化活性保持不变。铑氢配合物被检测为与水进行有效H/D交换的催化活性物种。当在D2O中进行甲酸的催化分解时,选择性地生成D2。这种有效的H/D交换以及在H2O中DCOOH催化分解中观察到的氘动力学同位素效应,为这种高效且选择性的分解过程提供了有价值的机理见解。