Sadakane Masahiro, Iimuro Yoshifumi, Tsukuma Daisuke, Bassil Bassem S, Dickman Michael H, Kortz Ulrich, Zhang Yi, Ye Shen, Ueda Wataru
Catalysis Research Center, Hokkaido University, N-21, W-10, 001-0021, Sapporo, Japan.
Dalton Trans. 2008 Dec 21(47):6692-8. doi: 10.1039/b810987g. Epub 2008 Oct 20.
The carbonyl-ruthenium substituted undecatungstosilicate alpha-SiW(11)O(39)Ru(II)(CO) () was isolated as a caesium salt and successfully characterized by using (183)W and (13)C NMR, elemental analysis, IR, UV-vis and cyclic voltammetry (CV). Polyanion represents the first example of a metal-carbonyl moiety being fully incorporated into the polyoxometalate (POM). As a result, the Ru(CO) moiety became redox active and was reversibly oxidized to the one-electron ruthenium(iii) derivative, alpha-SiW(11)O(39)Ru(III)(CO). This Ru(III)(CO) moiety was unexpectedly stable in aqueous solution compared to the organo-ruthenium carbonyl derivatives and could be detected by using UV-vis and in situ IR coupled with electrolysis. The oxidized ruthenium(iii) derivative slowly released CO in aqueous solution, resulting in the aqua species alpha-SiW(11)O(39)Ru(III)(H(2)O) and then the dimeric POM species by condensation. Furthermore, could be converted to the corresponding aqua polyanion by photo-irradiation.
羰基钌取代的十一钨硅酸根阴离子[α-SiW(11)O(39)Ru(II)(CO)]6-()以铯盐形式分离出来,并通过183W和13C核磁共振、元素分析、红外光谱、紫外可见光谱和循环伏安法(CV)成功表征。多阴离子代表金属羰基部分完全并入多金属氧酸盐(POM)的首个实例。结果,Ru(CO)部分变得具有氧化还原活性,并可逆地氧化为单电子钌(III)衍生物[α-SiW(11)O(39)Ru(III)(CO)]5-。与有机钌羰基衍生物相比,该Ru(III)(CO)部分在水溶液中意外地稳定,并且可以通过紫外可见光谱以及与电解联用的原位红外光谱检测到。氧化后的钌(III)衍生物在水溶液中缓慢释放CO,生成水合物种[α-SiW(11)O(39)Ru(III)(H2O)]5-,然后通过缩合生成二聚POM物种。此外,通过光照射可以将其转化为相应的水合多阴离子。