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羰基钌取代的α-凯吉型钨硅酸,[α-SiW(11)O(39)Ru(II)(CO)](6 -):合成、结构、氧化还原研究及反应活性

Carbonyl-ruthenium substituted alpha-Keggin-tungstosilicate, [alpha-SiW(11)O(39)Ru(II)(CO)](6-): synthesis, structure, redox studies and reactivity.

作者信息

Sadakane Masahiro, Iimuro Yoshifumi, Tsukuma Daisuke, Bassil Bassem S, Dickman Michael H, Kortz Ulrich, Zhang Yi, Ye Shen, Ueda Wataru

机构信息

Catalysis Research Center, Hokkaido University, N-21, W-10, 001-0021, Sapporo, Japan.

出版信息

Dalton Trans. 2008 Dec 21(47):6692-8. doi: 10.1039/b810987g. Epub 2008 Oct 20.

Abstract

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.

摘要

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。

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