首页> 外文期刊>Organometallics >Binuclear iron(I), ruthenium(I), and osmium(I) hexacarbonyl complexes containing a bridging benzene-1,2-dithiolate ligand. Synthesis, X-ray structures, protonation reactions, and EHMO calculations
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Binuclear iron(I), ruthenium(I), and osmium(I) hexacarbonyl complexes containing a bridging benzene-1,2-dithiolate ligand. Synthesis, X-ray structures, protonation reactions, and EHMO calculations

机译:双核铁(I),钌(I)和(I)六价羰基配合物,含有桥联的1,2-二硫代苯酚配体。合成,X射线结构,质子化反应和EHMO计算

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The dithiolate-bridged complexes [M-2(mu-bdt)(CO)(6)] (M = Fe (1), Ru (2), Os (3); bdt = benzene-1,2-dithiolate) have been prepared. X-ray diffraction studies have revealed that although the three compounds have analogous molecular structures their crystal structures are different as a result of different molecular packings. Complex 1 does not react with tetrafluoroboric acid in 1,2-dichloroethane, while compounds 2 and 3, under the same conditions, undergo protonation at the metal atoms to give the cationic hydride derivatives [M-2(mu-H)(mu-bdt)(CO)(6)][BF4] (M = Ru, Os). EHMO calculations have been used to rationalize the results of the protonation reactions. [References: 44]
机译:二硫醇盐桥接的复合物[M-2(mu-bdt)(CO)(6)](M = Fe(1),Ru(2),Os(3); bdt =苯-1,2-二硫醇盐)具有准备好了。 X射线衍射研究表明,尽管这三种化合物具有相似的分子结构,但由于分子堆积不同,它们的晶体结构也不同。配合物1在1,2-二氯乙烷中不与四氟硼酸反应,而化合物2和3在相同条件下在金属原子上质子化,得到阳离子氢化物衍生物[M-2(mu-H)(mu- bdt)(CO)(6)] [BF4](M = Ru,Os)。 EHMO计算已用于使质子化反应的结果合理化。 [参考:44]

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