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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >MONOTHIOCARBOXYLATE COMPLEXES OF OSMIUM(III) WITH FLUORO-THIOLATES AND DIMETHYLPHENYLPHOSPHINE CO-LIGANDS - X-RAY CRYSTAL STRUCTURES OF [OS(SR)(2)(SOCCH3)(PME(2)PH)(2)] (R=C6F5 OR C6F4H-4)
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MONOTHIOCARBOXYLATE COMPLEXES OF OSMIUM(III) WITH FLUORO-THIOLATES AND DIMETHYLPHENYLPHOSPHINE CO-LIGANDS - X-RAY CRYSTAL STRUCTURES OF [OS(SR)(2)(SOCCH3)(PME(2)PH)(2)] (R=C6F5 OR C6F4H-4)

机译:III(III)与氟-硫氰酸盐和二甲基苯基膦共配体的单硫代羧酸盐络合物-[OS(SR)(2)(SOCCH3)(PME(2)PH)(2)](R = C6F5)的X射线晶体结构C6F4H-4)

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Treatment of the pentacoordinated complexes [Os(SR)(3)(PMe(2)Ph)(2)] (R = C6F5 or C6F4H-4) with R'COSH (R' = CH3 or C6H5) in acetone gave the blue paramagnetic osmium(III) derivatives [Os(SC6F5)(2)(SOCR')(PMe(2)Ph)(2)] (1) and [Os(SC6F4H-4)(2) (SOCR')(PMe(2)Ph)(2)] (2). Mass spectrometric data are given. X-ray crystallography has shown that 1 (R' = CH3) and 2 (R' = CH3) have an octahedral structure with trans-thiolates, cis-phosphines and a chelating monothioacetate ligand. The electrochemical reduction of these compounds was studied by cyclic voltammetry in DMF. The potential at which the compounds undergo reduction was found to be nearly independent of the nature of the substituent group on the monothiocarboxylate ligand and slightly more dependent on the identity of the substituent group on the thiolate ligands, the reduction becoming easier for the more electron-withdrawing thiolate derivatives. [References: 13]
机译:用丙酮中的R'COSH(R'= CH3或C6H5)处理五配位配合物[Os(SR)(3)(PMe(2)Ph)(2)](R = C6F5或C6F4H-4)顺磁(III)衍生物[Os(SC6F5)(2)(SOCR')(PMe(2)Ph)(2)](1)和[Os(SC6F4H-4)(2)(SOCR')(PMe( 2)Ph)(2)](2)。给出了质谱数据。 X射线晶体学表明1(R′= CH 3)和2(R′= CH 3)具有八面体结构,具有反式硫代盐,顺式膦和螯合的单硫代乙酸盐配体。通过在DMF中的循环伏安法研究了这些化合物的电化学还原。发现化合物发生还原的电位几乎与单硫代羧酸盐配体上取代基的性质无关,而与硫醇盐配体上取代基的身份稍有相关,对于更多的电子,还原变得更加容易。提取硫醇盐衍生物。 [参考:13]

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