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首页> 外文期刊>Journal of Organometallic Chemistry >Reaction of ruthenium carbonyl chloride with iridium tetracarbonyl anion. Synthesis, crystal structure and characterisation of [Ru_2Ir_2H(CO)_(12)Cl]: a heterometallic tetranuclear butterfly cluster with chloride bridge
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Reaction of ruthenium carbonyl chloride with iridium tetracarbonyl anion. Synthesis, crystal structure and characterisation of [Ru_2Ir_2H(CO)_(12)Cl]: a heterometallic tetranuclear butterfly cluster with chloride bridge

机译:羰基氯化钌与四羰基铱阴离子反应。 [Ru_2Ir_2H(CO)_(12)Cl]:具有氯桥的多金属四核蝴蝶簇的合成,晶体结构和表征

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摘要

Reaction between [Ru_2(CO)_6Cl] and Na[Ir(CO)_4] in tetrahydrofuran (THF) yielded [Ru_2Ir_2H(CO)_(12)Cl], a new iridium-ruthenium mixed-metal cluster of possible catalytic interest. The cluster was characterised by ~1H-NMR and infrared spectroscopy and by single-crystal X-ray structure analysis. [Ru_2Ir_2H(CO)_(12)Cl] exhibits a butterfly arrangement of metal atoms, with three terminal carbonyls on each metal atom, chloride ligand in the bridging position, and hydride ligand at the Ir-Ir edge. The trinuclear ruthenium cluster [Ru_3(#mu#-Cl)_2(CO)_8(PPhMe_2)_2] was synthesised by reaction of [Ru_2(CO)_6Cl_4] with K[Ir(CO)_4] in THF, followed by ligand substitution with [PPhMe_2] in CH_2Cl_2 at ambient temperature. Determination of the structure by X-ray diffraction showed it to consist of an open trinuclear unit involving two metal-metal bonds. The open edge of the metal framework is supported by two symmetric bridging chloride ligands. Both phosphorus ligands are cis to the chlorine atoms and trans to the unique ruthenium atom.
机译:[Ru_2(CO)_6Cl]与Na [Ir(CO)_4]在四氢呋喃(THF)中的反应产生[Ru_2Ir_2H(CO)_(12)Cl],这是一种可能具有催化作用的新型铱-钌混合金属簇。通过〜1H-NMR和红外光谱以及单晶X射线结构分析对团簇进行表征。 [Ru_2Ir_2H(CO)_(12)Cl]呈金属原子蝶形排列,每个金属原子上具有三个末端羰基,桥连位置的氯化物配体,Ir-Ir边缘的氢化物配体。三核钌簇[Ru_3(#mu#-Cl)_2(CO)_8(PPhMe_2)_2]是通过[Ru_2(CO)_6Cl_4]与K [Ir(CO)_4]在THF中的反应合成的,然后进行配体反应室温下在CH_2Cl_2中用[PPhMe_2]取代。通过X射线衍射确定结构表明其由涉及两个金属-金属键的开放的三核单元组成。金属框架的开放边缘由两个对称的桥联氯化物配体支撑。两种磷配体对氯原子都是顺式的,而对独特的钌原子是反式的。

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