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首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis of mixed-valence trinuclear carbonylmanganese dithiolates: Promoting vacant coordination sites in tricarbonyl[(1-5-h)-pentadienyl]manganese
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Synthesis of mixed-valence trinuclear carbonylmanganese dithiolates: Promoting vacant coordination sites in tricarbonyl[(1-5-h)-pentadienyl]manganese

机译:混合价三核羰基羰基锰二硫酸盐的合成:促进三羰基[(1-5-h)-戊二烯基]锰中的空位配位点

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摘要

Mixed-valence complexes Mn_3(CO)_6(m-S(CH_2)nS-k~2-S'S')_3 n = 2, 3, and 4 were prepared upon reaction of tricarbonyl[(1-5-η)-pentadienyl]manganese with the respective alkanedithiols at room temperature in good yields. The three metal centers are bound by thiolate bridges with no metalemetal bonds; one manganese atom exhibits a formal oxidation state of t4; while the other two possess an oxidation state of +1. EPR and X-ray analysis showed an octahedral environment around the manganese centers.
机译:通过三羰基[(1-5-η)-戊二烯基]锰的反应制备混合价配合物Mn_3(CO)_6(mS(CH_2)nS-k〜2-S'S')_ 3 n = 2、3和4与各自的烷二硫醇在室温下以良好的收率。这三个金属中心被无金属键的硫醇盐桥键合。一个锰原子的形式氧化态为t4;而其他两个的氧化态为+1。 EPR和X射线分析显示锰中心周围为八面体环境。

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