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首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis and Reactivity of a Mononuclear Manganese(II) Complex Having Pseudo-Seven Coordination Environment
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Synthesis and Reactivity of a Mononuclear Manganese(II) Complex Having Pseudo-Seven Coordination Environment

机译:伪七配位环境的单核锰(II)配合物的合成与反应性

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Utilizing a planar five coordinating N3S2 ligand, 2,6-bis(2-methylthiophenyliminomethyl)pyridine, a pseudo 7-coordinated manganese(II) complex with two labile triflate anions in the axial positions was synthesized. The reaction of the manganese(II) complex with an oxidant, iodosylbenzene, produced a metastable high-valent manganese(IV)-oxo species at 0∩. The high-valent Mn(IV)-oxo intermediate was characterized with a UV-vis spectrophotometer and an electrospray ionization mass spectroscopy. Reactivity studies of the Mn(IV)=O species revealed that the intermediate is capable of oxygenating PPh3 and N-dealkylating N,N-dimethyl-toludine.
机译:利用平面五配位的N 3 S 2配体2,6-双(2-甲基硫代苯基亚氨基甲基)吡啶,合成了在轴向位置具有两个不稳定的三氟甲磺酸根阴离子的伪7-配位的锰(II)配合物。锰(II)配合物与氧化剂碘代苯的反应在0°产生亚稳的高价锰(IV)-氧代物种。用紫外可见分光光度计和电喷雾电离质谱对高价的Mn(IV)-氧代中间体进行了表征。对Mn(IV)= O物种的反应性研究表明,该中间体能够将PPh 3 N -去烷基化 N N -二甲基甲苯胺。

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