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Reactions of Zerovalent Ruthenium Complexes with Maleic Anhydride or Maleimides:Ligand Displacement vs Oxidative Cyclization

机译:Zeropalent钌配合物与马来酸酐或马来酰亚胺的反应:配体位移与氧化环化

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The reactions of Ru(eta~6-cot)(dmfm)_2(1;eta~6-cot = 1,3,5-cyclooctatriene,dmfm = dimethyl fumarate)and Ru(eta~4-cod)(eta~6-cot)(2;eta~4-cod = 1,5-cyclooctadiene)with maleic anhydride or maleimides were investigated.The former reaction gave a series of novel zerovalent complexes 4 via ligand displacement between dimethyl fumarate and added electron-deficient olefins.In contrast,oxidative cyclization proceeded in the latter case to afford divalent eta~5-pentadienyl complexes 5,which further reacted with CO giving tricarbonyl complex 6.
机译:Ru(eta〜6-cot)(dmfm)_2(1; eta; eta 6-cot = 1,3,5-环偶乙烯,dmfm =二甲基富马酸酯)和ru(eta〜4-cod)(eta〜6 - 调查 - 具有马来酸酐或马来酰亚胺的2; 2; ETA〜4-COD = 1.5-环辛二烯)。前反应通过二甲基富马酸酯之间的配体位移得到一系列新的Zeroportent络合物4并添加电子缺陷烯烃。相比之下,在后一种情况下进行氧化环化,得到二价Eta〜5-五戊基络合物5,其进一步与给予三羰基络合物6的共同反应。

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