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Arene Coordination to Yttrium(Ⅲ) via Carbon-Carbon Bond Formation

机译:碳-碳键形成芳烃配位至钇(Ⅲ)

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摘要

In contrast to the Hein chemistry discussed above, the biaryl couplings reported here do not involve any formal redox chemistry, since the yttrium center starts as Y(III) and finishes in the same oxidation level. This contrasts other lanthanoid arene systems that have been prepared via reductive sequences or by metal vapor techniques. Phenyl groups bridging lanthanoid metals are not well established, a few ex- amples of mononuclear σ-aryl complexes are known for yttrium but few have been structurally characterized. Reactivity studies of these dinuclear bis complexes are underway.
机译:与上面讨论的海因化学相反,此处报道的联芳基偶联不涉及任何形式的氧化还原化学,因为钇中心以Y(III)开头并以相同的氧化水平结束。这与通过还原序列或通过金属蒸气技术制备的其他镧系元素芳烃体系形成对比。桥联镧系金属的苯基尚未完全确立,钇的单核σ-芳基络合物的例子很少,但在结构上却很少。这些双核双配合物的反应性研究正在进行中。

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