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Olefin Metathesis With Ruthenium-Arene Catalysts Bearing N-Heterocyclic Carbene Ligands

机译:烯烃复分解含N-杂环配体的钌 - 芳烃催化剂

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In this chapter, we summarize the main results of our investigations on the ring-opening metathesis polymerization (ROMP) of cyclooctene catalyzed by various ruthenium (Ru)–arene complexes bearing imidazolin-2-ylidene, imidazolidin- 2-ylidene, or triazolin-5-ylidene ligands. Three major findings emerged from this study. First, we underscored the intervention of a photochemical activation step due to visible light illumination. Second, we established that the presence of an endocyclic double bond in the carbene ligand central heterocycle was not crucial to achieve high catalytic efficiencies. Third, we demonstrated that ortho-metallation of the N-heterocyclic carbene (NHC) ligand by the Ru center led to inactive catalysts.
机译:在本章中,我们总结了我们对由亚氨酰基-2- ylidene,咪唑酯蛋白-2- ylidene或三唑啉或三唑啉 - 咪唑啉 - 2- ylidene或三唑啉催化的各种钌(Ru)催化的环庚烯的开环复分解聚合(ROMP)对环辛酯的开环复分解聚合(ROMP)的主要结果。 5- ylidene配体。这项研究中出现了三个主要研究结果。首先,由于可见光照明,我们强调了光化学激活步骤的干预。其次,我们确实确定了卡宾配体中环杂环中环循环双键的存在对于实现高催化效率至关重要。第三,我们证明了Ru中心的N-杂环基石(NHC)配体的正交结果导致无活性催化剂。

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