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New indenylidene-type metathesis catalysts bearing unsymmetrical N-heterocyclic ligands with mesityl and nitrobenzyl substituents

机译:带有不对称的N-杂环配体和异丁基和硝基苄基取代基的新茚并型催化剂

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摘要

AbstractNew indenylidene-type second generation catalysts bearing modified unsymmetrically substituted N-heterocyclic carbene ligands were synthesized. The complexes contain an N-mesityl and N′-nitrobenzyl substituted NHC ligand. The precursors of free carbenes—imidazolinium salts—were obtained in an easy and environment-friendly way (under aqueous or neat conditions). The new catalysts were prepared by reaction of in situ generated carbenes with a 1st generation indenylidene catalyst, containing pyridine ligands instead of tricyclohexylphosphine. The complexes were tested in RCM, CM, and ene-yne metathesis model reactions in commercial-grade solvents in air. Their activities were compared with that of commercially available indenylidene catalyst. The structures of complexes and their stability were investigated using static DFT calculations with mixed basis set.
机译:摘要合成了带有改性的不对称取代的N-杂环卡宾配体的新型茚二烯型第二代催化剂。该配合物包含N-间苯二甲和N'-硝基苄基取代的NHC配体。游离碳烯的前体-咪唑啉鎓盐-以简单且环保的方式(在水性或纯净条件下)获得。通过使原位生成的碳烯与包含吡啶配体而不是三环己基膦的第一代茚基催化剂反应来制备新的催化剂。在空气中的商业级溶剂中,在RCM,CM和ene-yne复分解模型反应中对复合物进行了测试。将它们的活性与可商购的茚基亚烷基催化剂的活性进行了比较。使用带有混合基集的静态DFT计算研究了配合物的结构及其稳定性。

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