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Hydroalkylation of Aryl Alkenes with Organohalides Catalyzed by Molybdenum Oxido Based Lewis Pairs

机译:用氧化钼基对对催化的芳烃烷基的芳基烷基化芳基烷基化合物

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摘要

Three molybdenum(VI) dioxido complexes [MoO2(L)(2)] bearing Schiff base ligands were reacted with B(C6F5)(3)to afford the corresponding adducts [MoO{OB(C6F5)(3)}(L)(2)], which were fully characterized. They exhibit Frustrated Lewis-Pairs reactivity when reacting with silanes. Especially, the [MoO{OB(C6F5)(3)}(L)(2)] complex with L=2,4-dimethyl-6-((phenylimino)methyl)phenol proved to be active as catalyst for the hydroalkylation of aryl alkenes with organohalides and for the Atom-Transfer Radical Addition (ATRA) of organohalides to aliphatic alkenes. A series ofgem-dichloride andgem-dibromide compounds with potential for further derivatization were synthesized from simple alkenes and organohalides, like chloroform or bromoform, using low catalyst loading.
机译:三种钼(VI)二氧化硅络合物[MOO2(1)(2)]轴承席夫碱配体与B(C6F5)(3)反应,得到相应的加合物[MOO {OB(C6F5)(3)}(L)( 2),其完全表征。 当与硅烷反应时,它们表现出令人沮丧的刘易斯对反应性。 特别地,[Moo {Ob(C6F5)(3)}(L)(2)]络合物与L = 2,4-二甲基-6-((苯基咪唑酯-6-((苯基咪唑酯)甲基)苯酚被证明是活性作为催化剂的催化剂 芳基烯烃与有机卤化物和用于脂族烯烃的有机卤代的原子转移自由基添加(ATRA)。 使用低催化剂负载,通过简单的烯烃和有机卤化物合成具有进一步衍生化的潜力的OFEM-DEM-二溴-Dibromide化合物。

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