首页> 外文期刊>Organometallics >Low-melting dialkyl- and bis(polyfluoroalkyl)-substituted 1,1 '-methylenebis(imidazolium) and 1,1 '-methylenebis(1,2,4-triazolium) bis(trifluoromethanesulfonyl)amides: Ionic liquids leading to bis(N-heterocyclic carbene) complexes of palladium
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Low-melting dialkyl- and bis(polyfluoroalkyl)-substituted 1,1 '-methylenebis(imidazolium) and 1,1 '-methylenebis(1,2,4-triazolium) bis(trifluoromethanesulfonyl)amides: Ionic liquids leading to bis(N-heterocyclic carbene) complexes of palladium

机译:低熔点二烷基和双(多氟烷基)取代的1,1'-亚甲基双(咪唑鎓)和1,1'-亚甲基双(1,2,4-三唑鎓)双(三氟甲磺酰基)酰胺:导致双(N)的离子液体-杂环卡宾)钯配合物

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摘要

Ionic liquids with pincer dicationic nuclei, 2a-6a and 2b-6b, were prepared from either 1,1'-methylenebis(imidazole) or 1,1'-methylenebis(1,2,4-triazole) via quaternization with alkyl or polyfluoroalkyl halides under classical or microwave irradiation conditions. Palladium-catalyzed Heck cross-coupling reactions were performed successfully in the ionic liquid 3a. A single-crystal X-ray structure of a bis(N-heterocyclic carbene) complex of palladium (7) formed in the ionic liquid catalyst system supports its likelihood as the active catalyst.
机译:通过烷基或多氟烷基的季铵化作用,由1,1'-亚甲基双(咪唑)或1,1'-亚甲基双(1,2,4-三唑)制得具有夹钳状离子核的离子液体2a-6a和2b-6b经典或微波辐射条件下的卤化物。在离子液体3a中成功进行了钯催化的Heck交叉偶联反应。在离子液体催化剂体系中形成的钯(7)的双(N-杂环卡宾)配合物的单晶X射线结构证实了其作为活性催化剂的可能性。

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