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Synthesis of Heteroarylferrocenes by FriedlanderReaction and Their Spectral Properties

机译:弗里德兰德反应合成杂芳基二茂铁及其光谱性质

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A series of mono- and 1,1`-bis(heteroaryl)-substituted ferrocenes were prepared by employing Frielander reaction of acetyl- and 1,1`-diacetylferrocene with a series of o-aminoaldehydes. Reactions of 1,1`-diacetylferrocene with two equivalents of 1-aminonaphthalene-2-carbaldehyde and 8-aminoquinoline-7-carbaldehyde afforded a mixture of mono- and 1,1`-bis(heteroaryl)-substituted ferrocenes in a ratio of 1 : 3.1 - 3.8, while the reaction with 4-aminoacridine-3-carbaldehyde did not provide any characterizable product presumably due to the redox instability of the product induced by low reduction potential of benzo[b]-1,10-phenanthroline. Structural and optical properties of the compounds prepared were described.
机译:通过利用乙酰基和1,1′-二乙酰基二茂铁与一系列邻氨基醛的弗里兰德反应制备一系列的单和1,1′-双(杂芳基)取代的二茂铁。 1,1′-二乙酰基二茂铁与两个当量的1-氨基萘-2-甲醛和8-氨基喹啉-7-甲醛的反应得到单-和1,1-双(杂芳基)取代的二茂铁的混合物,其比率为1:3.1-3.8,而与4-氨基ac啶-3-甲醛的反应未提供任何可表征的产物,这可能是由于苯并[b] -1,10-菲咯啉的低还原电位所引起的产物的氧化还原不稳定。描述了所制备化合物的结构和光学性质。

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