首页> 外文期刊>The Journal of Organic Chemistry >2,6-Diacylnaphthalene-1,8:4,5-bis(dicarboximides): Synthesis, reduction potentials, and core extension
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2,6-Diacylnaphthalene-1,8:4,5-bis(dicarboximides): Synthesis, reduction potentials, and core extension

机译:2,6-二酰基萘-1,8:4,5-双(二甲酰亚胺):合成,还原电位和核心延伸

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摘要

2,6-Diacyl derivatives of naphthalene-1,8:4,5-bis(dicarboximide)s have been synthesized via Stille coupling reactions of the corresponding 2,6-distannyl derivative with acyl halides. Reaction of these diketones with hydrazine gave phthalazino[6,7,8,1-lmna]pyridazino[5,4,3-gh][3,8]phenanthroline-5,11(4H,10H) -dione fused-ring derivatives. The products were characterized by UV-vis absorption spectroscopy and electrochemistry, modeled using density functional theory calculations, and, in some cases, studied and compared using single-crystal X-ray diffraction.
机译:萘-1,8:4,5-双(二甲叉酰亚胺)的2,6-二酰基衍生物是通过相应的2,6-二苯甲醛衍生物与酰基卤的斯蒂勒偶联反应合成的。这些二酮与肼反应,得到酞嗪并[6,7,8,1-lmna]吡嗪并[5,4,3-gh] [3,8]菲咯啉-5,11(4H,10H)-二酮稠环衍生物。产品通过紫外可见吸收光谱和电化学进行表征,使用密度泛函理论计算进行建模,并在某些情况下使用单晶X射线衍射进行研究和比较。

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