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首页> 外文期刊>The Journal of Organic Chemistry >Synthesis of Bispyrenyl Sugar-Aza-Crown Ethers as New Fluorescent Molecular Sensors for Cu(II)
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Synthesis of Bispyrenyl Sugar-Aza-Crown Ethers as New Fluorescent Molecular Sensors for Cu(II)

机译:联吡啶双糖基氮杂-冠冕醚的合成作为Cu(II)的新型荧光分子传感器

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摘要

Two N-pyrenylacetamide-substituted sugar-aza-crown ethers have been synthesized as new fluorescent chemosensors. The designed ligands 1 and 2 exhibit fluorescence characteristics of a pyrene monomer and a dynamic excimer emission when compared to N-pyrenylacetamide as a model compound. Both ligands displayed a Cu2+-sensitive fluorescence quenching with a 1:1 stoichiometry and high stability constants (log K = 6.7 for 1 and 7.8 for 2). The quenching effect was rationalized on the basis of photoinduced electron transfer from the excited pyrene to the complexed Cu~(2+) cation, while the changes in excimer-to-monomer ratio were explained by a conformational analysis through DFT calculations. The predicted structure suggests that the Cu~(2+) cation is coordinated with the two carbonyl groups and the sugar-aza-crown ethers which rigidified the complex structure and placed the two pyrene moieties far apart.
机译:两种N-苯乙炔基乙酰胺取代的糖氮杂-冠醚已被合成为新型荧光化学传感器。与作为模型化合物的N-吡啶基乙酰胺相比,设计的配体1和2表现出a单体的荧光特征和动态受激准分子发射。两种配体均表现出Cu2 +敏感的荧光猝灭,化学计量比为1:1,并且具有较高的稳定性常数(log K = 6.7(1)和7.8(2))。在从激发的pyr到配位的Cu〜(2+)阳离子的光诱导电子转移的基础上,使猝灭效应合理化,同时通过DFT计算通过构象分析解释了准分子对单体比的变化。预测的结构表明,Cu〜(2+)阳离子与两个羰基和糖氮杂-冠状醚配位,使刚性结构复杂化,并使两个pyr部分相距较远。

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