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Selective d/π-electron Oxidation Behaviors of a FerroceneDerivative Dimerized by Hydrogen Bonds

机译:用氢键二聚铁密脱的选择性D /π-电子氧化行为

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Molecules showing both π-and d-electron oxidations enable to change their electronicstructures by alternating the π-d oxidized sites.Recently,much attention has been given to theπ-d oxidized character change by proton transfer,which could provide not only molecularbasedmultifunctional materials with multi-responses,but also fundamental understanding ofbiological activities based on proton coupled electron transfer (PCET).However,it is stillchallenging to construct such molecules,partially due to a difficulty to turn on and off the π-conjugation between π-and d-electron oxidized sites by the protonation/deprotonationbehaviors of molecules.Herein,I report that a ferrocene-substituted 2,3-dihydroquinazolinone(complexis a candidate of molecules,where the d-electron based oxidized state would beconverted to the π-electron based one accompanied by proton transfer (Figure 1).
机译:显示π-and电子氧化的分子使得通过交替π-d氧化位点来改变其电子结构。通常,通过质子转移给予氧化症状的氧化特性变化很多,这可以提供不仅提供分子的多官能材料多响应,也是基于质子耦合电子转移(PCET)的生物学活动的基本理解。但是,它是静止的构建这种分子,部分是由于难以打开和关闭π-and的π-缀合的π-电子氧化位点通过质子化/去质子化的分子。鉴定,我报告了一种二茂铁取代的2,3-二氢喹唑啉酮(复杂的分子候选物,其中基于D-Electron的氧化状态将被伴随地基于π-电子通过质子转移(图1)。

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