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首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Using the Negative Hyperconjugation Effect of Pentafluorosulfanyl Acceptors to Enhance Two-Photon Absorption in Push-Pull Chromophores
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Using the Negative Hyperconjugation Effect of Pentafluorosulfanyl Acceptors to Enhance Two-Photon Absorption in Push-Pull Chromophores

机译:使用五氟氟丁基受体的阴性超强凝固效果,以增强推拉发色团中的两光子吸收

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A series of first-generation pentafluorosulfanyl-substituted chromophores with high two-photon cross-sections is described. The pentafluorosulfanyl functional group is a very intriguing moiety that possesses not only a strong inductive effect due to its high electronegativity but also a sizable resonance acceptor constant due to negative hyperconjugation involving the sulfur(VI) center. This negative hyperconjugation effect imparts cationic character to the sulfurs, a feature that we exploit in the design of potent two-photon-absorbing systems where the pentafluorosulfanyl groups serve as strong terminal acceptors. Herein, we report five multibranched triarylamine-based dyes with two-photon absorption cross-sections ranging from 1100-2200 GM. This demonstrates for the first time that when coupled to a suitable donor, pentafluorosulfanyl acceptors are a viable molecular handle for designing large cross-sections in relatively small metal-free pi-conjugated systems.
机译:描述了一系列具有高双光子横截面的第一代五氟氟烷基取代的发色团。 五氟磺酰基官能团是一种非常有趣的部分,其不仅具有由于其高电负性而具有强的诱导效果,而且由于涉及硫(VI)中心的阴性高速缀合性,其具有可相同的共振受体恒定。 这种阴性高速谐波效果赋予硫磺的阳离子特征,这是我们利用在富氟磺基的有效的双光子吸收系统设计中的特征,其中五氟磺基基作为强末端受体。 在此,我们报告了五种基于多刺基三芳基胺的染料,其两种光子吸收横截面为1100-2200克。 这首次证明了当与合适的供体相结合时,五氟磺基烷基受体是用于在相对小的无金属PI缀合系统中设计大横截面的可行分子手柄。

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