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Unprecedented Charge-Transfer Complex of Fused Diporphyrin as Near-Infrared Absorption-Induced High-Aspect-Ratio Nanorods

机译:融合双卟啉的前所未有的电荷转移复合物,作为近红外吸收诱导的高纵横比纳米棒。

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摘要

Charge-transfer (CT) complexes of near-infrared absorbing systems have been unknown until now. Consequently, structural similarities between donor and acceptor are rather important to achieve this phenomenon. Herein, we report electron donors such as non-fused diporphyrin-anthracene (DP), zinc diporphyrin-anthracene (ZnDP) and fused zinc diporphyrin-anthracene (FZnDP) in which FZnDP absorbs in NIR region and permits a CT complex with the electron acceptor, perylene diimide (PDI) in CHCl3 exclusively. UV/Vis-NIR absorption, (HNMR)-H-1, NOESY and powder X-ray diffraction analysis demonstrated that the CT complex formation occurs by - stacking between perylene units in FZnDP and PDI upon mixing together in a 1:1 molar concentration in CHCl3, unlike non-fused ZnDP and DP. TEM and AFM images revealed that the CT complex initially forms nanospheres leading to nanorods by diffusion of CH3OH vapors into the CHCl3 solution of FZnDP/PDI (1:1 molar ratio). Therefore, these CT nanorods could lead to significant advances in optical, biological and ferroelectric applications.
机译:到目前为止,近红外吸收系统的电荷转移(CT)配合物还未知。因此,供体和受体之间的结构相似性对于实现这一现象非常重要。本文中,我们报道了电子供体,例如非融合二卟啉-蒽(DP),锌二卟啉-蒽(ZnDP)和熔融锌二卟啉-蒽(FZnDP),其中FZnDP在NIR区域吸收并允许与电子受体的CT络合物,仅在CHCl3中的in二酰亚胺(PDI)。 UV / Vis-NIR吸收,(HNMR)-H-1,NOESY和粉末X射线衍射分析表明,通过-以1:1摩尔浓度混合在一起,FZnDP和PDI中的per单元之间堆叠而形成CT络合物与非熔融的ZnDP和DP不同,它在CHCl3中的含量较高。 TEM和AFM图像显示,CT络合物最初通过将CH3OH蒸气扩散到FZnDP / PDI(1:1摩尔比)的CHCl3溶液中形成纳米球,从而形成纳米棒。因此,这些CT纳米棒可能会在光学,生物和铁电应用方面取得重大进展。

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