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萘二吲哚基马来酰亚胺染料的高拟斯托克斯位移

High Pseduo-Stoke's Shift of a Naphthalene-Bisindolylmaleimide Dye.

作者信息

Li Xiaochuan, Shan Dandan, Son Young-A

出版信息

J Nanosci Nanotechnol. 2016 Jan;16(1):856-60. doi: 10.1166/jnn.2016.11779.

Abstract

An energy transfer cassette was reported with energy donor and acceptor incorporated in one molecular. The two units (naphthalene and bisindolylmaleimide) were connected by covalent single bond. The intramolecular repulsion twisted the molecular conformation, thereby forcing the two units act as independent chromophores. Upon photoexcitation (λ = 280 nm), bright emission peak was observed around 583 nm. The intramolecular cascade energy transfer from the naphthalene moiety to the bisindolylmaleimide framework is efficient and the efficiency is estimated to be 86%, providing large pseudo-Stoke's shift (303 nm). At such a short separation, the orbital overlap interaction was completely isolated between chromophoric units. Computational study was carried out based on DFT. Further analysis of optimized structure and FMOs supports the efficient energy transfer in NBM. Favorable photophysical properties, such as efficient energy transfer, strong emission, and large Stoke's shift make it an attractive functional dye.

摘要

据报道,一种能量转移盒式结构将能量供体和受体整合在一个分子中。这两个单元(萘和双吲哚基马来酰亚胺)通过共价单键相连。分子内的排斥作用扭曲了分子构象,从而迫使这两个单元作为独立的发色团起作用。在光激发(λ = 280 nm)时,在583 nm左右观察到明亮的发射峰。从萘部分到双吲哚基马来酰亚胺骨架的分子内级联能量转移是高效的,效率估计为86%,提供了大的伪斯托克斯位移(303 nm)。在如此短的间距下,发色团单元之间的轨道重叠相互作用被完全隔离。基于密度泛函理论(DFT)进行了计算研究。对优化结构和前线分子轨道(FMO)的进一步分析支持了NBM中高效的能量转移。良好的光物理性质,如高效的能量转移、强烈的发射和大的斯托克斯位移,使其成为一种有吸引力的功能性染料。

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