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在功能化硼二吡咯亚甲基染料中,电子能量转移至受体的S2能级。

Electronic energy transfer to the S2 level of the acceptor in functionalised boron dipyrromethene dyes.

作者信息

Harriman Anthony, Mallon Laura J, Goeb Sébastien, Ulrich Gilles, Ziessel Raymond

机构信息

Molecular Photonics Laboratory, School of Chemistry, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Chemistry. 2009;15(18):4553-64. doi: 10.1002/chem.200802477.

Abstract

Taking the high road: Highly efficient electronic energy transfer takes place from a set of appended aryl polycyclic hydrocarbons to an expanded boron dipyrromethene (Bodipy)-based dye (see figure) despite negligible spectral overlap with the lowest-energy excited state localised on the acceptor.A multi-component array has been constructed around an expanded boron dipyrromethene (Bodipy) dye that absorbs and emits in the far-red region. One of the appendages is a perylene-based moiety that is connected to the boron atom of the terminal Bodipy by a 1,4-diethynylphenylene connector. Despite the fact that there is almost negligible spectral overlap between fluorescence from the perylene unit and absorption by the Bodipy residue, electronic energy transfer is rapid and essentially quantitative. It is concluded that at least half of the photons absorbed by perylene are transferred to the upper-lying singlet excited state (S(2)) associated with the Bodipy-based acceptor. The second appendage is a pyrene unit that is covalently linked to fluorene, through an ethynylene spacer, and to the boron atom of the Bodipy terminus, through a 1,4-diethynylphenylene connector. Pyrene absorbs and emits at higher energy than perylene and there is strong spectral overlap with the Bodipy-based S(2) state, and none with the corresponding S(1) state. Electronic energy transfer is now very fast and exclusively to the S(2) state of the acceptor. It is difficult to compute reasonable estimates for the rates of Coulombic energy transfer, because of uncertainties in the orientation factor, but the principle mechanism is believed to arise from electron exchange. Comparison with an earlier array built around a conventional Bodipy dye indicates that there are comparable electronic coupling matrix elements for the two systems. It is notable that pyrene is more strongly coupled to the Bodipy unit than perylene in both arrays. These new arrays function as highly effective solar concentrators.

摘要

另辟蹊径

尽管与受体上局域化的最低能量激发态的光谱重叠可忽略不计,但一组附加的芳基多环烃仍能高效地向一种基于扩展硼二吡咯亚甲基(Bodipy)的染料进行电子能量转移(见图)。围绕一种在远红区域吸收和发射的扩展硼二吡咯亚甲基(Bodipy)染料构建了一个多组分阵列。其中一个附属部分是基于苝的基团,它通过1,4 - 二乙炔基苯连接体与末端Bodipy的硼原子相连。尽管苝单元的荧光与Bodipy残基的吸收之间几乎没有光谱重叠,但电子能量转移迅速且基本定量。可以得出结论,苝吸收的光子中至少有一半转移到了与基于Bodipy的受体相关的较高单重激发态(S(2))。第二个附属部分是芘单元,它通过乙炔间隔基与芴共价连接,并通过1,4 - 二乙炔基苯连接体与Bodipy末端的硼原子相连。芘的吸收和发射能量高于苝,并且与基于Bodipy的S(2)态有很强的光谱重叠,而与相应的S(1)态没有重叠。现在电子能量转移非常快,且仅转移到受体的S(2)态。由于取向因子存在不确定性,难以计算库仑能量转移速率的合理估计值,但据信其主要机制源于电子交换。与围绕传统Bodipy染料构建的早期阵列相比,表明这两个系统具有相当的电子耦合矩阵元。值得注意的是,在这两个阵列中,芘与Bodipy单元的耦合都比苝更强。这些新阵列可作为高效的太阳能聚光器。

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