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Spectral Narrowing of UV-Visible Absorption and Emission Spectra of Anthracene-Derivatives in β-Cyclodextrin Nanocavity: Effects of Host/Guest Stoichiometry

机译:β-环糊精纳米腔中蒽衍生物的紫外可见吸收和发射光谱的光谱窄化:宿主/客体化学计量学的影响

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摘要

Cyclodextrins (CD) are cyclic oligosaccharides consisting of six or more D-glucopyranose units, the interior of which forms a hydrophobic cavity. In the present study, we employed the CD confinement effects as a tool to suppress an electronic decoherence of guest wavefunction by reducing intermolecular interactions between a guest molecule and the surrounding environment. Effects of host/guest stoichiometry on the decoherence suppresion were investigated by comparing native β-CD with trimethyl-β-CD that should form only a 1:1 complex. Both fluorecence and fluorecence-excitation spectra of inclusion complexes exhibited spectral narrowings only for the β-CD host, suggesting that the formation of barrel-type β-CD dimer plays a key role for the pronounced spectral narrowings.
机译:环糊精(CD)是由六个或更多D-吡喃葡萄糖单元组成的环状寡糖,其内部形成疏水腔。在本研究中,我们采用CD限制效应作为一种工具,通过减少来宾分子与周围环境之间的分子间相互作用来抑制来宾波函数的电子退相干。通过比较天然β-CD与应仅形成1:1配合物的三甲基-β-CD,研究了宿主/客体化学计量对去相干性抑制的影响。包合物的荧光光谱和荧光激发光谱都仅对β-CD主体显示光谱窄化,表明桶型β-CD二聚体的形成对于明显的光谱窄化起关键作用。

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