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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Characterization of guest molecule concentration dependent nanotubes of β-cyclodextrin and their secondary assembly: Study with trans-2-[4(dimethylamino)styryl]benzothiazole, a TICT-fluorescence probe
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Characterization of guest molecule concentration dependent nanotubes of β-cyclodextrin and their secondary assembly: Study with trans-2-[4(dimethylamino)styryl]benzothiazole, a TICT-fluorescence probe

机译:客体分子浓度依赖的β-环糊精纳米管及其二级组装的表征:使用反式-2- [4(二甲基氨基)苯乙烯基]苯并噻唑,一种TICT荧光探针进行研究

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The formation of nanotubes of β-cyclodextrins (β-CD) and their secondary assembly induced by trans-2-[4-(dimethylamino)styryl]benzothiazole (DMASBT) as a guest molecule has been explained using twisted intramolecular charge transfer (TICT) fluorescence, steady state fluorescence anisotropy, time-correlated single-photon counting fluorescence decay of DMASBT, atomic force microscopy and also transmission electron microscopy. It has been demonstrated that although at lower concentration of β-CD, DMASBT molecules form simple adduct of 1:1 stoichiometry but they form extended nanotubes at relatively high concentration of β-CD which further lead to the secondary assembly through intertubular hydrogen bondings forming rod-like structures. The changes in fluorescence properties of DMASBT yield critical aggregation concentration (CAC) of β-CD very close to 2.5 mM. The extent of formation of these supramolecular structures is dependent on the concentration of guest molecule. It has been observed that perchlorate ion (ClO_4~-) reduces the stability of supramolecular structures at higher concentration of it but at low concentration (<7 mM) it enhances the stability by providing the anchor sites for intermolec-ular hydrogen bonding between neighboring β-CD molecules. The polarity and viscosity dependent TICT fluorescence characteristics of DMASBT are exploited to determine the micropolarity and microviscosity of environment around it inside the nanotubes.
机译:使用扭曲分子内电荷转移(TICT)解释了反式-2- [4-(二甲基氨基)苯乙烯基]苯并噻唑(DMASBT)作为客体分子诱导的β-环糊精(β-CD)纳米管的形成及其次级组装荧光,稳态荧光各向异性,与时间相关的单光子计数DMASBT的荧光衰减,原子力显微镜以及透射电子显微镜。已经证明,虽然在较低的β-CD浓度下,DMASBT分子会形成化学计量比为1:1的简单加合物,但它们会以相对较高的β-CD浓度形成扩展的纳米管,进而通过管间氢键形成棒而导致二级组装类结构。 DMASBT荧光性质的变化产生了非常接近2.5 mM的β-CD临界聚集浓度(CAC)。这些超分子结构的形成程度取决于客体分子的浓度。已经观察到高氯酸根离子(ClO_4〜-)在较高浓度下会降低超分子结构的稳定性,但在低浓度(<7 mM)时会通过提供相邻β之间分子间氢键的锚定位点来增强稳定性。 -CD分子。利用DMASBT的极性和粘度依赖性的TICT荧光特性来确定纳米管内部环境的微极性和微粘度。

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