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3-乙酰基-4-氧代-6,7-二氢-12H-吲哚并[2,3-a]喹嗪在仿生反胶束纳米腔中的光物理研究:一种光谱学方法。

Photophysical study of 3-acetyl-4-oxo-6,7-dihydro-12H-indolo[2,3-a]quinolizine in biomimetic reverse micellar nanocavities: a spectroscopic approach.

作者信息

Mallick Arabinda, Haldar Basudeb, Maiti Subhendu, Bera Subhash Chandra, Chattopadhyay Nitin

机构信息

Department of Chemistry, Jadavpur University, Calcutta 700 032, India.

出版信息

J Phys Chem B. 2005 Aug 4;109(30):14675-82. doi: 10.1021/jp050511d.

Abstract

Photophysical properties of 3-acetyl-4-oxo-6,7-dihydro-12H-indolo[2,3-a]quinolizine (AODIQ), a bioactive molecule, has been investigated in well-characterized, monodispersed biomimicking nanocavities formed by sodium bis(2-ethylhexyl)sulfosuccinate (AOT) in heptane using steady-state and picosecond time resolved fluorescence and fluorescence anisotropy. The emission behavior of AODIQ is very much dependent upon the water/surfactant mole ratio (W), i.e., on the water pool size of the reverse micellar core. AODIQ exhibits a sharp decrease in fluorescence anisotropy with increasing W, implying that the overall motional restriction experienced by the molecule is decreased with increased hydration. Some of the depth-dependent relevant fluorescence parameters, namely, fluorescence maxima and fluorescence anisotropy (r), have been monitored for exploiting the distribution and microenvironment around the probe in the reverse micelles. Fluorescence spectral position and fluorescence quenching studies suggest that the probe does not penetrate into the reverse micellar core; rather it binds at the interfacial region. Quantitaive estimates of the micropolarity and microviscosity at the binding sites of the probe molecule have been determined as a function of W.

摘要

利用稳态和皮秒时间分辨荧光及荧光各向异性,对生物活性分子3-乙酰基-4-氧代-6,7-二氢-12H-吲哚并[2,3-a]喹嗪(AODIQ)在由双(2-乙基己基)磺基琥珀酸钠(AOT)在庚烷中形成的、具有良好表征的单分散仿生纳米腔中的光物理性质进行了研究。AODIQ的发射行为很大程度上取决于水/表面活性剂摩尔比(W),即取决于反胶束核的水池大小。随着W的增加,AODIQ的荧光各向异性急剧下降,这意味着分子所经历的整体运动限制随着水合作用的增加而降低。已监测了一些与深度相关的相关荧光参数,即荧光最大值和荧光各向异性(r),以探究反胶束中探针周围的分布和微环境。荧光光谱位置和荧光猝灭研究表明,探针不会渗透到反胶束核中;相反,它结合在界面区域。已根据W确定了探针分子结合位点处微极性和微粘度的定量估计值。

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