School of Chemistry, University of Hyderabad, Hyderabad 500046, India.
J Phys Chem B. 2009 Nov 19;113(46):15189-95. doi: 10.1021/jp906274a.
The aggregated state of the electron donor-acceptor molecule, 4-(9-anthryl)-N,N-dimethylaniline, abbreviated here as ADMA, has been studied by electronic absorption and fluorescence spectroscopy, microscopy, and crystallography. Self-assembled aggregates have been prepared by reprecipitation method under various conditions without using any stabilizing agent and characterized by different microscopic techniques. These studies reveal spherical and platelike morphologies and both amorphous and crystalline nature of the aggregates, whose sizes vary between 250 and 600 nm. The optical properties of these well-characterized aggregates have been studied and compared with those in molecular form. Intermolecular interaction in the aggregates induces remarkable change in the absorption and fluorescence properties of this dipolar system, and the formation of stable aggregates can be conveniently followed by monitoring the spectral response of the system as a function of time. Intramolecular charge transfer process, which dominates the photophysical behavior of this molecular system, could not be observed in the solid or aggregated state. The nature of the intermolecular interactions responsible for the formation and stabilization of the aggregates has been identified from the spectral and crystal structure data of the system. The results highlight the scope of broadening the spectral response of the present system by exploiting the advantageous optical properties of the aggregated state of the molecule.
电子给体-受体分子 4-(9-蒽基)-N,N-二甲基苯胺(简称 ADMA)的聚集态已通过电子吸收和荧光光谱、显微镜和晶体学进行了研究。在没有使用任何稳定剂的情况下,通过不同的沉淀方法在各种条件下制备了自组装聚集体,并通过不同的显微镜技术进行了表征。这些研究揭示了聚集体的球形和片状形态以及无定形和结晶性质,其尺寸在 250 至 600nm 之间变化。研究了这些特征良好的聚集体的光学性质,并将其与分子形式的光学性质进行了比较。聚集体中的分子间相互作用导致这个偶极体系的吸收和荧光性质发生显著变化,并且可以通过监测系统的光谱响应随时间的变化来方便地跟踪稳定聚集体的形成。在固态或聚集态下,不能观察到主导这个分子体系光物理行为的分子内电荷转移过程。从系统的光谱和晶体结构数据中确定了形成和稳定聚集体的分子间相互作用的性质。这些结果突出了通过利用分子聚集态的有利光学性质来拓宽本体系光谱响应的范围。