荧光
化学
激发态
光化学
电子顺磁共振
动态光散射
放松(心理学)
分子
动力学
密度泛函理论
化学物理
计算化学
纳米技术
纳米颗粒
核磁共振
材料科学
有机化学
光学
量子力学
物理
心理学
社会心理学
核物理学
作者
Elaine R. Sodre,Bruna C. Guido,Paulo Eduardo Narcizo de Souza,Daniel F. S. Machado,Valter H. Carvalho‐Silva,Juliano Alexandre Chaker,Claudia C. Gatto,José R. Corrêa,Talita de A. Fernandes,Brenno A. D. Neto
标识
DOI:10.1021/acs.joc.0c01805
摘要
An aggregation-induced emission enhancement (AIEE) effect in fluorescent lipophilic 2,1,3-benzothiadiazole (BTD) derivatives and their organic nanoaggregates were studied. A set of techniques such as single-crystal X-ray, dynamic light scattering (DLS), electron paramagnetic resonance (EPR), UV-vis, fluorescence, and density functional theory (DFT) calculations have been used to decipher the formation/break (kinetics), properties, and dynamics of the organic nanoaggregates of three BTD small organic molecules. An in-depth study of the excited-state also revealed the preferential relaxation emissive pathways for the BTD derivatives and the dynamics associated with it. The results described herein, for the first time, explain the formation of fluorescent BTD nanoaggregate derivatives and allow for the understanding of their dynamics in solution as well as the ruling forces of both aggregation and break processes along with the involved equilibrium. One of the developed dyes could be used at a nanomolar concentration to selectively stain lipid droplets emitting an intense and bright fluorescence at the red channel. The other two BTDs could also stain lipid droplets at very low concentrations and were visualized preferentially at the blue channel.
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