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Tunable molecular packing modes via H- or J-aggregates in the supramolecular helical nanostructures from an achiral C-3 symmetric molecule

  • 发布时间:2023-10-19
  • 点击次数:

  • 关键字:CHIRALITY; ASSEMBLIES; FLUORESCENCE; GELS; ENHANCEMENT; DISCOTICS; BREAKING; SYSTEMS; FILMS
  • 摘要:The self-assembly of a C-3-symmetric molecule benzene-1,3,5-tricarboxylate substituted with methyl cinnamate (BTECM) has been investigated by a reprecipitation method in H2O and cetyltrimethylammonium bromide (CTAB) aqueous solution, respectively. The nanostructures and characteristics of the assemblies were monitored by UV-Vis spectroscopy, fluorescence (FL) spectroscopy, circular dichroism (CD) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). It was found that helical nanostructures were successfully assembled from the achiral C-3 molecule BTECM. More importantly, the helices aggregated via different packing modes in H2O and CTAB aqueous solution. In H2O, the nanostructures underwent a process of particles, fibers and helices via H-type aggregate upon aging. In the case of CTAB aqueous solution (1.2 mM), the helices were translated from particles and the molecules were inclined to aggregate via the J-type mode. In addition, the aggregation process could be accelerated by raising the temperature proved by UV-Vis spectra. A molecular aggregation mechanism was proposed based on the experimental results.
  • 卷号:19
  • 期号:26
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