Strong fluorescence emission induced by supramolecular assembly and gelation: luminescent organogel from nonemissive oxadiazole-based benzene-1,3,5-tricarboxamide gelatorElectronic Supplementary Information (ESI) available: Synthetic and experimental details, X-ray diffractograms, H-bonded aggregate-state absorption and emission spectra, and original data for Fig. 1c and 2. See http://www.rsc.org/suppdata/cc/b3/b311648d/
Chemical Communications2003Iss. 1, pp. 70–70
Citations Over TimeTop 10% of 2003 papers
Abstract
Supramolecular aggregation of a novel nonfluorescent gelator yields highly luminescent organogels in aprotic organic solvents through intermolecular hydrogen bonding, which is a key motif for both self-assembly and photophysical process control.
Related Papers
- → Supramolecular Chemistry: A Toolkit for Soft Functional Materials and Organic Particles(2017)209 cited
- → Functional Supramolecular Architectures of Dipyrrin Complexes(2018)65 cited
- → Aromatic π–π driven supergelation, aggregation induced emission and columnar self-assembly of star-shaped 1,2,4-oxadiazole derivatives(2016)64 cited
- → Understanding the properties of dithienylethenes functionalized for supramolecular self-assembly: a molecular modeling study(2020)12 cited
- → Controlled Supramolecular Assembly of Gold (III) Amphiphiles in Aqueous Media(2022)4 cited