Abstract
The rational improvement of photophysical properties can be highly valuable for the discovery of novel organic fluorophores. Using our new design strategy guided by the oscillator strength, we developed a series of full-color-tunable furoindolizine analogs with improved molar absorptivity through the fusion of a furan ring into the indolizine-based Seoul fluorophore. The excellent correlation between the computable values (oscillator strength and theoretical S0-S1 energy gap) and photophysical properties (molar absorptivity and emission wavelength) confirmed the effectualness of our design strategy.
| Original language | English |
|---|---|
| Pages (from-to) | 15689-15693 |
| Number of pages | 5 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 54 |
| Issue number | 52 |
| DOIs | |
| State | Published - 21 Dec 2015 |
Bibliographical note
Publisher Copyright:© 2015 The Authors.
Keywords
- fluorescence
- molar absorptivity
- oscillator strength
- photophysical properties
- rational design