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Expanded Bodipy Dyes: Anion Sensing Using a Bodipy Analog with an Additional Difluoroboron Bridge

Ruslan Guliyev, Seyma Ozturk, Ertan Şahin, Engin Umut AKKAYA

ORGANIC LETTERS Cilt 14 · Sayı 6 · ss. 1528–1531 · 16.03.2012
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Özet

Oxalyl-tethered pyrroles can be doubly bridged with two difluoroboron chelating units to yield bright orange dyes. Interestingly, in polar organic solvents, the addition of fluoride and cyanide result in reversible detachment of the otherwise stable difluoroboron bridges, resulting in sharp changes in color. Thus, this novel compound behaves as a highly selective chromogenic sensor for fluoride and cyanide ions.

Atıf için künye

Guliyev, R., Ozturk, S., Şahin, E., & AKKAYA, E. U. (2012). Expanded Bodipy Dyes: Anion Sensing Using a Bodipy Analog with an Additional Difluoroboron Bridge. ORGANIC LETTERS, 14(6), 1528–1531. https://doi.org/10.1021/ol300260q

BibTeX
@article{guliyev2012-66547,
  author = {Guliyev, Ruslan and Ozturk, Seyma and Şahin, Ertan and AKKAYA, Engin Umut},
  title = {Expanded Bodipy Dyes: Anion Sensing Using a Bodipy Analog with an Additional Difluoroboron Bridge},
  journal = {ORGANIC LETTERS},
  year = {2012},
  volume = {14},
  number = {6},
  pages = {1528--1531},
  issn = {1523-7060},
  doi = {10.1021/ol300260q},
  url = {https://akademik.atauni.edu.tr/yayinlar/66547-expanded-bodipy-dyes-anion-sensing-using-a-bodipy-analog-with-an-additional}
}