A "turn-on" fluorescent probe based on BODIPY dyes for highly selective detection of fluoride ions. (June 2021)
- Record Type:
- Journal Article
- Title:
- A "turn-on" fluorescent probe based on BODIPY dyes for highly selective detection of fluoride ions. (June 2021)
- Main Title:
- A "turn-on" fluorescent probe based on BODIPY dyes for highly selective detection of fluoride ions
- Authors:
- Chen, Xi
Liu, Yu-Cong
Bai, Jiang
Fang, Hao
Wu, Fang-Ying
Xiao, Qiang - Abstract:
- Abstract: In the present paper, a novel difluoroboron dipyrromethene-based (BODIPY) fluorescent probe with a conjugated hydrazone group, named BDBH, was developed for the detection of F − with high selectivity and sensitivity. After addition of tetrabutylammonium fluoride (TBAF) into a BDBH solution, the fluorescence was "turned on", which displayed an 80-fold increasement of emission intensity. The wavelengths of excitation and emission were 518 nm and 613 nm respectively, which were free from the background interference. The titration of 1 H NMR (Nuclear Magnetic Resonance) indicated that the interaction involved hydrogen-bonding formation between the acidic H of –NH–CO group and F − at low concentration and deprotonation of N–H group at increasing concentration of fluoride. The theoretical calculations verified that once F − interacted with BDBH, the planarity and conjugation of BDBH enhanced, which resulted in a strong fluorescence emission at 613 nm. Furthermore, confocal fluorescence images of BDBH-incubated HeLa cells verified its potential application as an "off-on" sensor to monitor F− in living cells. Graphical abstract: A BODIPY-based fluorescence probe for fluoride detecting named BDBH was developed. It exhibited high selectivity and sensitivity for F − over other reactive anions, such as Cl −, Br −, I −, NO3 −, AcO −, H2 PO4 −, and HSO4 − . Preliminary application of BDBH in living cells fluorescence imaging was further verified its usage as an "Off-On" sensorAbstract: In the present paper, a novel difluoroboron dipyrromethene-based (BODIPY) fluorescent probe with a conjugated hydrazone group, named BDBH, was developed for the detection of F − with high selectivity and sensitivity. After addition of tetrabutylammonium fluoride (TBAF) into a BDBH solution, the fluorescence was "turned on", which displayed an 80-fold increasement of emission intensity. The wavelengths of excitation and emission were 518 nm and 613 nm respectively, which were free from the background interference. The titration of 1 H NMR (Nuclear Magnetic Resonance) indicated that the interaction involved hydrogen-bonding formation between the acidic H of –NH–CO group and F − at low concentration and deprotonation of N–H group at increasing concentration of fluoride. The theoretical calculations verified that once F − interacted with BDBH, the planarity and conjugation of BDBH enhanced, which resulted in a strong fluorescence emission at 613 nm. Furthermore, confocal fluorescence images of BDBH-incubated HeLa cells verified its potential application as an "off-on" sensor to monitor F− in living cells. Graphical abstract: A BODIPY-based fluorescence probe for fluoride detecting named BDBH was developed. It exhibited high selectivity and sensitivity for F − over other reactive anions, such as Cl −, Br −, I −, NO3 −, AcO −, H2 PO4 −, and HSO4 − . Preliminary application of BDBH in living cells fluorescence imaging was further verified its usage as an "Off-On" sensor to monitor F − . Image 1 Highlights: The first reported OFF-ON Fluorescent probe based on BODIPY dyes for F‾ detection through hydrogen-bond interaction. High selectivity and sensitivity, quick response to F‾. Biocompatible probe for detection of F‾ in living cells. … (more)
- Is Part Of:
- Dyes and pigments. Volume 190(2021)
- Journal:
- Dyes and pigments
- Issue:
- Volume 190(2021)
- Issue Display:
- Volume 190, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 190
- Issue:
- 2021
- Issue Sort Value:
- 2021-0190-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-06
- Subjects:
- F− -- Fluorescent turn on -- BODIPY -- Selectivity
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2021.109347 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23814.xml