Turn on fluorescent detection of hydrazine with a 1, 8-naphthalimde derivative. (December 2017)
- Record Type:
- Journal Article
- Title:
- Turn on fluorescent detection of hydrazine with a 1, 8-naphthalimde derivative. (December 2017)
- Main Title:
- Turn on fluorescent detection of hydrazine with a 1, 8-naphthalimde derivative
- Authors:
- Shi, Bingjie
He, Yangyang
Zhang, Panpan
Wang, Yulong
Yu, Mingming
Zhang, Hongyan
Wei, Liuhe
Li, Zhanxian - Abstract:
- Abstract: It is crucial to develop highly sensitive and selective probes toward hydrazine because it is a class of highly toxic and pollutant compound. Herein, using fracture of carbon carbon double bond and dissociation of amide by hydrazine, a novel off-on fluorescent probe was developed for hydrazine. The probe can quantitatively detect hydrazine in concentration range from 0 to 20 μM with the LOD of 140 nM. Further, it displayed excellent selectivity and anti-interference ability over many neutral molecules, metal ions, anions, and biological species. The ability to target lysosome and the response of hydrazine to this probe in a living cell was successfully tracked via fluorescence imaging. Graphical abstract: It is crucial to develop highly sensitive and selective probes toward hydrazine because it is a class of highly toxic and pollutant compound. Herein, using fracture of carbon carbon double bond and dissociation of amide by hydrazine, a novel off-on fluorescent probe was developed for hydrazine. The probe can quantitatively detect hydrazine in concentration range from 0 to 20 μM with the LOD of 140 nM. Further, it displayed excellent selectivity and anti-interference ability over many neutral molecules, metal ions, anions, and biological species. The response of hydrazine to this probe in a living cell was successfully tracked via fluorescence imaging. Highlights: A highly selective fluorescent probe for hydrazine shows off-on property. The probe can quantitativelyAbstract: It is crucial to develop highly sensitive and selective probes toward hydrazine because it is a class of highly toxic and pollutant compound. Herein, using fracture of carbon carbon double bond and dissociation of amide by hydrazine, a novel off-on fluorescent probe was developed for hydrazine. The probe can quantitatively detect hydrazine in concentration range from 0 to 20 μM with the LOD of 140 nM. Further, it displayed excellent selectivity and anti-interference ability over many neutral molecules, metal ions, anions, and biological species. The ability to target lysosome and the response of hydrazine to this probe in a living cell was successfully tracked via fluorescence imaging. Graphical abstract: It is crucial to develop highly sensitive and selective probes toward hydrazine because it is a class of highly toxic and pollutant compound. Herein, using fracture of carbon carbon double bond and dissociation of amide by hydrazine, a novel off-on fluorescent probe was developed for hydrazine. The probe can quantitatively detect hydrazine in concentration range from 0 to 20 μM with the LOD of 140 nM. Further, it displayed excellent selectivity and anti-interference ability over many neutral molecules, metal ions, anions, and biological species. The response of hydrazine to this probe in a living cell was successfully tracked via fluorescence imaging. Highlights: A highly selective fluorescent probe for hydrazine shows off-on property. The probe can quantitatively detect hydrazine in the concentration range from 0 to 20 μM. The detection limit on fluorescence response of the probe can be as low as 140 nM. … (more)
- Is Part Of:
- Dyes and pigments. Volume 147(2017)
- Journal:
- Dyes and pigments
- Issue:
- Volume 147(2017)
- Issue Display:
- Volume 147, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 147
- Issue:
- 2017
- Issue Sort Value:
- 2017-0147-2017-0000
- Page Start:
- 152
- Page End:
- 159
- Publication Date:
- 2017-12
- Subjects:
- Fluorescent probe -- Off-on -- 1, 8-naphthalimde -- Hydrazine -- Fluorescence imaging
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.2017.08.010 ↗
- 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:
- 4647.xml