A series of selective and sensitive fluorescent sensors based on a thiophen-2-yl-benzothiazole unit for Hg2+. (14th January 2016)
- Record Type:
- Journal Article
- Title:
- A series of selective and sensitive fluorescent sensors based on a thiophen-2-yl-benzothiazole unit for Hg2+. (14th January 2016)
- Main Title:
- A series of selective and sensitive fluorescent sensors based on a thiophen-2-yl-benzothiazole unit for Hg2+
- Authors:
- Mei, Qunbo
Tian, Ruqiang
Shi, Yujie
Hua, Qingfang
Chen, Chen
Tong, Bihai - Abstract:
- Abstract : Different types of fluorescent probes for Hg 2+ based on the 5-thiophen-2-yl-benzothiazole derivatives (TBT, CTBT, DTBT andNTBT ) were realized by changing the subsituents, including the fluorescence quenching probe, the fluorescence enhancement probe and the ratiometric fluorescent probe. Abstract : Different types of fluorescent probes for Hg 2+ based on the 5-thiophen-2-yl-benzothiazole derivatives (TBT, 2-thiophen-2-yl-benzothiazole;CTBT, 9-(5-benzothiazol-2-yl-thiophen-2-yl)-9 H -carbazole;DTBT, 2-(5-acenaphthen-5-yl-thiophen-2-yl)-benzothiazole; andNTBT, 6-(5-benzothiazol-2-yl-thiophen-2-yl)-2-hexyl-benzo[de]isoquinoline-1, 3-dione) were realized by changing the subsituents. Multisignaling changes were observed through UV-vis absorption and fluorescence spectra upon addition of Hg 2+ . The addition of Hg 2+ onTBT induced a remarkable OFF/ON-type fluorescence signaling behavior. With the introduction of electron-donating carbazole, the detection behavior ofCTBT was just the reverse of whatTBT displayed, while a ratiometric fluorescent probe based onDTBT for Hg 2+ was prepared by introducing the weak electron-drawing group acenaphthene. Moreover, the dichloromethane solution ofCTBT andDTBT showed a distinct color change from colorless to yellow with the addition of Hg 2+, which indicated that these two probes would facilitate the naked-eye detection of Hg 2+ . However, both UV-vis absorption and fluorescence spectra ofNTBT with strong electron-withdrawingAbstract : Different types of fluorescent probes for Hg 2+ based on the 5-thiophen-2-yl-benzothiazole derivatives (TBT, CTBT, DTBT andNTBT ) were realized by changing the subsituents, including the fluorescence quenching probe, the fluorescence enhancement probe and the ratiometric fluorescent probe. Abstract : Different types of fluorescent probes for Hg 2+ based on the 5-thiophen-2-yl-benzothiazole derivatives (TBT, 2-thiophen-2-yl-benzothiazole;CTBT, 9-(5-benzothiazol-2-yl-thiophen-2-yl)-9 H -carbazole;DTBT, 2-(5-acenaphthen-5-yl-thiophen-2-yl)-benzothiazole; andNTBT, 6-(5-benzothiazol-2-yl-thiophen-2-yl)-2-hexyl-benzo[de]isoquinoline-1, 3-dione) were realized by changing the subsituents. Multisignaling changes were observed through UV-vis absorption and fluorescence spectra upon addition of Hg 2+ . The addition of Hg 2+ onTBT induced a remarkable OFF/ON-type fluorescence signaling behavior. With the introduction of electron-donating carbazole, the detection behavior ofCTBT was just the reverse of whatTBT displayed, while a ratiometric fluorescent probe based onDTBT for Hg 2+ was prepared by introducing the weak electron-drawing group acenaphthene. Moreover, the dichloromethane solution ofCTBT andDTBT showed a distinct color change from colorless to yellow with the addition of Hg 2+, which indicated that these two probes would facilitate the naked-eye detection of Hg 2+ . However, both UV-vis absorption and fluorescence spectra ofNTBT with strong electron-withdrawing substituents showed no obvious change upon addition of Hg 2+ . It would be concluded that the electronic properties of the molecule was one of the vital factors in designing chemosensor molecules. … (more)
- Is Part Of:
- New journal of chemistry. Volume 40:Number 3(2016:Mar.)
- Journal:
- New journal of chemistry
- Issue:
- Volume 40:Number 3(2016:Mar.)
- Issue Display:
- Volume 40, Issue 3 (2016)
- Year:
- 2016
- Volume:
- 40
- Issue:
- 3
- Issue Sort Value:
- 2016-0040-0003-0000
- Page Start:
- 2333
- Page End:
- 2342
- Publication Date:
- 2016-01-14
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c5nj02259b ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 852.xml