Rhodol Derivatives as Selective Fluorescent Probes for the Detection of HgII Ions and the Bioimaging of Hypochlorous Acid. Issue 2 (6th December 2017)
- Record Type:
- Journal Article
- Title:
- Rhodol Derivatives as Selective Fluorescent Probes for the Detection of HgII Ions and the Bioimaging of Hypochlorous Acid. Issue 2 (6th December 2017)
- Main Title:
- Rhodol Derivatives as Selective Fluorescent Probes for the Detection of HgII Ions and the Bioimaging of Hypochlorous Acid
- Authors:
- Li, Ling
Wang, Shu
Lan, Hongxia
Gong, Guiyi
Zhu, Yifan
Tse, Yu Chung
Wong, Keith Man‐Chung - Abstract:
- Abstract: Two sensors, 1 with a spirolactone group and2 with a spirolactam group containing a phenyl isothiocyanate moiety, based on rhodol, were designed and synthesized in order to obtain materials with excellent optical properties for the detection of environmentally and biologically important Hg 2+ and hypochlorous acid (HClO) ions. The crystal structure of1 revealed two moieties, a rhodamine‐like portion with a spirolactone and a fluorescein‐like portion without a spirolactone. In the absence of analyte, 1 produced an optical output with a maximum absorption and emission at 475 and 570 nm, respectively, which was attributed to the fluorescein‐like moiety without a spirolactone. In contrast, the rhodamine‐like moiety containing a spirolactone was activated by the addition of H + or Hg 2+ ions, and1 yielded new absorption and emission peaks at 530 and 612 nm, respectively. Further functionalization with a phenyl isothiocyanate group afforded2, a fluorescent probe for HClO. High selectivity and sensitivity towards the hypochlorite ion were anticipated, owing to the stoichiometric and irreversible formation of a thiosemicarbazide group, which led to dramatic fluorescence responses. With good functionality at physiological pH, probe2 was successfully used to image HClO in HeLa cells. Abstract : Get the picture : A series of rhodol derivatives with extended π conjugation are reported to give selective sensing properties. Those functionalized with a phenyl isothiocyanate groupAbstract: Two sensors, 1 with a spirolactone group and2 with a spirolactam group containing a phenyl isothiocyanate moiety, based on rhodol, were designed and synthesized in order to obtain materials with excellent optical properties for the detection of environmentally and biologically important Hg 2+ and hypochlorous acid (HClO) ions. The crystal structure of1 revealed two moieties, a rhodamine‐like portion with a spirolactone and a fluorescein‐like portion without a spirolactone. In the absence of analyte, 1 produced an optical output with a maximum absorption and emission at 475 and 570 nm, respectively, which was attributed to the fluorescein‐like moiety without a spirolactone. In contrast, the rhodamine‐like moiety containing a spirolactone was activated by the addition of H + or Hg 2+ ions, and1 yielded new absorption and emission peaks at 530 and 612 nm, respectively. Further functionalization with a phenyl isothiocyanate group afforded2, a fluorescent probe for HClO. High selectivity and sensitivity towards the hypochlorite ion were anticipated, owing to the stoichiometric and irreversible formation of a thiosemicarbazide group, which led to dramatic fluorescence responses. With good functionality at physiological pH, probe2 was successfully used to image HClO in HeLa cells. Abstract : Get the picture : A series of rhodol derivatives with extended π conjugation are reported to give selective sensing properties. Those functionalized with a phenyl isothiocyanate group can serve as a fluorescent probe for bioimaging of endogenous HClO within HeLa cells. … (more)
- Is Part Of:
- ChemistryOpen. Volume 7:Issue 2(2018)
- Journal:
- ChemistryOpen
- Issue:
- Volume 7:Issue 2(2018)
- Issue Display:
- Volume 7, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 7
- Issue:
- 2
- Issue Sort Value:
- 2018-0007-0002-0000
- Page Start:
- 136
- Page End:
- 143
- Publication Date:
- 2017-12-06
- Subjects:
- chemosensor -- fluorescence -- hypochlorous acid -- mercury -- rhodol
Chemistry -- Periodicals
540
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2191-1363 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/open.201700154 ↗
- Languages:
- English
- ISSNs:
- 2191-1363
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5894.xml