Journal
POLYMER CHEMISTRY
Volume 6, Issue 23, Pages 4279-4289Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5py00390c
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [51173044]
- Research Innovation Program of SMEC [14ZZ065]
- Shanghai Pujiang Program [14PJ1402600]
- State Key Laboratory of Materials-Oriented Chemical Engineering
- Fundamental Research Funds for the Central Universities
Ask authors/readers for more resources
We herein reported a click strategy to fabricate two kinds of colorimetric and turn-on fluorescent dual-modal mercury sensors (PEG-DMS) based on the styryl BODIPY scaffold attached to a hydrophilic polymer PEG, where the PEG chain could effectively improve the water solubility of these two mercury sensors and mean that their Hg2+ detection could be performed in pure water, while their corresponding small molecular precursor DMS could only detect Hg2+ in the mixed medium with a large amount of organic solvent. It is interesting that PEG-DMS exhibits an excellent spectral response to Hg2+ by inhibiting the intramolecular charge transfer (ICT) effect from the Hg2+ specific ligand, dithia-dioxa-aza cyclo-pentadecane, to the BODIPY core. Upon addition of Hg2+, a significant fluorescence enhancing property in conjunction with a visible colorimetric change can be observed. These two sensors are highly selective for Hg2+ over other common cations, whereas PEG-DMS1 with one Hg2+ binding ligand exhibits higher sensitivity than PEG-DMS2 with two Hg2+ binding ligands. Additionally, the sensor could be used as a potential imaging reagent for the detection of Hg2+ uptake in HeLa cells as revealed by confocal laser scanning microscopy (CLSM).
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available