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Highly sensitive and selective fluorescent monomer/polymer probes for Hg2+ and Ag+ recognition and imaging of Hg2+ in living cells
The detection of heavy metals such as Hg 2+ and Ag + is important and urgent. In this work, – NO 2 /– NH 2 /C=S boron dipyrromethene small molecular derivatives were synthesized at first. Then they were incorporated into polymer chains. The macromolecular fluorescent probes were obtained via Sonogas...
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Published in: | Analytical and bioanalytical chemistry 2020-02, Vol.412 (4), p.881-894 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The detection of heavy metals such as Hg
2+
and Ag
+
is important and urgent. In this work, – NO
2
/– NH
2
/C=S boron dipyrromethene small molecular derivatives were synthesized at first. Then they were incorporated into polymer chains. The macromolecular fluorescent probes were obtained via Sonogashira reaction using the small molecular probes as building blocks. The as-prepared small-molecule fluorescent probe
BO3
exhibits high sensing performance for Hg
2+
. By introducing it into macromolecules, the sensing ability still remains, and even more, the recognition performance is improved. The macromolecular fluorescent probes
P1
,
P2
, and
P3
also have high recognition ability for Ag
+
with a binding ratio of 2:1 (metal ion to probe ratio). Through the study of the sensing mechanism and the recycling experiments, it is found that the probes responded by the photo-induced electron transfer mechanism and can be recycled and reused. At the same time,
BO3
,
P2
, and
P3
show excellent recognition performance for Hg
2+
in living cells and zebrafish. Living cell imaging experiments indicated that these fluorescent probes had good cell membrane permeability and low cytotoxicity, and could realize bioimaging of Hg
2+
. Therefore, the application value of these fluorescent probes could be enlarged.
Graphical abstract |
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ISSN: | 1618-2642 1618-2650 |
DOI: | 10.1007/s00216-019-02297-w |