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A bis-benzimidazole PMO ratiometric fluorescence sensor exhibiting AIEE and ESIPT for sensitive detection of Cu 2 .

Authors :
Hao X
Han S
Zhu J
Hu Y
Chang LY
Pao CW
Chen JL
Chen JM
Haw SC
Source :
RSC advances [RSC Adv] 2019 May 02; Vol. 9 (24), pp. 13567-13575. Date of Electronic Publication: 2019 May 02 (Print Publication: 2019).
Publication Year :
2019

Abstract

A novel bis-benzimidazole organic siloxane precursor (BBM-Si) was prepared, and was combined with tetraethylorthosilicate (TEOS) as a mixed Si source. Then, bridged periodic mesoporous organosilica (BBM-PMO) spherical nanoparticles were synthesized by co-condensation using cetyltrimethylammonium bromide (CTAB) as structure directing agent. The optical properties showed that BBM qualifies as an "aggregation induced emission enhanced" (AIEE) molecule, exhibiting characteristics of excited-state intramolecular proton transfer (ESIPT), such as a large Stokes shift and dual fluorescence emission. For the BBM-PMO materials, the silica skeleton provides a rigid environment that limits molecular rotation, resulting in improved fluorescence emission. In particular, the BBM-PMOs exhibited dual emission of the enol and keto forms, achieving a ratiometric response to Cu <superscript>2+</superscript> with high sensitivity and selectivity in a broad pH range. Additionally, the limit of detection was as low as 7.15 × 10 <superscript>-9</superscript> M in aqueous solution. The X-ray absorption near-edge spectroscopy (XANES) showed the coordination structure through the interaction between copper ions and N atoms of benzimidazole in the BBM-PMO coordinated to Cu <superscript>2+</superscript> . These results demonstrate that BBM-PMO hybrid materials have potential applications in the fields of bio-imaging and environmental monitoring.<br />Competing Interests: There are no conflicts to declare.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2046-2069
Volume :
9
Issue :
24
Database :
MEDLINE
Journal :
RSC advances
Publication Type :
Academic Journal
Accession number :
35519599
Full Text :
https://doi.org/10.1039/c9ra00892f