| Literature DB >> 28717898 |
Kun-Peng Wang1, Ju-Peng Chen1, Si-Jie Zhang1, Yang Lei1, Hua Zhong2, Shaojin Chen1, Xin-Hong Zhou1, Zhi-Qiang Hu3.
Abstract
The thiophene-modified rhodamine 6G (GYJ) has been synthesized as a novel chemosensor. The sensor has sufficiently high selectivity and sensitivity for the detection of Fe3+ and Al3+ ions (M3+) by fluorescence and ultraviolet spectroscopy with a strong ability for anti-interference performance. The binding ratio of M3+-GYJ complex was determined to be 2:1 according to the Job's plot. The binding constants for Fe3+ and Al3+ were calculated to be 3.91 × 108 and 5.26 × 108 M-2, respectively. All these unique features made it particularly favorable for cellular imaging applications. The obvious fluorescence microscopy experiments demonstrated that the probes could contribute to the detection of Fe3+ and Al3+ in related cells and biological organs with satisfying resolution. Graphical abstract GYJ has high selectivity and sensitivity for the detection of Fe(III) and Al(III) with the binding ratio of 2:1.Entities:
Keywords: Al3+; Cells; Fe3+; Fluorescence probe; Rhodamine 6G; Spirolactam opening
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Year: 2017 PMID: 28717898 DOI: 10.1007/s00216-017-0490-8
Source DB: PubMed Journal: Anal Bioanal Chem ISSN: 1618-2642 Impact factor: 4.142