4.5 Article

A dual-functional Co(II) coordination polymer luminescent sensor: turn-off sensing acetylacetone and rare turn-on detection of ascorbic acid

期刊

INORGANICA CHIMICA ACTA
卷 527, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2021.120546

关键词

Coordination polymer (CP); Fluorescent sensor; Ascorbic acid; Acetylacetone

资金

  1. foundation of Key Sci-entific and Technological Project of Henan Province [212102210295, 212102310178]
  2. Henan Provincial Key Scientific Research Projects of Higher Education Institutions [19A150044]
  3. Nanhu Scholars Pro-gram for Young Scholars of XYNU

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This study presents a new Co(II) coordination polymer based on a semi-rigid tricarboxylate acid, which shows excellent chemical stability and can act as a fluorescent probe for sensitive detection of ascorbic acid and acetylacetone. The material exhibited high performance, sensitivity, selectivity, and reusability in the proposed sensing systems, with detection limits as low as 2.60 nM and 57.5 μM. The possible mechanisms were also discussed in detail.
One new Co(II) coordination polymer was prepared by the hydrothermal method based on a semi-rigid tricarboxylate acid, 4-(2',3'-dicarboxylphenoxy) benzoic acid (H3L) as [H(2)bpe][Co(HL)(2)(bpe)(H2O)(2)]center dot(H2O)(4) (1) (bpe = 1,2-bis(4-pyridyl) ethylene). This compound has been characterized by single crystal and powder X-ray diffraction, elemental analysis, IR spectra, thermogravimetric analysis, and fluorescent properties. In particular, it is found that compound 1 possesses excellent chemical stability. More importantly, this material could act as a novel turn-on fluorescent probe for highly selectively sensitizing ascorbic acid (AA) and turn-off' sensor for recognizing acetylacetone (Hacac) in the aqueous phase. Both proposed sensing systems showed excellent performance with high sensitivity and selectivity as well as good reusability. The detection limits are as low as 2.60 nM and 57.5 mu M, respectively. In addition, the possible mechanism were detailedly discussed.

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