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https://hdl.handle.net/2445/154386| Title: | Selective detection of Cu2+ and Co2+ in aqueous media: asymmetric chemosensors, crystal structure and spectroscopic studies |
| Author: | Dogaheh, Samira Gholizadeh Khanmohammadi, Hamid Sañudo Zotes, Eva Carolina |
| Keywords: | Fluorescència Ions metàl·lics Estructura cristal·lina (Sòlids) Fluorescence Metal ions Layer structure (Solids) |
| Issue Date: | 15-May-2017 |
| Publisher: | Elsevier B.V. |
| Abstract: | Two new azo-azomethine receptors, H2L1 and H2L2, containing hydrazine, naphthalene and different electron withdrawing groups, Cl and NO2, have been designed and synthesized for qualitative and quantitative detection of Cu2+ and Co2+ in aqueous media. The crystal structure of H2L1 is reported. The H2L1 was used as a chemosensor for selective detection of trace amount of Cu2+ in aqueous media. H2L2 was also applied to naked-eye distinction of Cu2+ and Co2+ from other transition metal ions in aqueous media. Detection limit of Cu2+ is 1.13 mu M and 1.26 mu M, in water, for H2L1 and H2L2, respectively, which are lower than the World Health Organization (WHO) recommended level. The binuclear Cu2+ and Co2+ complexes of the receptors have been also prepared and characterized using spectroscopic methods and MALDI-TOF mass analysis. Furthermore, the binding stoichiometry between the receptors upon the addition Cu2+ and Co2+ has been investigated using Job's plot. Moreover, the fluorescence emission spectra of the receptors and their metal complexes are also reported. (C) 2017 Elsevier B.V. All rights reserved. |
| Note: | Versió postprint del document publicat a: https://doi.org/10.1016/j.saa.2017.02.017 |
| It is part of: | Spectrochimica Acta Part A-Molecular and Biomolecular Spectroscopy, 2017, vol. 179, p. 32-41 |
| URI: | https://hdl.handle.net/2445/154386 |
| Related resource: | https://doi.org/10.1016/j.saa.2017.02.017 |
| ISSN: | 1386-1425 |
| Appears in Collections: | Articles publicats en revistes (Química Inorgànica i Orgànica) |
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| 674322.pdf | 1.3 MB | Adobe PDF | View/Open |
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