Fluorimetric detection of phosphates in water using a disassembly approach: a comparison of FeIII-, ZnII-, MnII- and MnIII-salen complexes

Abstract: Details of the reaction sequence used for the fluorimetric detection of phosphates by disassembly of transition metal Schiff base complexes were investigated for [FeIII(salen)(H2O)]+, [ZnII(salen)], [MnII(salen)(H2O)2], and [MnIII(salen)(H2O)]+. The reactivity of these compounds towards phosphorus oxoanions of differing charge, number of donor atoms and steric hindrance was detected by UV/Vis and fluorescence spectroscopy in both aprotic organic and aqueous media. Selectivity of [FeIII(salen)(H2O)]+ towards pyrophosphate over all other tested phosphorus‐containing analytes was strongly supported. [ZnII(salen)] showed a faster reactivity but was much less selective. In contrast, [MnIII(salen)(H2O)]+ proved to be more stable than the iron complex but generally showed little reactivity towards phosphorus oxoanions. The influence of the charge of the central atom was investigated using the MnII analogue [MnII(salen)(H2O)2]. As expected, the reduced charge resulted in a reactivity comparable to the ZnII complex in organic solution but lead to hydrolysis of the complex in water. Finally, the reaction products of [FeIII(salen)(H2O)]+ with phosphates were characterized by IR spectroscopy and mass spectrometry, providing further insights into the reaction mechanism of the disassembly process

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
Zeitschrift für anorganische und allgemeine Chemie. - 646, 13 (2020) , 933-939, ISSN: 1521-3749

Keyword
Komplexe
Phosphate
Detektion
Fluoreszenz
Mangan
Eisen
Zink

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2020
Creator

DOI
10.1002/zaac.202000045
URN
urn:nbn:de:bsz:25-freidok-1658219
Rights
Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 11:00 AM CEST

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Associated

Time of origin

  • 2020

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