Four super water-stable lanthanide-organic frameworks with active uncoordinated carboxylic and pyridyl groups for selective luminescence sensing of Fe(3.)
Four super water-stable isostructural lanthanide-organic frameworks, [Ln(HL)(H2O)2]n·2H2O (1-Ln) (Ln = Eu, Tb, Nd and Sm), have been successfully synthesized under hydrothermal conditions with 3,5-di(2,4-dicarboxylphenyl)pyridine (H4L) and Ln(NO3)3·6H2O. 1-Ln shows a novel 2D layered structure with...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2015-08, Vol.44 (29), p.13325-13330 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Four super water-stable isostructural lanthanide-organic frameworks, [Ln(HL)(H2O)2]n·2H2O (1-Ln) (Ln = Eu, Tb, Nd and Sm), have been successfully synthesized under hydrothermal conditions with 3,5-di(2,4-dicarboxylphenyl)pyridine (H4L) and Ln(NO3)3·6H2O. 1-Ln shows a novel 2D layered structure with uncoordinated carboxylic and pyridyl groups pointing to the interior of interlayer channels. The luminescent properties of 1-Eu in the solid state and one steeped in aqueous solution have been measured, which show excellent luminescence and good luminescent stability in water. Next 1-Eu was chosen as a probe for sensing different metal ions. Consequently, 1-Eu exhibits a highly selective response to Fe(3+) through the luminescence quenching effect in aqueous solutions. The probable mechanisms of the quenching effects have been investigated in detail. |
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ISSN: | 1477-9234 |
DOI: | 10.1039/c5dt01421b |