Synthesis and characterisation of new tripodal lanthanide complexes and investigation of their optical and magnetic propertiesElectronic supplementary information (ESI) available: NMR, SEM-EDS, ESI-mass, PXRD, emission and FT-IR spectra and magnetic studies. CCDC 1515525-1515528. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7dt02556d
This paper presents the synthesis of a tripodal ligand (H 3 L) via the Schiff base condensation of N , N -diethylsalicylaldehyde and tris(2-aminoethyl)amine. The neutral complexes of type [EuL], [GdL] and [DyL] were synthesized and characterized by FT-IR, SEM-EDS, PXRD, single crystal X-ray diffract...
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Sprache: | eng |
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Zusammenfassung: | This paper presents the synthesis of a tripodal ligand (H
3
L)
via
the Schiff base condensation of
N
,
N
-diethylsalicylaldehyde and tris(2-aminoethyl)amine. The neutral complexes of type [EuL], [GdL] and [DyL] were synthesized and characterized by FT-IR, SEM-EDS, PXRD, single crystal X-ray diffraction, CHN analysis and high resolution ESI-MS. X-ray crystallographic studies demonstrated that the heptadentate ligand incorporating a cavity pre-organized by hydrogen bonding binds the Ln(
iii
) ions to yield a face capped octahedral coordination geometry with three-fold symmetry. Photoluminescence studies show a typical Ln(
iii
) absorption character for the three complexes, with [EuL] demonstrating considerably stronger lanthanide-based luminescence peaks, and a Eu(
iii
) centered luminescence lifetime of 0.144 ± 0.01 ms. Temperature/field-dependent DC and temperature/frequency-dependent AC magnetic measurements carried out for the Dy(
iii
) complex indicated obvious magnetic anisotropy and suggested slow relaxation behaviour with considerable quantum tunnelling of the magnetization contribution.
The neutral complexes of type [EuL], [GdL] and [DyL] incorporating a heptadentate tripodal ligand were synthesized and their optical and magnetic properties have been investigated. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c7dt02556d |