Repozytorium

Lanthanide(III) complexes of N4O4 Schiff base macrocycle: luminescence and formation of heterodinuclear d-f complexes.

Autorzy

Paula Gawryszewska

Jerzy Lisowski

Rok wydania

2012

Czasopismo

Inorganica Chimica Acta

Numer woluminu

383

Strony

220-229

DOI

10.1016/j.ica.2011.11.012

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

The new macrocyclic Schiff base lanthanide(III) complexes of the formula [Ln(H 4 L)Cl 3 ]·nH 2 O (Ln=Pr(III), Nd(III), Sm(III), Gd(III), Dy(III), Ho(III), Er(III), Tm(III), Yb(III) and Lu(III)) have been synthesized in the template condensation of 1,3-diamino-2-hydroxypropane and 2,6-diformyl-4-methylphenol in the presence of the appropriate Ln(III) chlorides. The obtained compounds have been characterized in solution by NMR spectroscopy, and the 1 H and 13 C NMR spectra of [Pr(H 4 L)Cl 3 ]·H 2 O, [Nd(H 4 L)Cl 3 ]·H 2 O, [Sm(H 4 L)Cl 3 ]·H 2 O and [Yb(H 4 L)Cl 3 ]·4H 2 O complexes have been assigned on the basis of COSY, NOESY and HMQC techniques. The analysis of isotropic shifts of the paramagnetic Ln(III) derivatives indicate the unsymmetrical coordination of the lanthanide(III) ions within the macrocyclic ligand H 4 L. 1 H NMR spectroscopy has also been used to follow transformation of the [Ln(H 4 L)] 3+ complexes into heterodinuclear derivatives, [LnCo(H 2 L)] 3+ and [LnCo(HL)] 2+ . Emission and excitation spectra as well as luminescence decay time measurements (at 293 and 77K) were used to characterize the photophysical properties of the mononuclear Eu(III), Gd(III) and Yb(III) [Ln(H 4 L)Cl 3 ]·nH 2 O complexes in solid-state. Energy transfer from the ligand to the Yb(III) ions has been proved at both room temperature and 77K. The f–f luminescence of Nd(III) and Er(III) was not observed neither by the excitation through the ligand ( 1 π– 1 π ) nor the lanthanide ion absorption transitions both at 293 and 77K. In the case of Eu(III) complex the energy transfer only occurs at 77K, while at room temperature a thermally activated back energy transfer process from 5 D 0 Eu(III) excited state to the ligand triplet states has been proposed. The 4f–4f emission spectrum of Eu(III) in a low site symmetry with the dominating 5 D 07 F 4 transition has been demonstrated for the first time.

Słowa kluczowe

macrocycles, lanthanide complexes, Heterodinuclear complexes, NMR, photoluminescence

Adres publiczny

http://dx.doi.org/ 10.1016/j.ica.2011.11.012

Strona internetowa wydawcy

http://www.elsevier.com

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