Slow Magnetic Relaxation and Luminescence Properties in Tetra β-Diketonate Lanthanide(III) Complexes

Author:

Speed Saskia1ORCID,Tubau Ànnia1ORCID,Vicente Ramon1ORCID,Castro Eva1,Font-Bardia Mercè2

Affiliation:

1. Departament de Química Inorgànica i Orgànica, Universitat de Barcelona, Martí i Franquès 1-11, E-08028 Barcelona, Spain

2. Departament de Mineralogia, Cristal·lografia i Dipòsits Minerals and Unitat de Difracció de R-X, Centre Científic i Tecnològic de la Universitat de Barcelona (CCiTUB), Universitat de Barcelona, Solé i Sabarís 1-3, E-08028 Barcelona, Spain

Abstract

The reaction of [Ln(btfa)3(H2O)2] (btfa- = 4,4,4-trifluoro-1-phenyl-1,3-butanedionate) with additional 4,4,4-trifluoro-1-phenyl-1,3-butanedione (Hbtfa) and acridine (Acr) in ethanol allows the isolation of the mononuclear compounds HAcr[Nd(btfa)4]·EtOH, (1) and HAcr[Ln(btfa)4], Ln = Dy (2) and Yb (3); HAcr+ = acridinium cation. Magnetic measurements indicate that complexes 1–3 show field-induced single-ion magnet behavior with anisotropy energy barriers and preexponential factors of Ueff = 20.7 cm−1, τ0 = 24.5 × 10−8 s; Ueff = 40.5 cm−1, τ0 = 8.6 × 10−10 s and Ueff = 22.7 cm−1, τ0 = 8.4 × 10−8 s, for 1–3 respectively. The solid-state luminescence emission in the NIR region shows efficient energy transfer from the 4,4,4-trifluoro-1-phenyl-1,3-butanedionate ligands to the central Ln3+ ion in the case of compounds 1 and 3.

Funder

Ministry of Economy, Industry and Competitiveness

Publisher

MDPI AG

Subject

Materials Chemistry,Chemistry (miscellaneous),Electronic, Optical and Magnetic Materials

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