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Issue 4, 2017
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Lanthanide complexes involving multichelating TTF-based ligands

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Abstract

The reaction between the 2-{TTF-fused-1H-benzimidazol-2-yl}pyridine alkylated with either the di-(pyrazol-1-yl)-4-pyridyl (L1) or dimethyl-2,2′-bipyridine (L2) moiety and 1 equiv. of Ln(hfac)3·2H2O (LnIII = DyIII and YbIII) leads to three dinuclear complexes of formula [Yb2(hfac)6(L1)]·2(CH2Cl2)·C6H14 (1) and [Ln2(hfac)6(L2)]·CH2Cl2 (LnIII = YbIII (2) and DyIII (3)). The X-ray structures highlight square antiprism (D4d symmetry) and spherical tricapped trigonal prism (D3h) for the eight- and nine-coordinated lanthanide ions, respectively. Irradiation of the lowest-energy HOMO → LUMO ILCT absorption band induced a 2F5/22F7/2 Yb-centered emission for 1 and 2. Both YbIII ions displayed similar emissions in 2 while two distinct emissions, attributed to the two YbIII ions because of their different coordination environments, were observed in 1. Slow magnetic relaxation is detected by dynamic magnetic measurements for 3 with a measured relaxation time τ0 = 3.7(1.3) × 10−7 s and an energy barrier Δ = 39.6(2) cm−1. Taking into account the environment of both DyIII ions in 3, it was expected that both metallic centers displayed similar dynamic magnetic behavior. The latter was rationalized by ab initio CASSCF/SI-SO calculations.

Graphical abstract: Lanthanide complexes involving multichelating TTF-based ligands

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Supplementary files

Article information


Submitted
30 Nov 2016
Accepted
10 Jan 2017
First published
12 Jan 2017

Inorg. Chem. Front., 2017,4, 604-617
Article type
Research Article

Lanthanide complexes involving multichelating TTF-based ligands

S. Speed, M. Feng, G. Fernandez Garcia, F. Pointillart, B. Lefeuvre, F. Riobé, S. Golhen, B. Le Guennic, F. Totti, Y. Guyot, O. Cador, O. Maury and L. Ouahab, Inorg. Chem. Front., 2017, 4, 604
DOI: 10.1039/C6QI00546B

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