A New Nitronyl‐Nitroxide Ligand for Designing Binuclear Ln III Complexes: Syntheses, Crystal Structures, Magnetic and EPR Studies - Archive ouverte HAL
Article Dans Une Revue European Journal of Inorganic Chemistry Année : 2022

A New Nitronyl‐Nitroxide Ligand for Designing Binuclear Ln III Complexes: Syntheses, Crystal Structures, Magnetic and EPR Studies

Résumé

A new nitronyl-nitroxide ligand (H2L) featuring alcoholic and phenolic groups has been synthesised starting from 2-hydroxy-3-(hydroxymethyl)-5-methylbenzaldehyde (A). Using this ligand, three 2p–4 f binuclear complexes have been obtained and crystallographically characterized: [Ln2(HL)2(hfac)4], (Ln=Gd 1, Tb 2, Dy 3). Apart from the desired compounds, two by-products have been isolated as a molecular alloy containing an intermediate bearing hydroxylamino and N-oxide groups, i. e. (1-hydroxy-2-(2-hydroxy-3-(hydroxymethyl)-5-methylphenyl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazole 3-oxide, B, and the imino-nitroxide derivative, C. This system was characterized by single crystal X-ray diffraction, UV-VIS and EPR spectroscopy. During the synthesis of compounds 1–3, two other complexes have been obtained and characterized: [Ln(C)(hfac)3] (4, Ln=Tb) and [Ln2(A−H)2(hfac)4] (5, Ln=Tb), where (A−H) results from the deprotonation of the phenolic group in A. The synthetic procedure was optimized in order to obtain pure 1–3 complexes. The cryomagnetic properties of compounds 1–3 have been investigated. Continuous-wave (CW) electron paramagnetic resonance (EPR) measurements were carried out at X- and Q-band for compound 1. Time-dependent experiments were performed at three magnetic fields. Phase memory times, Tm, were found to be about 1000 ns at 6 K.
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Dates et versions

hal-03689254 , version 1 (30-06-2022)

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Mihai Răducă, Daniel Martins, Cristian Spinu, Mihaela Hillebrand, Floriana Tuna, et al.. A New Nitronyl‐Nitroxide Ligand for Designing Binuclear Ln III Complexes: Syntheses, Crystal Structures, Magnetic and EPR Studies. European Journal of Inorganic Chemistry, 2022, 2022 (16), pp.e202200128. ⟨10.1002/ejic.202200128⟩. ⟨hal-03689254⟩
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