Modulation of the spin crossover behaviour in four manganese(III) complexes through cation-anion interactions

Abstract

Here we report the synthesis, structural and magnetic characterization of a series of manganese(III) monomers, formulated as [Mn(L)]X with X = PF6¯ (1), BF4¯ (2), I¯ (3) and Br¯/NO3¯ (4). These four compounds have been prepared with a Schiff base ligand (H2L) formed by 1:2 condensation of eugenol scaffold aldehyde and N,N′-bis(3-aminopropyl)ethylene-diamine. The structure of compounds 1-4 shows in all cases the presence of the same [MnIII(L)]+ cation surrounded by different X ¯ anions. Interestingly, the anions play a key role in determining not only the symmetry and cation-anion packing, which are quite different in compound 1 compared to compounds 2-4, but also the magnetic properties of the [MnIII(L)]+ cation. Variable temperature magnetic measurements show that in compound 1 the MnIII centre is in the high spin S = 2 state at any temperature, whereas compounds 2-4 show a smooth and incomplete spin crossover (SCO) from the low spin (S = 1) to the high spin (S = 2) ground state in the temperature range 200-400 K. At 400 K the high spin fractions are around 31 %, 27 % and 42 % for compounds 2-4, respectively. Isothermal magnetization measurements at low temperatures confirm the spin ground states in all cases. The magnetic data can be very well reproduced with a simple monomeric S = 2 (in 1) or S = 1 (in 2 4, for the low spin state) model with a zero field splitting (ZFS) contribution (and a very weak intermolecular antiferromagnetic interaction in 2 and 4). Additionally, a detailed analysis of the structural parameters in compounds 2-4 shows that the Mn-N bond distances, the continuous Shape parameters, the trigonal distortion angles (Φ) and the octahedral distortion parameters (Σ) show a significant increase when the temperature is increased from 100 to 398 K, confirming the presence of an incomplete SCO between 100 and 398 K in compounds 2-4.