A Mn(iii) single ion magnet with tridentate Schiff-base ligands.

Single ion magnet behaviour is reported for a mononuclear Mn(iii) ion with tridentate Schiff-base ligands which exhibits a tetragonal Jahn-Teller elongation along the Namine-Mn-Namine axis and crystallises with two crystallographically distinct Mn(iii) cations (unit A and unit B). While magnetic measurements show a large and negative axial zero-field splitting (D = -4.73 cm(-1)), HF-EPR reveal two distinct large axial Ds (D = -4.60 cm(-1) for unit A and D = -4.18 cm(-1) for unit B), thus resulting in the largest D known to date for a Mn(iii) single ion magnet. AC magnetic measurements at 2000 Oe allowed determination of the energy barrier for spin reversal (10.19 K) and spin reversal relaxation time (1.476 × 10(-6) s) for the Mn(iii) ion. Computational studies were used to characterise the electronic structure and substantiate the zero field splitting in the Mn(iii) complex.

Slow magnetic relaxation mechanisms in erbium SIMs.

The magnetic properties of two similar Er(3+) complexes have been investigated. [Er(tpm)3(bipy)] (Htpm = 1,1,1-trifluoro-5,5-dimethyl-2,4-hexanedione and bipy = 2,2'-bipyridine) displays thermally activated slow relaxation of magnetisation under a zero direct-current (DC) field. Under an applied HDC field of 1000 G, [Er(tpm)3(bipy)] exhibits two thermally activated processes with energy barriers of 9 and 40 K, while [Er(tfa)3(bipy)] (Htfa = 4,4,4-trifluoro-1-(2-furyl)-1,3-butanedione) shows only one activated process with a barrier of 15 K. Both compounds are luminescent in the solid state, emitting in the near IR region.

Effect of the capping ligand on luminescent erbium(III) ß-diketonate single-ion magnets.

Erbium complexes featuring ß-diketonate ligand 2,4-hexanedione (Hh) and N,N-donor-ligands 2,2'-bipyridine (bipy), 5-nitro-1,10-phenanthroline (5NO2phen) and bathophenanthroline (bath) have been synthesized. The structures of the ternary complexes [Er(h)3(bipy)], [Er(h)3(5NO2phen)] and [Er(h)3(bath)] have been determined by single crystal X-ray diffraction. Excitation of the complexes in the ultraviolet region (337 nm) led to near infrared (NIR) luminescence at 1532 nm characteristic of the trivalent erbium ion in the three compounds, with an improved antenna effect in the 5-nitro-1,10-phenanthroline complex. The AC susceptibility studies conducted at frequencies ranging from 33 to 9995 Hz and at temperatures in the 1.7 to 10 K range revealed that the application of a static magnetic field induces a slow magnetic relaxation in all three compounds. The complex with the bulkier capping ligand (bathophenanthroline) exhibits the highest energy barrier U/k(B) = 23 K.

Ferromagnetic order in aged Co-doped TiO2 anatase nanopowders.

This paper reports on the ferromagnetic properties of aged Ti(1-x)CoxO(2-delta) anatase nanopowders with different Co contents (0.03 < or = x < or = 0.10). It is shown for the first time that aged Co:TiO2 anatase samples retain rather high values of magnetization (M), remanence (Mr) and coercivity (Hc) which provide strong evidence for a preserved long-range ferromagnetic order. Room temperature M, Mr and Hc values were measured in the ranges of [0.05, 0.79] microB/Co, [0.044, 0.096] microB/Co and [366.7,494.8]Oe, respectively, which are in the same range as in general reported either for newly prepared thin films or nanoparticles.