A {Gd12Na6} Molecular Quadruple-Wheel with a Record Magnetocaloric Effect at Low Magnetic Fields and Temperatures.

Reaction of Gd(OAc)3·4H2O, salicylaldehyde and CH3ONa in MeCN/MeOH affords [Gd12Na6(OAc)25(HCO2)5(CO3)6(H2O)12]·9H2O.0.5MeCN (1·9H2O.0.5MeCN), whose structure describes a quadruple-wheel consisting of two {Na3} and two {Gd6} rings. The magnetic properties of 1 reveal very weak antiferromagnetic interactions between the GdIII ions, which give rise to a record magnetocaloric effect at low applied magnetic fields and low temperatures. The magnetic entropy change reaches -ΔSm= 29.3 J kg-1 K-1 for full demagnetization from B = 1 T at T = 0.5 K.

A ferromagnetically coupled pseudo-calixarene [Co16] wheel that self-assembles as a tubular network of capsules.

Reaction of Co(OAc)2·4H2O and Hsal in a basic MeCN solution affords the hexadecanuclear wheel [Co16(sal)16(OAc)16]·16MeCN (1·16MeCN) that displays ferromagnetic nearest neighbour exchange and has pseudo-calixarene character. Symmetry equivalent wheels self-assemble to form remarkable tubular networks of capsules in the extended structure.

Constructing "Closed" and "Open" {Mn8} Clusters.

Use of the 1,3,5-tri(2-hydroxyethyl)-1,3,5-triazacyclohexane ligand, LH3, in manganese chemistry affords access to two structurally related {Mn8} clusters: a "closed" {MnIII 6MnII 2} puckered square wheel of formula [Mn8L2(LH)O3(OH)2(MeO)2Br(imH)(H2O)3](Br)3 (1; imH = imidazole) and an "open" {MnIII 8} rod of formula [MnΙΙΙ 8L2O4(aibH)2(aib)2(MeO)6(MeOH)2](NO3)2 (2, aibH = 2-amino-isobutyric acid). In each case the triaza ligands, L/LH, direct the formation of {Mn3} triangles with their N atoms preferentially bonding to the Jahn-Teller axes of the MnIII ions. Subsequent self-assembly is dependent on the anion of the Mn salt and the identity of the organic coligand employed-the terminally bonded imidazole and the chelating/bridging amino acid. The {Mn3} triangles fold up on themselves in 1, forming a wheel. However, the syn, syn-bridging carboxylates in 2 prevent this from happening, instead directing the formation of a linear rod. Magnetic susceptibility and magnetization measurements reveal competing ferro- and antiferromagnetic interactions in both complexes, the exchange being somewhat weaker in 1 due to the presence of MnII ions.

A [Mn18] wheel-of-wheels.

A [Mn18] wheel of wheels is obtained from the reaction of MnBr2·4H2O and LH3 in MeOH. The metallic skeleton reveals two asymmetric [MnIII6MnII2] square wheels connected into a larger wheel via two MnII ions. Magnetic susceptibility and magnetisation data reveal competing exchange interactions, supported by computational studies.

The first amino acid bound manganese-calcium clusters: a {[MnCa]2} methylalanine complex, and a [MnCa] trigonal prism.

An amino acid containing octanuclear heterometallic {[MnCa]2} cluster has been synthesized, alongside a structurally-related trigonal prismatic [MnCa]2+ cage.

Dodecanuclear [Mn6(III)Ln6(III)] species: synthesis, structures and characterization of magnetic relaxation phenomena.

The use of H3L (= 2-(ß-naphthalideneamino)-2-hydroxymethyl-1-propanol) in mixed-metal manganese-lanthanide carboxylate cluster chemistry has led to the isolation of two new dodecametallic heteronuclear isostructural [Mn6(III)Ln6(III)] complexes (Ln = Gd, Dy), with the Dy analogue displaying temperature and frequency dependent out-of-phase signals suggesting possible single molecule magnetism behaviour.

A family of [Mn(III)6Ln(III)2] rod-like clusters.

Employment of H3L (= 2-(ß-naphthalideneamino)-2-hydroxymethyl-1-propanol) in mixed-metal manganese-lanthanide cluster chemistry has led to the isolation of five new octametallic heteronuclear isostructural [Mn(III)6Ln(III)2] complexes. More specifically, the reaction of Mn(ClO4)2·6H2O with H3L and the corresponding lanthanide nitrate in MeCN in the presence of a base, NEt3, yielded four complexes with the general formula [Mn(III)6Ln(III)2O2(OH)2(H2O)2(HL)6(NO3)6]·6MeCN·0.5H2O (Ln: Gd, 1·6MeCN·0.5H2O; Tb, 2·6MeCN·0.5H2O; Dy, 3·6MeCN·0.5H2O; Er, 4·6MeCN·0.5H2O). Furthermore, the Y(III) analogue, [Mn(III)6Y(III)2O2(OH)2(H2O)2(HL)6(NO3)6]·6MeCN·0.5H2O (5·6MeCN·0.5H2O), was also synthesized in the same manner. All five clusters describe a central rod-like topology consisting of four face-sharing defective cubane metallic units, forming a planar hexametallic [Mn(III)4Ln(III)2] core, which is further capped by two Mn(III) ions. Dc magnetic susceptibility studies in the 5-300 K range for complexes 1-5 reveal the presence of dominant antiferromagnetic exchange interactions within the metallic clusters, while ac magnetic susceptibility measurements show temperature and frequency dependent out-of-phase signals for the Dy(III) analogue (3·6MeCN·0.5H2O), suggesting potential single molecule magnetism character. Furthermore, the Y(III) analogue yielded a diamagnetic ground-state for the [Mn(III)6] core, thus proving that the SMM character displayed by 3·6MeCN·0.5H2O is due to the presence of the Dy(III) centres.