Influence of antisymmetric exchange interaction on quantum tunneling of magnetization in a dimeric molecular magnet Mn6

We present magnetization measurements on the single molecule magnet Mn6, revealing various tunnel transitions inconsistent with a giant-spin description. We propose a dimeric model of the molecule with two coupled spins S=6, which involves crystal-field anisotropy, symmetric Heisenberg exchange interaction, and antisymmetric Dzyaloshinskii-Moriya exchange interaction. We show that this simplified model of the molecule explains the experimentally observed tunnel transitions and that the antisymmetric exchange interaction between the spins gives rise to tunneling processes between spin states belonging to different spin multiplets.Comment: 5 pages, 4 figure

Pseudopeptidic ligands: exploring the self-assembly of isopthaloylbisglycine (H2IBG) and divalent metal ions

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Assessment of How Natural Stand Structure for Narrow Endemic Cedrus brevifolia Henry Supports Silvicultural Treatments for Its Sustainable Management

Cedrus brevifolia Henry is a narrow endemic tree species of Cyprus flora. The objectives of this study are to develop silvicultural treatments for the conservation of the species formations based on the stand structure analysis of C. brevifolia natural forest and to present the characteristics of the first application of the treatments through silvicultural interventions. Six structural types were distinguished in C. brevifolia formations in the study area located in the state forest of Paphos. For each structural type, six circular plots of approximately 500 m2 were established. In each plot, various measurements and estimations were recorded. Then, silvicultural interventions were applied in the plots of the mixed C. brevifolia formations. In the formations of C. brevifolia a great number of trees grow in the understory. In the very productive and in the poorly productive sites C. brevifolia occurs only in pure formations. The basal area of C. brevifolia in pure formations ranges from 19.04 m2·ha-1 in poorly productive sites to 38.49 m2·ha-1 in fairly productive sites. Cedrus brevifolia is the most competitive species of the study area as a result of both shade tolerance and the wide range of its site sensitivity behavior. The climax of the study area are the pure stands of C. brevifolia having an understory of Quercus alnifolia Poech and a sparse occurrence of Pinus brutia Ten., mainly in moderately productive sites. Forest practice has to, as much as possible, unite species formations in order to create extensive areas of C. brevifolia formations

Assembling hexagonal‐bipyramidal {Mn8Zn2} and {Mn8Zn4} clusters

Reaction between Mn(NO3)2 ⋅ 6H2O, Zn(NO3)2 ⋅ 6H2O, 1,3,5-tri(2-hydroxyethyl)-1,3,5-triazacyclohexane (H3L) and pyrazole in MeOH under basic conditions leads to the formation of the decanuclear complex [MnIII6MnII2ZnII2(L)2(pyr)4O4(OH)4(NO3)2 (MeOH)2(H2O)4](NO3)2 ⋅ Η2Ο (1 ⋅ Η2Ο). The metallic core of the cationic cluster consists of a central hexagonal-bipyramidal {MnIII4MnII2ZnII2} unit connected to two peripheral trivalent Mn centers arranged in a “trans” fashion, with one MnIII center lying above and one MnIII center below the hexagonal plane. Replacing Mn(NO3)2 ⋅ 6H2O with MnBr2 ⋅ 4H2O and repeating the same reaction leads to the formation of the related, neutral decanuclear complex [MnIII6MnII2ZnII2(L)2(pyr)4O4(OH)4Br4(H2O)2] (2), displaying the same metallic core as 1. Addition of THF to the reaction mixture that produces (2) affords the neutral dodecanuclear complex [MnIII6MnII2ZnII4(L)2(pyr)6O4(OH)4Br6(H2O)4] ⋅ 8THF (3 ⋅ 8THF), whose metallic skeleton retains the central hexagonal-bipyramidal {MnIII4MnII2ZnII2} unit found in 1 and 2 but is now connected to two peripheral {MnIIIZnII} units. Magnetic susceptibility and magnetization measurements carried out in the T=2–300 K temperature range and in fields up to B=7.0 T for all three complexes reveal dominant antiferromagnetic exchange interactions

Attempting to understand (and control) the relationship between structure and magnetism in an extended family of Mn-6 single-molecule magnets

International audienceThe synthesis and characterisation of a large family of hexametallic [Mn-6(III)] Single-Molecule Magnets of general formula [(Mn6O2)-O-III(R-sao)(6)(X)(2)(Sol)(4-6)] (where R = H, Me, Et; X = -O2CR'(R' = H, Me, Ph etc) or Hal(-); sol = EtOH, MeOH and/or H2O) are presented. We show how deliberate structural distortions of the [Mn3O] trinuclear moieties within the [Mn-6] complexes are used to tune their magnetic properties. These findings highlight a qualitative magneto-structural correlation whereby the type (anti- or ferromagnetic) of each Mn-2 pairwise magnetic exchange is dominated by the magnitude of each individual Mn-N-O-Mn torsion angle. The observation of magneto-structural correlations on Such large polymetallic complexes is rare and represents one of the largest studies of this kind