Valence tautomeric transformation in the [CrCo] compound: exploration of cooperative interactions.

A crystal containing the heterometallic Cr-ligand-Co cluster with an unpaired electron on the ligand as a structural unit is examined. The developed model which describes the magnetic and polarizability characteristics of this crystal takes into account that the electron residing on the ligand can be transferred to the Co-ion, thus converting the diamagnetic ls-CoIII ion into the paramagnetic hs-CoII one. Since this transformation is accompanied by electron density redistribution and elongation of the Co-N bond lengths, the vibronic interaction of the Co-ion with totally symmetric displacements of the nearest surroundings and cooperative dipole-dipole and electron-deformational interactions are accounted for as well. The exchange interactions between the CrIII ion and the electron localized on the ligand as well as in the CrIII-hs-CoII pair are also included in consideration; the parameters of these interactions are estimated within the framework of the DFT method. Bistability in the magnetic and polarization characteristics is predicted for certain strengths of intra- and intercluster interactions in the crystal under study. Within the framework of the developed approach an explanation of the observed magnetic properties of the [Cr(SS-cth)(Co(RR-cth)(µ-dhbq))](PF6)2Cl crystal is given.

Charge-transfer-induced spin transitions in crystals containing cyanide-bridged Co-Fe clusters: role of intra- and intercluster interactions.

A theoretical model has been developed to explain at the electronic level the charge-transfer-induced spin transition (CTIST) in crystals based on cyano-bridged binuclear Fe-Co clusters. The CTIST is considered as a cooperative phenomenon (phase transformation) driven by the long-range electron-deformational interaction via the acoustic phonons field that is taken into account within the mean field approach. The model for CTIST includes also the metal-metal electron transfer and intracluster magnetic exchange. The conditions that favor the CTIST are discussed. The qualitative explanation of the experimental data is given.

A model of spin crossover in manganese(III) compounds: effects of intra- and intercenter interactions.

A microscopic approach to the problem of cooperative spin crossover in the [MnL2]NO3 crystal, which contains Mn(III) ions as structural units, is elaborated on, and the main mechanisms governing this effect are revealed. The proposed model also takes into account the splitting of the low-spin 3T1 (t(2)(4)) and high-spin 5E (t(2)(3)e) terms by the low-symmetry crystal field. The low-spin → high-spin transition has been considered as a cooperative phenomenon driven by interaction of the electronic shells of the Mn(III) ions with the all-around full-symmetric deformation that is extended over the crystal lattice via the acoustic phonon field. The model well explains the observed thermal dependencies of the magnetic susceptibility and the effective magnetic moment.