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Lanthanide phthalocyaninates with paramagnetic REE(III) ions reveal single-molecular magnetic (SMM) behaviour [1,2]. The magnetic properties of usual double- or triple-decker sandwich complexes can be tuned by increasing the number of decks. Earlier in our group it was shown that triple-decker phthalocyaninates (1) with one terminal crown-substituted deck is capable for dimerization in solution in the presence of potassium ions [3]. In the present work we proved the formation of such sextuple-decker sandwich complex in solid state by single crystal XRD. The yttrium complex was chosen as diamagnetic reference for later investigations. The solvates (1)2*(KBPh4)¬4•4(CH3CN)•7(CHCl3) were obtained by slow diffusion of KBPh4 in CH3CN into the solution of (1) in CHCl3 at 25 °C. The structural characteristics of the dimer suggest the possibility of the magnetic-dipolar f-f interaction between the ions at M1 and M2 cites, as well as additional weaker coupling between ions at M2 and M2' cites, which can be later observed in the case of isostructural complexes with Tb(III) and Dy(III). Acknowledgements: This work was supported by the grants of leading scientific schools NSh-3867.2018.3 and Russian Science Foundation 18-73-00246. [1] H. Wang, B. W. Wang, Y. Bian, S. Gao and J. Jiang. (2016). Coord. Chem. Rev., 306, 195–216. [2] R.J. Holmberg, M.A. Polovkova, A. G. Martynov, Y. G. Gorbunova, M. Murugesu (2016). Dalton Trans, 45, 9320–9327. [3] A. G. Martynov, O. V. Zubareva, Y. G. Gorbunova, S. G. Sakharov and A. Y. Tsivadze. (2009). Inorg. Chim. Acta, 362, 11–18.
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