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Two polynuclear mixed-valence manganese clusters, [Mn13] and [Mn16], containing mixed chelating ligands were synthesized and structurally characterized. The alternating current (AC) susceptibilities of both complexes reveal nonzero frequency-dependent out-of-phase (χM′′) signals. [ABSTRACT FROM AUTHOR]

The slow diffusion reaction of octacyanometallate [MoV(CN)8]3-, lanthanide ions (Gd-Lu), and 1,10-phenanthroline (phen) in CH3CN/H2O has yielded eight isostructural one-dimensional chains, [LnIII(phen)2(H2O)MoV(CN)8]2[(n-C4H9)4N](NO3)·2CH3CN·4H2O (Ln = Gd(1), Tb(2), Dy(3), Ho(4), Er(5), Tm(6), Yb(7), Lu(8)), in which [LnIII(phen)2(H2O)]3+ and [MoV(CN)8]3- units are linked alternatively through cyanide groups, generating left- and right-handed helices. Interestingly, 1-8 undergo a resolvation-recrystallization process upon prolonging the diffusion-reaction time, together with the valence change from V to IV of Mo center and structural dimensionalities switching from helical chains to trinuclear clusters, (Hphen)2.5[LnIII0.5(phen)(H2O)][MoIV(CN)8]·1.5CH3CN (Ln = Gd(9), Tb(10), Dy(11), Ho(12), Er(13), Tm(14), Yb(15), Lu(16)). Magnetic studies of 1-16 revealed the typical effects induced by single-ion magnetic anisotropy and/or the population of low-lying excited states, and 11 and 13 showed extraordinary field-induced slow magnetic relaxations. [ABSTRACT FROM AUTHOR]