Synthesis of Isomeric Tb3+-Phthalocyanine Double-Decker Complexes Depending on the Difference in the Direction of Coordination Plane and Their Magnetic Properties

A C-4h symmetrically substituted phthalocyanine, 1,8,15,22-tertrakis(2,4-dimethylpent-3-oxy)phthalocyanine (H(2)TdMPPc), was used to synthesize Tb3+-phthalocyanine double-decker complexes ([Tb(TdMPPc)(2)]s). Because H(2)TdMPPc has C-4h symmetry, S,S, R,R, and meso isomers of [Tb(TdMPPc)(2)] were obtained depending on the difference in the direction of the coordination plane of two C-4h-type phthalocyanines with respect to a central Tb3+ ion. We investigated the physical properties of these [Tb(TdMPPc)(2)] isomers, including their single-ion magnetic properties, and found that the spin-reversal energy barrier (U-eff) of the meso isomer was apparently higher than that of the enantiomers. Detailed crystal structural analyses indicated that the meso isomer has a more symmetrical structure than do the enantiomers, thereby suggesting that the higher U-eff of the meso isomer originated from the more highly symmetrical structure.