Abstract
Three heterometallic dinuclear compounds, [MIIDyIII(L)(Pc)(ROH)]·ROH (R = CH3, M = Ni (1), Zn (2); R = C2H5, M = Zn (3)), were stepwise synthesized based on phthalocyanine (H2Pc) and one tripodal Schiff-base ligand 1,1,1-tris[(salicylideneamino)methyl]ethane (H3L). All of them have been studied structurally and magnetically. The six-coordinate MII ion and the seven-coordinate DyIII ion are bridged by two phenolic oxygen atoms to form an MII-LnIII heterodinuclear unit. Magnetic measurements indicate that the ferromagnetic NiII-DyIII interaction is operative in compound 1 and all three compounds exhibit the field-induced slow relaxation of magnetizations. In particular, compounds 2 and 3 have the improved magnetic performance. Ab initio calculations indicate that the weak NiII-DyIII interaction decreases the energy barrier, while the replacement of the paramagnetic NiII ion by the diamagnetic ZnII in compound 2 and 3 not only controls the magnetic interaction but also alters the local magnetic axes of DyIII ions to optimize the magnetic relaxation behavior.
Sign-in/Register to access full text options 
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
