Abstract

AbstractFour complexes based on rare earth biradicals [Ln(hfac)3(NITPhmbis)2]2 {Ln = La (1), Nd (2), Gd (3), Tb (4); hfac = hexafluoroacetylacetone; NITPhmbis = [1,3‐bis(1′‐oxyl‐3′‐oxido‐4′,4′,5′,5′‐tetramethyl‐4,5‐hydro‐1H‐imidazol‐2‐yl)benzene]} were successfully synthesized under appropriate conditions. Single‐crystal structures show that 1 is a mononuclear two spin complex and 2–4 are mononuclear three spin complexes, in which a NITPhmbis molecule acts as a bidentate ligand with one coordinated lanthanide ion. The four complexes are isomorphous, the coordination number around the lanthanide ion is eight, and the polyhedron is a 4,4‐bicappped trigonal prism. For lanthanum(III) complex 1, the temperature dependence of the magnetic susceptibility indicates that weakly antiferromagnetically coupled radicals exist (Jrad–rad = –1.2 cm–1). In the case of neodymium(III) complex 2, its magnetic behavior gives antiferromagnetic NdIII–radical interactions, whereas for complexes 3 and 4, static magnetic properties show that the GdIII and TbIII ions interact ferromagnetically with the radical. The dynamic magnetic properties of 4 were also measured, and 4 was found to exhibit slow relaxation of the magnetization at low temperature.

Full Text
Paper version not known

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

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.