合成了1个稀土金属Tb-氮氧自由基配合物Tb(hfac)3(NITPhOH)2(hfac:六氟乙酰丙酮;NIT-PhOH:2-(4-羟基苯基)-4,4,5,5-四甲基咪唑啉-3-氧化-1-氧基自由基).X-射线单晶衍射分析结果表明,该化合物属正交晶系I222空间群,晶胞参数a=1.228 2(3)nm,b=2.874 0(6)nm,c=3.255 1(7)nm,α=β=γ=90°.Tb(Ⅲ)离子为八配位模式,2个氮氧自由基以单齿端基配体的形式分别以氮氧基团的氧原子与Tb(Ⅲ)离子配位,形成了十二面体的结构.配合物的变温磁化率研究显示,配合物中Tb(Ⅲ)离子与氮氧自由基之间存在弱的铁磁相互作用.
A novel complex [Tb(hfac)3(NITPhOH)2] was synthesized and characterized structurally and magnetically(hfac=hexa uoroacetylacetonate,NITPhOH=2-(4′-hydroxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide).It crystallizes in Orthorhombic,space group I222,with a=1.228 2(3) nm,b=2.874 0(6) nm,c=3.255 1(7) nm.Each Tb(Ⅲ) ion is coordinated by two oxygen atoms from two NITPhOH radicals and six oxygen atoms from three different hfac anions to form eight-coordinated dodecahedron geometry.The variable magnetic measurement shows that there is weak ferro magnetic interaction between Tb(Ⅲ) ion and NITPhOH radical.