采用甲基嘧啶基取代的Ullman氮氧自由基2M5PmyNIT与过渡金属镍(Ⅱ)离子进行配位,得到了一个双核的四自旋配合物[Ni(hfac)2]2(2M5PmyNIT)2.2CHCl3(其中2M5PmyNIT=2-(2′-甲基-5′-嘧啶基)-4,4,5,5-四甲基咪唑啉-3-氧化-1-氧基自由基,hfac=1,1,1,5,5,5-六氟乙酰丙酮).X-射线单晶衍射分析表明,在一个分子中,2个2M5PmyNIT自由基作为桥联配体,连接了2个Ni(hfac)2单元,形成双核四自旋配合物.变温磁化率的研究表明,Ni(Ⅱ)离子和直接配位的氮氧自由基之间存在着强的反铁磁相互作用.
A four-spin complex [Ni (hfac)2]2 (2M5PmyNIT)2 . 2CHCl2 (2M5PmyNIT = 2- (5' -2' - methylpyrimidyl )-4,4,5,5-tetramethylimidazoline-l-oxyl-3-oxide, hfac = 1,1,1,5,5,5- hexafluoro- acetylaceonate) was synthesized using a methylpyrimidyl substituted nitroxide rad- ical. The single crystal X-ray analysis reveals that two 2M5PmyNIT radicals act as bridging ligand linking two Ni(hfac)2 units together. The magnetic study shows that there exists strong magnetic interaction between Ni( Ⅱ ) ions and directly bonded radicals.