化学
一氧化氮介导的自由基聚合
吡啶
部分
结晶学
磁化率
配体(生物化学)
铁磁性
感应耦合
反铁磁性
立体化学
离子
衍生工具(金融)
药物化学
自由基聚合
有机化学
凝聚态物理
聚合
受体
物理
经济
量子力学
金融经济学
生物化学
聚合物
作者
Hong-Wei Song,Jiao Lu,Xiaotong Wang,Licun Li
标识
DOI:10.1002/zaac.202300090
摘要
Abstract Two new Cu−Ln 1D coordination chains with formula [Ln(hfac) 3 Cu(hfac) 2 (NIT‐3Py‐5‐3Py)(H 2 O)] n (Ln III =Gd 1 , Dy 2 ; hfac=hexafluoroacetylacetonate, NIT‐3Py‐5‐3Py=2‐(5‐(3‐pyridyl)‐3‐pyridyl)‐4,4,5,5‐tetramethylimidazoline‐1‐oxyl‐3‐oxide) were successfully constructed by means of a new nitronyl nitroxide radical ligand containing two pyridine groups. In these two complexes, the radical ligand binds two Cu II ions through its two pyridine groups to produce 1D chain while the aminoxyl moiety of the radical is bound to a Ln (III) ion. Direct‐current magnetic susceptibility investigations indicate that ferromagnetic exchanges are dominant and magnetic susceptibility data of Gd derivative are analyzed using a magnetic model, indicating that Cu‐NO coupling through pyridine group and Gd‐NO direct exchange are ferromagnetic interactions. There is no magnetic relaxation behavior for Dy analogue.
科研通智能强力驱动
Strongly Powered by AbleSci AI