化学
镍
铜
乙二胺
电子顺磁共振
结晶学
八面体
无机化学
晶体结构
磁化率
循环伏安法
配体(生物化学)
钴
氮气
金属
电化学
高分子化学
物理化学
有机化学
物理
受体
生物化学
核磁共振
电极
作者
Pavel Kopel,Zdeněk Trávnı́ček,Libor Kvı́tek,Zdeněk Černošek,Grzegorz Wrzeszcz,Jaromı́r Marek
标识
DOI:10.1080/0095897021000039034
摘要
Copper, cobalt and nickel complexes with nitrogen donor ligands and trithiocyanurate dianion (ttcH2-) have been prepared and characterized by elemental analysis, electronic and EPR (copper complexes) spectra, and magnetic susceptibility measurements over the temperature range 78-291 K. Some of the complexes have also been studied by thermal analysis and by cycle voltammetry. Structures of the complexes have been proposed on the basis of magnetic and spectral properties. Two copper complexes of compositions Cu(bpy)(ttcH) and Cu(phen)(ttcH), where bpy=2,2'-bipyridine, phen=1,10-phenanthroline, are probably polymeric, whereas the copper complex with N,N'-bis(3-aminopropyl)ethylenediamine (bapen) of composition [Cu(bapen)ttcH)]·2H2O is mononuclear. We assume distorted octahedral structures for nickel complexes. A single crystal X-ray analysis of [Ni(bappn)(ttcH)]·5H2O shows that the central nickel atom is coordinated by tetradentate nitrogen ligand N,N'-bis(3-aminopropyl)-1,3-propanediamine and coordination is completed by sulfur and nitrogen atoms of trithiocyanurate dianion.
科研通智能强力驱动
Strongly Powered by AbleSci AI