首页> 外文期刊>European journal of inorganic chemistry >Two New Iron(II) Spin-Crossover Complexes with N4O2 Coordination Sphere and Spin Transition around Room Temperature
【24h】

Two New Iron(II) Spin-Crossover Complexes with N4O2 Coordination Sphere and Spin Transition around Room Temperature

机译:具有N4O2配位球和室温自旋转变的两种新型铁(II)自旋交叉配合物

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

The reaction of iron(II) acetate with the tetradentate Schiffbase like ligand H2L1 {[3,3]-[4,5-dihydroxy-1,2-phenylenebis( iminomethylidyne)bis(2,4-pentanedion)]} leads to the formation of the complex [FeL1(MeOH)]. Reaction of this complex with pyridine (py) or N,N-dimethylaminopyridine (dmap) leads to the two N4O2-coordinated complexes [FeL1(py)2]·py (1) and [FeL1(dmap)2]·MeOH·0.5dmap (2). Both complexes are spin-crossover compounds that were characterised by using magnetic measurements, X-ray crystallography and temperature-dependent 1H NMR spectroscopy. Special attention was given to the role of the two hydroxy groups on the phenyl ring in the formation of a hydrogen- bonding network and the influence of this network on the spin-transition properties. Although only a gradual spin crossover was observed for both complexes, the transition temperature was shifted to higher temperatures relative to that of the complexes with no additional hydroxy groups at the Schiff base like ligand. The hydrogen-bonding network was responsible for this effect
机译:乙酸铁(II)与四齿席夫碱类似配体H2L1 {[3,3]-[4,5-二羟基-1,2-亚苯基双(亚氨基甲基二炔)双(2,4-戊二酮)]}的反应导致形成配合物[FeL1(MeOH)]。该络合物与吡啶(py)或N,N-二甲基氨基吡啶(dmap)的反应生成两个N4O2配位的络合物[FeL1(py)2]·py(1)和[FeL1(dmap)2]·MeOH·0.5 dmap(2)。两种络合物均为自旋交联化合物,其特征在于使用磁测量,X射线晶体学和温度依赖性1H NMR光谱进行表征。特别注意苯环上的两个羟基在氢键网络形成中的作用以及该网络对自旋转变性质的影响。尽管两种配合物仅观察到逐渐的自旋交叉,但相对于在席夫碱样配体上没有额外羟基的配合物,转变温度转移到更高的温度。氢键网络是造成这种效应的原因

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号