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首页> 外文期刊>Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry >SYNTHESIS, CHARACTERISATION AND ELECTROCHEMICAL BEHAVIOUR OF SOME NICKEL(II) COMPLEXES WITH LINEAR AND TRIPODAL TETRADENTATE LIGANDS DERIVED FROM SCHIFF BASES
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SYNTHESIS, CHARACTERISATION AND ELECTROCHEMICAL BEHAVIOUR OF SOME NICKEL(II) COMPLEXES WITH LINEAR AND TRIPODAL TETRADENTATE LIGANDS DERIVED FROM SCHIFF BASES

机译:席夫夫碱衍生的线性和四方齿四齿齿配位镍(II)配合物的合成,表征和电化学行为

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A number of new six-coordinate Ni(II) complexes with linear and tripodal tetradentate ligands having the general formula [Ni(H2L)(H2O)(2)]Cl-2 . xH(2)O have been synthesized. Microanalysis, molar conductance, IR spectra, thermogravimetric analysis, magnetic measurements, and electronic spectra have been used to elucidate their structure. The experimental data show that the ligands are bonded in a non-deprotonated form and are coordinated in a tetradentate manner, the other axial sites being occupied by the aquo molecules. On the basis of electronic results it is concluded that tripodal ligands exert the strongest ligand field and the ligand substituents affect the ligand field strength which increases with the electron donating effect of the R group. The electrochemical behaviour of the nickel(II) complexes was determined by cyclic voltammetry which shows that chelate structure, ligand geometry and electron donating effect of the ligand substituents are among the factors influencing the redox potentials of the complexes. Also, we note that the ligands used in the present study can stabilize both the nickel(I) and the nickel(III) states. [References: 34]
机译:许多具有通式[Ni(H2L)(H2O)(2)] Cl-2的具有线性和三脚形四齿配体的新型六配位Ni(II)配合物。 xH(2)O已合成。微观分析,摩尔电导,IR光谱,热重分析,磁测量和电子光谱已用于阐明其结构。实验数据表明,配体以非去质子化形式键合并以四齿方式配位,其他轴向位点被水分子占据。根据电子结果,可以得出结论,三脚架配体发挥最强的配体场,并且配体取代基影响配体场强度,该强度随R基团的电子给予作用而增加。镍(II)配合物的电化学行为通过循环伏安法测定,表明螯合物的结构,配体几何形状和配体取代基的供电子作用是影响配合物氧化还原电位的因素。另外,我们注意到本研究中使用的配体可以稳定镍(I)和镍(III)态。 [参考:34]

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