摘要
在成桥活化配合物反应机理基础上,Ogarl,P.Benson等人,根据中心离子的结构和成桥基配体的性质,用配位场理论,研究报导了水中配合物间电子转移反应的动力学行为。本文,在混合溶剂中配合物间电子转移反应机理研究的基础上,探索了非桥基配体Cl<sup>-</sup>和H<sub>2</sub>O,对H<sub>2</sub>O、H<sub>2</sub>O—McOH、H<sub>2</sub>O—DMF等溶剂中Cis-[Co(cn)<sub>2</sub>Cl<sub>2</sub>]<sup>+</sup>和Cis-[Co(cn)<sub>2</sub>(OH<sub>2</sub>)Cl]<sup>2+</sup>和Fe(Ⅱ)间电子转移反应的影响。实验发现:相同条件下。
Investigations have been made in the effect of nonbridging ligands on the electron transfer reactions between Cis-[Co(en)_2Cl_2]^+ or Cis-[Co(en)_2(OH_2)Cl]^(2+) and iron(Ⅱ), and the effect of nonbridging ligand (Cl^- and H_2O) on the apparent rate constants of the reactions have also been expounded using spectrochemical series of ligand and crystal field stabilization energy.
出处
《化学研究与应用》
CAS
CSCD
1991年第2期70-74,共5页
Chemical Research and Application