摘要
由Ru2(μ-O2CCH3)4Cl为前体配合物,采用羧酸置换反应,合成了两种氧原子作为电子供体的功能性双核噻吩羧酸钌(Ⅱ,Ⅲ)配合物[Ru2(μ-O2CR4(MeOH)2]PF6(O2CR-=3-噻吩甲酸,3-噻吩乙酸)。通过元素分析、红外光谱对配合物进行了表征。通过循环伏安法考察了该配合物的电化学性质,结果表明,其氧化还原电位比较低,相较于2-噻吩羧酸配合物跟更容易发生聚合反应。
The displacement reaction of Ru2(μ-O2CCH3)4Cl was lewis base ligand leading to the formation of O-donor ruthenium complex of [Ru2(μ-O2CR4(MeOH)2]PF6 has been synthesized and characterized by elemental analysis,IR and UV-vis absorption spectroscopies.The electrochenical properties of ruthenium(Ⅱ,Ⅲ) complex have been studied by means of cyclic voltametry.The redox potential was greater than 1.5rmV(vs.Ag/AgCl).They were better candidates for polymerization than thiophen-2-carboxylate ruthenium complex.
出处
《化工新型材料》
CAS
CSCD
北大核心
2010年第6期87-88,共2页
New Chemical Materials
关键词
双核钌配合物
羧酸置换
光电材料
光谱电化学
ruthenium(Ⅱ
Ⅲ) complex
carboxylic acid displacement
exchange reaction
optical-electro material
spectroelectrochemistry