摘要
水溶液中Eu^(3+)与meso-四(4-磺苯基)卟啉(TPPS)不易形成卟啉络合物,但在乙酸、酒石酸、丙二酸等共存时,在循环伏安图上可得一对Eu^(3+)还原-氧化的可逆或准可逆峰,此峰与Eu^(3+)在NaClO_4底液中的还原峰相比,峰电位正移,峰电流增高。从6种Eu^(3+)-羧酸络合物与TPPS共存时的实验中证明这些络合物并没有和TPPS形成三元络合物,而是吸附在汞电极上的TPPS产生电催化作用。
It is difficult to synthesize the complexes of rare earth ions with meso-tetra(4-sulfophenyl)porphyrin(TPPS)in aqueous solution. Eu(Ⅲ)can form complexes with carboxylic acids, such as acetic,tartaric, malonic, gluconic, citric acids and EDTA with different stability constants,and exhibits irreversible or quasi-reversible redox peaks in cyclic voltammograms. TPPS, which adsorbed on Hg electrode,exerts catalytic effect on the redox behvior of Eu(Ⅲ)-acetic, tartaric, malonic acid complexes by changing the irreversible process to a reversible one, but the Eu(Ⅲ)-TPPS complex was not formed.The mechanism of such a catalytic effect has been discussed.
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
1996年第5期786-789,共4页
Chemical Journal of Chinese Universities
基金
国家自然科学基金
关键词
电催化作用
铕
配合物
TPPS
TPPS,Eu(Ⅲ)-carboxylic acid complex, Electro-catalytic effect