摘要
含有铁卟啉化合物活性中心的细胞色素P-450和其它过氧化物酶具有重要的生物化学功能。本文讨论了铁卟啉模型物模拟这些酶功能的反应机理。通过与已知的过氧化物中氧氧键均裂机理的比较,以及对大部分溶液反应的研究,表明在过氧化物(包括过氧酸)与铁卟啉生成活性中间体(?Fe=O^+)的过程中,氧氧键的异裂机理占主导地位。过氧化物如同其它氧化剂受物(如烯烃)一样,能快速地直接与?FeO^+反应。以铁卟啉为催化剂的过氧化物反应体系为我们提供了研究模拟催化酶的人工模型体系。
The enzymes cytochrome P-450 and other peroxidases which contain iron-porphyrin
active centre play a key role in hydrogen peroxide removal from biological systems. The
mechanistic studies on this reaction catalyzed by model iron porphyrins have been
discussed herein. In the active intermediate ('iron-oxene' porphyrin) forming step, a
general base catalyzed heterolytic-type cleavage of oxygen-oxygen bond scheme is
consistent with most of experiment results from direct observations of reactions in
solution and the comparisons with thermolysis studies of peroxides, which is well known
homolytic. A direct, rapid reaction of peroxides with iron-oxene intermediate can take
place. Peroxides react as substrate as well as oxidant. Those systems could provide us
convenient models to study the enzyme catalase.
出处
《化学学报》
SCIE
CAS
CSCD
北大核心
1989年第1期49-56,共8页
Acta Chimica Sinica
