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Dioxygen Activation by Mononuclear Nonheme Iron(II) Complexes Generates Iron-Oxygen Intermediates in the Presence of an NADH Analogue and Proton

Authors
Hong, S (Hong, Seungwoo)Lee, YM (Lee, Yong-Min)Shin, W (Shin, Woonsup)Fukuzumi, S (Fukuzumi, ShunichNam, W (Nam, Wonwoo)
Issue Date
Oct-2009
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.131, no.39, pp 13910 - 13910
Pages
1
Journal Title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume
131
Number
39
Start Page
13910
End Page
13910
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/148005
DOI
10.1021/ja905691f
ISSN
0002-7863
1520-5126
Abstract
One primary goat in biomimetic research is to understand mechanisms of dioxygen activation, structures of reactive intermediates, and reactivities of the intermediates involved in catalytic oxidation reactions by metalloenzymes, such as heme and nonheme iron oxygenases. In this communication, we have reported the first example of generating nonheme iron(III)-hydroperoxo and iron(IV)-oxo complexes by activating O(2) with a biologically important electron donor, an NADH analogue, and an acid. The formation of iron(ill)-hydroperoxo and iron(IV)-oxo complexes was found to depend on the supporting ligands. We have also demonstrated that high-spin nonheme iron(II) complexes with a low oxidation potential are able to bind and activate O(2) to generate, the iron-oxygen intermediates.
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