Photochemical reactions leading to NO and NOx generation

被引:73
作者
Ford, PC [1 ]
Wecksler, S [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
关键词
photochemistry; nitric oxide; transition metal; metal nitrosyls; porphyrins; salens; chromium/manganese nitrito complexes; cyclams; iron sulfur nitrosyls; two photon excitation;
D O I
10.1016/j.ccr.2004.10.022
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Studies in this laboratory are concerned with elucidating chemical mechanisms relevant to roles played by nitrogen monoxide and other NO, species in mammalian bioregulation and immunology. Dynamic photochemical techniques have proved very useful in probing these mechanisms. We also have interest in strategies to deliver NO to biological targets upon demand for such goals as the sensitization of gamma-radiation damage in hypoxic tissue. One such strategy would be to employ a precursor that displays relatively low thermal reactivity but is photochemically active to release NO. This proposition has led us to investigate the flash and continuous photolysis kinetics of a number of different nitrosyl complexes and other NO and NO, precursors such as metal nitrito complexes. The systems probed include several ruthenium salen and porphyrin nitrosyls, manganese(III) and chromium(III) nitrito complexes, ferri- and ferro-heme models and proteins, and iron-sulfur-nitrosyl clusters known as the Roussin's anions (e.g. Fe2S2(NO)(4)(2-)) and esters (e.g., Fe-2(mu-SR)(2)(NO)(4), where R is an organic functional group). An overview of these studies is presented. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1382 / 1395
页数:14
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