Nitrite to nitric oxide interconversion by heme FeII complex assisted by [CuI(tmpa)]+

被引:2
作者
Turias, Francesc [1 ,2 ,3 ]
Sola, Miquel [1 ,2 ]
Falivene, Laura [3 ]
Cavallo, Luigi [3 ]
Poater, Albert [1 ,2 ]
机构
[1] Univ Girona, Inst Quim Computac & Catalisi, Campus Montilivi, Girona 17071, Catalonia, Spain
[2] Univ Girona, Dept Quim, Campus Montilivi, Girona 17071, Catalonia, Spain
[3] King Abdullah Univ Sci & Technol, Phys Sci & Engn Div, KAUST Catalysis Ctr, Thuwal 239556900, Saudi Arabia
关键词
Iron catalyst; Copper catalyst; Heme; Nitrite; Nitric oxide; Cytochrome c oxidase; ASSEMBLY MEDIATED NITRITE; ELECTRONIC-STRUCTURE; HEME/COPPER; THERMOCHEMISTRY; REDUCTASE; TETRAKIS(2,6-DIFLUOROPHENYL)PORPHYRINATE(2-); PSEUDOPOTENTIALS; CHEMISTRY; DIOXYGEN; BIOLOGY;
D O I
10.1007/s11224-015-0670-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The present computational study complements the recent experimental efforts by Karlin and coworkers to describe the interconversion of nitrite to nitric oxide by means of an iron porphyrin complex together with a Cu chemical system, i.e., the iron(II) complex (F8TPP)Fe-II [F8TPP = tetrakis(2,6-difluorophenyl)porphyrinate(2-)] and a preformed copper(II)-nitrito complex [(tmpa)Cu-II(NO2)][B(C6F5)(4)] [tmpa = tris(2-pyridylmethyl)amine], being the latter an oxidized species of [(tmpa)Cu-I(MeCN)](+). By DFT calculations, we unravel how the reduction of nitrite to nitric oxide takes place through a mu-oxo heme-Fe-III-O-Cu-II complex, following a mimetic path as in the cytochrome c oxidase. Mayer bond order (MBO) and energy decomposition analyses are used to analyze the bonding strength of such nitro derivatives to either copper or iron.
引用
收藏
页码:409 / 417
页数:9
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