Nitric oxide cation, formation

The most important physiological nitrogen substrate of peroxidases is undoubtedly nitric oxide. In 1996, Ishiropoulos et al. [252] suggested that nitric oxide is able to interact with HRP Compounds I and II. Glover et al. [253] measured the rate constants for the reactions of NO with HRP Compounds I and II (Table 22.2) and proposed that these reactions may occur in in vivo inflammatory processes. The interaction of NO with peroxidases may proceed by two ways through the NO one-electron oxidation or the formation of peroxidase NO complexes. One-electron oxidation of nitric oxide will yield nitrosonium cation NO+ [253,254], which is extremely unstable and rapidly hydrolyzed to nitrite. On the other hand, in the presence of high concentrations of nitric oxide and the competitor ligand Cl, the formation of peroxidase NO complexes becomes more favorable. It has been shown [255]... 

Ionic compounds consist of positive ions (cations) and negative ions (anions) hence, ionic compounds often consist of a metal and nonmetal. The electrostatic attraction between a cation and anion results in an ionic bond that results in compound formation. Binary ionic compounds form from two elements. Sodium chloride (NaCl) and sodium fluoride (NaF) are examples of binary ionic compounds. Three elements can form ternary ionic compounds. Ternary compounds result when polyatomic ions such as carbonate (C032 ), hydroxide (OH-), ammonium (NH4+), form compounds. For example, a calcium ion, Ca2+, combines with the carbonate ion to form the ternary ionic compound calcium carbonate, CaC03. Molecular compounds form discrete molecular units and often consist of a combination of two nonmetals. Compounds such as water (H20), carbon dioxide (C02), and nitric oxide (NO) represent simple binary molecular compounds. Ternary molecular compounds contain three elements. Glucose ( 12 ) is a ternary molecular compound. There are several distinct differences between ionic and molecular compounds, as summarized in Table 1.2. 

The features of initiation of free radical reactions in polymers by dimers of nitrogen dioxide are considered. The conversion of planar dimers into nitrosyl nitrate in the presence of amide groups of macromolecules has been revealed. Nitrosyl nitrate initiates radical reactions in oxidative primary process of electron transfer with formation of intermediate radical cations and nitric oxide. As a result of subsequent reactions, nitrogen-containing radicals are produced. The dimer conversion has been exhibited by estimation of the oxyaminoxyl radical yield in characteristic reaction of p-benzoquinone with nitrogen dioxide on addition of aromatic polyamide and polyvinylpyrrolidone to reacting system. The isomerisation of planar dimers is efficient in their complexes with amide groups, as confirmed by ab initio calculations. 

Regulation of Nitric Oxide Synthase Role of Oxygen Radicals and Cations in Nitric Oxide Formation... 

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