Английская Википедия:Azo violet

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Шаблон:Chembox Шаблон:PH indicator template

Azo violet (Magneson I;[1] p-nitrobenzeneazoresorcinol) is an azo compound with the chemical formula C12H9N3O4. It is used commercially as a violet dye and experimentally as a pH indicator, appearing yellow below pH 11, and violet above pH 13.[2] It also turns deep blue in the presence of magnesium salt in a slightly alkaline, or basic, environment.[3][4] Azo violet may also be used to test for the presence of ammonium ionsШаблон:Citation needed. The color of ammonium chloride or ammonium hydroxide solution will vary depending upon the concentration of azo violet used. Magneson I is used to test Be also; it produces an orange-red lake with Be(II) in alkaline medium.[5]

Properties

Файл:Aqueous azo violet (Magneson I).jpg
Azo violet at pH ~7.

The intense color from which the compound gets its name results from irradiation and subsequent excitation and relaxation of the extended π electron system across the R-N=N-R' linked phenols. Absorption of these electrons falls in the visible region of the electromagnetic spectrum. Azo violet's intense indigo color (λmax 432 nm) approximates Pantone R: 102 G: 15 B: 240.

Synthesis

Azo violet can be synthesised by reacting 4-nitroaniline with nitrous acid (generated in situ with an acid and a nitrite salt) to produce a diazonium intermediate. This is then reacted with resorcinol, dissolved in a sodium hydroxide solution, via an azo coupling reaction.

Файл:Azo Violet Synthesis.svg

This is consistent with the generalized strategy for preparing azo dyes.

Файл:Generalized Azo Dye Synthesis.jpeg


Reactivity

Файл:Tautomerization of Azo Violet.jpg
Tautomerization of Azo Violet

The chemical character of azo violet may be attributed to its azo group (-N=N-), six-membered rings, and hydroxyl side groups. Due to steric repulsions, azo violet is most stable in the trans-configuration, but isomerization of azo dyes by irradiation is not uncommon. The para-position tautomerization of azo violet provides mechanical insight into the behavior of the compound in an acidic environment, and thus its use as a basic pH indicator.

The predicted 1H-NMR of pure azo violet shows the hydroxyl protons as the most deshielded and acidic protons. The participation of these hydroxyl groups' electron-donation to the conjugated π system likewise influences azo violet's λmax and pKa value.

Pure Azo Violet NMR
Pure Azo Violet NMR

Шаблон:-

References

Шаблон:Reflist