- Method for dyeing keratinous fibres using an aminoindole in combination with a quinone derivative
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Method for dyeing keratinous fibres, characterized in that at least one composition (A) containing at least one aminoindole in a medium appropriate for dyeing is applied to these fibres, the application of the composition (A) being preceded or followed by the application of a composition (B) containing, in a medium appropriate for dyeing, at least one quinone derivative chosen from ortho- or para-benzoquinones, ortho- or para-benzoquinone monoimines or diimines, 1,2- or 1,4-naphthoquinones, ortho- or para-benzoquinone sulphonimides, α,ω-alkylene-bis-1,4-benzoquinones, or 1,2- or 1,4-naphthoquinone monoimines or diimines, the aminoindoles and the quinone derivatives being chosen such that the difference in redox potential ΔE between the redox potential Ei of the aminoindoles, determined at pH 7 in a phosphate medium on a vitreous carbon electrode by voltametry, and the redox potential Eq of the quinone derivative, determined at pH 7 in a phosphate medium by polarography on a mercury electrode relative to the saturated calomel electrode, in such that
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- Process for dyeing keratinous fibres with a hydroxyindole in combination with a quinone derivative; and novel 1,4-benzoquinones
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Process for dyeing keratinous fibres, comprising the step of applying to these fibres at least one composition A containing, in a medium appropriate for dyeing, at least one mono- or di-hydroxyindole the application of the composition A being preceded or followed by the application of a composition B containing, in a medium appropriate for dyeing, at least one quinone derivative chosen from ortho- or para-benzoquinones, monoimines or diimines of ortho- or para-benzoquinones, 1,2- or 1,4-naphthoquinones, sulphonimides of ortho- or para-benzoquinones, α, ω-alkylene-bis-1,4-benzoquinones, or 1,2- or 1,4-naphthoquinone-monoimines or -diimines; the mono- or di-hydroxyindoles and the quinone derivatives being chosen such that the oxidation-reduction potential difference ΔE between the oxidation-reduction potential Ei of the mono- or di-hydroxyindoles, determined at pH 7 in a phosphate medium on a vitreous carbon electrode by voltametry, and the oxidation-reduction potential Eq of the quinone derivative determined at pH 7 in a phosphate medium by polarography on a mercury electrode and relative to a saturated calomel electrode is such that
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- SYNTHESIS OF A MODEL PHOTOSYNTHETIC SYSTEN OF THE "COVERED" TYPE BASED ON MESOPORPHYRIN II
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The synthesis of a porphyrinquinone compound of the "covered" type based on mesoporphyrin II was accomplished.Spectral investigations of the compound obtained were carried out.
- Borovkov, V. V.,Evstigneeva, R. P.,Mirakova, E. V.,Rozynov, B. V.
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p. 1144 - 1148
(2007/10/02)
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- SYNTHESIS OF POLYCYCLIC SULFONES
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The diene synthesis between 2-isopropenyl-2-thiolene 1,1-dioxide and benzo-, naphtho-, and anthraquinones was used as a convenient method for the production of polycyclic sulfones, including those modeling the structures of natural biologically active compounds.It was established that the cycloaddition of alkylthio- and alkylsulfonylbenzoquinones and the corresponding naphthoquinones is highly regioselective.
- Tolstikov, G. A.,Shul'ts, E. E.,Vafina, G. F.,Spirikhin, L. V.,Panasenko, A. A.
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p. 1109 - 1121
(2007/10/02)
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