A\*~\*'-bi-(2H-1,4-benzothiazine) shows striking photochromism and thermochromism. The color change is thermally and photochemically reversible. The photochromism can be ascribed to the cis-tram isomerization about the central double bond, the yellow tram isomer being more stable. The quantum yield
Studies on Heterocyclic Colouring Matters Part II: Δ2,2′ -Bi (2H-1, 4-benzothiazines)
✍ Scribed by B. L. Kaul
- Book ID
- 102855450
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- German
- Weight
- 751 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
A novel one‐step ‘Inverse Indigo Synthesis’ of the Δ^2,2′^‐bi(3,4‐dihydro‐3‐oxo‐2__H__‐1, 4‐benzothiazine) chromophore is described. Structure, substitution reactions, mechanism of formation, colour and other relevant properties of this system have been investigated in relation to known thioindigos. A synthesis of the basic skeleton of one of the ‘Trichosiderins’, the colouring matters of human red hair, is reported.
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