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Cationic dyes delocalized

The positive charge of cationic dyes may be either localized or delocalized. In 1, the positive charge is localized on an ammonium group ... [Pg.44]

Cationic dyes with delocalized charge are classified with the methine dyes (see Section 2.6). They may be viewed as vinylogous amidinium salts 3 [1] ... [Pg.45]

Cationic dyes form positively charged dye ions by dissociation, and the positive electric charge is delocalized over the entire molecule. They are usually di- and triarylmethine dyes such as C.I. Basic Green 4, 42000 [569-64-2] (31), which are also known as triarylmethane dyes or triaryl carbenium ions [15], oxazine dyes such as C.I. Basic Blue 3, 51005 [2787-91-9] (32), orthiazine dyes. [Pg.470]

The positive charge is here an integral part of the chromophoric system and the dyes are termed delocalized cationic dyes. [Pg.110]

So-called delocalized cationic azo dyes are another type ia which the positive charge is delocalized (or distributed) across the dye cation. Basic Blue 54 (132) (2-amiao-6-methoxybenzothiazole coupled to /V, /V-dimethy1 ani1 ine and then quarternized with dimethyl sulfate) is an example of this class which can also be considered as a diazamethine dye. [Pg.454]

Basic Red 22 (134), which contains 1 part ia 7 of the yellowish red 1,4-dimethyl isomer, Basic Red 29 (135), and Basic Yellow 25 (136) are all examples of delocalized cationic azo dyes. Dyes of this type can also be synthesized by Hbnig s oxidative coupling reaction of heteroaromatic hydrazones with tertiary aromatic amines. [Pg.454]

Delivery receipt, 25 330 Delocalized cationic azo dyes, 9 423 Delta-3-carene (A-3-carene), 24 499 8-alumina, 2 404, 406t Delta coke, 22 704 8-damascone, 24 570... [Pg.250]

In the diazahemicyanine dye 2, the positive charge is delocalized across the dye cation. [Pg.44]

Such bonding implies that chelation of the proton with the azo group increases the accessibility of the electron pair involved in the hydrogen bond with the cotton. The chelation of a metal ion would probably result in the formation of a more stable chelate ring but would also introduce the probability of delocalizing the electron pair as well as converting the dye to a cation. [Pg.101]


See other pages where Cationic dyes delocalized is mentioned: [Pg.72]    [Pg.43]    [Pg.49]    [Pg.254]    [Pg.294]    [Pg.125]    [Pg.869]    [Pg.86]    [Pg.323]    [Pg.325]    [Pg.265]    [Pg.466]    [Pg.768]    [Pg.366]    [Pg.106]    [Pg.150]    [Pg.323]    [Pg.325]    [Pg.84]    [Pg.67]    [Pg.496]    [Pg.429]    [Pg.222]    [Pg.339]    [Pg.84]   
See also in sourсe #XX -- [ Pg.110 ]




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