The Cyanine Dyes and Related Compounds, Volume 18
The Chemistry of Heterocyclic Compounds, since its inception, has been recognized as a cornerstone of heterocyclic chemistry. Each volume attempts to discuss all aspects – properties, synthesis, reactions, physiological and industrial significance – of a specific ring system. To keep the series up-to-date, supplementary volumes covering the recent literature on each individual ring system have been published. Many ring systems (such as pyridines and oxazoles) are treated in distinct books, each consisting of separate volumes or parts dealing with different individual topics. With all authors are recognized authorities, the Chemistry of Heterocyclic Chemistry is considered worldwide as the indispensable resource for organic, bioorganic, and medicinal chemists.
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B The Constitution of Cyanine
F The Constitution of Kryptocyanine
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2-methyl 2-methylbenzothiazole ethiodide 2,2'-carbocyanine 4-linked quinoline absorption maximum acetic anhydride acid alcohol aldehyde alkiodide alkyl analogue Aniline aqueous bathochromic shift benzoselenazole benzothiazole benzothiazole series benzoxazole Brit bromide Brooker carbocyanines CH:CH chain Chem chloride converted corresponding cyanines cyclic derivative dimethin dimethinmerocyanines Eastman Kodak Eastman Kodak Co equation ethanol ethiodide ethyl orthoacetate ethyl orthoformate F. L. White gave Gevaert Photo-Producten N.V. give heterocyclic hydrochloride I.G. Farbenind Ilford Ltd iodide isocyanine Kendall ketomethylene compound Kiprianov lepidine maxima merocyanines methin methincyanine method methotoluene-/>-sulphonate methylene base minutes molecule mols mono-ionic nitrogen atoms nucleus ortho-ester patent piperidine potassium prepared by boiling prepared by condensing prepared by heating pyridine Quaternary Salt Residues quinaldine quinaldine ethiodide quinoline R=Et R=Me reaction reactive methyl group recrystallised rhodanine sensitising sensitising action sensitising maximum similarly sodium acetate substituted symmetrical synthesised thia thiacarbocyanine thiazole thiazoline toluene-/>-sulphonate triethylamine triethylamine in ethanol trimethin trimethincyanines trinuclear dyes unsubstituted unsymmetrical X=Br Y=CH:CH Y=Se