Collect. Czech. Chem. Commun.
1970, 35, 857-866
https://doi.org/10.1135/cccc19700857
Reactivity of organic azo compounds. IX. Tautomerism of some azohydroxy compounds
J. Schrieber, J. Socha and K. Rothschein
Crossref Cited-by Linking
- Antonov Liudmil, Deneva Vera, Kurteva Vanya, Nedeltcheva Daniela, Crochet Aurelien, Fromm Katharina M.: Controlled tautomerism – switching caused by an “underground” anionic effect. RSC Adv. 2013, 3, 25410. <https://doi.org/10.1039/c3ra45326j>
- Wojciechowski K., Szymczak A.: The research of the azo–hydrazone equilibrium by means of AM1 method based on the example of an azo dye – the Schäffer salt derivative. Dyes and Pigments 2007, 75, 45. <https://doi.org/10.1016/j.dyepig.2006.05.016>
- Amaike Masato, Kobayashi Hideki, Sakurai Kazuo, Shinkai Seiji: Novel Attempts to Change the Colour of Dye Molecules Utilizing the Aggregation Mode of Saccharides. Supramolecular Chemistry 2002, 14, 245. <https://doi.org/10.1080/10610270290026158>
- Amaike Masato, Kobayashi Hideki, Shinkai Seiji: Molecular Design of Low Molecular-weight Aqueous Gels Bearing an Azo-hydrazone Tautomeric Group Useful as a Solvent Polarity Probe. Chemistry Letters 2001, 30, 620. <https://doi.org/10.1246/cl.2001.620>
- Wojciechowski Krzysztof, Szadowski Jerzy: Effect of the sulphonic group position on the properties of monoazo dyes. Dyes and Pigments 2000, 44, 137. <https://doi.org/10.1016/S0143-7208(99)00085-6>
- Isak Stefan J, Eyring Edward M, Spikes John D, Meekins Patricia A: Direct blue dye solutions: photo properties. Journal of Photochemistry and Photobiology A: Chemistry 2000, 134, 77. <https://doi.org/10.1016/S1010-6030(00)00248-3>
- Bajpai P. K., Pal Biswajit, Baul T. S. Basu: Structure of some arylazophenols and arylazonaphthols in the solid state: A resonance Raman study. J Raman Spectroscopy 1995, 26, 217. <https://doi.org/10.1002/jrs.1250260303>
- Antonov Liudmil, Stoyanov Stefan: Resolution of overlapping UV-visible absorption bands: Quantitative analysis of tautomeric equilibria. Analytica Chimica Acta 1995, 314, 225. <https://doi.org/10.1016/0003-2670(95)00281-4>
- Stoyanov Stefan, Antonov Liudmil, Soloveytchik Boriana, Petrova Veselina: Quantitative analysis of tautomeric equilibrium in 1-phenylazo-4-naphthols—a new approach. Dyes and Pigments 1994, 26, 149. <https://doi.org/10.1016/0143-7208(94)85008-9>
- Fanghänel E., Tschötsch C. K. J., Richter A. M.: Heterocyclisch substituierte Arendiazoniumsalze mit erweiterter spektraler Empfindlichkeit. II. 4‐(1‐Heterocycliden‐2,3‐diaza‐prop‐2‐en‐3‐yl)‐benzendia‐zoniumtetrafluoroborate. J. Prakt. Chem. 1990, 332, 43. <https://doi.org/10.1002/prac.19903320106>
- Mustroph Heinz: Über die Azo‐Hydrazon‐Tautomerie. Zeitschrift fuer Chemie 1987, 27, 281. <https://doi.org/10.1002/zfch.19870270803>
- Haessner R., Mustroph H., Borsdorf R.: 1H‐NMR‐spektroskopische Untersuchungen zur Azo‐Hydrazon‐Tautomerie in substituierten 1‐Phenylazo‐2‐naphtholen. J. Prakt. Chem. 1985, 327, 555. <https://doi.org/10.1002/prac.19853270405>
- Haessner R., Mustroph H., Epperlein J.: Untersuchungen zum photochemischen Ausbleichverhalten von tautomeriefähigen Azofarbstoffen. V. Oxidation substituierter 1‐Phenylazo‐2‐naphthole durch Singulettsauerstoff in polymerer Matrix. J. Prakt. Chem. 1983, 325, 943. <https://doi.org/10.1002/prac.19833250610>
- Jacques P.: Characteristic Raman bands for Azo and hydrazone structures. J Raman Spectroscopy 1982, 12, 102. <https://doi.org/10.1002/jrs.1250120117>
- Mustroph H., Bartel R.: Untersuchungen zum UV/Vis‐Spektralverhalten von Azofarbstoffen. VI. Zum Einfluß von Substituenten auf die Farbe von Derivaten des 1‐Phenylazo‐2‐naphthols. J. Prakt. Chem. 1982, 324, 743. <https://doi.org/10.1002/prac.19823240507>
- Ball P., Nicholls C.H.: Azo-hydrazone tautomerism of hydroxyazo compounds—a review. Dyes and Pigments 1982, 3, 5. <https://doi.org/10.1016/0143-7208(82)80010-7>
- Yoshida Tooru: An X-Ray Photoelectron Spectroscopic Study of Several Hydroxy Azo Compounds. Bulletin of the Chemical Society of Japan 1980, 53, 498. <https://doi.org/10.1246/bcsj.53.498>
- Balli Heinz, Gunzenhauser Sigmund: Valenzisomerisierungsversuche an substituierten 2‐Phenyl‐4‐phenylazo‐benzotriazolen: Grenzen der Boulton‐Katritzky‐Umlagerung. Helvetica Chimica Acta 1978, 61, 2628. <https://doi.org/10.1002/hlca.19780610734>
- Jacques Patrice, Goursot Annick, Faure Jean: Conformational analysis of some ortho-hydroxyazoic dyes by the PCILO method. Chemical Physics 1977, 26, 301. <https://doi.org/10.1016/0301-0104(77)87055-9>
- Hellrung Bruno, Balli Heinz: Azidiniumsalze. 16. Mitteilung [1]. Struktur‐Reaktivitätsbeziehungen in Serien quartärer N‐Heteroaromaten: Kinetik der Reaktion heterocyclischer Azidiniumsalze mit Sulfit‐Ionen. Helvetica Chimica Acta 1976, 59, 140. <https://doi.org/10.1002/hlca.19760590116>
- Hempel R., Morgenstern J., Viola H., Mayer R.: Untersuchung der Tautomerie p‐substituierter 4‐Phenylazo‐1‐naphthole. J. Prakt. Chem. 1976, 318, 983. <https://doi.org/10.1002/prac.19763180615>
- Millefiori S., Zuccarello F., Millefiori A., Guerrera F.: Tautomerism in arylazonaphthols by dipole moment analysis. Tetrahedron 1974, 30, 735. <https://doi.org/10.1016/S0040-4020(01)97159-5>
- SCHREIBER J., SOCHA J., ROTHSCHEIN K.: ChemInform Abstract: REAKTIVITAET ORGANISCHER AZOVERBINDUNGEN 9. MITT. TAUTOMERIE EINIGER AZOHYDROXY‐VERBINDUNGEN (VON BENZOL UND NAPHTHALIN). Chemischer Informationsdienst. Organische Chemie 1970, 1. <https://doi.org/10.1002/chin.197052181>