Tautomerism of anthraquinones: XI. 1-amino-4-hydroxyanthraquinone
The disperse dye red 2C regarded as 1-amino-4-hydroxy-9,10-anthraquinone is not a 9,10-anthraquinone derivative. It is characterized by a keto-enol and amino-imine tautomerism, and it consists of equilibrium mixtures of tautomers and conformers containing 4-amino-9-hydroxy-1,10-, 9 amino-4-hydroxy-1...
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Veröffentlicht in: | Russian journal of organic chemistry 2010-05, Vol.46 (5), p.655-660 |
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creator | Fain, V. Ya Zaitsev, B. E Ryabov, M. A |
description | The disperse dye red 2C regarded as 1-amino-4-hydroxy-9,10-anthraquinone is not a 9,10-anthraquinone derivative. It is characterized by a keto-enol and amino-imine tautomerism, and it consists of equilibrium mixtures of tautomers and conformers containing 4-amino-9-hydroxy-1,10-, 9 amino-4-hydroxy-1,10-, 9 amino-10-hydroxy-1,4-anthraquinones, 9 hydroxy-1,10-anthraquinone 10-imine, and also their conformers with a single intramolecular hydrogen bond. The significant differences in the absorption spectra known for this dye originate from the dissimilar isomeric composition of the samples of this dye prepared or purified by various procedures |
doi_str_mv | 10.1134/S107042801005009X |
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The significant differences in the absorption spectra known for this dye originate from the dissimilar isomeric composition of the samples of this dye prepared or purified by various procedures</description><identifier>ISSN: 1070-4280</identifier><identifier>EISSN: 1608-3393</identifier><identifier>DOI: 10.1134/S107042801005009X</identifier><language>eng</language><publisher>Dordrecht: Dordrecht : SP MAIK Nauka/Interperiodica</publisher><subject>Chemistry ; Chemistry and Materials Science ; Organic Chemistry</subject><ispartof>Russian journal of organic chemistry, 2010-05, Vol.46 (5), p.655-660</ispartof><rights>Pleiades Publishing, Ltd. 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c312t-2993919b28cc0fa500b0bf6470fd1de265c144b3f375627c5dfcd8dace1493bd3</citedby><cites>FETCH-LOGICAL-c312t-2993919b28cc0fa500b0bf6470fd1de265c144b3f375627c5dfcd8dace1493bd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S107042801005009X$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S107042801005009X$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids></links><search><creatorcontrib>Fain, V. Ya</creatorcontrib><creatorcontrib>Zaitsev, B. E</creatorcontrib><creatorcontrib>Ryabov, M. A</creatorcontrib><title>Tautomerism of anthraquinones: XI. 1-amino-4-hydroxyanthraquinone</title><title>Russian journal of organic chemistry</title><addtitle>Russ J Org Chem</addtitle><description>The disperse dye red 2C regarded as 1-amino-4-hydroxy-9,10-anthraquinone is not a 9,10-anthraquinone derivative. It is characterized by a keto-enol and amino-imine tautomerism, and it consists of equilibrium mixtures of tautomers and conformers containing 4-amino-9-hydroxy-1,10-, 9 amino-4-hydroxy-1,10-, 9 amino-10-hydroxy-1,4-anthraquinones, 9 hydroxy-1,10-anthraquinone 10-imine, and also their conformers with a single intramolecular hydrogen bond. The significant differences in the absorption spectra known for this dye originate from the dissimilar isomeric composition of the samples of this dye prepared or purified by various procedures</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Organic Chemistry</subject><issn>1070-4280</issn><issn>1608-3393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLQzEQhYMoWKs_wJX3D6TOJLmPuCvFFxRctIXuQm4efeC90aQF--9NqRsRXM0M53zD4RByizBC5OJ-hlCDYA0gQAkgl2dkgBU0lHPJz_OeZXrUL8lVSlsAECj4gIzner8LnYub1BXBF7rfraP-3G_60Lv0UCxfRwVS3eWbCro-2Bi-Dr9M1-TC6_fkbn7mkCyeHueTFzp9e36djKfUcGQ7yqTkEmXLGmPA65yxhdZXogZv0TpWlQaFaLnndVmx2pTWG9tYbRwKyVvLhwRPf00MKUXn1UfcdDoeFII6dqD-dJAZdmJS9vYrF9U27GOfY_4L3Z0gr4PSq9yMWswYIAdsSlGC4N8ME2dU</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>Fain, V. Ya</creator><creator>Zaitsev, B. 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It is characterized by a keto-enol and amino-imine tautomerism, and it consists of equilibrium mixtures of tautomers and conformers containing 4-amino-9-hydroxy-1,10-, 9 amino-4-hydroxy-1,10-, 9 amino-10-hydroxy-1,4-anthraquinones, 9 hydroxy-1,10-anthraquinone 10-imine, and also their conformers with a single intramolecular hydrogen bond. The significant differences in the absorption spectra known for this dye originate from the dissimilar isomeric composition of the samples of this dye prepared or purified by various procedures</abstract><cop>Dordrecht</cop><pub>Dordrecht : SP MAIK Nauka/Interperiodica</pub><doi>10.1134/S107042801005009X</doi><tpages>6</tpages></addata></record> |
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title | Tautomerism of anthraquinones: XI. 1-amino-4-hydroxyanthraquinone |
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