Studies on Phenothiazinyl Radicals
During the course of numerous studies on phenothiazine radicals, it has been indicated by electron spin resonance (ESR) method that neutral phenothiazinyl radical which is rather unstable can be produced from phenothiazine by several methods. However, any work has not been published regarding the el...
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Veröffentlicht in: | Chemical & pharmaceutical bulletin 1973/01/25, Vol.21(1), pp.211-214 |
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description | During the course of numerous studies on phenothiazine radicals, it has been indicated by electron spin resonance (ESR) method that neutral phenothiazinyl radical which is rather unstable can be produced from phenothiazine by several methods. However, any work has not been published regarding the electronic absorption spectrum of these radicals. This may be chiefly because, as seen in general, measuring and assigning the spectrum of such unstable radical are seriously prevented from coexistence of various radical decay products. In this note we shall report the electronic absorption spectra of non-substituted and 1-methylsubstituted phenothiazinyl radicals which are generated in degassed dimethylsulfoxide-acetic anhydride mixture. By referring to the ESR spectra in the same systems and by performing theoretical calculations on the electronic transition of the radicals, a brief comment will be given to the assignment of the new absorption maxima in the electronic absorption spectra. |
doi_str_mv | 10.1248/cpb.21.211 |
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However, any work has not been published regarding the electronic absorption spectrum of these radicals. This may be chiefly because, as seen in general, measuring and assigning the spectrum of such unstable radical are seriously prevented from coexistence of various radical decay products. In this note we shall report the electronic absorption spectra of non-substituted and 1-methylsubstituted phenothiazinyl radicals which are generated in degassed dimethylsulfoxide-acetic anhydride mixture. By referring to the ESR spectra in the same systems and by performing theoretical calculations on the electronic transition of the radicals, a brief comment will be given to the assignment of the new absorption maxima in the electronic absorption spectra.</description><identifier>ISSN: 0009-2363</identifier><identifier>EISSN: 1347-5223</identifier><identifier>DOI: 10.1248/cpb.21.211</identifier><language>eng</language><publisher>Tokyo: The Pharmaceutical Society of Japan</publisher><ispartof>Chemical and Pharmaceutical Bulletin, 1973/01/25, Vol.21(1), pp.211-214</ispartof><rights>The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 1973</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4371-f39551e7c9251e0283ba3d9f2d8a80f8c2e20854854be8fa490ce58b4db647ff3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids></links><search><creatorcontrib>KAMIYA, MAMORU</creatorcontrib><creatorcontrib>MITSUI, TAKEHIRO</creatorcontrib><creatorcontrib>AKAHORI, YUKIO</creatorcontrib><title>Studies on Phenothiazinyl Radicals</title><title>Chemical & pharmaceutical bulletin</title><addtitle>Chem. 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By referring to the ESR spectra in the same systems and by performing theoretical calculations on the electronic transition of the radicals, a brief comment will be given to the assignment of the new absorption maxima in the electronic absorption spectra.</description><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1973</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LAzEQhoMoWKsXf0HRm7A1M0k2yVGKVaGg-HEO2Wxit9TdmmwP9debpX7AyzyHeZiBl5BzoFNArq7dppoi5MABGQHjshCI7JCMKKW6QFayY3KS0opSFFSyEbl46bd149OkaydPS992_bKxX027W0-ebd04u06n5Chk-LMfjsnb_PZ1dl8sHu8eZjeLwnEmoQhMCwFeOo0ZFBWrLKt1wFpZRYNy6JEqwXMqr4LlmjovVMXrquQyBDYml_u7m9h9bn3qzarbxja_NMCFlrJEDdm62lsudilFH8wmNh827gxQM3RgcgcGIWeQZ3t5lXr77v9UG_vGrf2gghZq0OF3wP92aaPxLfsG6zhkwQ</recordid><startdate>1973</startdate><enddate>1973</enddate><creator>KAMIYA, MAMORU</creator><creator>MITSUI, TAKEHIRO</creator><creator>AKAHORI, YUKIO</creator><general>The Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>1973</creationdate><title>Studies on Phenothiazinyl Radicals</title><author>KAMIYA, MAMORU ; MITSUI, TAKEHIRO ; AKAHORI, YUKIO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4371-f39551e7c9251e0283ba3d9f2d8a80f8c2e20854854be8fa490ce58b4db647ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1973</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KAMIYA, MAMORU</creatorcontrib><creatorcontrib>MITSUI, TAKEHIRO</creatorcontrib><creatorcontrib>AKAHORI, YUKIO</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Chemical & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KAMIYA, MAMORU</au><au>MITSUI, TAKEHIRO</au><au>AKAHORI, YUKIO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on Phenothiazinyl Radicals</atitle><jtitle>Chemical & pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>1973</date><risdate>1973</risdate><volume>21</volume><issue>1</issue><spage>211</spage><epage>214</epage><pages>211-214</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><abstract>During the course of numerous studies on phenothiazine radicals, it has been indicated by electron spin resonance (ESR) method that neutral phenothiazinyl radical which is rather unstable can be produced from phenothiazine by several methods. However, any work has not been published regarding the electronic absorption spectrum of these radicals. This may be chiefly because, as seen in general, measuring and assigning the spectrum of such unstable radical are seriously prevented from coexistence of various radical decay products. In this note we shall report the electronic absorption spectra of non-substituted and 1-methylsubstituted phenothiazinyl radicals which are generated in degassed dimethylsulfoxide-acetic anhydride mixture. By referring to the ESR spectra in the same systems and by performing theoretical calculations on the electronic transition of the radicals, a brief comment will be given to the assignment of the new absorption maxima in the electronic absorption spectra.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><doi>10.1248/cpb.21.211</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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title | Studies on Phenothiazinyl Radicals |
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