{"title":"Radiation mechanisms—XI","authors":"Martyn C.R. Symons, Donald N. Zimmerman","doi":"10.1016/0020-7055(76)90028-0","DOIUrl":null,"url":null,"abstract":"<div><p>Exposure of aqueous glasses containing carbonate enriched in <sup>13</sup>CO<sub>3</sub><sup>2−</sup> gave <sup>.</sup>OH and e<sub><em>t</em></sub><sup>−</sup> as major primary products at 77 K, but <sup>.</sup>CO<sub>2</sub><sup>−</sup> and CȮ<sub>3</sub><sup>−</sup> features together with <sup>13</sup>C satellite lines grew strongly on annealing above 77 K. Alkaline solutions gave mainly <sup>.</sup>O<sup>−</sup> and e<sub><em>t</em></sub><sup>−</sup>, but on annealing a new radical, tentatively identified as CȮ<sub>4</sub><sup>3−</sup>, was detected. This had E.S.R. parameters comparable with those for <sup>13</sup>CȮ<sub>3</sub><sup>−</sup>, but with a smaller anisotropy in both A(<sup>13</sup>C) and <em>g</em>. This species is thought to result from addition of <sup>.</sup>O<sup>−</sup> to CO<sub>3</sub><sup>2−</sup></p><p>Solutions is methanol (CD<sub>3</sub>OD) gave mainly D<sub>2</sub>ĊOD, e<sub><em>t</em></sub><sup>−</sup>, and <sup>.</sup>CO<sub>2</sub><sup>3−</sup> radicals, but CȮ<sub>3</sub><sup>−</sup> grew in strongly on annealing.</p><p>Neutral aqueous glasses containing formate ions gave HĊO and ĊO<sub>2</sub><sup>−</sup> in addition to <sup>.</sup>OH radicals, together with a broad feature tentatively assigned to HĊO<sub>2</sub><sup>2−</sup> or HĊO(OH)<sup>−</sup> radical. These features were better defined in alkali glasses (HĊO<sub>2</sub><sup>2−</sup>) and in 6 mol dm<sup>−3</sup> sulphuric acid glasses [HĊO(OH)<sup>−</sup>]. Features for <sup>13</sup>CO<sub>2</sub><sup>−</sup> were clearly resolved in the former, but in the acidic glasses a larger <sup>13</sup>C hyperfine coupling suggested <sup>13</sup>ĊO(OH). The formly radical was also detected in the scidic glasses but not in the alkaline media. The mechanisms of the reactions leading to these intermediates are discussed and compared with those for aqueous nitrite solutions.</p></div>","PeriodicalId":100688,"journal":{"name":"International Journal for Radiation Physics and Chemistry","volume":"8 5","pages":"Pages 595-601"},"PeriodicalIF":0.0000,"publicationDate":"1976-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-7055(76)90028-0","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal for Radiation Physics and Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0020705576900280","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
Exposure of aqueous glasses containing carbonate enriched in 13CO32− gave .OH and et− as major primary products at 77 K, but .CO2− and CȮ3− features together with 13C satellite lines grew strongly on annealing above 77 K. Alkaline solutions gave mainly .O− and et−, but on annealing a new radical, tentatively identified as CȮ43−, was detected. This had E.S.R. parameters comparable with those for 13CȮ3−, but with a smaller anisotropy in both A(13C) and g. This species is thought to result from addition of .O− to CO32−
Solutions is methanol (CD3OD) gave mainly D2ĊOD, et−, and .CO23− radicals, but CȮ3− grew in strongly on annealing.
Neutral aqueous glasses containing formate ions gave HĊO and ĊO2− in addition to .OH radicals, together with a broad feature tentatively assigned to HĊO22− or HĊO(OH)− radical. These features were better defined in alkali glasses (HĊO22−) and in 6 mol dm−3 sulphuric acid glasses [HĊO(OH)−]. Features for 13CO2− were clearly resolved in the former, but in the acidic glasses a larger 13C hyperfine coupling suggested 13ĊO(OH). The formly radical was also detected in the scidic glasses but not in the alkaline media. The mechanisms of the reactions leading to these intermediates are discussed and compared with those for aqueous nitrite solutions.