R. Newman, C. G. Freeman, M. McEwan, R. Claridge, L. F. Phillips
{"title":"某些脂肪胺的汞致敏发光","authors":"R. Newman, C. G. Freeman, M. McEwan, R. Claridge, L. F. Phillips","doi":"10.1039/TF9716701360","DOIUrl":null,"url":null,"abstract":"Rate constants for quenching of 253.7 nm fluorescence and quantum efficiencies for emission of luminescence during mercury-sensitized photolysis have been measured for methylamine, ethylaminc, n-propylamine, isopropylamine, n-butylamine, isobutylamine, tert-butylamine, sec-butylamine, dimethylamine, diethylamine, trimethylamine and triethylamine. From the variation of luminescent efficiency with the structure of the amine we conclude that the main process competing with luminescence, during the reaction of Hg(3Po) with an amine, is normally the abstraction of an α-hydrogen atom. Strong σ*→n fluorescence was observed during 253.7 nm irradiation of trimethylamine, triethylamine and tri-n-propylamine.","PeriodicalId":23290,"journal":{"name":"Transactions of The Faraday Society","volume":"67 1","pages":"1360-1364"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1039/TF9716701360","citationCount":"21","resultStr":"{\"title\":\"Mercury-sensitized luminescence of some aliphatic amines\",\"authors\":\"R. Newman, C. G. Freeman, M. McEwan, R. Claridge, L. F. Phillips\",\"doi\":\"10.1039/TF9716701360\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Rate constants for quenching of 253.7 nm fluorescence and quantum efficiencies for emission of luminescence during mercury-sensitized photolysis have been measured for methylamine, ethylaminc, n-propylamine, isopropylamine, n-butylamine, isobutylamine, tert-butylamine, sec-butylamine, dimethylamine, diethylamine, trimethylamine and triethylamine. From the variation of luminescent efficiency with the structure of the amine we conclude that the main process competing with luminescence, during the reaction of Hg(3Po) with an amine, is normally the abstraction of an α-hydrogen atom. Strong σ*→n fluorescence was observed during 253.7 nm irradiation of trimethylamine, triethylamine and tri-n-propylamine.\",\"PeriodicalId\":23290,\"journal\":{\"name\":\"Transactions of The Faraday Society\",\"volume\":\"67 1\",\"pages\":\"1360-1364\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1039/TF9716701360\",\"citationCount\":\"21\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Transactions of The Faraday Society\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/TF9716701360\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transactions of The Faraday Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/TF9716701360","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Mercury-sensitized luminescence of some aliphatic amines
Rate constants for quenching of 253.7 nm fluorescence and quantum efficiencies for emission of luminescence during mercury-sensitized photolysis have been measured for methylamine, ethylaminc, n-propylamine, isopropylamine, n-butylamine, isobutylamine, tert-butylamine, sec-butylamine, dimethylamine, diethylamine, trimethylamine and triethylamine. From the variation of luminescent efficiency with the structure of the amine we conclude that the main process competing with luminescence, during the reaction of Hg(3Po) with an amine, is normally the abstraction of an α-hydrogen atom. Strong σ*→n fluorescence was observed during 253.7 nm irradiation of trimethylamine, triethylamine and tri-n-propylamine.