S. Mataka*, 又賀 駿太郎, W. Lin, 李 偉華, M. Tashiro, 田代 昌士, Kazufumi Takahashi, 高橋 和文, T. Hatta, 八田 泰三, A. Torii, 鳥井 昭美, シュンタロウ マタカ, リ イカ, マサシ タシロ, カズフミ タカハシ, タイゾウ ハッタ, アケミ トリイ
{"title":"4,7 -二(烷氧基取代)苯基- 1,2,5 -噻二唑(3,4 -c)吡啶的吸收和荧光光谱","authors":"S. Mataka*, 又賀 駿太郎, W. Lin, 李 偉華, M. Tashiro, 田代 昌士, Kazufumi Takahashi, 高橋 和文, T. Hatta, 八田 泰三, A. Torii, 鳥井 昭美, シュンタロウ マタカ, リ イカ, マサシ タシロ, カズフミ タカハシ, タイゾウ ハッタ, アケミ トリイ","doi":"10.15017/17192","DOIUrl":null,"url":null,"abstract":"A series of 4, 7-Di (alkoxy-substituted) phenyl-1,2,5-thiadiazolo[3, 4-c]pyridines were prepared and their absorption and fluorescence spectre were obatined. These compounds showed a large stokes shift of 115-135 nm arid 6-aryl derivatives and 6-alkoxycarbonyl opes are strongly fluorescent in a solid state. and 1, 2, 5-oxadiazolo[3, 4-c]pyridine are strongly fluorescent in a solid state and, as a dyestuff, the for-mer is superior to the latter in the durablity.`) As a part of our studies on fluorescent heterocycles, we now report on the fluorescence of alkoxy-substituted 4, 6, 7-tri- and 4, 7-diaryl-1, 2, 5-thiadiazolo[3, 4-c]pyridines.","PeriodicalId":11722,"journal":{"name":"Engineering sciences reports, Kyushu University","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1990-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Absorption and Fluorescence Spectra of 4, 7-Di (alkoxy-substituted) pheny1-1, 2, 5-thiadiazolo (3, 4-c) pyridine\",\"authors\":\"S. Mataka*, 又賀 駿太郎, W. Lin, 李 偉華, M. Tashiro, 田代 昌士, Kazufumi Takahashi, 高橋 和文, T. Hatta, 八田 泰三, A. Torii, 鳥井 昭美, シュンタロウ マタカ, リ イカ, マサシ タシロ, カズフミ タカハシ, タイゾウ ハッタ, アケミ トリイ\",\"doi\":\"10.15017/17192\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A series of 4, 7-Di (alkoxy-substituted) phenyl-1,2,5-thiadiazolo[3, 4-c]pyridines were prepared and their absorption and fluorescence spectre were obatined. These compounds showed a large stokes shift of 115-135 nm arid 6-aryl derivatives and 6-alkoxycarbonyl opes are strongly fluorescent in a solid state. and 1, 2, 5-oxadiazolo[3, 4-c]pyridine are strongly fluorescent in a solid state and, as a dyestuff, the for-mer is superior to the latter in the durablity.`) As a part of our studies on fluorescent heterocycles, we now report on the fluorescence of alkoxy-substituted 4, 6, 7-tri- and 4, 7-diaryl-1, 2, 5-thiadiazolo[3, 4-c]pyridines.\",\"PeriodicalId\":11722,\"journal\":{\"name\":\"Engineering sciences reports, Kyushu University\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1990-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Engineering sciences reports, Kyushu University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15017/17192\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Engineering sciences reports, Kyushu University","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15017/17192","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Absorption and Fluorescence Spectra of 4, 7-Di (alkoxy-substituted) pheny1-1, 2, 5-thiadiazolo (3, 4-c) pyridine
A series of 4, 7-Di (alkoxy-substituted) phenyl-1,2,5-thiadiazolo[3, 4-c]pyridines were prepared and their absorption and fluorescence spectre were obatined. These compounds showed a large stokes shift of 115-135 nm arid 6-aryl derivatives and 6-alkoxycarbonyl opes are strongly fluorescent in a solid state. and 1, 2, 5-oxadiazolo[3, 4-c]pyridine are strongly fluorescent in a solid state and, as a dyestuff, the for-mer is superior to the latter in the durablity.`) As a part of our studies on fluorescent heterocycles, we now report on the fluorescence of alkoxy-substituted 4, 6, 7-tri- and 4, 7-diaryl-1, 2, 5-thiadiazolo[3, 4-c]pyridines.