Synthesis of 6-(4-diethylamino)phenyl-2-oxo-2H-pyran-3-carbonitorile derivatives and their fluorescence in solid state and in solutions

Autor: Masayori Hagimori, Ho-Hsiang Wei, Chen-Kuen Tai, Tzenge-Lien Shih, Shinich Kawashima, Keisuke Kawashima, Naoko Mizuyama, Kenichirou Yokota, Bo-Cheng Wang, Zhi-Shuan Huang, Shih-Chun Tseng, Jian-Wei Lu, Yoshinori Tominaga, Kuen-Da Wu, Mika Suzuta, Yasuhisa Nishimura, San-Lang Wang, Chieh-Yu Chen
Rok vydání: 2012
Předmět:
Zdroj: Dyes and Pigments. 92:1069-1074
ISSN: 0143-7208
Popis: One-pot synthesis of a new 2-pyrone dye ( 3a ) by the reaction of 4-diethylamino-acetophenone ( 1 ) with methyl 2-cyano-3,3-bis(methylsulfanyl)acrylate ( 2 ) in the presence of sodium hydroxide as the base was carried out in DMSO. Compound 4a was synthesized by the replacement of methylsulfanyl group of 3a with dimethylamine at 4-position of pyrone ring. Similarly, compound 5a was prepared via the reaction of 3a with diethyl malonate. Compounds 3a–5a exhibited the following fluorescence in the solid state: red ( 3a ), green ( 4a ), and orange ( 5a ). In addition, it was revealed that 2-pyrone dyes exhibit fluorescence in various solvents and show positive solvatochromism. Compounds 3a and 5a exhibited intense fluorescence in chloroform and dichloromethane (fluorescence quantum yield Φ : 0.94–0.95). In contrast, compound 4a exhibited intense fluorescence in polar solvents (methanol: Φ = 0.92). These 2-pyrone dyes have the potential for applications in various fields.
Databáze: OpenAIRE