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Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes
Taku Shoji1, Yukino Ariga2, Daichi Ito2
1Department of Chemical Biology and Applied Chemistry, College of Engineering, Nihon University, Koriyama 963-8642, Fukushima, Japan. shoji.taku@nihon-u.ac.jp.
Abstract:
2-Aryl-6-pyrrolidinylazulenes bearing 1,3-diester substituents were synthesized and found to display distinct fluorescence in the solid state. In contrast, the decarboxylated analogues were entirely non-emissive. Photophysical measurements revealed that fluorescence efficiency is primarily governed by the radiative rate constant, while the nonradiative rate remains relatively constant, indicating that activation of the radiative channel underlies the observed emission in the solid state.
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