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出 处:《Chinese Journal of Chemistry》2012年第8期1741-1747,共7页中国化学(英文版)
摘 要:A simple method for the synthesis of new bithienylethenes bearing a functional group on the cyclopentene moi- ety is developed. Three new photochromic compounds (4a, 4b, 4c) have been successfully synthesized through this simple method, and exhibit good photochromic properties with alternate irradiation of ultraviolet and visible light. Furthermore, the fluorescence of compound 4a, which bears a quinoline unit on the cyclopentene, can be modulated via optic and proton dual inputs. Upon excitation by 320 nm light, 4a emits a strong fluorescence at 404 nm. After irradiation with 254 nm light, the emission intensity is reduced due to the fluorescence resonance energy transfers (FRET) from quinoline unit to bithienylethene unit. Moreover, on addition of H~, the fluorescence is quenched completely due to the protonation of the quinoline. In addition, both the FRET and protonation process are reversi- ble, which indicates a potential application in molecular switches and logic gates.A simple method for the synthesis of new bithienylethenes bearing a functional group on the cyclopentene moi- ety is developed. Three new photochromic compounds (4a, 4b, 4c) have been successfully synthesized through this simple method, and exhibit good photochromic properties with alternate irradiation of ultraviolet and visible light. Furthermore, the fluorescence of compound 4a, which bears a quinoline unit on the cyclopentene, can be modulated via optic and proton dual inputs. Upon excitation by 320 nm light, 4a emits a strong fluorescence at 404 nm. After irradiation with 254 nm light, the emission intensity is reduced due to the fluorescence resonance energy transfers (FRET) from quinoline unit to bithienylethene unit. Moreover, on addition of H~, the fluorescence is quenched completely due to the protonation of the quinoline. In addition, both the FRET and protonation process are reversi- ble, which indicates a potential application in molecular switches and logic gates.
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