Novel Fluorescent 2-(1,2,3-Triazolyl)Adenine Analogs
XXII IRT Abstract Book 2016
Ērika Bizdēna, Andrejs Šišuļins, Zigfrīds Kapilinskis, Dace Cīrule, Māris Turks

Push-pull purine derivatives are attractive as sensors and reporters for biological applications. Recently the fluorescent purines as materials for electronic devices have also been developed. 1 Different combinations of electron donor and acceptor substituents allow fluorescence emission tuning in the range of 350-450 nm, making the purines good candidates for the construction of OLED devices. 1 Earlier we have reported that N6-substituted 2-triazolyl-adenine nucleosides exhibit strong fluorescence with emission maxima around 400 nm and quantum yields up to 53%. 2 The aim of this research was to synthesize 9-alkyl purines with electron donor at C(6) and 4- substituted 1,2,3-triazol-1 -yl group as acceptor at C(2) and investigate their fluorescence properties.


Keywords
Fluorescent adenine analogs, CuAAC, push-pull purines

Bizdēna, Ē., Šišuļins, A., Kapilinskis, Z., Cīrule, D., Turks, M. Novel Fluorescent 2-(1,2,3-Triazolyl)Adenine Analogs. In: XXII IRT Abstract Book, France, Paris, 18-22 July, 2016. Paris: 2016, pp.212-213.

Publication language
English (en)
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