Selective fluorescent and colorimetric recognition of cyanide via altering hydrogen bonding interaction in aqueous solution and its application in bioimaging
Autor: | Yen Leng Pak, Xin Zhou, Zhixue Liu, Jaemee Kim, K.M.K. Swamy, Juyoung Yoon, Sunjung Jo |
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Rok vydání: | 2016 |
Předmět: |
Aqueous solution
010405 organic chemistry Chemistry Hydrogen bond Process Chemistry and Technology General Chemical Engineering Cyanide Imine 010402 general chemistry Photochemistry 01 natural sciences Fluorescence 0104 chemical sciences chemistry.chemical_compound Intramolecular force Pyrene Selectivity |
Zdroj: | Dyes and Pigments. 128:256-262 |
ISSN: | 0143-7208 |
DOI: | 10.1016/j.dyepig.2016.02.007 |
Popis: | In this paper, we report a new pyrene imine derivative which bears a relatively rigid intramolecular hydrogen bonding pocket, for fluorescent and colorimetric sensing of cyanide. In CH3CN solution, the chemosensor displayed distinct fluorescent and UV absorption changes towards CN−, C H 3 C O 2 − , F−, and H 2 P O 4 − . Notably, in an aqueous CH3CN medium (10%, v/v), the selectivity towards cyanide over other various anions were observed with an obvious fluorescence enhancement and colorimetric change. Thus, we demonstrated that the selectivity of the pyrene based chemosensor towards anions can be optimized via controlling hydrogen bonding interactions in different solvent systems. Finally the application of the chemosensor in fluorescent imaging cellular cyanide variation was demonstrated with living HeLa cells. |
Databáze: | OpenAIRE |
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