Add time:07/14/2019         Source:sciencedirect.com

We designed and synthesized a tri-(2-picolyl) amine (TPA) functionalized triarylborane, 1-(6-(4-(dimesitylboryl)phenyl)pyridin-2-yl)-N,N-bis(pyridin-2-ylmethyl)methanamine (PB2). The photophysical properties of PB2 were thoroughly explored. Moreover, PB2 can capture CN− and F− in aqueous solution through strong chelation induced by the synergy of a boron atom and metal ion gripped by TPA to display entirely different fluorogenic responses such as fluorescence enhancement for CN− and fluorescence quenching for F−. The results of TOF-MS-EI analysis and theoretical calculations indicate that the complexing of PB2 with CN− formed a 2-to-2 adduct with a stabilized configuration, resulting in strong emission. The complexing of PB2 with F− formed a 1-to-1 adduct with a loose configuration, resulting in weak emission. In pure water, the detection limit of PB2 for CN− is 0.79 μM, and in H2O/THF (1:9 v/v) system, the detection limits of PB2 for CN− and F− can reach 0.39 and 2.12 μM, respectively, indicating its potential application for effective detection and discrimination of CN− and F−.

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