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Deprotonation-Triggered Stokes Shift Fluorescence of an Unexpected Basic-Stable Metal–Organic Framework

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https://figshare.com/articles/dataset/Deprotonation_Triggered_Stokes_Shift_Fluorescence_of_an_Unexpected_Basic_Stable_Metal_Organic_Framework/2219134
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A new three-dimensional porous metal–organic framework, JUC-119, constructed by a pyrene-based dendritic organic linker, H8TIAPy (H8TIAPy = 1,3,6,8-tetrakis­(3,5-isophthalic acid)­pyrene), and Eu­(III) has been synthesized successfully. JUC-119 shows unexpected stability under a wide range of basic conditions from 0 to 0.01 M NaOH. Furthermore, with two carboxyl groups uncoordinated in each ligand, the crystals of JUC-119 show deprotonation-triggered Stokes shift fluorescence under basic conditions. As the concentration of base increases from 0 to 0.01 M NaOH, the luminescence emission of JUC-119 becomes gradually red shifted from 455 to 485 nm. In addition, the Stokes shift shows a good linear relationship to −log­[OH–], which makes JUC-119 promising for base sensing.
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