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Preparation of Highly Porous Coordination Polymer Coatings on Macroporous Polymer Monoliths for Enhanced Enrichment of Phosphopeptides
Published on: July 14, 2015
Integration of intrinsic proton conduction and guest-accessible nanospace into a coordination polymer
Daiki Umeyama1, Satoshi Horike, Munehiro Inukai
1Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Kyoto 615-8510, Japan.
Abstract:
We report the synthesis and characterization of a coordination polymer that exhibits both intrinsic proton conductivity and gas adsorption. The coordination polymer, consisting of zinc ions, benzimidazole, and orthophosphate, exhibits a degree of flexibility in that it adopts different structures before and after dehydration. The dehydrated form shows higher intrinsic proton conductivity than the original form, reaching as high as 1.3 × 10(-3) S cm(-1) at 120 °C. We found that the rearranged conduction path and liquid-like behavior of benzimidazole molecules in the channel of the framework afforded the high proton conductivity. Of the two forms of the framework, only the dehydrated form is porous to methanol and demonstrates guest-accessible space in the structure. The proton conductivity of the dehydrated form increases by 24 times as a result of the in situ adsorption of methanol molecules, demonstrating the dual functionality of the framework. NMR studies revealed a hydrogen-bond interaction between the framework and methanol, which enables the modulation of proton conductivity within the framework.
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