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• W3204577935 endingPage "5952" @default.
• W3204577935 startingPage "5952" @default.
• W3204577935 abstract "Mesitylene was used as a core in seven new tritopic nitrogen containing linkers. Three of the linkers, each containing three nitrile groups, were obtained through Suzuki, Sonogashira and Heck-type coupling reactions. Next, these were converted to tetrazol-5-yl moieties by the cycloaddition of sodium azide to the nitrile functionalities. The last linker, containing three 1,2,3-triazol-4-yl moieties, was synthesized by the Huisgen cycloaddition of phenyl azide to the corresponding alkyne. The latter was obtained via a Corey-Fuchs reaction sequence from the previously reported formyl derivative. As the proof of concept for their potential in MOF design, one of the nitriles was used to build an Ag-based network." @default.
• W3204577935 created "2021-10-11" @default.
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• W3204577935 date "2021-09-30" @default.
• W3204577935 modified "2023-10-05" @default.
• W3204577935 title "Nitrogen-Based Linkers with a Mesitylene Core: Synthesis and Characterization" @default.
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• W3204577935 doi "https://doi.org/10.3390/molecules26195952" @default.
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• W3204577935 hasPublicationYear "2021" @default.
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