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• W4328049116 abstract "As intelligent probes, dynamic and controllable molecular switches are useful tools for probing and intervening in life processes. However, the types and properties of molecular switches are still relatively single and often can only make two actions: “off” and “on”. Therefore, the development of novel molecular switches with multiple colors and multiple instructions is very challenging. Herein, we propose a novel strategy based on the instability of the Lewis acid–base pair (boron (B) and nitrogen (N)), such as introducing the Schiff base (C═N) group into the aminoborane skeleton and preparing the novel molecular switches BN-HDZ and BN-HDZ-N. These two molecules were found to have good multicolor fluorescence switching capability for methanol. Surprisingly, the compound BN-HDZ-N shows unprecedented visual identification for the butanol isomers and could be made into a portable strip for simple and rapid visual identification of the four isomers of butanol, promising an alternative to conventional Lucas reagents. This provides a novel strategy for the design and fabrication of novel multicolor-tunable molecular switches with visual identification of isomers." @default.
• W4328049116 created "2023-03-22" @default.
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• W4328049116 date "2023-03-21" @default.
• W4328049116 modified "2023-10-16" @default.
• W4328049116 title "Multicolor Adjustable B–N Molecular Switches: Simple, Efficient, Portable, and Visual Identification of Butanol Isomers" @default.
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• W4328049116 doi "https://doi.org/10.1021/acs.analchem.2c05045" @default.
• W4328049116 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36942711" @default.
• W4328049116 hasPublicationYear "2023" @default.
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