A kind of potassium ion fluorescent probe and its preparation method and application
A fluorescent probe, potassium ion technology, applied in fluorescence/phosphorescence, chemical instruments and methods, luminescent materials, etc., can solve problems such as great influence, and achieve the effects of environmental sensitivity, high detection accuracy, and good water solubility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0055] The preparation method of the fluorescent probe of the present invention is: compound I and compound II are synthesized by a known method, and then the two react to obtain a potassium ion fluorescent probe, specifically:
[0056] Add compound I (0.35 mmol) and compound II (0.3 mmol) into 10 mL of absolute ethanol, heat to reflux, react for 10 hours and then cool to room temperature. The reaction solution was evaporated and concentrated under reduced pressure to obtain a crude product, which was purified by column chromatography (silica gel, dichloromethane / methanol=1:2, v / v) to obtain a red solid compound with a yield of 92.2%, and its structure is as follows:
[0057]
[0058] Such as figure 1 For the determination of the high-resolution mass spectrum of the product, the high-resolution mass spectrometry results: Calcd.[M-I] - :611.3639; found value[M-I] - :611.3755.
Embodiment 2
[0060] Add compound I (0.3 mmol) and compound II (0.3 mmol) into 10 mL of anhydrous methanol, heat to reflux, react for 5 hours and then cool to room temperature. The reaction solution was evaporated and concentrated under reduced pressure to obtain a crude product, which was purified by column chromatography (silica gel, dichloromethane / methanol=1:2, v / v) to obtain a red solid compound with a yield of 93.4%, and its high-resolution mass spectrum Measurement result: Calcd.[M-I] - :611.3639; found value[M-I] - :611.3734.
Embodiment 3
[0062] Add compound I (0.6 mmol) and compound II (0.3 mmol) into 15 mL of anhydrous acetonitrile, heat to reflux, react for 12 hours and then cool to room temperature. The reaction solution was evaporated and concentrated under reduced pressure to obtain a crude product, which was purified by column chromatography (silica gel, dichloromethane / methanol=1:2, v / v) to obtain a red solid compound with a yield of 92.4%, and its high-resolution mass spectrum Measurement result: Calcd.[M-I] - :611.3639; found value[M-I] - :611.3688.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com