Related Experiment Video
Updated: Jan 31, 2026

Fluorescence-Based Detection of FEN1 Nuclease Activity and Screening of Small-Molecule Inhibitors
Published on: June 27, 2025
Optically active crown ether-based fluorescent sensor molecules: A mini-review.
Ildikó Móczár1, Péter Huszthy1
1Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, Budapest, Hungary.
This review highlights fluorescent optically active crown ethers for enantiomeric recognition and cation binding. Fluorescence spectroscopy is key for studying these advanced chemosensors.
Area of Science:
- Supramolecular Chemistry
- Analytical Chemistry
- Organic Chemistry
Background:
- Crown ethers are cyclic molecules known for cation binding.
- Optically active crown ethers possess chirality, enabling enantioselective interactions.
- Fluorescent crown ethers act as chemosensors, signaling analyte binding through changes in fluorescence.
Purpose of the Study:
- To review fluorescent optically active crown ethers for enantiomeric recognition.
- To explore their inorganic cation complexation properties.
- To highlight the application of fluorescence spectroscopy in studying these compounds.
Main Methods:
- Literature review of fluorescent optically active crown ethers.
- Investigation of enantiomeric recognition using fluorescence spectroscopy.
- Analysis of inorganic cation complexation via fluorescence changes.
Main Results:
- Fluorescent optically active crown ethers demonstrate significant enantiomeric recognition capabilities.
- These sensors can also bind inorganic cations, with binding influenced by the crown ether structure and fluorophore.
- Fluorescence spectroscopy proves to be a sensitive and versatile tool for evaluating these properties.
Conclusions:
- Fluorescent optically active crown ethers are effective chemosensors for chiral recognition and cation sensing.
- The combination of crown ether cavity, chirality, and fluorophore design is crucial for sensor performance.
- Fluorescence spectroscopy is indispensable for the development and application of these advanced molecular sensors.
Related Concept Videos
Crown Ethers
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Review and Preview
Percentiles are a type of fractile that partition data into...
Review and Preview
Properties of Enantiomers and Optical Activity
Structure and Nomenclature of Ethers
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
Classification of Ethers
Based on their attached substituent...

