Related Experiment Video
Updated: Feb 24, 2026

Author Spotlight: Characterizing DNA G-Quadruplex by Bis-3-Chloropiperidine Based Chemical Mapping
Published on: May 12, 2023
A Cr(VI) selective probe based on a quinoline-amide calix[4]arene
Juliane F Ferreira1, Izilda A Bagatin1
1Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Departamento de Química, Laboratório de Química de Calixarenos, Espectroscopia Molecular e Catálise, Universidade Federal de São Paulo, Rua Prof. Arthur Riedel, 275, CEP 09972-270 Diadema, SP, Brazil.
A novel quinoline-amide calix[4]arene receptor selectively detects hazardous dichromate (Cr2O72-) and mercury (Hg2+) ions. This sensor exhibits high selectivity for dichromate, making it a promising tool for environmental monitoring.
Area of Science:
- Supramolecular Chemistry
- Analytical Chemistry
- Materials Science
Background:
- Development of selective chemosensors for hazardous anions and cations is crucial for environmental safety.
- Calix[4]arene scaffolds offer a versatile platform for designing host molecules with specific binding properties.
Purpose of the Study:
- To synthesize and characterize a new quinoline-amide calix[4]arene receptor.
- To investigate the receptor's sensing capabilities for various hazardous anions and metal ions.
- To evaluate the selectivity and sensitivity of the receptor for target analytes.
Main Methods:
- Synthesis of the quinoline-amide calix[4]arene receptor.
- UV-vis and fluorescence spectroscopy for sensing studies.
- Proton Nuclear Magnetic Resonance (NMR) spectroscopy for anion-binding investigations.
Main Results:
- The synthesized receptor demonstrated selective sensing for dichromate (Cr2O72-) and mercury (Hg2+) ions.
- Higher association constants were observed for dichromate compared to mercury ions.
- Fluorescence measurements indicated high selectivity for dichromate over other tested anions and cations, with a low limit of detection (7.36×10-6 moldm-3).
- Proton NMR studies confirmed strong interactions between the dichromate anion and the receptor's NH and CH groups, attributed to hydrogen bonding.
Conclusions:
- The quinoline-amide calix[4]arene receptor is a highly selective and sensitive sensor for dichromate ions.
- The receptor's design, incorporating hydrogen-bond donor groups, enhances anion binding affinity.
- This receptor shows significant potential for the selective detection of Cr(VI) in environmental samples.

