Related Experiment Video
Updated: Jul 15, 2025

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
Published on: December 29, 2016
Chalcogen Bonding Catalysis: Tellurium, the Last Frontier?
1Institute of Chemistry of Strasbourg, UMR 7177-LASYROC, CNRS and Strasbourg University, 4 rue Blaise Pascal, 67000, Strasbourg, France.
Chalcogen bonding, a non-covalent interaction, is increasingly used in catalysis. Tellurium-based catalysts show superior Lewis acid properties and are highlighted for their catalytic applications.
Area of Science:
- Supramolecular Chemistry
- Catalysis
- Materials Science
Background:
- Chalcogen bonding (ChB) is a non-covalent interaction involving chalcogen atoms acting as Lewis acids.
- This interaction, similar to halogen bonding, enables precise structural organization in solid and solution states.
- ChB is recognized as a novel activation mode in catalysis, with growing applications.
Purpose of the Study:
- To review the Lewis acid properties of tellurium-based derivatives in solution.
- To summarize the current state of applications of tellurium-based chalcogen bonding in catalysis.
Main Methods:
- Literature review focusing on chalcogen bonding.
- Analysis of Lewis acid properties of tellurium compounds.
- Summary of catalytic applications of tellurium-based ChB.
Main Results:
- Tellurium-based chalcogen bonding catalysts exhibit significant Lewis acid characteristics.
- These tellurium derivatives often outperform lighter chalcogen (sulfur, selenium) counterparts in catalysis.
- Numerous examples demonstrate the effectiveness of ChB in catalytic processes.
Conclusions:
- Tellurium-based compounds are highly effective as Lewis acids in chalcogen bonding catalysis.
- The unique properties of tellurium-based ChB catalysts warrant further investigation and application.
- Chalcogen bonding, particularly with tellurium, represents a promising frontier in catalytic science.
More Related Videos
04:09Demonstrating the Simplicity and In Situ Temperature Monitoring of the Mechanochemical Synthesis of Metal Chalcogenides Suitable for Thermoelectrics
Published on: August 30, 2024
12:30Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
Related Concept Videos
Predicting Molecular Geometry
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Complexation Equilibria: The Chelate Effect
Valence Bond Theory
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.