Related Experiment Video
Updated: Jun 11, 2025

Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives
Published on: January 19, 2016
Fluorination of antimonene hexagons
Michael Fickert1, Rebeca Martinez-Haya2, Diego López-Alcalá2
1Department of Chemistry and Pharmacy and Joint Institute of Advanced Materials and Processes (ZMP) Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) Fürth, 90762, Germany.
Researchers explored fluorination of 2D antimonene using plasma and etching methods. This study confirms fluorine bond stability, enabling future modifications of heavy 2D pnictogens.
Area of Science:
- Materials Science
- Nanotechnology
- Surface Chemistry
Background:
- Two-dimensional (2D) materials offer unique electronic and physical properties.
- Antimonene, a heavy 2D pnictogen, shows promise for novel applications.
- Controlled surface functionalization is key to tailoring material properties.
Purpose of the Study:
- To investigate the fluorination of 2D antimonene synthesized via a colloidal bottom-up approach.
- To explore the efficacy of microwave-induced plasma and reactive ion etching for antimonene fluorination.
- To confirm the stability of the resulting fluorine-antimonene bonds.
Main Methods:
- Synthesis of 2D antimonene using a colloidal bottom-up method.
- Fluorination using microwave-induced plasma with CF4.
- Fluorination using reactive ion etching with CF4.
- Density Functional Theory (DFT) calculations to assess bond stability.
Main Results:
- Successful fluorination of 2D antimonene hexagons was achieved.
- Both microwave-induced plasma and reactive ion etching proved effective fluorination strategies.
- DFT calculations corroborated the stability of the fluorine-antimonene bonds.
Conclusions:
- Fluorination of 2D antimonene is feasible using established plasma and etching techniques.
- The generated fluorine bonds on antimonene are stable.
- This research opens avenues for creating novel halogen-derivative 2D pnictogen materials.
More Related Videos
10:10Application of Elemental Lanthanides in the Selective C-F Activation of Trifluoromethylated Benzofulvenes Providing Access to Various Difluoroalkenes
Published on: July 28, 2018
05:34Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes
Published on: December 16, 2019
Related Concept Videos
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
VSEPR Theory and the Effect of Lone Pairs
Hybridization of Atomic Orbitals I
VSEPR Theory and the Basic Shapes
The Aufbau Principle and Hund's Rule
Hybridization of Atomic Orbitals II