Related Experiment Video
Updated: Dec 6, 2025

Author Spotlight: Functionalizing Metal-Organic Frameworks: Advancements, Challenges, and the Power of Post-Synthetic Ligand Exchange
Published on: June 23, 2023
Strong Affinity of Triazolium-Appended Dipyrromethenes (TADs) for BF4
Charles Guérin1, Zhan Zhang1, Ludivine Jean-Gérard1
1ICBMS-UMR 5246, Université de Lyon, Université Claude Bernard Lyon 1, Campus Lyon-Tech la Doua, Bâtiment Lederer, 1, Rue Victor Grignard, 69622 Villeurbanne, France.
Abstract:
Because BF4- is a labile, non- or weakly coordinating anion, it is generally chosen by chemists who do not want the anion to interfere with the associated cation. Herein, we demonstrate that BF4- actually strongly binds to triazole-appended dipyrromethenes (TADs). In particular, HETCOR NMR experiments and DFT calculations were used to rationalize the results observed with anion titrations. Hence, special care should be taken when considering that BF4- is innocent.
More Related Videos
06:44From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Published on: March 24, 2018
12:05Preparation of Hydrophobic Metal-Organic Frameworks via Plasma Enhanced Chemical Vapor Deposition of Perfluoroalkanes for the Removal of Ammonia
Published on: October 10, 2013
Related Concept Videos
Molecular Shape and Polarity
Intermolecular Forces
VSEPR Theory and the Effect of Lone Pairs
Hybridization of Atomic Orbitals I
Hybridization of Atomic Orbitals II
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene