Related Experiment Video
Updated: Sep 9, 2025

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
Published on: March 24, 2018
Does the Presence of Sigma Holes Affect the Way Neutral Ligands Attach to a Halonium Cation?
1Faculty of Chemistry, Wroclaw University of Science and Technology, Wybrzeze Wyspianskiego 27, 50-370, Wroclaw, Poland.
Abstract:
This study explores the fundamental nature of interactions between halonium cations-modeled as fragments of real crystal structures-and Lewis bases, with hydrogen cyanide (HCN) serving as a representative ligand. Two types of halonium cation monomers, namely the iodonium ion of adamantylideneadamantane and ethynyl(phenyl)-λ3-iodane, along with their chlorine and bromine analogues, are examined. Complexes formed with HCN molecules are investigated using quantum chemical calculations and topological analyses of electron density. The findings indicate that the σ-hole plays a decisive role in directing both the geometry and strength of these noncovalent interactions. Systems featuring a single σ-hole exhibit reduced stabilization upon additional ligand coordination, often weakening the primary halogen bond. In contrast, cations with two σ-holes can accommodate up to three or four HCN molecules without compromising the integrity of the original halogen bonds. Nevertheless, the most favorable configuration remains the directional binding of two ligands to two distinct σ-holes.
More Related Videos
09:37Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
12:43The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique
Published on: November 28, 2016
Related Concept Videos
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Molecular Orbital Theory II
Alkyl Halides
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
ortho–para-Directing Deactivators: Halogens
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...