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Related Concept Videos

Halogens03:01

Halogens

23.5K
Group 17 elements, known as halogens, are nonmetals. At room temperature, fluorine and chlorine are gases, bromine is a liquid, and iodine a solid. Astatine is a highly unstable radioactive element, so currently, most of its properties are unknown due to its short half-life. Tennessine is a synthetic element also predicted to be in this group. 
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Peptide Bonds02:43

Peptide Bonds

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A peptide bond covalently attaches amino acids through a dehydration reaction. One amino acid's carboxyl group and another amino acid's amino group combine, releasing a water molecule. The resulting bond is the peptide bond. The products that such linkages form are peptides. As more amino acids join this growing chain, the resulting chain is a polypeptide. Each polypeptide has a free amino group at one end. This end has the N-terminal, or the amino-terminal, and the other end has a free...
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Bond Energies and Bond Lengths02:49

Bond Energies and Bond Lengths

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Stable molecules exist because covalent bonds hold the atoms together. The strength of a covalent bond is measured by the energy required to break it, that is, the energy necessary to separate the bonded atoms. Separating any pair of bonded atoms requires energy — the stronger a bond, the greater the energy required to break it.
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Bonding in Metals02:32

Bonding in Metals

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Metallic bonds are formed between two metal atoms. A simplified model to describe metallic bonding has been developed by Paul Drüde called the “Electron Sea Model”. 
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Ionic Bonds00:42

Ionic Bonds

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Overview
When atoms gain or lose electrons to achieve a more stable electron configuration they form ions. Ionic bonds are electrostatic attractions between ions with opposite charges. Ionic compounds are rigid and brittle when solid and may dissociate into their constituent ions in water. Covalent compounds, by contrast, remain intact unless a chemical reaction breaks them.
Opposing Charges Hold Ions Together in Ionic Compounds
Ionic bonds are reversible electrostatic interactions between ions...
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Valence Bond Theory02:45

Valence Bond Theory

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Overview of Valence Bond Theory
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Updated: Jan 28, 2026

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
06:44

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

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Halogen bonding as a supramolecular dynamics catalyst.

Patrick M J Szell1, Scott Zablotny1, David L Bryce2

  • 1Department of Chemistry and Biomolecular Sciences & Centre for Catalysis Research and Innovation, University of Ottawa, Ottawa, ON, K1N 6N5, Canada.

Nature Communications
|February 24, 2019
PubMed
Summary
This summary is machine-generated.

Halogen bonding significantly enhances molecular dynamics in solid crystals by lowering rotational energy barriers for methyl groups. This effect is more pronounced than hydrogen bonding, suggesting halogen bonds can act as tunable catalysts for molecular processes.

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Area of Science:

  • Solid-state chemistry
  • Molecular dynamics
  • Supramolecular chemistry

Background:

  • Dynamic processes are crucial in functional molecules like catalysts and enzymes.
  • Understanding how intermolecular interactions influence molecular motion is key to designing new materials.

Purpose of the Study:

  • To investigate the impact of halogen bonding on molecular dynamics in solid-state cocrystals.
  • To compare the catalytic effect of halogen bonding with hydrogen bonding on methyl group rotation.

Main Methods:

  • Deuterium NMR relaxation experiments were used to study molecular dynamics.
  • Density functional theory (DFT) calculations were employed to understand the underlying mechanisms.

Main Results:

  • Halogen bonding reduced the rotational activation energy of methyl groups by 56% in 2,3,5,6-tetramethylpyrazine cocrystals.
  • Hydrogen bonding resulted in a 36% reduction in rotational activation energy.
  • DFT calculations revealed that halogen bonding destabilizes staggered and stabilizes gauche conformations, lowering the rotational energy barrier.

Conclusions:

  • Halogen bonding acts as a superior catalyst for molecular dynamics compared to hydrogen bonding in this system.
  • The catalytic efficiency of halogen bonding is tuneable and depends on the strength of the halogen bond donor.
  • Halogen bonding can play a significant role in both the assembly of molecular structures and the promotion of dynamical processes.