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Related Concept Videos

Hydrogen Bonds01:04

Hydrogen Bonds

9.2K
A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
9.2K
Exceptions to the Octet Rule02:55

Exceptions to the Octet Rule

29.1K
Many covalent molecules have central atoms that do not have eight electrons in their Lewis structures. These molecules fall into three categories:
29.1K
Valence Bond Theory02:45

Valence Bond Theory

33.0K
Overview of Valence Bond Theory
33.0K
Introduction to Functional Groups02:08

Introduction to Functional Groups

27.8K

Functional groups are group of atoms with specific chemical properties that occur within organic molecules and sometimes denoted as “R”. Functional groups are found along the carbon backbone of macromolecules can form chains or rings of carbon atoms. Functional groups can “functionalize” a compound by enabling it to adopt different physical and chemical properties.  
Types of common functional groups
The table below summarizes some of the major functional...
27.8K
ortho–para-Directing Deactivators: Halogens01:24

ortho–para-Directing Deactivators: Halogens

5.7K
Halogens are ortho–para directors. They are more electronegative than carbon. Therefore, as ring substituents, they can withdraw electrons through the inductive effect and deactivate the aromatic ring towards electrophilic substitution. Halogens also have an electron-donating resonance effect on the ring, which influences the orientation of the incoming electrophile. If an electrophile attacks at the ortho or the para position, the halogen donates electrons and stabilizes the intermediate...
5.7K
Halogenation of Alkenes02:46

Halogenation of Alkenes

16.2K
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
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.
16.2K

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Related Experiment Video

Updated: Aug 28, 2025

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

Published on: March 24, 2018

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Halogen bonding regulated functional nanomaterials.

Jie Zheng1, Ady Suwardi1, Claris Jie Ee Wong2

  • 1Institute of Materials Research and Engineering, ASTAR (Agency for Science, Technology and Research) Fusionopolis Way, Innovis, #08-03 Singapore 138634 Singapore zheng_jie@imre.a-star.edu.sg lohxj@imre.a-star.edu.sg lizb@imre.a-star.edu.sg.

Nanoscale Advances
|September 22, 2022
PubMed
Summary
This summary is machine-generated.

Halogen bonding, a powerful non-covalent interaction, drives self-assembly for advanced nanomaterials. This review highlights its applications in molecular recognition, catalysis, and functional materials.

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Area of Science:

  • Supramolecular Chemistry
  • Materials Science
  • Crystal Engineering

Background:

  • Non-covalent interactions are key to fabricating supramolecular architectures.
  • Halogen bonding is a potent non-covalent bond gaining traction in nanomaterial design.
  • This review focuses on recent advancements in halogen bonding for self-assembly.

Purpose of the Study:

  • To review the latest studies on halogen bonding-induced self-assembly.
  • To discuss the fundamental aspects and engineering applications of halogen bonding in nanomaterials.
  • To highlight the potential of halogen bonding in crystal and materials engineering.

Main Methods:

  • Review of recent scientific literature on halogen bonding and self-assembly.
  • Analysis of studies focusing on nanomaterial fabrication via halogen bonding.
  • Discussion of applications including molecular recognition, sensing, and organocatalysis.

Main Results:

  • Halogen bonding offers high directionality and controllable interaction strength for nanomaterial design.
  • It provides a facile platform for synthesizing diverse nanomaterials.
  • Applications span molecular recognition, sensing, organocatalysis, and multifunctional materials.

Conclusions:

  • Halogen bonding is a powerful tool for designing and synthesizing functional nanomaterials.
  • Its controllable nature facilitates applications in advanced materials and supramolecular chemistry.
  • Further exploration promises innovations in areas like sensing and catalysis.