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Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
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Hydrogen Bonds

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...
Hydrogen Bonds00:26

Hydrogen Bonds

Hydrogen BondsHydrogen bonds are weak attractions between atoms that have formed other chemical bonds. One of these atoms is electronegative, like oxygen, and has a partial negative charge. The other is a hydrogen atom that has bonded with another electronegative atom and has a partial positive charge.Hydrogen Bonds Control the World!Because hydrogen has very weak electronegativity when it binds with a strongly electronegative atom, such as oxygen or nitrogen, electrons in the bond are...
Aromatic Hydrocarbon Anions: Structural Overview01:18

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Neutral hydrocarbons like cyclopentadiene with an odd number of carbon atoms and one intervening CH2 group in the ring are not aromatic. Cyclopentadiene with 4 π electrons does not satisfy the 4n + 2 π electron rule. Additionally, the intervening CH2 group is sp3 hybridized and lacks a vacant p orbital, thereby interrupting the overlap of p orbitals in a continuous manner and preventing the delocalization of π electrons throughout the ring.
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Characteristics and Nomenclature of Homopolymers01:00

Characteristics and Nomenclature of Homopolymers

Polymers that are made up of identical monomer units are called homopolymers. Only one repeating unit is involved in the construction of the homopolymer structure. For example, as depicted in Figure 1, polypropylene is a homopolymer constituted of propylene monomers. Here, the only repeating unit in the polymer chain is propylene.
π Molecular Orbitals of 1,3-Butadiene01:24

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Conjugated dienes have lower heats of hydrogenation than cumulated and isolated dienes, making them more stable. The enhanced stabilization of conjugated systems can be understood from their π molecular orbitals.
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Microfluidic-based Synthesis of Covalent Organic Frameworks (COFs): A Tool for Continuous Production of COF Fibers and Direct Printing on a Surface
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Rapidly Diversifying Hydrogen-Bonded Organic Frameworks With Permanent Porosity.

Taito Hashimoto1, Ichiro Hisaki1

  • 1Division of Chemistry, Graduate School of Engineering Science, The University of Osaka, Toyonaka, Osaka, Japan.

Angewandte Chemie (International Ed. in English)
|July 13, 2026
PubMed
Summary

Hydrogen-bonded organic frameworks (HOFs) have advanced significantly, offering sustainable materials with tunable properties. This review covers HOF evolution, focusing on porosity, structure-property relationships, and multicomponent designs.

Keywords:
hydrogen bondpi‐conjugated moleculeporous molecular crystal

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Area of Science:

  • Materials Science
  • Chemistry
  • Crystallography

Background:

  • Hydrogen-bonded organic frameworks (HOFs) represent a significant advancement in porous molecular crystals (PMCs).
  • HOFs offer advantages like fewer defects and precise structure-property analysis due to reversible bonding.
  • They are recognized for their potential as sustainable materials.

Purpose of the Study:

  • To review the evolution of HOFs, particularly those with permanent porosity, over the past 15 years.
  • To analyze HOFs based on the molecular structures of their constituent molecules (tectons).
  • To highlight distinctive aspects including permanent porosity, isostructural libraries, and multicomponent HOFs.

Main Methods:

  • Review of scientific literature on HOF synthesis and characterization.
  • Analysis of HOF structures derived from diverse tectons (benzene derivatives, polycyclic aromatics, macrocycles).
  • Focus on concepts like permanent porosity, isostructural/isoreticular HOFs, and multicomponent HOFs.

Main Results:

  • HOFs synthesized from a wide range of tectons exhibit diverse structures and properties.
  • Permanent porosity in both rigid and flexible HOFs is crucial for porous material applications.
  • Isostructural HOFs enable the creation of continuous libraries, while multicomponent HOFs allow for function tuning.

Conclusions:

  • HOFs have undergone significant development, driven by diverse tecton choices and structural concepts.
  • The ability to precisely control structure-property relationships makes HOFs highly promising.
  • Future directions include leveraging multicomponent HOFs for novel functionalities and enhanced material design.