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Network Covalent Solids02:18

Network Covalent Solids

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Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
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Cyclohexane does not exist in a planar form due to the high angle and torsional strain it would experience in the planar structure. Instead, it adopts non-planar chair and boat conformations.
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Life on Earth is carbon-based, as all macromolecules that make up living organisms contain carbon atoms. All organic compounds have a carbon backbone. Each carbon atom is tetravalent and can bond with four other atoms, making it an extraordinarily flexible component of biological molecules. Because carbon’s valence electrons are stable, it rarely becomes an ion. As the carbon chain increases in length, structural modifications such as ring structures, double bonds, and branching side...
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Metallic solids such as crystals of copper, aluminum, and iron are formed by metal atoms. The structure of metallic crystals is often described as a uniform distribution of atomic nuclei within a “sea” of delocalized electrons. The atoms within such a metallic solid are held together by a unique force known as metallic bonding that gives rise to many useful and varied bulk properties.
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Related Experiment Video

Updated: Aug 26, 2025

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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Soft 2D Covalent Organic Framework with Compacted Honeycomb Topology.

Chenglong Liu1, Zhenzhu Wang1, Lei Zhang1

  • 1State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, China.

Journal of the American Chemical Society
|October 6, 2022
PubMed
Summary

Researchers synthesized a novel soft 2D covalent organic framework (S-COF) with a unique compacted honeycomb structure. This breakthrough expands the possibilities for developing advanced S-COF materials.

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Synthesis of Single-Crystalline Core-Shell Metal-Organic Frameworks
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Area of Science:

  • Materials Science
  • Organic Chemistry
  • Nanotechnology

Background:

  • Covalent Organic Frameworks (COFs) are crystalline porous polymers.
  • Existing COFs are typically rigid, limiting their structural diversity.
  • Soft COFs (S-COFs) offer potential for novel topological structures.

Purpose of the Study:

  • To synthesize a novel imine-based soft 2D covalent organic framework (S-COF).
  • To achieve a unique compacted honeycomb topology in an S-COF.
  • To explore the structural properties and formation mechanism of this new S-COF.

Main Methods:

  • Utilized a helically folded ditopic flexible linker and a trigonal building block for synthesis.
  • Characterized the S-COF structure using transmission electron microscopy (TEM), atomic force microscopy (AFM), and powder X-ray diffraction (PXRD).
  • Confirmed structural integrity and properties via thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FT-FTIR), and circular dichroism (CD) measurements.

Main Results:

  • Successfully synthesized a 2D S-COF with a previously unachieved compacted honeycomb topology.
  • The flexible skeleton enabled spontaneous formation of a nonporous, compacted structure via intramolecular π-stacking.
  • Demonstrated the unique topological structure through comprehensive material characterization.

Conclusions:

  • This study reports the first experimental realization of a compacted honeycomb topology in S-COFs.
  • The findings open new avenues for designing and synthesizing advanced S-COF materials.
  • Significantly expands the scope and potential applications of covalent organic frameworks.