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Related Concept Videos

Network Covalent Solids02:18

Network Covalent Solids

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.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
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Coordination Number and Geometry

For transition metal complexes, the coordination number determines the geometry around the central metal ion. Table 1 compares coordination numbers to molecular geometry. The most common structures of the complexes in coordination compounds are octahedral, tetrahedral, and square planar.
Metallic Solids02:37

Metallic Solids

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.
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability. Many...
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Structural Isomerism

Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
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Ionic Crystal Structures

Ionic crystals consist of two or more different kinds of ions that usually have different sizes. The packing of these ions into a crystal structure is more complex than the packing of metal atoms that are the same size.
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Valence Bond Theory

Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...

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Two cuprous cyanide polymorphs: diamond net versus 3,4-connected net.

Xian-Ming Zhang1, Ying-Lian Qing, Hai-Shun Wu

  • 1School of Chemistry & Material Science, Shanxi Normal University, Linfen 041004, People's Republic of China. zhangxm@dns.sxnu.edu.cn

Inorganic Chemistry
|February 27, 2008
PubMed
Summary

Hydrothermal reactions yielded two cuprous cyanide polymorphs. These compounds share similar hexagonal layers but exhibit distinct supramolecular arrangements, offering new insights into crystal engineering.

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Area of Science:

  • Materials Science
  • Crystallography
  • Inorganic Chemistry

Background:

  • Cuprous cyanide compounds are of interest due to their diverse structural possibilities.
  • Understanding the factors controlling polymorphism is crucial for materials design.

Purpose of the Study:

  • To synthesize and characterize new cuprous cyanide polymorphs.
  • To investigate the structural differences between polymorphs generated under similar conditions.

Main Methods:

  • Hydrothermal synthesis was employed to generate crystalline materials.
  • Single-crystal X-ray diffraction was used for structural determination.

Main Results:

  • Two distinct polymorphs of cuprous cyanide were successfully synthesized.
  • Both polymorphs feature hexagonal [Cu2(CN)3](-) layers.
  • The polymorphs differ in their supramolecular assembly of these layers.

Conclusions:

  • Hydrothermal conditions can lead to the formation of multiple cuprous cyanide polymorphs.
  • Subtle changes in reaction conditions can influence supramolecular packing.
  • This study provides a foundation for exploring structure-property relationships in cuprous cyanide materials.