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Related Concept Videos

Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

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Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
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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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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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Valence Bond Theory

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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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Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
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Metallic Solids

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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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Updated: Jan 8, 2026

Chemical Synthesis of Porous Barium Titanate Thin Film and Thermal Stabilization of Ferroelectric Phase by Porosity-Induced Strain
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Titanium phosphate glasses: Beyond tetrahedral network structures.

Esther Girón Lange1,2, Randall E Youngman3, Bruce G Aitken3

  • 1Department of Physics, University of Bath, Bath BA2 7AY, United Kingdom.

The Journal of Chemical Physics
|December 22, 2025
PubMed
Summary
This summary is machine-generated.

Titanium phosphate glasses exhibit structural variability, with decreasing P-O-P bonds and increasing titanium coordination as titanium content rises. This structural flexibility is key to their glass formation.

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Area of Science:

  • Materials Science
  • Solid-State Chemistry
  • Glass Science

Background:

  • Titanium phosphate glasses are an atypical glass-forming system.
  • Understanding their structure is crucial for developing new materials.
  • Previous studies lack detailed structural insights into these glasses.

Purpose of the Study:

  • To elucidate the structure of titanium phosphate glasses (TiO2)x(P2O5)1-x.
  • To determine the composition dependence of structural motifs.
  • To provide a benchmark for future glass structure investigations.

Main Methods:

  • Combined neutron and high-energy X-ray diffraction.
  • Solid-state 31P nuclear magnetic resonance (NMR) spectroscopy.
  • Raman spectroscopy and ab initio molecular dynamics simulations.

Main Results:

  • Decreasing P-O-P bonds from 23% to 11% with increasing TiO2 content.
  • Increasing Ti-O coordination number from 5.32(7) to 5.49(7).
  • Prevalence of five- and six-coordinated titanium and coexistence of O(II) and O(III) oxygen atoms.

Conclusions:

  • Structural variability, including Ti coordination and oxygen environments, drives vitrification.
  • Phosphate groups form P-O(II)-Ti and P-O(III)-2Ti connections.
  • These findings offer insights into glass formation in systems with higher-coordinated polyhedra.