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Formal Charges02:42

Formal Charges

In some cases, there are seemingly more than one valid Lewis structures for molecules and polyatomic ions. The concept of formal charges can be used to help predict the most appropriate Lewis structure when more than one reasonable structure exists.
Acid Strength and Molecular Structure03:05

Acid Strength and Molecular Structure

Binary Acids and Bases
In the absence of any leveling effect, the acid strength of binary compounds of hydrogen with nonmetals (A) increases as the H-A bond strength decreases down a group in the periodic table. For group 17, the order of increasing acidity is HF < HCl < HBr < HI. Likewise, for group 16, the order of increasing acid strength is H2O < H2S < H2Se < H2Te. Across a row in the periodic table, the acid strength of binary hydrogen compounds increases with increasing...
Structural Isomerism02:34

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.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Valence Bond Theory02:42

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...
Resonance and Hybrid Structures02:16

Resonance and Hybrid Structures

According to the theory of resonance, if two or more Lewis structures with the same arrangement of atoms can be written for a molecule, ion, or radical, the actual distribution of electrons is an average of that shown by the various Lewis structures.
Resonance Structures and Resonance Hybrids
The Lewis structure of a nitrite anion (NO2−) may actually be drawn in two different ways, distinguished by the locations of the N–O and N=O bonds.
Polymer Classification: Architecture01:14

Polymer Classification: Architecture

Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...

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Related Experiment Video

Updated: Jul 9, 2026

Synthesis and Microdiffraction at Extreme Pressures and Temperatures
07:26

Synthesis and Microdiffraction at Extreme Pressures and Temperatures

Published on: October 7, 2013

Structural and bonding changes in cesium iodide at high pressures.

E Knittle, R Jeanloz

    Science (New York, N.Y.)
    |January 6, 1984
    PubMed
    Summary

    Cesium iodide transforms structurally and electronically under high pressure. It becomes a semiconductor around 60 gigapascals and may turn metallic near 100 gigapascals.

    Area of Science:

    • Solid-state physics
    • Materials science
    • High-pressure physics

    Background:

    • Cesium iodide (CsI) is an ionic salt at ambient conditions.
    • Understanding material behavior under extreme pressure is crucial for fundamental science and technological applications.

    Purpose of the Study:

    • To investigate the structural and electronic properties of cesium iodide under high pressure.
    • To determine the pressure-induced phase transitions and changes in electronic band structure.

    Main Methods:

    • High-pressure experiments utilizing diamond anvil cells.
    • Analysis of structural changes and electronic band gap evolution.

    Main Results:

    • Cesium iodide undergoes a second-order structural transformation from B2 to body-centered tetragonal at 40 gigapascals.

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    Combining Chemical Cross-linking and Mass Spectrometry of Intact Protein Complexes to Study the Architecture of Multi-subunit Protein Assemblies
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  • The electronic band gap of CsI decreases significantly with increasing pressure, transitioning from an insulator to a semiconductor.
  • Extrapolation suggests CsI may become metallic at pressures around 100 gigapascals.
  • Conclusions:

    • High pressure dramatically alters the properties of cesium iodide, inducing a phase transition and semiconductor behavior.
    • These findings provide insights into the pressure-dependent electronic and structural evolution of ionic materials.
    • Similar phenomena may occur in other alkali halides at comparable high-pressure regimes.