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Related Concept Videos

Lewis Structures of Molecular Compounds and Polyatomic Ions02:54

Lewis Structures of Molecular Compounds and Polyatomic Ions

To draw Lewis structures for complicated molecules and molecular ions, it is helpful to follow a step-by-step procedure as outlined:
Polyprotic Acids03:38

Polyprotic Acids

Acids are classified by the number of protons per molecule that they can give up in a reaction. Acids such as HCl, HNO3, and HCN that contain one ionizable hydrogen atom in each molecule are called monoprotic acids. Their reactions with water are:
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...
Titration of a Polyprotic Acid02:08

Titration of a Polyprotic Acid

A polyprotic acid contains more than one ionizable hydrogen and undergoes a stepwise ionization process. If the acid dissociation constants of the ionizable protons differ sufficiently from each other, then the titration curve for such polyprotic acid generates a distinct equivalence point for each of its ionizable hydrogens. Therefore, titration of a diprotic acid results in the formation of two equivalence points, whereas the titration of a triprotic acid results in the formation of three...
Titration of Polyprotic Base with a Strong Acid01:18

Titration of Polyprotic Base with a Strong Acid

The titration of a polyprotic base such as sodium carbonate with a strong acid such as hydrochloric acid results in two equivalence points on the titration curve. At the first equivalence point, the carbonate ions in the base are completely converted to bicarbonate ions. The second equivalence point corresponds to the complete conversion of bicarbonate ions to carbonic acid, which dissociates into carbon dioxide and water. The region before the first equivalence point corresponds to the...
Titration of Polyprotic Acids with a Strong Base01:23

Titration of Polyprotic Acids with a Strong Base

Titration of a polyprotic acid, which contains multiple ionizable protons, involves distinct dissociation steps, each with its own dissociation constant (Ka). Each successive Ka is weaker than the previous one. In the titration of a polyprotic acid like sulfurous acid with a strong base such as sodium hydroxide, the base first neutralizes the initial ionizable proton, forming an intermediate species (e.g., hydrogen sulfite ions). This step's titration curve resembles that of a weak monoprotic...

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Related Experiment Video

Updated: Jul 20, 2026

Synthesis of High Purity Nonsymmetric Dialkylphosphinic Acid Extractants
12:06

Synthesis of High Purity Nonsymmetric Dialkylphosphinic Acid Extractants

Published on: October 19, 2017

K(UO)Si2O6: a pentavalent-uranium silicate.

Chih-Shan Chen1, Shang-Fan Lee, Kwang-Hwa Lii

  • 1Department of Chemistry, National Central University, Chungli, Taiwan 320, ROC.

Journal of the American Chemical Society
|September 1, 2005
PubMed
Summary

Scientists synthesized the first pentavalent-uranium silicate using a high-temperature, high-pressure hydrothermal method. This novel material features a unique 3-D framework with specific silicate rings and uranium-oxygen chains, confirmed by magnetic susceptibility and XPS analysis.

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In situ FTIR Spectroscopy as a Tool for Investigation of Gas/Solid Interaction: Water-Enhanced CO2 Adsorption in UiO-66 Metal-Organic Framework
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U2O5 Film Preparation via UO2 Deposition by Direct Current Sputtering and Successive Oxidation and Reduction with Atomic Oxygen and Atomic Hydrogen
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In situ FTIR Spectroscopy as a Tool for Investigation of Gas/Solid Interaction: Water-Enhanced CO2 Adsorption in UiO-66 Metal-Organic Framework
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Published on: February 1, 2020

Area of Science:

  • Inorganic Chemistry
  • Materials Science
  • Solid-State Chemistry

Background:

  • Uranium silicates are rare, with limited understanding of uranium's higher oxidation states in such compounds.
  • High-temperature, high-pressure synthesis methods are crucial for exploring novel inorganic materials.

Purpose of the Study:

  • To synthesize and characterize the first pentavalent-uranium silicate.
  • To elucidate the structural and electronic properties of this new compound.
  • To confirm the valence state of uranium in the synthesized material.

Main Methods:

  • High-temperature, high-pressure hydrothermal synthesis.
  • X-ray Photoelectron Spectroscopy (XPS) for valence state determination.
  • Magnetic susceptibility measurements for electronic property analysis.

Main Results:

  • Successful synthesis of a novel pentavalent-uranium silicate.
  • Characterization of a unique 3-D framework composed of SiO4 tetrahedra and UO4/1O2/2 chains.
  • Confirmation of pentavalent uranium (U(V)) using XPS and magnetic susceptibility data.

Conclusions:

  • The first pentavalent-uranium silicate has been synthesized, expanding the known chemistry of uranium compounds.
  • The structural and electronic properties provide insights into the behavior of high-valent uranium in silicate frameworks.
  • This work opens avenues for exploring other high-oxidation-state actinide materials.