Related Experiment Video
Updated: Aug 10, 2026

High Pressure Single Crystal Diffraction at PX^2
Published on: January 16, 2017
Refinement of the structure of beta-U4O9
1Chemical Crystallography, University of Oxford, Chemical Research Building, Mansfield Road, OX1 3TA, England.
Beta-uranium oxide (Beta-U4O9) exhibits a superlattice structure derived from the fluorite arrangement of uranium dioxide (UO2). Additional oxygen atoms are located in specific clusters within this structure, refined using neutron diffraction data.
Area of Science:
- Solid-state chemistry
- Crystallography
- Materials science
Background:
- Beta-uranium oxide (Beta-U4O9) is a superlattice structure.
- It is based on the fluorite arrangement of uranium dioxide (UO2).
Purpose of the Study:
- To refine the crystal structure of Beta-U4O9.
- To understand the accommodation of additional oxygen atoms in the UO2-based structure.
Main Methods:
- Single-crystal neutron diffraction data was utilized.
- Structure refinement was performed following established procedures.
Main Results:
- The U atoms are positioned similarly to those in UO2.
- Additional O atoms occupy cuboctahedral clusters with 43m symmetry.
- These clusters are centered on 12-fold sites within the I43d cubic space group.
Conclusions:
- The refined structure provides detailed insights into Beta-U4O9.
- This work clarifies the crystallographic arrangement of oxygen in this superlattice structure.
Related Concept Videos
Covalently Linked Protein Regulators
These groups modify specific amino acids in a protein.
Protein Complexes with Interchangeable Parts
The SCF ubiquitin ligase is a protein complex of five individual proteins. This complex attaches ubiquitin to other target proteins to mark them for degradation. In order to...
Hydroboration-Oxidation of Alkenes
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
Protein Folding Quality Check in the RER
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism

