Related Experiment Video
Updated: Jun 4, 2025

Activating Molecules, Ions, and Solid Particles with Acoustic Cavitation
Published on: April 11, 2014
Revisiting the Optical Spectrum of the Plutonyl Ion (PuO2)2+ in 1 M HClO4
1MS 70A3317, Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Abstract:
The analysis of the solution absorption spectrum of the plutonyl ion in an aqueous environment was given by Eisenstein and Pryce (E&P) in 1968. In 2011 a new spectrum was published of the (PuO2)2+ ion in 1 M HClO4. We have been provided with the original data of this spectrum and have found in the data a previously unreported low-lying transition at 7385 cm-1 which we have assigned as a magnetic dipole transition. We have fit most of the near-infrared and optical transitions with Gaussian fits and tabulated a new energy level list up to 22,000 cm-1 which mostly agrees with the data of E&P. We assumed a crystal field of D∞h (only axial symmetry) and utilized the intensity calculations published for the isoelectronic (NpO2)1+ ion using a complete basis set for the 5f2 problem including the Coulombic, spin-orbit as well as the crystal field Hamiltonian. Our results differ substantially from those of E&P. Subsequently, we used a truncated Hamiltonian to try to establish the effects of assuming the σ antibonding orbitals are at such high energies that we can ignore their contributions to the lower lying φ and δ orbitals.
More Related Videos
09:18Laser-heating and Radiance Spectrometry for the Study of Nuclear Materials in Conditions Simulating a Nuclear Power Plant Accident
Published on: December 14, 2017
12:22Speciation and Bioavailability Measurements of Environmental Plutonium Using Diffusion in Thin Films
Published on: November 9, 2015
Related Concept Videos
The Aufbau Principle and Hund's Rule
UV–Vis Spectroscopy: Molecular Electronic Transitions
Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview
Crystal Field Theory - Tetrahedral and Square Planar 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,...
Hybridization of Atomic Orbitals II
UV–Vis Spectroscopy of Conjugated Systems
One of the factors influencing λmax is the extent...