Related Experiment Video
Updated: May 22, 2026

Preparing an Isotopically Pure 229Th Ion Beam for Studies of 229mTh
Published on: May 3, 2019
Spectroscopic and energetic properties of thorium(IV) molecular clusters with a hexanuclear core
Monica Vasiliu1, Karah E Knope, L Soderholm
1Chemistry Department, The University of Alabama, Shelby Hall, Box 870336, Tuscaloosa, Alabama 35487-0336, USA.
Abstract:
The spectral and energetic properties of three polynuclear thorium(IV) molecular complexes Th(6)(OH)(4)O(4)(H(2)O)(6)(HCOO)(12)·nH(2)O (1), Th(6)(OH)(4)O(4)(H(2)O)(6)(CH(3)COO)(12)·nH(2)O (2), and Th(6)(OH)(4)O(4)(H(2)O)(6)(ClCH(2)COO)(12)·4H(2)O (3) have been studied. Each complex has a hexanuclear core with six 9-coordinate Th(IV) cations bridged by four μ(3)-hydroxo and four μ(3)-oxo groups. The +12 core is stabilized by twelve bridging carboxylate functionalized organic acid (formate, acetate, and chloroacetate) units. The calculated (1)H NMR chemical shifts for the four μ(3)-hydroxo, water, and formate protons are reported and compared to the experimental values. The vibrational frequencies were calculated to aid in the assignment of the observed Raman bands. The Mulliken and NBO (natural bond orbital) charges are calculated for the Th clusters. The Th atoms are positive and the bridging O and O(H) are negative. The analysis of the calculated highest-occupied and lowest-unoccupied molecular orbitals (HOMO and LUMO) is reported. The average water complexation energies, the gas phase, the aqueous and dimethylsulfoxide (DMSO) acidities were predicted, and the Th clusters are found to be mild to strong acids in gas phase yet they behave as weak acids in solution.
More Related Videos
07:24Hyperspectral Imaging as a Tool to Study Optical Anisotropy in Lanthanide-Based Molecular Single Crystals
Published on: April 14, 2020
08:54Vibrational Spectra of a N719-Chromophore/Titania Interface from Empirical-Potential Molecular-Dynamics Simulation, Solvated by a Room Temperature Ionic Liquid
Published on: January 25, 2020
Related Concept Videos
Electron Configuration of Multielectron Atoms
Valence Bond Theory
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
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,...
Atomic Spectroscopy: Absorption, Emission, and Fluorescence
Crystal Field Theory - Octahedral Complexes
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...