Related Experiment Video
Updated: Dec 25, 2025

Characterization of Calcification Events Using Live Optical and Electron Microscopy Techniques in a Marine Tubeworm
Published on: February 28, 2017
Infrared Studies of Aragonite, Calcite, and Vaterite Type Structures in the Borates, Carbonates, and Nitrates
Abstract:
Infrared absorption spectra have been obtained on the alkali nitrates, the divalent metal carbonates, and the rare earth borates which assume the aragonite, calcite, or vaterite crystal structures. It was observed that similar structures give rise to analogous spectra except for the carbonate and borates having the vaterite structure. The marked differences observed in these latter spectra are discussed. Frequency shifts produced by cation substitution are ascribed to repulsion between closed electron shells of oxygen atoms. It is concluded that this repulsive force determines the structure type in the rare earth borates.
Related Concept Videos
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
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...
VSEPR Theory and the Basic Shapes
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,...
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Infrared (IR) Spectroscopy: Overview
Different compounds display unique properties due to their...

