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This book is concerned with recent experimental and theoretical work dealing with phenomena created by the transient dipoles and polarizabilities produced by intermolecular interactions. The for mer produce absorption from the microwave to the optical regions of the spectrum and the latter produce Rayleigh and Raman scattering; such absorption and scattering would be absent without collisions. Static properties, such as dielectric constant, refractive index, and Kerr effect, also exhibit the effects of induced dipoles and polarizabilities. The first observation of an infrared absorption spectrum pro duced by the collisions of molecules which ordinarily do not have an allowed dipole transition was reported in 1949 (Crawford, Welsh, and Locke). The first observation of depolarized Rayleigh spectra due to collisions in atomic gases appeared in 1968 (McTague and Birnbaum). However, it was not until 1977 that the first conference dealing with collision-induced phenomena was organized by J. D. Poll at the University of Guelph. This conference was mainly concerned with studies of collision-induced absorption in gases. Light scat tering received more attention at the second meeting of the colli sion-induced community in 1978, at the E. Fermi Summer School on "Intermolecular Spectroscopy and Dynamical Properties of Dense Sys tems," organized by J. Van Kranendonk. However, the emphasis was still on collision-induced absorption in compressed gases, although some work on liquids, solid H , and related subjects such as ro 2 tational relaxation was included. The third induced phenomena con ference, organized by F.
Recent advances in high pressure diamond anvil cell techniques and synchrotron radiation characterization methods have enabled investigation of a wide range of materials properties in-situ under extreme conditions. High pressure studies have made significant contribution to our understanding in a number of scientific fields, e.g. condensed matter physics, chemistry, Earth and planetary sciences, and material sciences. Pressure, as a fundamental thermodynamic variable, can induce changes in the electronic and structural configuration of a material, which in turn can dramatically alter its properties. The novel phases and new compounds existing at high pressure have improved our basic understanding of bonding and interactions in condensed matter. This dissertation focuses on how pressure affects materials' bonding and electronic structures in two types of systems: hydrogen rich molecular compounds and strongly correlated transition metal oxides. The interaction of boranes and hydrogen was studied using optical microscopy and Raman spectroscopy and their hydrogen storage potential is discussed in the context of practical applications. The pressure-induced behavior of the SiH4 + H2 binary system and the formation of a newly formed compound SiH4(H2)2 were investigated using a combination of optical microscopy, Raman spectroscopy and x-ray diffraction. The experimental work along with DFT calculations on the electronic properties of the compound up to the possible metallization pressure, indicated that there are strong intermolecular interactions between SiH4 and H2 in the condensed phase. By using a newly developed synchrotron x-ray spectroscopy technique, we were able to follow the evolution of the 3d band of a 3d transition metal oxide, Fe2O3 under pressure, which experiences a series of structural, electronic and spin transitions at approximately 50 GPa. Together with theoretical calculations we revisited its electronic phase transition mechanism, and found that the electronic transitions are reflected in the pre-edge region.