Infrared and Raman Spectra of Li+, Na+, K+ and Mg2+ complexes of amides have been studied and assignments made of low frequency bands characteristic of metal—oxygen polyhedra (in the case of Li+, asymmetric stretching is around 400 cm−1). Infrared spectra of pyridine and CH3CN complexes with characteristic MN bands are reported. Analysis of the spectra of linear OM
+O (M = H, D or Li) systems in sparteine-N16-oxide sesquiperchlorate has established the D∞h
symmetry of the group with the characteristic OLi+O asymmetric stretching mode around 400 cm−1. Crown ether complexes of Li+ show characteristic LiO4 bands around 400 cm−1. Crystalline oxides of Li with well-defined LiO4 tetrahedra also exhibit the 400 cm−1 band due to LiO stretching. Oxide glasses show low frequency bands characteristic of the metal—oxygen polyhedra. These bands are shown to be useful in determining the nature of cation coordination in a variety of systems.
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