Magic Angle Spinning and Truncated Field Concept in NMR

Abstract

In order to thoroughly comprehend and adequtely interpret NMR data, it is necessary to perceive the complex structure of spin Hamiltonian. Although NMR principles have been extensively discussed in a number of distinguished introductory publications, it still remains difficult to find illustrative graphical models revealing the tensorial nature of spin interaction. Exposure of the structure standing behind mathematical formulas can clarify intangible concepts and provide a coherent image of basic phenomena. This approach is essential when it comes to hard to manage, time-dependent processes such as Magic Angle Spinning (MAS), where the anisotropic character of the spin system interactions couple with experimentally introduced time evolution processes. The presented work concerns fundamental aspects of solid state NMR namely: the uniqueness of the tetrahedral angle and evolution of both dipolar D and chemical shield σ coupling tensors under MAS conditions.