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NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...

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3.1 <strong>IN</strong>TRODUCTION<br />

- 31 -<br />

CHAPTER 3<br />

NARROW<strong>IN</strong>G THE NUCLEAR RESONANCE SPECTRUM BY<br />

MACROSCOPIC SAMPLE ROTATION<br />

In Chapter 2 the various line-broadening interactions which<br />

exist in solids, and metals in particular, have been considered.<br />

In many liquids and solids the situation is different: motion of<br />

the nuclear spins averages out the secular line broadening mechan-<br />

ism. ' The internal motion may be described by a correlation funct-<br />

ion f(v) with a mean correlation time Tc. If Tc is short and less<br />

than T2 (the characteristic time describing the dephasing of spins<br />

in the rotating frame) the spin vectors will execute a random walk<br />

in the rotating frame and only slowly accumulate a phase difference<br />

relative to the mean resonance frequency vo. In the extreme case<br />

the secular interactions become so inefficient that the width of<br />

the resonance spectrum is determined by the homogeneity of the<br />

magnetic field across the sample and lifetime broadening.<br />

The above discussion is concerned with microscopic motion with-<br />

in a particular sample. Similar arguments apply when studying<br />

the effect of a macroscopic rotation of the sample about a unique<br />

axis, but there are a few important differences. Unlike random<br />

internal motion, macroscopic rotation only causes averaging over<br />

the plane of rotation and not over inter-nuclear distances. Macro-<br />

scopic motion is a very slow process by molecular standards and<br />

involves a single frequency of motion. Although Fourier analysis

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