Magic angle spinning

In <a href="/facts/Solid-state_NMR/cumWwN7Y">solid-state NMR</a> <a href="/facts/Spectroscopy/mj71FuNK">spectroscopy</a>, magic-angle spinning (MAS) is a technique routinely used to produce better resolution NMR spectra. MAS NMR consists in spinning the sample (usually at a frequency of 1 to 130 <a href="/facts/KHz/6Wshj5qm">kHz</a>) at the <a href="/facts/Magic_angle/Ep1mgIXB">magic angle</a> θm (ca. 54.74°, where cos2θm=1/3) with respect to the direction of the <a href="/facts/Magnetic_field/Ta8Ev588">magnetic field</a>.
Three main interactions responsible in solid state NMR (<a href="/facts/Dipolar_coupling/nLA5Nwlo">dipolar</a>, <a href="/facts/Chemical_shift_anisotropy/VoCY7s7R">chemical shift anisotropy</a>, <a href="/facts/Solid-state_nuclear_magnetic_resonance/cumWwN7Y">quadrupolar</a>) often lead to very broad and featureless NMR lines. However, these three interactions in solids are orientation-dependent and can be averaged to some extent by MAS:

<ul><li>The nuclear dipolar interaction has a 
 
 
 
 3
 
 cos
 
 2
 
 
 ⁡
 θ
 −
 1
 
 
 {\displaystyle 3\cos ^{2}\theta -1}
 
 dependence, where 
 
 
 
 θ
 
 
 {\displaystyle \theta }
 
 is the angle between the internuclear axis and the main magnetic field. As a result, the dipolar interaction vanish at the magic angle θm and the interaction contributing to the line broadening is removed. Even though all internuclear vectors cannot be all set to the magic angle, rotating the sample around this axis produces the same effect, provided the frequency is comparable to that of the interaction. In addition, a set of spinning sidebands appear on the spectra, which are sharp lines separated from the isotropic resonance frequency by a multiple of the spinning rate.</li>
<li>The <a href="/facts/Chemical_shift_anisotropy/VoCY7s7R">chemical shift anisotropy</a> (CSA) represents the orientation-dependence of the chemical shift. <a href="/facts/Solid-state_nuclear_magnetic_resonance/cumWwN7Y">Powder patterns</a> generated by the CSA interaction can be averaged by MAS, resulting to one single resonance centred at the isotropic chemical shift (centre of mass of the powder pattern).</li>
<li>The quadrupolar interaction is only partially averaged by MAS leaving a residual secondary quadrupolar interaction.</li></ul>
In solution-state NMR, most of these interactions are averaged out because of the rapid time-averaged molecular motion that occurs due to the thermal energy (molecular tumbling).

The spinning of the sample is achieved via an impulse air <a href="/facts/Turbine/gqosKCkI">turbine</a> mechanism, where the sample tube is lifted with a frictionless <a href="/facts/Air_bearing/BKwNfmVY">compressed gas bearing</a> and spun with a gas drive. Sample tubes are hollow cylinders coming in a variety of outer diameters ranging from 0.70 to 7 mm, mounted with a turbine cap. The rotors are typically made from zirconium oxide, although other ceramic materials (<a href="/facts/Silicon_nitride/58X9QPQJ">silicon nitride</a>) or polymers (<a href="/facts/Poly(methyl_methacrylate)/CnCRBo5F">poly(methyl methacrylate)</a> (PMMA), <a href="/facts/Polyoxymethylene/TFrYKSx7">polyoxymethylene</a> (POM)) can be found. Removable caps close the ends of the sample tube. They are made from a range of materials typically <a href="/facts/Polychlorotrifluoroethylene/tw7UJfcB">Kel-F</a>, <a href="/facts/Vespel/A1CUrsDh">Vespel</a>, or <a href="/facts/Zirconium_dioxide/d2RN7wGQ">zirconia</a> and <a href="/facts/Boron_nitride/kumlPQRg">boron nitride</a> for an extended temperature range.
Magic-angle spinning was first described in 1958 by <a href="/facts/Edward_Raymond_Andrew/M9tphD6A">Edward Raymond Andrew</a>, A. Bradbury, and R. G. Eades and independently in 1959 by I. J. Lowe. The name "magic-angle spinning" was coined in 1960 by Cornelis J. Gorter at the AMPERE congress in Pisa.

Magic angle spinning open-in-new

Magic angle spinning