The Relation of NMR to Other Kinds of Spectroscopy

Nuclear magnetic resonance spectroscopy involves transitions between possible energy levels of magnetic nuclei in an applied magnetic field (see Figure 9-21). The transition energies are related to the frequency of the absorbed radiation by the familiar equation ΔE−hνΔ. An important difference between nmr and other forms of spectroscopy is that ΔE is influenced by the strength of the applied field. This should not be surprising, because if we are to measure the energy of changing the direction of alignment of a magnetic nucleus in a magnetic field, then the stronger the field the more energy will be invloved.

Nuclear spin (symbolized as I) is a quantized property that correlates with nuclear magnetism such that when I is zero the nucleus has no spin and no magnetic properties. Examples are 12C and 16O. Several nuclei of particular interest to organic chemists - 1H, 13C, 15, 19, and 31P - have spin of 1/2. With I=1/2 there are only two magnetic energy states of the nucleus in a magnetic field. These states are designated with the spin quantum numbers +1/2 and −1/2. The difference in energy between these states, ΔE, is given by

or

in which h is Planck's constant, ν is in hertz, γ is a nuclear magnetic constant called the gyromagnetic ratio,10, and H is the magnetic field strength at the nucleus. In general, H will not be exactly equal to Ho, the applied magnetic field and, as we will see, this difference leads to important chemical information. Each kind of nucleus (1H, 13C, 15N, etc.) has its own γ value and, consequently, will undergo transitions at different frequencies at any particular value of H. This should become clearer by study of Figure 9-24.

There are several modes of operation of an nmr spectrometer. First and most common, we hold νν constant and vary (or "sweep") HoHo. Close to ν=γH , energy is absorbed by the nuclei and the current flow from the transmitter increases until ν is exactly equal to γH. Further increase of HoHo makes ν<γHo and the current flow decreases. The form of the energy-absorption curve as a function of Ho when Ho is changed very slowly is shown in Figure 9-25a. The peak is centered on the point where ν=γH. When Ho is changed more rapidly, transient effects are observed on the peak, which are a consequence of the fact that the nuclei do not revert instantly from the −1/2 to +1/2 state. The resulting

Figure 9-25: Comparison of sweep rates on nmr absorption curves; (a) 500-sec sweep, (b) 50-secsec , (c) 10-sec sweep, The "ringing" in the faster sweep curves is a transient effect that has a small effect on the position of the peak and none on the integral.

phenomenon is called "ringing" and is shown in Figures 9-25b and 9-25c. Evidence of ringing also will be seen on peaks of Figure 9-23.

An alternative method of running an nmr spectrometer is to hold the magnetic field constant and to sweep the transmitter frequency through the resonances. This mode of operation is more like other forms of spectroscopy and gives the same line shapes as sweeping the field (Figure 9-25).

What energy is associated with a 1H nmr transition? The magnitude of this energy may be calculated from the relationship between energy and wavelength (frequency) of the absorbed radiation. That is,

The frequency ν is the operating frequency of the spectrometer, which we will take as 60MHz or 6×10⁷ Hz (cycles sec−1), and the velocity of light is 3×10⁸ m sec−1. Hence

This is a very small energy difference, which means that only very few more of the nuclei are in the more stable +1/2 state than in the less stable −1/2 state. The equilibrium constant K for −1/2⇌+1/2 calculated from Equation 4-2 for 25^o  and neglecting possible entropy effects is 1.000010!

مواضيع ذات صلة

Spectroscopic Properties of Alkynes

Spectroscopic Properties of Alkenes

Application of Chemical Shifts to Structure Determination

Correlations Between Structure and Chemical Shifts

Electronegativity and Chemical Shifts

Effects of Carbon Bond Type

Mass Spectroscopy

Hydrogen Bonding

Chemical Exchange

Proton-Proton Splittings and Conformational Analysis

Spin-Spin Splitting - What We Observe

Proton-Proton Splittings and Chemical Exchange