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Introduction to Nanotechnology

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i 3.4. SPECTROSCOPY 69<br />

NMR involves the interaction of a nucleus possessing a nonzero nuclear spin I<br />

with an applied magnetic field Bapp <strong>to</strong> give the energy-level splitting in<strong>to</strong> 21 + 1 lines<br />

with the energies<br />

E, = fiyBappm (3.15)<br />

where y is the gyromagnetic ratio, sometimes called the mugne<strong>to</strong>gyric ratio,<br />

characteristic of the nucleus, and rn assumes integer or half-integer values in the<br />

range -I < m < +I depending on whether I is an integer or a half-integer. The<br />

value of y is sensitive <strong>to</strong> the local chemical environment of the nucleus, and it is<br />

cus<strong>to</strong>mary <strong>to</strong> report the chemical shift S of y relative <strong>to</strong> a reference value yR, that is,<br />

S = (y - yR)/yR. Chemical shifts are very small, and are usually reported in parts<br />

per million ( ppm). The most favorable nuclei for study are those with I = i, such as<br />

H, 19F, 3'P, and 13C; the latter iso<strong>to</strong>pe is only 1.1% abundant.<br />

Fullerene molecules such as C,, and C70 are discussed in Chapter 5. The wellknown<br />

buckyball C,, has the shape of a soccer ball with 12 regular pentagons and<br />

20 hexagons. The fact that all of its carbon a<strong>to</strong>ms are equivalent was determined<br />

unequivocally by the 13C NMR spectrum that contains only a single narrow line. In<br />

contrast <strong>to</strong> this, the rugby-ball-shaped C,, fullerene molecule, which contains 12<br />

pentagons (2 regular) and 25 hexagons, has five types of carbons, and this is<br />

confirmed by the 13C NMR spectrum presented at the <strong>to</strong>p of Fig. 3.34. The five<br />

NMR lines from the a, b, c, d, and e carbons, indicated in the upper figure, have the<br />

intensity ratios 10 : 10 : 20 : 20 : 10 corresponding <strong>to</strong> the number of each carbon type<br />

in the molecule. Thus NMR provided a confirmation of the structures of these two<br />

fullerene molecules.<br />

Electron paramagnetic resonance (EPR), sometimes called electron spin resonance<br />

(ESR), detects unpaired electrons in transition ions, especially those with odd<br />

numbers of electrons such as Cu2+ (3d9) and Gd3+ (4f7). Free radicals such as those<br />

associated with defects or radiation damage can also be detected. The energies or<br />

resonant frequencies are three orders of magnitude higher than NMR for the same<br />

magnetic field. A different notation is employed for the energy E, = gpBBa,,m,<br />

where pB is the Bohr magne<strong>to</strong>n and g is the dimensionless g fac<strong>to</strong>r, which has the<br />

value 2.0023 for a free electron. For the unpaired electron with spin S = on a free<br />

radical EPR measures the energy difference AE = - E-1,2 between-the levels<br />

rn = *$, <strong>to</strong> give a single-line spectrum at the energy level<br />

(3.16)<br />

Equations (3.15) and (3.16) are related through the expression gpB = Ay. If the<br />

unpaired electron interacts with a nuclear spin of magnitude I, then 21 + 1 hyperfine<br />

structure lines appear at the energies<br />

(3.17)

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