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Esr Spectros

ESR spectroscopy detects unpaired electrons in a sample by applying a magnetic field and microwave radiation. The resonance condition is satisfied when the microwave frequency is equal to the Larmor precession frequency of the electron spins in the applied field. ESR operates at lower magnetic fields and higher frequencies than NMR due to the electron's larger magnetic moment. The ESR spectrum provides information about electron-nucleus couplings and relaxation rates that is analogous to NMR.

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Umendra Khokhar
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476 views

Esr Spectros

ESR spectroscopy detects unpaired electrons in a sample by applying a magnetic field and microwave radiation. The resonance condition is satisfied when the microwave frequency is equal to the Larmor precession frequency of the electron spins in the applied field. ESR operates at lower magnetic fields and higher frequencies than NMR due to the electron's larger magnetic moment. The ESR spectrum provides information about electron-nucleus couplings and relaxation rates that is analogous to NMR.

Uploaded by

Umendra Khokhar
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© © All Rights Reserved
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Electron Spin Resonance (ESR) Spectroscopy

(Electron Paramagnetic Resonance, EPR)


The principles of ESR are quite analogous to those of NMR.
Thus the electron has an intrinsic magnetic moment
e = -geS
where g = 2.0023, e = eh/4%mc = 9.2741 10-24J T-1 (Bohr
magneton), and S =
The first order Zeeman Effect
splits the two ms states of the
unpaired electrons in a
paramagnetic material.

ms=+1/2

g B

ms= -1/2
B

The resonance condition is therefore h = gB, but since the


magnetic moment of an electron is 2-3 orders of magnitude
greater than that of a magnetic nucleus an ESR spectrometer
operates with smaller magnetic fields and higher frequencies
than an NMR spectrometer.


Compare a 300 MHz NMR spectrometer with a standard (Xband) ESR spectrometer
NMR

3 108 Hz

and B = 4.5 Tesla

ESR

9 109 Hz

and B = 0.3 Tesla

Higher frequency (microwave) radiation requires different


technology for ESR spectrometers.

The klystron is the source of microwave radiation of fixed


frequency

The cavity (corresponds to the NMR probe) is a hollow


rectangular or cylindrical box, the dimensions of which are
matched to the wavelength of the microwaves so that the sample
(which is ins erted in a quartz nmr-like tube) is held in a region
where the magnetic field component of the radiation is
maximized and the electric field is minimized.
The spectrometer is tuned so that the waveguides and cavity
contain standing waves, and the detector records a constant
intensity.
When the magnetic field is swept to achieve the resonance
condition, radiation is absorbed by the sample, and a small
decrease in radiation intensity should be observed at the
detector.
Since it is much more efficient to detect an AC signal in the
presence of a large DC background, the magnetic field is
modulated (typically at 100 KHz) by means of coils embedded
in the walls of the cavity.

This generates a signal that looks like the first derivative of the
absorption line.

Any sample that contains unpaired electrons can, in principle,


yield an ESR (EPR) spectrum.

Free radicals (organic and inorganic)

triplet states of molecules with diamagnetic ground states

transition metal, lanthanide, and actinide complexes with


unpaired d or f electrons.

Spectra are commonly recorded on solutions or on solids (single


crystals, polycrystalline powders, frozed glasses, etc.)
The observable characteristics of an ESR spectrum are

The position of the signal (analog of the NMR chemical


shift)

The pattern of electron-nucleus hyperfine coupling (analog


of NMR spin coupling)

The line-shapes and -widths (relaxation rates, exchange


effects, anisotropy as in NMR)

The position of an ESR signal is defined by the effective gvalue, i.e. by

g=

h
eB

g-values are determined by careful measurement of the


frequency and magnetic field, or more commonly by using a
reference of known g-value.
A very common reference is the stable free radical
diphenylpicrylhydrazyl
(C6H5)2NN(&){C6H2(NO2)3}
for which g = 2.0036
In liquid samples the average (isotropic) value of g is found; in
solid samples g is often isotropic (gx , gy , gz).
The g-value of a free electron is 2.0023, and the g-values of
most free radicals are very close to this value, since the unpaired
electron has very little orbital contribution to the magnetic
moment. (carbon-based radicals, spin-orbit coupling very small).
So, the g-value of a radical has little significance.
On the other hand, g-values for ESR spectra of dn and fn
complexes can differ greatly from 2.00, because of spin-orbit
coupling.


Recall that g=2.0 is the (anomalous) proportionality between the


spin angular momentum and magnetic moment of an electron (in
Bohr Magnetons). The corresponding proportionality between
the orbital angular momentum and magnetic moment is 1.0.
Thus the effective g for an electron in a dn complex say will
depend upon how much orbital angular momentum contributes
to the magnetic moment, and whether this orbital contribution
acts in parallel or is opposed to the spin angular momentum.
Hunds 3rd rule states that the ground state of a dn complex is the
one with minimum J (=L-S) if the shell is less than half-full, and
maximum J (=L+S) if the shell is more than half full.
So for a V4+ (d1) compound we expect g < 2.00 (typically 1.9)
For Cu2+ (d9) g > 2.00 (typically 2.2)
For Mn2+ (d5, L=0) g = 2.00

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