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Lecture 2 1 H Nuclear Magnetic Resonance

Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

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Page 1: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Lecture 2 1H Nuclear Magnetic Resonance

Page 2: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Time

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Gas Chromatograph of Molecular Hydrogen at –100 °C

Thermoconductivity Detector

1 2

Page 3: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

• If the two components are collected separately and re-injected, the following is observed:

Page 4: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

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Gas Chromatograph of Peak 1

Page 5: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

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Gas Chromatograph of Peak 2

Page 6: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Peak 1 + O2 H2O; Peak 2 + O2 H2O

Peak 1 + Ni H2 Peak 2 + Ni H2

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Page 7: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Whats going on?

Page 8: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Whats going on?

Ortho Hydrogen Para Hydrogen

O/P = 1:1 at 80 K

Page 9: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

S

N

The magnetic moment of a spinning nucleus is colinear with the axis of spin

For a nucleus with a spin of 1/2, only two orientations in a magnetic field are allowed

Page 10: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12
Page 11: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Processional frequency, , is proportional to the magnetic field strength, H

= H

For 1H For 13C

At 14,000 Gauss (1.4Tesla) = 60 MHz = 14 MHz

At 70,500 Gauss (7.05 Tesla) = 300 MHz = 70 MHz

At 141000 Gauss (14.1 Tesla) = 600 MHz = 140 MHz

1 Hz = 1 cycle/second

Page 12: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

E

Energy difference between the two states

0 H

Magnetic field strength

Since the energy of the two states are different, so must be their populations

Page 13: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

For resonance to occur, the processional frequency of the nucleus, must equal the radiofrequency, . In a continuous wave spectrometer (now hardly ever used), the following occurs:

Considering the excess nuclei in the ground state only …

Page 14: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12
Page 15: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

In a pulsed experiment, the frequency generator provides all frequencies simultaneously; only those frequencies present in the precessing nuclei interact causing those nuclei to to tip in the same manner. The angle of tip depends on the duration and the intensity of the rf signal.

During this condition of resonance, some nuclei absorb rf energy and are transported into their excited state. Their contribution to the resulting net magnetic moment is lost.

If the rf frequency is sufficiently intense, and short in duration, the protons respond by pressessing about the field generated by the rf field.

Once the rf is turned off, these nuclei continue to precess about the external field. Suppose an intense rf field is maintained long enough to cause the protons to precess one quarter turn (90 °)about the rf field.

Page 16: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

N

S

Before the rf pulse

Consider a set of identical nuclei

Page 17: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

rf generator

signal coil

N

S

Just after the 90 ° rf pulse

Page 18: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Resultant moment

When the rf is turned off

detector coil

rf coil

NS

Page 19: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

z

x

y

H

NS

Receiver coil

Page 20: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

time

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rece

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-1

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Receiver coil output with time

Page 21: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

The resulting magnetic moment of the protons will precess about the xy plane at some frequency .

Suppose now we simply examine how the magnitude of the resulting magnetic moment of the protons varies with time. To do this we need to precess with the resulting moment about the xy plane at the same frequency. This is called the rotating frame of reference.

This is like being on a merry go round on a stationary horse watching the other horses go up and down. To us the motion is simple an up and down motion. To an observer who is not on the merry go round, the motion of the horses going up and down is complicated by the fact that they are also moving in a circular direction.

Page 22: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Remembering that = H, local field inhomogeneities about H will cause to vary with time

x

y

x

y

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y

y y y

xxx

t = 0 t = t1 t = t2

Page 23: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

time

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Net magnetic moment detected by the detector coil

No magnetic inhomogeneity With magnetic homogeneity

Page 24: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

The rate by which the magnetic moment decays in the xy plane is first order and is described by a rate constant, k2 (s-1). The reciprocal of k2 is a time constant, T2. It is the time necessary for H of the nuclei to decay to 1/e (1/2.71= 0.36) of the original value, Ho. Generally the magnetization can be thought to be completely gone after 5T2

First order process ln(H/Ho) = - k2t; when t = 1/k2

ln(H/Ho) = -1 and H/Ho = e-1

T2 is also referred to as transverse relaxation and it refers to the loss of magnetization in the xy plane

Page 25: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

H

NS

Receiver coil

Once magnetization is lost in the xy plane, how is it re-established in the z direction?

Page 26: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Equilibrium condition

Page 27: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

The buildup of magnitization in the z direction is also a first order process. It is characterized by the rate constant k1; the reciprocal of k1 is T1, the spin lattice relaxation time. It is the time necessary to build magnitization in the z direction to it equilibrium value.

The process of tipping the nuclei 90 ° results in absorption of energy and this energy must be dissipated into the environment.

T1 is referred to as spin lattice relaxation because the nucleus in relaxing must transfer its energy to a component in the lattice with the same frequency. Buildup of magnitization is considered complete after 5 T1

ln(Hze-Hzo) = -k1t; when t = 1/k1 (T1)

ln(Hze- Hzo) = -1

(Hze- Hzo) = e-1

Page 28: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Magnitude of T1 and T2

T1 values vary depending on the local environment of the nucleus in question. Typical values for protons is seconds or less; much longer times are observed for 13C.

T2 values depend on the magnetic inhomogeneity

T1 values are generally much longer than T2

Page 29: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

T1 are dependent on the type of nucleus. It can range from 10-2 to 100 sec.

For protons it is of the order of a few seconds but can be longer.

For solids it can be of the order of days.

For spin lattice relaxation to occur, there needs to be certain magnetic moments cause by spinning dipoles or other magnetic fileds that have a magnetic component with the same frequency as the processional frequency of the nucleus in question. This provides a mechanism for relaxation or energy transfer to occur. The magnetic field fall off rapidly with distance so these field need to be in close proximity.

Page 30: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12
Page 31: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12
Page 32: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12
Page 33: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Suppose now that instead of only one kind of nucleus, we have two kinds, with different processional frequencies. Let say that they are related in the following fashion: 1 = ; 2 = 3, but equal in number.

Following the 90 ° pulse, the following results:

Page 34: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

H

NS

Receiver coil

Page 35: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

H

NS

Receiver coil

ω 3 ω

Page 36: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

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Page 37: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

Fourier analysis of this free induction decay results (fid) in the two frequencies that lead up to this beat pattern.

In NMR the beat pattern is caused by magnetic moments precessing at different frequencies.

Fourier transform simply identifies the frequencies needed to reproduce the fid signal. It does so by an algorithm called fast Fourier transform.

Page 38: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12
Page 39: Lecture 2 1 H Nuclear Magnetic Resonance. Gas Chromatograph of Molecular Hydrogen at –100 °C Thermoconductivity Detector 12

For a 1H nucleus precessing at 300 MHz, what is the relative

populations of nuclei in the ground (g)and excited states (e)?

Ne/Ng = e-H/RT

-H/RT = h/kT since h is the energy of a photon of frequency and R = k*(Avogadros Number)

h/kT = 6.62*10-34 Js *300*106 s-1/ 1.38*10-23 J/K* 300 K

h/kT = 0.000048; e-0.000048 = 0.999952/1 or 999952/106

the difference is 48 nuclei in a total of /2*106 nuclei

1 mmol of 1H nuclei = 6*1023 *0.001*24/106 = 144*1014 excess nuclei in the ground state