Transcript Nuclear Magnetic Resonance Spectroscopy Renee Y. Becker Valencia Community College CHM 2011C The Use of NMR Spectroscopy • Used to determine relative location of atoms within.

Nuclear Magnetic Resonance
Spectroscopy
Renee Y. Becker
Valencia Community College
CHM 2011C
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The Use of NMR Spectroscopy
• Used to determine relative location of atoms
within a molecule
• Most helpful spectroscopic technique in organic
chemistry
• Related to MRI in medicine (Magnetic Resonance
Imaging)
• Maps carbon-hydrogen framework of molecules
• Depends on very strong magnetic fields
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Nuclear Magnetic Resonance Spectroscopy
•
1H
or 13C nucleus spins and the internal magnetic field
aligns parallel to or against an aligned external magnetic
field (See Figure 13.1)
• Applying an external magnetic field, Bo, the proton or
nucleus will orient parallel or anti-parallel to the
orientation of the external field.
– The parallel orientation of the proton or nucleus is lower in energy
than the anti-parallel orientation.
• Radio energy of exactly correct frequency (resonance)
causes nuclei to flip into anti-parallel state
•
Energy needed is related to molecular environment
(proportional to field strength, Bo ) – see Figure 13.2
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Nuclear Magnetic Resonance Spectroscopy (1H)
• The energy of the radiation required is within the
radio frequency range.
• The energy required is dependent upon the
nucleus and the strength of the magnetic field.
• A proton in a magnetic field of 1.41 telsa requires
a E.M. radiation of 60 MHz to resonate.
– E = 2.4 x 10-5 kJ/mol
– I.R. energies  48 kJ/mol
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The Nature of NMR Absorptions
• Electrons in bonds shield nuclei from magnetic field
• Different signals appear for nuclei in different
environments
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1H
13C
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The NMR Measurement
• The sample is dissolved in a solvent that does not
have a signal itself and placed in a long thin tube
• The tube is placed within the gap of a magnet and
spun
• Radiofrequency energy is transmitted and
absorption is detected
• Species that interconvert give an averaged signal
that can be analyzed to find the rate of conversion
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Chemical Shifts
• The relative energy of resonance of a particular nucleus
resulting from its local environment is called chemical
shift
• NMR spectra show applied field strength increasing from
left to right
• Left part is downfield right part is upfield
• Nuclei that absorb on upfield side are strongly shielded.
• Chart calibrated versus a reference point, set as 0,
tetramethylsilane [TMS]
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Chemical Shifts
• Let’s consider the just the proton (1H) NMR.
• 60 MHz NMR experiments are carried out with a constant
RF of 60 MHz and the magnetic field is varied. When a
spin-flip occurs (resonance), it is detected by an R.F.
receiver.
Bare proton
Proton in organic molecule
Ho
Ho’ > Ho
Increasing magnetic field strength
Increased shielding of nucleus
Downfield
Upfield
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Measuring Chemical Shift
• Numeric value of chemical shift: difference between
strength of magnetic field at which the observed
nucleus resonates and field strength for resonance of
a reference
– Difference is very small but can be accurately
measured
– Taken as a ratio to the total field and multiplied by
106 so the shift is in parts per million (ppm)
• Absorptions normally occur downfield of TMS, to
the left on the chart
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Measuring Chemical Shift
observed shift ( Hz )
chemical shift( ) 
spectrometer frequency( MHz )
Remember: the chemical shift is in ppm.
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1H
NMR Spectroscopy and Proton Equivalence
• Proton NMR is much more sensitive than 13C and
the active nucleus (1H) is nearly 100 % of the
natural abundance
• Shows how many kinds of nonequivalent
hydrogens are in a compound
• Equivalent H’s have the same signal while
nonequivalent are different
– There are degrees of nonequivalence
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Chemical Shifts in 1H NMR Spectroscopy
• Lower field signals are H’s attached to sp2 C
• Higher field signals are H’s attached to sp3 C
• Electronegative atoms attached to adjacent C cause
downfield shift (deshielding)
– Decreases electron density around protons
• See Tables 13-2 and 13-3 for a complete list
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• The most important perturbation of the NMR
frequency for applications of NMR is the
'shielding' effect of the surrounding electrons. In
general, this electronic shielding reduces the
magnetic field at the nucleus (which is what
determines the NMR frequency).
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Integration of 1H NMR Absorptions: Proton Counting
• The relative intensity of a signal (integrated area) is
proportional to the number of protons causing the signal
• This information is used to deduce the structure
• For example in ethanol (CH3CH2OH), the signals have the
integrated ratio 3:2:1
• For narrow peaks, the heights are the same as the areas and
can be measured with a ruler
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Integration of 1H NMR Absorptions: Proton Counting
• This is proportional to the relative number of protons
causing each signal.
– An integration ratio of 1.5:1 is consistent with a 6:4
ratio of protons as with a 3:2 ratio of protons.
– How many signals would you expect from the 1H NMR
spectrum of chloromethyl methyl ether, ClCH2OCH3,
and what would you expect the signal area ratios to be?
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Spin-Spin Splitting in 1H NMR Spectra
• Peaks are often split into multiple peaks due to
interactions between nonequivalent protons on
adjacent carbons, called spin-spin splitting
• The splitting is into one more peak than the
number of H’s on the adjacent carbon (“n+1 rule”)
• The set of peaks is a multiplet (2 = doublet, 3 =
triplet, 4 = quartet)
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Rules for Spin-Spin Splitting
• Equivalent protons do not split each other
• The signal of a proton with n equivalent
neighboring H’s is split into n + 1 peaks
• Protons that are farther than two carbon
atoms apart do not split each other
– Unless a pi system can be used to tunnel
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13.12 More Complex Spin-Spin Splitting Patterns
• Spectra can be more complex due to overlapping
signals, multiple nonequivalence
• Example: trans-cinnamaldehyde
H
O
H
H
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p-bromotoluene
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Analysis of NMR Spectra
• The NMR spectra provides the following information that
can assist in the determination of chemical structure
– The number of signals
– The chemical shift
– The intensity of the signal (area under each peak)
– The splitting of each signal
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