Hybridoma Technology ( Production , Purification , and Application )
use of nmr in structure ellucidation
1. Use of NMR in Structure
Elucidation
Presented By:
Anuradha Verma
Research Scholar
2. Overview
• NMR is a sensitive, non-destructive method
for elucidating the structure of organic
molecules
• Information can be gained from the hydrogens
(proton NMR, the most common), carbons
(13C NMR) or other elements like 31P, 15N, 19F.
3. Making NMR work
• Not all protons absorb at the same field values
• Either magnetic field strength or radio
frequency must be varied
• Frequency/field strength at which the proton
aďsorďs tells soŵethiŶg aďout the protoŶ’s
surroundings
4. In a magnetic field the states have different energies
Alignment with the magnetic field (called ) is
lower energy than against the magnetic field
(called ). How much lower it is, depends on the
strength of the magnetic field
5. • Energy difference linearly depends on field
strength
E
proton spin state
(higher energy)
E = h x 300 MHz E = h x 500 MHz
7.05 T 11.75 T
Bo
proton spin state
(lower energy)
Graphical relationship between
magnetic field (B o) and frequency (
for 1H NMR absorptions
at no magnetic field,
there is no difference beteen
- and - states.
0 T
6. NMR Signals
• The number of signals shows how many different
kinds of protons are present.
• The location of the signals shows how shielded or
deshielded the proton is.
• The intensity of the signal shows the number of
protons of that type.
• Signal splitting shows the number of protons on
adjacent atoms.
7. Chemical shift
• Protons in different environments absorb at
different field strengths (for the same frequency)
• Different environment = different electron density
around the H
8. Location of Signals
• More electronegative atoms
deshield more and give larger
shift values.
• Effect decreases with distance.
• Additional electronegative
atoms cause increase in
chemical shift.
13. O-H and N-H Signals
• Chemical shift depends on concentration.
• Hydrogen bonding in concentrated solutions deshield
the protons, so signal is around 3.5 for N-H and 4.5
for O-H.
• Proton exchange between the molecules broaden the
peak.
14. Hydroxyl Proton
• Ultrapure samples of
ethanol show splitting.
• Ethanol with a small
amount of acidic or basic
impurities will not show
splitting.
15. N-H Proton
• Moderate rate of exchange.
• Peak may be broad.
16. Identifying the O-H or N-H Peak
• Chemical shift will depend on concentration and
solvent.
• To verify that a particular peak is due to O-H or N-H,
shake the sample with D2O.
• Deuterium will exchange with the O-H or N-H
protons.
• On a second NMR spectrum the peak will be absent,
or much less intense.
18. Intensity of Signals
• The area under each peak is proportional to
the number of protons.
• Shown by integral trace.
19. Spin-Spin Splitting
• Nonequivalent protons on adjacent carbons have
magnetic fields that may align with or oppose the
external field.
• This magnetic coupling causes the proton to absorb
slightly downfield when the external field is reinforced
and slightly upfield when the external field is opposed.
20. The N + 1 Rule
If a signal is split by N equivalent protons,
it is split into N + 1 peaks.
=>
23. Range of Magnetic Coupling
• Equivalent protons do not split each other.
• Protons bonded to the same carbon will split
each other only if they are not equivalent.
• Protons on adjacent carbons normally will
couple.
• Protons separated by four or more bonds will not
couple.
24. Coupling Constants
• Distance between the peaks of multiplet
• Measured in Hz
• Not dependent on strength of the external field
• Multiplets with the same coupling constants may
come from adjacent groups of protons that split each
other.
26. Complex Splitting
• Signals may be split by adjacent protons, different
from each other, with different coupling constants.
• Example:
Ha of styrene which is split by an adjacent H trans to it
(J = 17 Hz) and an adjacent H cis to it (J = 11 Hz).
C C
H
H
a
H
c
b
27. General Regions of Chemical Shifts
-Disubstitutid aliphatic
Aromatic and heteroaromatic
Aldehydic
Olefinic
Aliphatic alicyclic
-Substituted aliphatic
Acetylenic
-Monosubstituted aliphatic
10 9 8 7 6 5 4 3 2 1 0 = TMS
CH3-CH2-CH2-CH2-CH2-CH=CH-CH2-CH=CH-CH2-CH2-CH2-CH2-CH2-CH2-CH2-COOCH2
HOCH
HOCH2
42. Summary
•The magnetic nucleus may assume any one of ( 2 I + 1)
orientations with respect to the directions of the applied
magnetic field.
•Therefore, a proton (1/2) will be able to assume only one
of two possible orientations that correspond to energy
levels of + or - H in an applied magnetic field, where H
is the strength of the external magnetic field.
43. Summary
•If proper v is introduced, the Wo will be resonance with
the properly applied radio frequency and the proton will
absorb the applied frequency and will be raised to the
high energy spin state.
•Even though the external magnetic field strength (Ho)
applied to the molecule is the same, the actual magnetic
field strength exerted to the protons of the molecule are
different if the protons are in the different electronic
chemical environment.
45. Structure Determination by NMR
• Biological molecules such as proteins and nucleic acids can be large
and complex. They can easily exceed 2000 atoms.
• Knowing their structure is critical in understanding the relationship
between structure and function.
• X-ray crystallography is an excellent method to determine detailed 3D
structures of even some of the largest biological molecules.
• However, it has some significant difficulties. Getting crystals and the
obtained structure may not be biologically relevant.
• NMR can be used to determine 3D structure and dynamics in solution!
It’s liŵitatioŶ is ŵoleĐular size. Hoǁeǀer, this is ĐhaŶgiŶg.
46. • Large molecules with numerous atoms nuclear magnetic moment
does not permit the determination of these fundamental parameters
easily.
• Some 1D spectra are far too complex for interpretation because
signals overlap heavily.
• e.g. cholesterols, protein spectra
47. How 2D NMR is useful?
Nonequivalent proton groups can have nearly the same chemical shift and/or
complex splitting patterns making 1D NMR spectra complicated even for
relatively simple molecules.
The introduction of additional spectral dimensions simplifies the spectra and
provides more information.
Two-dimensional (2D) NMR techniques can be used to solve such sophisticated
structural problems.
2-D spectra simplify the complexity arising from overlapping of peaks.
Simplification of NMR spectra makes their interpretation easier and sometimes
the only way possible.
The interaction of nuclear spins (1H with 1H, 1H with 13C, etc.) are plotted in two
dimensions
48. • In 2-D spectra the intensity is plotted as a
function of two frequencies, usually represented
as F1 and F2. F1 and F2 are Fourier transformed
frequency axis from a time domain signal.
49. H-H Correlation Spectroscopy (COSY)
• In a COSY experiment, the chemical shift range
of the proton spectrum is plotted on both axis.
50. • COSY spectrum of a molecule containing just one
type of protons HX.
• COSY spectrum of a hypothetical molecule
containing just two protons, HA and HX, which are
not coupled
51. • COSY spectrum of a hypothetical molecule containing just two types
of protons, HA and HX, which are coupled
• Signals on the diagonal divides the spectrum in two equal halves.
Signals symmetrical to the diagonal called cross signals (peaks).
• The cross signals originate from nuclei that exchanged magnetization
during the mixing time. They indicate an interaction of these two
nuclei. The cross signals contain the information of 2D NMR spectra.
52. • If there had been no coupling, their
magnetizations would not have given rise to off-diagonal
peaks.
• COSY spectrum shows which pairs in a molecule
are Đoupled (thro’ ďond Đoupling, henĐe
connectivity).
• From a single COSY spectrum it is possible to
trace out the whole coupling network in the
molecule.
54. • 31P-NMR allowed the measurement of the
intracellular pH of the muscle, resting or
fatigued, through the shift of the frequency of
the Pi peak
• The major phosphate metabolites of muscle are:
ATP, PCr, Pi. ATP and PCr occur at high
concentrations in normal resting muscle,
whereas the appearance of Pi indicates fatigue.
55. 31P-Spectroscopy of Heart Muscle
• 31P spectrum of beating rat heart shows the
Pi, PCr, and ATP resonances