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Summary Nuclear magnetic resonance (NMR)

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Drug design and mechanisms of drug action - 1st semester Includes bullet points, key diagrams and images

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  • June 8, 2023
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NMR

NMR Theory

 Nuclei have the property of spin
 Spin quantum number (I)
 I=1/2 as a proton
 Nuclei have a positive charge so generate a magnetic field
 Magnetic spin quantum number is direction of spin
 m=2I+1
 Magnetic field Bo provides the energy difference
 Energy difference is small and allows spin flip
 NMR measures the relaxation from excited state to ground state
 Use 9.4T (400MHz) or biological 21.1T (900MHz)




Spectrum

 Frequency (resonance) observed is dependant on the proton environment
 Nucleus is affected by Bo but electrons also have a magnetic field which modifies
this

, Reference Compounds

 TMS- tetramethylsilane
 Chemical shift δ=0
 It’s protons are very high field as they are very shielded
 Can calculate δ using TMS
 δ= v-v0/v0 where v0=reference resonance and v=observed resonance
 Independent of magnetic strength

NMR Solvents

 CDCL3 δ=7.2
 DMSO δ=2.5 and around 3 there’s a water peak as hygroscopic

Interpreting NMR Spectra

Peak Positions (Chemical Shift δ)

 Generally number of environments= number of different peaks
 δ depends on degree of branching as you get electronic effects of neighbouring
atoms
 δ CH>CH2>CH3
 CH3 is most up field- EWG reduce shielding and resonance so moves it down field
 More electronegative atoms increases resonance as electron density decreases
(shielding)
 Can extend down an alkyl chain




Hydroxyl Groups

 δ depends on the solvent as more dilute means a smaller
chemical shift as less hydrogen bonds
 High concentrations decreases electron density, deshields
the group and gives a higher frequency
 In carboxylic acids they can dimerise through hydrogen
bonding giving δ=10-12

CH2 In a Chain

 Neighbouring carbon is electronegative so protons are deshielded and shifted
down field
 δ=1.3-2.0ppm

CH In A Chain

 δ=1.7-2.5ppm

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