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NMR Nuclear Magnetic Resonance
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1 H, 13 C, 15 N, 19 F, 31 P
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One Level is more populated than the other Therefore a Resulting Net Magnetization will be Macroscopically Observable
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CW Continous Wave
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The Exact Resonance Frequency Varies with the Chemical and Electronical Environment of the Nucleus – This is Called the Chemical Shift (measured in ppm)
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The Chemical Shift is Measured Relative to a Reference or ‘Standard’ ppm ‘parts per million’ =( - ref )/ ref * 10 6 The most common standard for 1 H and 13 C NMR is TMS Tetramethylsilan CH 3 CH 3 – Si - CH 3 CH 3
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NMR is ‘quantitative’ The intensity is measured as the integral below the resonance signal. The intensities are proportional to the number of protons, that contribute to the signal.
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A – B B – A – B C – B – A Each Particular Arrangement of Nuclei has a Characteristic Coupling Pattern n Neighbors – (n+1) Lines
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CH 3 CH 2 No spin-spin coupling is observed if: 1.protons are separated by four or more single bonds, i.e., 2.H-C-C-C-H 3.protons are equivalent, i.e.,within a CH 3 or CH 2 group example
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Pick the molecule that gives rise to the following 1 H NMR spectrum!
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Assign the Signals to the Correct Hydrogens
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(almost) pure D Glucose ~50% - 50% D Glucose
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FT NMR ‘Pulse Echo’ NMR ‘Broadband Excitation’ Record ‘Transient Response’ FID Free Induction Decay Extract Frequencies by Fourier Transform to get NMR Spectrum
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More Complex Experiments Measurement of Relaxation Times (‘Lifetimes’) Inversion Recovery
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13 C NMR Spectroscopy Sensitivity low: only 1.1% natural abundance Complicated 1 H coupling pattern, no couplings between 13 Cs (due to low abundance) S/N can be improved by 1 H ‘broadband decoupling’ and FT averaging
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3 J HH coupling constants contain Geometrical Information on Torsion Angles ‘Karplus Relation’
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COSY Correlated SpectroscopY Two Dimensional NMR Spectroscopy A Signal as a function of two times becomes after 2D FT Spectrum as a function of two frequencies Usually presented as ‘contour plot’
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Cyclosporin A
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HNHN HH HH CH 3 / etc
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‘complex’ spectra can be resolved using 2dimensional NMR methods
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