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Spectroscopy 3: Magnetic Resonance CHAPTER 15. Conventional nuclear magnetic resonance Energies of nuclei in magnetic fields Typical NMR spectrometer.

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Presentation on theme: "Spectroscopy 3: Magnetic Resonance CHAPTER 15. Conventional nuclear magnetic resonance Energies of nuclei in magnetic fields Typical NMR spectrometer."— Presentation transcript:

1 Spectroscopy 3: Magnetic Resonance CHAPTER 15

2 Conventional nuclear magnetic resonance Energies of nuclei in magnetic fields Typical NMR spectrometer The chemical shift (effect of nearby nuclei) Fine structure (nuclear spin-spin coupling) Pulsed techniques in FT-NMR

3 The 1 H-NMR low-resolution spectrum of ethanol

4 Fig 15.6 The 1 H-NMR high-res spectrum of ethanol Integrated signal singlet quartet triplet 1 3 2 Fine structure

5 Fine Structure Each magnetic nucleus may contribute to the local field of adjacent nuclei ∴ Resonance frequencies are modified Strength of interaction given by the coupling constant, J (Hz) J is independent of applied mag field, B o

6 Margin pg 526 n equivalent nuclei split adjacent spin(s) into n+1 lines with intensity distribution given by Pascal’s triangle :

7 Fig 15.15 Origin of the 1:2:1 triplet in the proton resonance of a –CH 3 group from coupling with –CH 2 protons e.g., CH 3 CH 2 OH ⇇⇉ ⇆ ⇄ B0B0 ⇉ ⇇ ⇆ ⇄

8 Fig 15.16 Origin of the 1:3:3:1 quartet in the proton resonance of a -CH 2 from coupling with -CH 3 protons e.g., CH 3 CH 2 OHB0B0

9 Spectrum 1Empiricial formula C 4 H 8 O

10 Spectrum 2Empiricial formula C 4 H 8 O 2

11 Spectrum 3Contains C, H, OMW = 72

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