Relaxation, Multi pulse Experiments and 2D NMR
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1 Relaxation, Multi pulse Experiments and 2D NMR
2 To Do s Read Chapter 6 Complete the end of chapter problems; 6 1, 6 2, 6 3, 6 5, 6 9 and Read Chapter 15 and do as many problems as you can.
3 Relaxation in NMR In NMR, the term relaxation describes several processes by which nuclear magnetization prepared in a non equilibrium state to the equilibrium distribution. e -t/t T: relaxation time constant Short T Fast relaxation Broad peak Long T Slow relaxation Sharp peak
4 T1 and T2 Relaxation Net magnetization M 0 at thermal equilibrium, Followed by a 90 RF excitation pulse M xy = zero M z = M 0 M xy = M 0 M z = zero T1 >= T2 Decay of M xy (time constant T2), and recovery of M z (time constant T1) T2: spin-spin relaxation T1: spin-lattice relaxation
5 Relaxation Mechanisms T1 (Spin Lattice relaxation or longitudinal relaxation) Magnetic field fluctuation by nearby magnetically active nuclei Most effective when they occur at the Larmor precession frequency T2 (Spin spin relaxation or transverse relaxation) Energy transfer within the spin system or spin diffusion
6 Inversion Recovery Experiment τ = 0
7 T1 and Structural Information r CH, r HH T1 τ c : time required for molecule to rotate one radian Rotation τ c T1
8 Chlorobenzene Quaternary carbon r CH T1 Slower relaxation
9 Other Examples Slower relaxation C1(3) Quaternary carbon C5 C2 C4(6) Relaxed by H5 and CH3
10 T1 and Anisotropic Motion Rotation τ c T1
11 T1 and Segment Motion H-bonding with each other Rotation τ c T1
12 Solvent Suppression Selective saturation Selective relaxation Selective excitation and detection
13 Solvent Suppression by Selective Relaxation Solvent molecules are generally smaller in size than the molecules of interest. Thus, solvent protons and carbons relax more slowly. Use π t D π/2 Acquire where t D is set such that the solvent is nulled.
14 Summary of Common 2D NMR Techniques?
15 COSY (Correlation Spectroscopy) Proton proton correlation through J coupling Use two 90 degree pulses, (π/2)x t1 (π/2)x Acquire FID Fourier Transform 2 dimensional NMR
16 Magnetization Changes in COSY Experiment FID FID
17 COSY of CHCl 3 t 1 FT FT t 2 A collection of FIDs
18 COSY of Methyl Acetate 1D 1 H-NMR COSY
19 J coupled Spin System J AX f 2 Diagonal axis f 1
20 COSY of β Chloroacrylic acid Stacked plot Contour plot
21 Typical COSYs are Recorded in Lower Digital Resolution
22 Predicted COSY for 1 Nitropropane a Cross peaks c b a b c Diagonal peaks
23 Ethyl Benzene
24 Annulene Start with a proton with only one cross peak, and trace the connectivity.
25 Citronellol Virtual coupling Diastereotopic H4s Diastereotopic H2s Allylic coupling
26 HMQC (Hetronuclear Multiple-Quantum Correlation): A modern equivalent of HETCOR The HMQC (Heteronuclear Multiple-Quantum Correlation) experiment is a heteronuclear correlation technique that offers a means of identifying 1-bond H-C connectivities within a molecule.
27 HMQC Example
28 Unknown (IHD = 4) -CH 3 5H X-CH 2 2H 4H 2H
29 Unknown CH DEPT135 CH 2 DEPT90 C CH 3 Normal 13 C-NMR
30 Unknown Two CH 2 overlapping
31 Chapter 6 Problems 6.1(a) -CH 2 -CH 2 -CH 2 -CH 2 -CH 3
32 Unknown 2 (C 6 H 10 O) (IHD = 2) 1642
33 Unknown 2 3 alkene protons 1H 1H 2H 1H 2H 2H 1H
34 Unknown 2 DEPT135 DEPT90 CH CH2 CH2 CH CH2 CH2
35 Unknown 2 1H 1H Diastereotopic CH2 Allylic coupling to CH2
36 Unknown 2 CH CH 2 2 CH
37 Unknown 2
38 HMBC (Heteronuclear Multiple Bond Correlation) HMBC is closely related to HMQC and operates in essentially the same manner. In this case, however, the sequence timings are optimized for much smaller coupling constants and therefore seeks the correlations across more than one bond that arise from so-called long-range couplings. In HMBC, direct one-bond correlations are suppressed. This gives connectivity information much like a proton-proton COSY. H H H C C - C H H H C C - C
39 Easy Unknown 3-Methyl-2-Pentanone
40 3-Methyl-2-Pentanone, Predicted HMBC 3-H 5-H 6-H 2-H 4-H 4-H
41 HMBC example
42
43 Unknown, C 11 H 12 O, IR & MS A ketone? M-15 IHD = 6
44 Unknown, C 11 H 12 O, 1 H- and 13 C-NMR CH2 CH3 CH3, CH2, C and C=O C=O 4CH + 2C C Ortho splitting pattern! 6H 4H 2H
45 Unknown, C 11 H 12 O, HMQC CH3 CH2 C
46 Unknown, C 11 H 12 O, HMBC CH2 is adjacent to CH3 and C=O CH3 CH2 C=O C=O is close to aromatic proton CH2 is NOT correlated with aromatic CH
47 MS, IR and UV/Vis Data 1 H, 13 C NMR, DEPT C H correlation from HSQC H H correlation from COSY Check assignment of diastereotopic protons using COSY and HSQC Assemble substructures using COSY data Combine substructures using long range H C data from HMBC Check all working structures for consistency with 2D NMR data
48 Use NOE and NOESY data to determine stereochemistry
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