multidimensional nmr experiments · 2014. 8. 2. · running two nmr experiments – but it is...
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Multidimensional NMR Experiments
Chem 4010/5326:Organic Spectroscopic Analysis
© 2015 Andrew Harned
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2D NMR SpectroscopyGeneral Information
– More complicated experiments to set up than 1H and 13C– Changes in pulses (#, length, angles, mixing times, etc.)– Observe effects based on relationship of nuclei
**Can be homonuclear (same nuclei) (e.g. H–H) or heteronuclear (different nuclei) (e.g. H–C, H–P, etc.)**
– Will only go over the what the experiments tell you and how to interpret, and only for the most common and widely used for solving organic structures
– DEPT, H–H COSY, HMQC (HETCOR), HMBC, INADEQUATE– There is a whole alphabet soup of other experiments (both 1D and 2D)
– EXSY, TOCSY, HOHAHA, INEPT, WATERGATE, and many more
http://www.chem.ox.ac.uk/spectroscopy/nmr/acropage.htm
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2D NMR SpectroscopyNumber of Protons on Carbon
– Used to be known as APT (Attached Proton Test)– DEPT is 1H-detected; APT is 13C-detected
– Tells you how many protons are attached to a particular carbon– negative peaks = CH2
– positive peaks = CH and CH3 (distinguishable with further processing)
– “missing” peaks = carbons w/o protons– With a little help from IR and chemical shift of 1H and 13C, can get a rough idea of molecular weight
DEPT (Distortionless Enhancement by Polarisation Transfer)
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2D NMR SpectroscopyNumber of Protons on Carbon
= Carbon spectrum = ↓ CH2 ↑ CH, CH3
= ↑ CH
135ºpulse
90ºpulse
DEPT (Distortionless Enhancement by Polarisation Transfer)
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– Tells you which protons are coupled to one another– Very useful when peaks are overlapping in 1H NMR and you are unable to calculate coupling constants, or when there are a lot of similar coupling constants– Cross peaks are coupled to each other
– Newer method is DQF (Double Quantum Filtered)-COSY– same information, but looks “cleaner”
2D NMR SpectroscopyWho is Talking to Who?
1H–1H COSY (Correlation Spectroscopy)
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2D NMR SpectroscopyWho is Talking to Who?
1H1H
4H2H 2H 1H
3H3H
2H
– Overlapping protons and a lot of similar coupling constants
Raffinose–a trisaccharide
1H–1H COSY (Correlation Spectroscopy)
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2D NMR SpectroscopyWho is Talking to Who?
Raffinose–a trisaccharide
1H–1H COSY (Correlation Spectroscopy)
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2D NMR SpectroscopyWho is Talking to Who?
4H
1H
1H2H2H1H
3H3H
2H
1H–1H COSY (Correlation Spectroscopy)
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2D NMR SpectroscopyWho is Talking to Who?
– DQF-COSY: Double Quantum Filtered COSY – cleans up the spectrum by reducing noncoupled systems (e.g. CH3 singlets)
1H–1H COSY (Correlation Spectroscopy)
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2D NMR SpectroscopyWho is Talking to Who?
– DQF-COSY: Double Quantum Filtered COSY – cleans up the spectrum by reducing noncoupled systems (e.g. CH3 singlets)
1H–1H COSY (Correlation Spectroscopy)
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2D NMR SpectroscopyWho is Talking to Who?
C6H10O2
1H–1H COSY (Correlation Spectroscopy)
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2D NMR SpectroscopyWho is Talking to Who?
1H–1H COSY (Correlation Spectroscopy)
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– Tells you which protons are coupled to one another– Very useful when peaks are overlapping in 1H NMR and you are unable to calculate coupling constants, or when there are a lot of similar coupling constants– Cross peaks are coupled to each other
Recall...1H–1H COSY
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– Tells you which protons are coupled to one another– Very useful when peaks are overlapping in 1H NMR and you are unable to calculate coupling constants, or when there are a lot of similar coupling constants– Cross peaks are coupled to each other
Recall...1H–1H COSY
4H
1H
1H
2H2H1H
3H
3H
2H
This can still causeambiguities!
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2D NMR SpectroscopyWho is Talking to Who?
– Tells you which protons are in the same spin system (a continuous chain of spin-spin coupled protons)
– Magnetization from HA is transferred to HB, which then transfers to HC and on down the line
– Can be run as either a 1D or 2D experiment– Running as a 1D experiment greatly simplifies spectra with severe signal
overlap– Related experiment (HOHAHA) gives essentially the same information– Can also observe one-bond 1H–13C couplings (HMQC-TOCSY,
hetero-TOCSY, HEHAHA) - will not discuss
1H–1H TOCSY (Total Correlation Spectroscopy)
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1D TOCSYSpin System Identification
– Irradiate at frequency of proton of interest– Wait a period of time (typically 20 to 400 ms) and then collect
1D spectrum– Only observe protons to which magnetization has been transferred– Short periods of time (20 ms) will only give rise to “single step”
transfers; longer periods of time allow magnetization to propagate further
α- and β-lactose
1H–1H TOCSY (Total Correlation Spectroscopy)
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1D TOCSYSpin System Identification
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1D TOCSY
Claridge, T. D. W. High-Resolution NMR Techniques in Organic Chemistry, 2nd Ed., Elsevier, 2009.
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1D TOCSY
Claridge, T. D. W. High-Resolution NMR Techniques in Organic Chemistry, 2nd Ed., Elsevier, 2009.
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2D TOCSYSpin System Identification
– Cross peaks are in the same spin system
COSY TOCSY
Claridge, T. D. W. High-Resolution NMR Techniques in Organic Chemistry, 2nd Ed., Elsevier, 2009.
1H–1H TOCSY (Total Correlation Spectroscopy)
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2D TOCSY– Cross peaks are in the same spin system
Claridge, T. D. W. High-Resolution NMR Techniques in Organic Chemistry, 2nd Ed., Elsevier, 2009.
Intermediate in biomimetic synthesis of manzamine
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2D TOCSY– Cross peaks are in the same spin system
Claridge, T. D. W. High-Resolution NMR Techniques in Organic Chemistry, 2nd Ed., Elsevier, 2009.
Intermediate in biomimetic synthesis of manzamine
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2D TOCSY– Cross peaks are in the same spin system
Claridge, T. D. W. High-Resolution NMR Techniques in Organic Chemistry, 2nd Ed., Elsevier, 2009.
Intermediate in biomimetic synthesis of manzamine
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– Conceptually the same as the homonuclear decoupling experiment mentioned earlier, but allows multiple frequencies to be decoupled at the same time
New DevelopmentsDeconvolution via MDEC
J. Am. Chem. Soc. 2009, 131, 15994–15995
(a) 1H NMR(b) irr @ H-1(c) irr @ H-1/H-7(d) irr @ H-1/H-3a/H-7
H-2 (dddd)
H-2 (app dt)
H-2 (dd, J = 3.3, 12.2 Hz)X !
X !
X !
MDEC (Multi Frequency Homonuclear Decoupling)
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New DevelopmentsDeconvolution via MDEC
J. Am. Chem. Soc. 2009, 131, 15994–15995
(a) 1H NMR(b) 1D-TOCSY irr @ H-3(c) 1D-TOCSY irr @ H-3 with MDEC @ H-1b, H-2b, H-3
H-2aX !
X !
X !
1D-TOCSY-MDEC
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2D NMR SpectroscopyWho is Talking to Who?
– HETCOR (Heteronuclear Correlation)– older experiment; 13C-detected
– HMQC (Heteronuclear Multiple Quantum Correlation) and HSQC (Heteronuclear Single Quantum Correlation)
– newer experiments; 1H-detected; largely replaced HETCOR– Both give same information, experimentally very different– Peaks have one-bond coupling (i.e. attached directly)– Compliments DEPT– Particularly useful for diastereotopic protons
1H–13C COSY
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2D NMR SpectroscopyWho is Talking to Who?
HMQC
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2D NMR SpectroscopyWho is Talking to Who?
DiastereotopicProtons
HMQC
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2D NMR SpectroscopyWho is Talking to Who?
Can “see into” multiplets
HMQC
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2D NMR SpectroscopyWho is Talking to Who?
HMQC
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2D NMR Spectroscopy
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2D NMR Spectroscopy
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2D NMR Spectroscopy
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2D NMR SpectroscopyWho is Talking to Who?
– COLOC (Correlated spectroscopy for Long range Couplings)– older experiment; 13C-detected
– HMBC (Heteronuclear Multiple Bond Coherence)– newer experiment; 1H-detected; completely replaced COLOC
– Both give same information, experimentally very different– Peaks have two- or three-bond coupling– “Sees through” heteroatoms and quaternary carbons– Can be very complicated, but is very powerful
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2D NMR SpectroscopyWho is Talking to Who?
– HETCOR (Heteronuclear Correlation)– older experiment; 13C-detected
– HMQC (Heteronuclear Multiple Quantum Correlation) and HSQC (Heteronuclear Single Quantum Correlation)
– newer experiments; 1H-detected; largely replaced HETCOR– Both give same information, experimentally very different– Peaks have one-bond coupling (i.e. attached directly)– Compliments DEPT– Particularly useful for diastereotopic protons
1H–13C COSY (Long Range)
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2D NMR SpectroscopyWho is Talking to Who?
HMQC
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2D NMR SpectroscopyWho is Talking to Who?
HMBC
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2D NMR SpectroscopyWho is Talking to Who?
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2D NMR SpectroscopyWho is Talking to Who?
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2D NMR SpectroscopyWho is Talking to Who?
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2D NMR SpectroscopyWho is Talking to Who?
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2D NMR SpectroscopyWho is Talking to Who?
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2D NMR SpectroscopyWho is Talking to Who?
– INADEQUATE (Incredible Natural Abundance Double Quantum Transfer Experiment)– tells what carbons are attached to each other– if you know what type of carbon it is (C, C=O, CH, CH2, CH3, etc.) from DEPT, you can almost write down the entire gross structure by running two NMR experiments
– BUT it is 13C–13C coupling– probability of one 13C is 0.01– two next to each other 0.01x0.01 = 0.0001
(~1 molecule in 10,000)– Need lots of sample and instrument time to overcome– In our facility: 80% v/v, overnight, 500 MHz = nothing
13C–13C COSY
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2D NMR SpectroscopyWho is Talking to Who?
INADEQUATE
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2D NMR SpectroscopyWho is Talking to Who?
– Cross peaks show up as doublets = JCC – Diagonal is midway between the two doublets
5 4 1 9 103 11 2 15 126,714
INADEQUATE
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2D NMR SpectroscopyCH C CH CH2 C CH2
CH3,CH3,CH2,CH3
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2D NMR SpectroscopyCH C CH CH2 C CH2
CH3,CH3,CH2,CH3
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2D NMR Spectroscopy
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2D NMR Spectroscopy
C C,CH
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2D NMR Spectroscopy
C CCH CH CH2 CH2 CH3CH3 x2
![Page 51: Multidimensional NMR Experiments · 2014. 8. 2. · running two NMR experiments – BUT it is 13C–13C coupling – probability of one 13C is 0.01 – two next to each other 0.01x0.01](https://reader033.vdocuments.mx/reader033/viewer/2022060817/609652e1efc29154bb73c808/html5/thumbnails/51.jpg)
2D NMR Spectroscopy
C CCH CH CH2 CH2 CH3CH3 x2
WhichIsomer?
![Page 52: Multidimensional NMR Experiments · 2014. 8. 2. · running two NMR experiments – BUT it is 13C–13C coupling – probability of one 13C is 0.01 – two next to each other 0.01x0.01](https://reader033.vdocuments.mx/reader033/viewer/2022060817/609652e1efc29154bb73c808/html5/thumbnails/52.jpg)
2D NMR Spectroscopy
![Page 53: Multidimensional NMR Experiments · 2014. 8. 2. · running two NMR experiments – BUT it is 13C–13C coupling – probability of one 13C is 0.01 – two next to each other 0.01x0.01](https://reader033.vdocuments.mx/reader033/viewer/2022060817/609652e1efc29154bb73c808/html5/thumbnails/53.jpg)
2D NMR Spectroscopy