Title: 13CNMR, 2DNMR, and MRI
113C-NMR, 2D-NMR, and MRI
- Lecture Supplement
- Take one handout from the stage
2Midterm Exam 2
- Date Monday May 21
- Time 500-650 PM
- Topics All of spectroscopy (mass spectrometry ?
today) - Location last name A-La in Haines 39
- last name Le-Z in Moore 100
- Calculators not allowed
- Question and Answer Session
- Lecture time, Monday May 21
- Submit questions to harding_at_chem.ucla.edu
- Label as Question for QA
- Deadline for possible inclusion noon Sunday May
20 - Extra Office Hours
- Saturday 3-5 PM, Young Hall 3077F (Steve Joiner)
- Sunday ???
313C-NMR
- Is NMR limited to 1H?
- Any nucleus with I ? 0 can be observed
- I ? 0 when nucleus has odd number of protons or
odd number of neutrons - Includes 1H, 2H, 13C, 19F, 29Si, 31P, 127I, etc.
- Examples
- 19F 9 protons, 10 neutrons 100 natural
abundance - 31P 15 protons, 16 neutrons 100 natural
abundance
- 13C-NMR
- Carbon is backbone of organic molecules so
13C-NMR has high potential, but... - Low natural abundance 13C 1.1 (12C 98.9
but has 6 protons and 6 neutrons) - Low probability that photon absorption causes
spin flip 1.6 compared to 1H - Result 13C spin flip much harder to observe than
1H spin flip - Modern NMR spectrometers have overcome these
problems 13C-NMR now routine
413C-NMR
- What can we deduce about molecular structure from
13C-NMR spectrum? - NMR fundamentals are the same regardless of
nucleus - Information from carbon NMR spectrum
- Number of signals equivalent carbons and
molecular symmetry - Chemical shift presence of high EN atoms or pi
electron clouds - Integration ratios of equivalent carbons
- Coupling number of neighbors
513C-NMR Number of Signals
- Number of 13C-NMR signals reveals equivalent
carbons - One signal per unique carbon type
- Reveals molecular symmetry
- Examples
CH3CH2CH2CH2OH
CH3CH2OCH2CH3
2 x CH3 equivalent
No equivalent carbons Four 13C-NMR signals
2 x CH2 equivalent
Two 13C-NMR signals
Symmetry exists when of 13C-NMR signals lt of
carbons in formula
613C-NMR Position of Signals
- Position of signal relative to reference
chemical shift - 13C-NMR reference TMS 0.00 ppm
- 13C-NMR chemical shift range 0 - 250 ppm
- Downfield shifts caused by electronegative atoms
and pi electron clouds
Example
HOCH2CH2CH2CH3
OH does not have carbon ? no 13C-NMR OH signal
713C-NMR Position of Signals
- Trends
- RCH3 lt R2CH2 lt R3CH
- EN atoms cause downfield shift
- Pi bonds cause downfield shift
- CO 160-210 ppm
It is not necessary to memorize this table. It
will be given on an exam if necessary.
813C-NMR Integration
- 1H-NMR Integration reveals relative number of
hydrogens per signal - 13C-NMR Integration reveals relative number of
carbons per signal - Rarely useful due to slow relaxation time for 13C
- Relaxation time important phenomenon for MRI
913C-NMR Spin-Spin Coupling
- Spin-spin coupling of nuclei causes splitting of
NMR signal - Only nuclei with I ? 0 can couple
- Examples 1H with 1H, 1H with 13C, 13C with 13C
- 1H NMR splitting reveals number of H neighbors
- 13C-NMR limited to nuclei separated by just one
sigma bond no pi bond free spacers
- Conclusions
- Carbon signal split by attached hydrogens (one
bond coupling) - No other coupling important
1013C-NMR Spin-Spin Coupling
1H-13C Splitting Patterns
- Carbon signal split by attached hydrogens
- N1 splitting rule obeyed
Triplet
Doublet
Quartet
Singlet
Example
1113C-NMR Spin-Spin Coupling
Simplification of Complex Splitting Patterns
- Broadband decoupling all C-H coupling is
suppressed - All split signals become singlets
- Signal intensity increases less time required to
obtain spectrum
1213C-NMR Spin-Spin Coupling
Distortionless Enhancement by Polarization
Transfer (DEPT)
- Assigns each 13C-NMR signal as CH3, CH2, CH, or C
13Two-Dimensional NMR (2D-NMR)
- Basis interaction of nuclear spins (1H with 1H,
1H with 13C, etc.) plotted in two dimensions - Applications
- Simplifies analysis of more complex or ambiguous
cases such as proteins - Obtain structural information not accessible by
one-dimensional NMR methods - Techniques include
Correlation Spectroscopy (COSY) Heteronuclear
Correlation Spectroscopy (HETCOR) Heteronuclear
Multiple-Quantum Coherence (HMQC) Nuclear
Overhauser Effect Spectroscopy (NOESY) Incredible
Natural Abundance Double Quantum Transfer
Experiment (INADEQUATE) Many others
142D-NMR
COSY Correlation of 1H-1H coupling
Sucrose 1H-NMR
Sucrose 1H-NMR
- Examples
- H6 and H5 are coupled
- Identify H8 by its coupling with H9
152D-NMR
HMQC Correlation of spin-spin coupling between
1H and nuclei other than 1H such as 13C
Sucrose 1H-NMR
- No diagonal
- Example
- Which carbon bears H6?
Sucrose 13C-NMR
16Magnetic Resonance Imaging (MRI)
- Basis Spin-excited nuclei relax at a rate
dependent on their environment - Environmental factors bonding to other atoms,
solvent viscosity, etc. - Photons released upon excitation are detected
- 1H relaxation times varies with tissue type
(brain, bone, etc.) - Therefore tissues may be differentiated by NMR
- Timeline
- 1971 First MRI publication Tumor Detection by
Nuclear Magnetic Resonance - Science, 1971, 171, 1151
- 2002 22,000 MRI instruments in use 6 x 107 MRI
exams performed - 2003 Nobel Prize in Physiology or Medicine to
Paul Lauterbur and Peter Mansfield - for their discoveries concerning
magnetic resonance imaging - http//nobelprize.org
17Magnetic Resonance Imaging (MRI)NMR and MRI Use
Similar Instruments
Powerful magnets
18Magnetic Resonance Imaging (MRI)MRI Images
Quite Different from NMR Spectra!