TABLE 12.7 Common 2D NMR experiments and their applications.2D NMR experiment
Application
Advantages
Limitations
Comments
COSY (correlated
spectroscopy)
Provides 2 and 3 bond
1 H
1 H
connectivity
Simple to run, resolves
overlapped protonresonances. Minimumamount required 1–2
m
g
Greater than three bond
correlations cannot beobserved
Any ambiguity in the
1D
1 H
assignment
should be followed bya COSY
TOCSY (total
correlatedspectroscopy)
Provides 2, 3, 4 and 5
bond
1 H
1 H
correlations
Simple to run, provides
long through-bondconnectivites.Minimum amountrequired 2–5
m
g
Sometimes, some long
bond correlation maynot be observed. Highpower may berequired for thespin lock pulse
Confirms the COSY as
signments or can beperformed instead ofa COSY. Used foridentifying contiguousproton spin systems
NOESY (NOE
spectroscopy)
Reveals through space
interactions
Stereochemical
questions can beanswered forappropriate molecules
Not a simple experiment to
perform. Data can becomplicated due toexchange peaks Insensitive
Only used where
appropriate
ROESY (rotating frame
noe spectroscopy)
Same as NOESY,
through-spaceinteractions
Same as NOESY plus can
distinguish betweenexchange and ROE peaks
Same as NOESY and
also insensitive
Same as NOESY
HMQC (heteronuclear
multiple quantumcorrelation) or HSQC(heternuclear singlequantum correlation)
Provides 1 bond
1 H
13
C
or
1 H
15
N
correlation
Can identify all the
protonated carbonsand nitrogens in amolecule
Less sensitive experiment
due to low sensitivity of 13
C
and
15
N
Compound
requirement is highMinimum 20
m
g or more
Can assist in identifying
complete unknowns,unexpected productsor metabolites
HMBC (heteronuclear
multiple bondcorrelation)
Provides 2 to 3 bonds
1 H
13
C
and
1 H
15
N
correlation.
Crucial for identifying
nonprotonatedcarbons and nitrogens
Most insensitive
experiment. 100
m
g
and higher amount ofmaterial required
Useful for complete
unknowns,unexpected productsand metabolites
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