Multinuclear NMR Spectroscopy

3 NMR tubes

Multinuclear NMR spectroscopy is the name given to the study of NMR active nuclei of elements other than just 1H (proton) or 13C (carbon). In fact the second most sensitive nucleus for NMR work is ... 19F! Our research has resulted in us obtaining a wide range of fluorine spectra, and of other nuclei, below you will find examples of 19F, 31P, 77Se, 119Sn, 199Hg data amongst others. Since this is an area not well covered in standard NMR textbooks, we also provide some of the relevant background/theory and calculators, such as the interactive Pascal's triangle j-coupling pattern calculator, on our nmr primer page.

These pages are slowly evolving, they will be expanded to include new spectra, data and relevant links, as they become available to us. Note: In most cases clicking on a spectrum will display a larger version.]

The 19F NMR spectra of C6F3H2Br.

The spectrum below was obtained for a sample of the partially fluorinated aromatic compound 1-bromo,3,4,5-trifluorobenzene. In this molecule there are two different chemical environments for the fluorine nuclei, that is the fluorine atoms in the 3 and 5 positions (blue in the diagram) are in one similar environment, while the C-4 fluorine (para to the bromine) is in its own unique environment. Consider either F-3 or F-5, this nucleus will couple with the adjacent F-4 nucleus, to give a doublet, and also with the neighbouring proton, which splits this signal again to generate a doublet of doublets. The single, unique fluorine, F-4, will couple with the two equivalent fluorine nuclei (F3 and F5) to give a triplet, and also with the two chemically equivalent protons so this signal appears as a triplet of triplets.

19-F NMR spectrum showing a doublet of doublets and triplet of triplets
The 19F NMR spectrum of 1-Br,3,4,5-trifluorobenzene

The 19F NMR spectra of CF3CH2OCF2CF2H.

The spectrum below is for the fluoroether compound shown in the picture below. Because of free-rotation around the C-C bonds there are three different chemical environments for the fluorine nuclei; the CF3 group, the OCF2 fluorines and the CF2H fluorines. Consistent with this the spectrum shows 3 signals, in the relative intensity ratio (integrals) 3:2:2. The first of these signals, a ca. -75 ppm, is a triplet because of coupling to the adjacent 2 protons [2nI+1 => triplet]. The most negative signal, at ca. -137 ppm, is a doublet of triplets (see expansion) which arises from coupling to the singlet proton (to give a doublet) and then the two fluorine nuclei on the neighbouring carbon (to give the triplet part of the pattern) so generating a doublet of triplets overall. The middle signal arises from the two fluorines of the central OCF2 group.

19-F NMR spectrum showing three multiplets
The 19F NMR spectrum of CF3CH2OCF2CF2H

The 199Hg NMR spectra of Hg(CF=CF2)2 and Hg(CF=CF(CF3))2.

The spectrum below is of Hg(CF=CF2)2, also shown below. In this molecule all three fluorines of each trifluorovinyl group are chemically inequivalent to each other, but the same either side of the mercury centre, so the mercury signal is split into a triplet of triplet of triplets. [Click on the spectrum to see a larger version.]

199-Hg NMR spectrum showing a triplet of triplet of triplets
The 199Hg NMR spectrum of Hg(CF=CF2)2

The 199-Hg NMR spectrum shown below is for Hg(CF=CF(CF3))2. Compared with the molecule above, one of the fluorines of each group has been replaced by a CF3 group, so now the coupling pattern is a triplet of triplet of septets. However, the septet coupling is not very well resolved, even in the most intense, central portion of the spectrum the weakest outer lines (1:6:15:20:15:6:1) of the septet are difficult to pick out.

NMR spectrum showing a triplet of triplet of septets
The 199Hg NMR spectrum of Hg(CF=CF(CF3))2

The 31P and 19F NMR spectra of Ph2P(i-C3F7).

The spectra below are for a sample of Ph2P(i-C3F7). In this molecule there are two fuorine environments in the ratio 1:6, so the 31P NMR spectrum is a doublet of septets, as shown below. [Click on the spectrum to see a larger version.] However these are not completely separated, so there is some overlap in the centre of the pattern. The 19F NMR spectrum has two signals, reflecting the fact that there are two fluorine environments. The intense peak is due to the six fluorine nuclei of the two CF3 groups, which couple to the other fluorine, and the phosphorus to give a doublet of doublets. The weaker signal arises from the unique single fluorine environment, which shows coupling to the phosphorus and the six fluorines of the CF3 groups, so appears as a doublet of septets.

31P NMR spectrum showing a doublet of septets
31P NMR spectrum of Ph2P(i-C3F7)
NMR spectrum showing an intense doublet of doublets and a weaker doublet of septets
19F NMR spectrum of Ph2P(i-C3F7)

77Se NMR spectrum of Ph2P(Se)CH2CH2P(Se)Ph2.

The selenium NMR spectrum of the selenide of dppe bis(diphenylphospino)ethane is shown below. 77Se is of low abundance, only 7.6% (or 0.076), so there is the possibility of a molecule possessing either none, one or two Se-77 nuclei. The probability of these can be calculated in the following way:

Neither selenium is 77: 0.924 x 0.924 = 0.854, or 85.4%
One selenium is 77:     2 x 0.076 x 0.924 = 0.140 or 14%
Both seleniums are 77 : 0.076 x 0.076 = 0.006 or 0.6%

Of course when neither selenium atom is 77Se there can be no 77-Se NMR spectrum. Conversely, the chance of both seleniums being 77Se is so low (0.6%) that we can effectively ignore it. This leaves us with the molecules in which one of the two seleniums is spin-active. In such molecules the two phosphorus atoms will be different - one is connected to a spin-active selenium, the other is not, so the selenium NMR signal is split into a widely separated doublet by the phosphorus nucleus to which it is directly bound (1J(SeP)) and also by the more distant, other phosphorus nucleus (4J(SeP)), so a doublet of doublets is observed, as shown below.

77Se NMR spectrum and inset an expansion, showing a doublet of doublets
77Se NMR spectrum of Ph2P(Se)CH2CH2P(Se)Ph2

Links to other sites

The following sites are worth a visit:

Site Menu
Fluorine Events
Nov 2014
Su 
Mo 
Tu 
We 
Th 
Fr 
Sa 
      
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30

Days with events are highlighted, click, or hover on them for more details. Click here for the diary.

Visitor Number

655499
54.237.235.12

Fluorine Group News
The crystal structure of [FeCp(CO)2(CCl=CF2)]

[FeCp(CO)2(CCl=CF2)]
One of the first organometallic chlorodifluorovinyl complexes to be prepared.

Click for other news

Fluorine@Manchester
HFC-134a cylinder, a solvent for enzyme reactions

HFCs for biological transformations
Jason Micklefield's group pioneered the use of HFCs as solvents for enzymatic reactions.

Fluorine in Society
water beads on a surface

Repelency coatings
Many water repellency treatments for clothes and equipment, such as coats, shoes and tents, are based on fluorochemicals.