Complex coupling

In all of the examples of spin-spin coupling that we have seen so far, the observed splitting has resulted from the coupling of one set of hydrogens to just one neighboring set of hydrogens. When a set of hydrogens is coupled to two or more sets of nonequivalent neighbors, the result is a phenomenon called complex coupling. A good illustration is provided by the ¹H-NMR spectrum of methyl acrylate:

First, let's first consider the H_c signal, which is centered at 6.21 ppm. Here is a closer look:

With this enlargement, it becomes evident that the Hc signal is actually composed of four sub-peaks. Why is this? H_c is coupled to both H_a and H_b , but with two different coupling constants. Once again, a splitting diagram (or tree diagram) can help us to understand what we are seeing. H_a is trans to H_c across the double bond, and splits the H_c signal into a doublet with a coupling constant of ³J_ac = 17.4 Hz. In addition, each of these H_c doublet sub-peaks is split again by H_b (geminal coupling) into two more doublets, each with a much smaller coupling constant of ²J_bc = 1.5 Hz.

The result of this `double splitting` is a pattern referred to as a doublet of doublets, abbreviated `dd`.

The signal for H_a at 5.95 ppm is also a doublet of doublets, with coupling constants ³J_ac= 17.4 Hz and ³J_ab = 10.5 Hz.

The signal for H_b at 5.64 ppm is split into a doublet by H_a, a cis coupling with ³J_ab = 10.4 Hz. Each of the resulting sub-peaks is split again by H_c, with the same geminal coupling constant ²J_bc = 1.5 Hz that we saw previously when we looked at the H_c signal. The overall result is again a doublet of doublets, this time with the two `sub-doublets` spaced slightly closer due to the smaller coupling constant for the cis interaction. Here is a blow-up of the actual H_bsignal:

When a proton is coupled to two different neighboring proton sets with identical or very close coupling constants, the splitting pattern that emerges often appears to follow the simple `n + 1 rule` of non-complex splitting. In the spectrum of 1,1,3-trichloropropane, for example, we would expect the signal for H_b to be split into a triplet by H_a, and again into doublets by H_c, resulting in a 'triplet of doublets'.

H_a and H_c are not equivalent (their chemical shifts are different), but it turns out that ³J_ab is very close to ³J_bc. If we perform a splitting diagram analysis for H_b, we see that, due to the overlap of sub-peaks, the signal appears to be a quartet, and for all intents and purposes follows the n + 1 rule.

For similar reasons, the H_c peak in the spectrum of 2-pentanone appears as a sextet, split by the five combined H_b and H_d protons. Technically, this 'sextet' could be considered to be a 'triplet of quartets' with overlapping sub-peaks.

In practice, however, all three aromatic proton groups have very similar chemical shifts and their signals overlap substantially, making such detailed analysis difficult. In this case, we would refer to the aromatic part of the spectrum as a multiplet.

When we start trying to analyze complex splitting patterns in larger molecules, we gain an appreciation for why scientists are willing to pay large sums of money (hundreds of thousands of dollars) for higher-field NMR instruments. Quite simply, the stronger our magnet is, the more resolution we get in our spectrum. In a 100 MHz instrument (with a magnet of approximately 2.4 Tesla field strength), the 12 ppm frequency 'window' in which we can observe proton signals is 1200 Hz wide. In a 500 MHz (~12 Tesla) instrument, however, the window is 6000 Hz - five times wider. In this sense, NMR instruments are like digital cameras and HDTVs: better resolution means more information and clearer pictures (and higher price tags!)

مواضيع ذات صلة

Spectroscopic Properties of Alkynes

Spectroscopic Properties of Alkenes

Application of Chemical Shifts to Structure Determination

Correlations Between Structure and Chemical Shifts

Electronegativity and Chemical Shifts

Effects of Carbon Bond Type

Mass Spectroscopy

Hydrogen Bonding

Chemical Exchange

Proton-Proton Splittings and Conformational Analysis

Spin-Spin Splitting - What We Observe

Proton-Proton Splittings and Chemical Exchange