By James Ashenhurst
UV-Vis Spectroscopy: Absorbance of Carbonyls
Last updated: September 29th, 2016
In our last post we showed that molecules with C-C pi (π) bonds absorb light in the UV-visible region, which promotes electrons from (bonding) π orbitals to (anti bonding) π* orbitals.
We saw that
- the energy required for the transition depends mostly on the extent of conjugation (i.e. the number of consecutive pi bonds, roughly speaking).
- an alkene with little or no conjugation (e.g. ethene, CH2=CH2) possesses a large energy gap (ΔE) between the bonding and anti bonding orbitals, which requires more energetic (shorter wavelength) photons for excitation. For ethene, maximum absorbance occurs at about 170 nm, in the UV region.
- as conjugation increases, the energy gap ΔE decreases, pushing the wavelength of maximum absorbance (λmax) toward the visible (less energetic photons, longer wavelength) . For example, β-carotene (the orange pigment in carrots) with 11 conjugated pi bonds, absorbs in the visible (λmax = 470 nm).
Because the post was so damn long, we never got around to addressing a key question: does this apply to other types of pi bonds as well?
For example, do C=O pi bonds also absorb light in the UV/visible region?
- The short answer is: yes.
- The medium sized answer is: yes, but the main transition of interest is not a pi-pi* transition – it’s slightly different.
The long answer is.. well, here’s the long answer.
Absorbance of C=O bonds
Let’s start with one of the simplest compounds with a C=O bond: 2-propanone, otherwise known as acetone.
Question: Does acetone absorb UV or visible light?
Answer: You betcha. Here’s the UV-Vis absorption spectrum for 2-propanone (acetone).
[The key piece of information to glean from that spectrum is that there is an absorbance maximum at about 275 nm, in the ultraviolet.]
If you have an astonishingly good memory you may recall from the last post (or from my introduction above) that the absorption max for ethene (CH2=CH2) is about 170 nm.
An absorption around 275 nm means that longer wavelength and therefore less energetic photons are required for this transition.
Doesn’t that seem weird?
If anything, C=O π bonds are stronger than C=C π bonds. [You can look it up]. Wouldn’t you reasonably expect *more* energy to be required to promote an electron from pi(π) to pi* (π*)?
Now: as we’ll see in a minute, there is a pi to pi* ( π→π*) transition for acetone in the UV, but that peak at 275 nm is NOT a pi to pi* transition. It’s a transition from a non-bonding orbital (n) to the pi* orbital (n→π*).
Carbonyl (C=O) Groups Tend To Show Weak Absorbances At (Roughly) 300 nm That Correspond To Transitions Between Non-Bonding Orbitals and Pi* Orbitals
Huh? Let’s look at a simple molecular orbital drawing of acetone.
[This is a somewhat simplified picture. For a more detailed MO diagram for that also includes a more thorough discussion about the nature of the non-bonding orbitals, I highly recommend Reusch’s online textbook entry here. ]
A few important things to note:
- Carbonyl groups contain non-bonding electrons that are in an orbital intermediate in energy between the bonding pi orbital and the anti bonding pi* orbital. These orbitals are absent in typical alkenes such as ethylene [CH2=CH2] [note 1]
- Being higher in energy, transitions between electrons in the non-bonding orbital to the pi* orbital have a smaller ΔE and therefore absorb at longer wavelength.
- It is this (n→π*) transition which is responsible for the peak at around 275 nm.
What About Pi to Pi* Transitions for C=O?
So what about the pi to pi* transition? Doesn’t that happen too?
Glad you asked. If you take a quick look back at the UV-Vis absorption spectrum of acetone, above, you’ll note that the X-axis gets cut off around 240 nm or so. There’s a reason for that (mwah-ah-ah).
If you zoom out, you’ll see that there’s a much stronger transition around 190 nm. [I went looking for a decent full-size UV spectrum of acetone, and the diagram below is the best I could find. I didn’t make this image and it is not my intellectual property. I found it here. ]
So as it turns out, that “peak” at 275 nm (n→π*) we were looking at turns out to be a molehill, next to the (π→π*) mountain at about 195 nm in the deeper UV.
In other words, the (n→π*) transition at 275 nm that we’ve spent so much time talking about is very weak relative to the (π→π*) transition. [sometimes a term called “epsilon, ε” is used to denote this difference in magnitude of absorption].
Why might that be? It has to do with differences in orbital overlap. In order for an electron to transition from one orbital to another, two conditions must be met.
- First, as previously discussed, the orbital has to interact with a photon of appropriate energy ΔE.
- Second, there has to be significant overlap between the orbitals in space. We generally don’t discuss this for (π→π*) and (σ→σ*) transitions because each pair of bonding and anti bonding orbitals occupies the same region of space. If you look back to the diagram for the location of the n orbitals in acetone compared to the location of the pi* orbitals, you might notice that they are essentially at right angles to each other. Poor orbital overlap means that even if the electron has sufficient energy ΔE to make the transition, the transition is considerably less likely to occur since the excited electron will be less likely to be occupying an area of space corresponding to the higher-energy orbital. [Extra detail: you might recall that orbitals are 3-dimensional volumes where the probability of encountering an electron is 95%. Therefore, there is some electron density outside of the volumes we typically consider “orbitals”]
Carbonyls Also Participate in Conjugation
Carbonyls can also participate in conjugation with C-C pi bonds. This leads to an increase in the overall λmax of the molecule. For instance, the absorbance of the alkene 2-methyl pent-2-ene is below 200 nm, as is the π→π* absorbance of 4-methyl pentane-2-one (below).
In mesityl oxide, where the alkene and C=O group are in conjugation with each other, the absorption maximum moves to longer wavelength at 228 nm. This is similar to the difference between the absorbance of ethene (174 nm) and butadiene (217 nm).
[Additional note] The absorbance maximum can be sensitive to the identity of the solvent as well as the identity of the substituents on the alkene. For carbonyls, generally more polar solvents lead to higher λmax values, as does the presence of substituents (such as methyl groups) on the alkene.
The Bottom Line
Absorbance in the rough neighbourhood of 270-300 nm is common for molecules containing a C=O group (such as ketones and aldehydes) and this corresponds to a (n→π*) transition.
These absorbances tend to be weak, relative to (π→π*) transitions. Still, observing this absorbance can be an important clue in the structure determination of unknown compounds.
In the next post we’ll go into practical details of using UV-Vis in structure determination.
[Again, for a more in depth look on the subject of C=O absorbance, go to Reusch. We’re really skimming the surface here, but it is enough for our purposes.]
Bonus Topic: Azo Dyes
Since we’re on the subject, let’s briefly explore another system where both n→π* and π→π* transitions are observed: azo dyes.
Azo dyes are the kind of thing that you’ve likely seen a million times without specifically knowing what they are.
For example, the yellow color of highway markings? That’s Pigment Yellow 10.
Azo dyes are commonly used in colouring textiles, plastics, and many other substances not intended for human consumption (they’re generally banned as food additives).
The key structural feature of an azo compound is a N=N linkage. One of the simplest azo compounds is azobenzene, where each nitrogen is connected to an aromatic ring. Slight modifications to the benzene ring can dramatically modify the color of the molecule. Aniline Yellow, discovered in 1861, was the first azo compound to find commercial use as a dye, and countless derivatives of azobenzene have been synthesized since then. [The synthesis is via diazo coupling – we won’t get into that here].
Here’s the UV-Vis spectrum of Aniline Yellow, as calculated by ChemTube 3D.
Note how it is qualitatively similar to that of acetone: a strong absorbance on the left (towards the UV) and a weak absorbance on the right (towards the visible).
In contrast to acetone, however, where the weak absorbance is at 260 nm, the weak absorbance in Aniline Yellow is in the visible region of the spectrum at about 460 nm. It is this absorbance at 460 nm that is responsible for the color of Aniline Yellow.
By analogy to acetone, the weak transition is an (n→π*) transition and the strong transition around 360 nm is a π→π* transition.
What’s even more interesting about azobenzenes and their derivatives (e.g. Aniline Yellow) is the phenomenon of photoisomerization, where absorption of specific frequencies of light can lead to isomerization of trans isomers to cis isomers and vice-versa.
Absorbance of UV light by trans-azobenzene (a π→π* transition) leads to isomerization to cis-azobenzene. Contrariwise, absorbance of visible light (blue light) by cis-azobenzene (the n→π* transition) results in conversion back to the trans-isomer [so does leaving cis-azobenzene in the dark, a process known as thermal relaxation]. The mechanism for this process is still not completely settled.
Pretty neat that you can target a specific isomer merely by changing the frequency of light. [note 2]
[note 1] It should be noted that non-bonding orbitals are present in species such as the allyl cation, allyl anion, and other ions of odd-numbered pi systems.
[note 2] The discovery of this process has led to some interesting applications. I know of one research group that made a series of azo polymers that could be spin coated onto glass slides. Application of a UV laser onto the surface resulted in the formation of a diffraction grating, which was permanent until either erased with a blue laser, or through heating the polymer to its glass transition temperature. The Department of Naval Research funded them to build optical computers that would erase themselves in the event of a system failure (e.g. warplane shot down over enemy territory, etc.).