Molecular electronic transitions take place when electrons in a molecule are excited from one energy level to a higher energy level. The energy change associated with this transition provides information on the structure of a molecule and determines many molecular properties such as colour. The relationship between the energy involved in the electronic transition and the frequency of radiation is given by Planck's relation.
Organic molecules and other molecules
The electronic transitions in organic compounds and some other compounds can be determined by ultraviolet–visible spectroscopy, provided that transitions in the ultraviolet (UV) or visible range of the electromagnetic spectrum exist for this compound. Electrons occupying a HOMO of a sigma bond can get excited to the LUMO of that bond. This process is denoted as a σ → σ* transition. Likewise promotion of an electron from a π-bonding orbital to an antibonding π orbital* is denoted as a π → π* transition. Auxochromes with free electron pairs denoted as n have their own transitions, as do aromatic pi bond transitions. Sections of molecules which can undergo such detectable electron transitions can be referred to as chromophores since such transitions absorb electromagnetic radiation (light), which may be hypothetically perceived as color somewhere in the electromagnetic spectrum. The following molecular electronic transitions exist:
In addition to these assignments, electronic transitions also have so-called bands associated with them. The following bands are defined: the R-band from the German radikalartig or radical-like, the K-band from the German Konjugierte or conjugated, B-band from benzoic and the E-band from ethylenic (system devised by A. Burawoy in 1930). For example, the absorption spectrum for ethane shows a σ → σ* transition at 135 nm and that of water a n → σ* transition at 167 nm with an extinction coefficient of 7,000. Benzene has three aromatic π → π* transitions; two E-bands at 180 and 200 nm and one B-band at 255 nm with extinction coefficients respectively 60,000, 8,000 and 215. These absorptions are not narrow bands but are generally broad because the electronic transitions are superimposed on the other molecular energy states.
- Morrill, Terence C.; Silverstein, Robert M.; Bassler, G. Clayton (1981). Spectrometric identification of organic compounds. New York: Wiley. ISBN 0-471-02990-4.
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- Burawoy, A. (1930). "Licht-Absorption und Konstitution, I. Mitteil.: Homöopolare organische Verbindungen". Berichte der deutschen chemischen Gesellschaft (A and B Series). 63: 3155. doi:10.1002/cber.19300631130
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