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Mass spectrometry[change | change source]
In mass spectrometry, an α-cleavage occurs when molecules break apart within a mass spectrometer. A mass spectrum tells the size and elements found in each molecule fragment. Chemists use their understanding of how molecules break apart to guess the structure of the original molecule. Many different molecules break apart with α-cleavage inside the mass spectrometer. Many times, α-cleavage explains the resulting mass spectra.
As an example of a mechanism of alpha cleavage, an electron is knocked off an atom (usually by electron collision) to form a radical cation. Electrons are most likely to be removed in the following order: 1) lone pair electrons, 2) pi bond electrons, 3) sigma bond electrons.
One of the lone pair electrons moves down to form a pi bond with an electron from an adjacent (alpha) bond. The other electron from the bond moves to an adjacent atom (not one adjacent to the lone pair atom) creating a radical. This creates a double bond adjacent to the lone pair atom (oxygen is a good example) and breaks (cleaves) the bond that lost the two electrons that were removed.
Photochemistry[change | change source]
References[change | change source]
- Hathaway, Bruce A. (2005). Organic chemistry the easy way. Woodbury, N.Y: Barron's Educational Series. p. 315. ISBN 0-7641-2794-2.
- "α-cleavage (alpha-cleavage)". IUPAC Compendium of Chemical Terminology (Gold Book). IUPAC. Retrieved 2008-07-08.
- Todd, J. F. J. (1991). "Recommendations for nomenclature and symbolism for mass spectroscopy (including an appendix of terms used in vacuum technology). (Recommendations 1991)". Pure and Applied Chemistry 63 (10): 1541. doi:10.1351/pac199163101541.
- International Union of Pure and Applied Chemistry. "α-cleavage (alpha-cleavage)". Compendium of Chemical Terminology Internet edition.
- Verhoeven, J. W. (1996). "Glossary of terms used in photochemistry (IUPAC Recommendations 1996)". Pure and Applied Chemistry 68 (12): 2223. doi:10.1351/pac199668122223.