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photorearrangement

Photoisomerization involving changes in the arrangement of the atoms within the molecular species. It may lead to unstable isomers that react further by, e.g., dehydrogenation, deprotonation, or other reactions.
Note:
Examples are photorearrangements of alkenes (other than cis-trans photoisomerization), of cyclohex-2-enones, of endoperoxides, of thioarenes, the di-π-methane rearrangement and others.
Source:
PAC, 2007, 79, 293 (Glossary of terms used in photochemistry, 3rd edition (IUPAC Recommendations 2006)) on page 398
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Cite as:
IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. doi:10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: doi:10.1351/goldbook.PT07460.
Original PDF version: http://www.iupac.org/goldbook/PT07460.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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