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Solvent assisted photochemical formation of a new keto[3,3]paracyclophaneopen access

Authors
Shin, Ho SukMoon, Da YoonAn, SejinPark, Bong Ser
Issue Date
Jun-2022
Publisher
Royal Society of Chemistry
Keywords
Benzoic Acid; Phenols; Electron Transfer; Paracyclophane; Phenol Moiety; Photochemicals; Protic Solvents; [carbonyl; Photolysis
Citation
Organic & Biomolecular Chemistry, v.20, no.21, pp 4303 - 4308
Pages
6
Indexed
SCIE
SCOPUS
Journal Title
Organic & Biomolecular Chemistry
Volume
20
Number
21
Start Page
4303
End Page
4308
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/2971
DOI
10.1039/d2ob00660j
ISSN
1477-0520
1477-0539
Abstract
Photolysis of a phenacyl benzoate tethered with a phenol leads to a very efficient release of benzoic acid, which is suggested to occur by electron transfer and/or proton transfer from the remote phenol moiety to the triplet excited carbonyl. Photolysis of the compound in protic solvents forms a new keto[3,3]paracyclophane.
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