Photocatalytic degradation of 4-chlorophenol. 1. The hydroquinone pathway

Citation
Xj. Li et al., Photocatalytic degradation of 4-chlorophenol. 1. The hydroquinone pathway, J ORG CHEM, 64(23), 1999, pp. 8509-8524
Citations number
107
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
00223263 → ACNP
Volume
64
Issue
23
Year of publication
1999
Pages
8509 - 8524
Database
ISI
SICI code
0022-3263(19991112)64:23<8509:PDO41T>2.0.ZU;2-M
Abstract
Complete mineralization of 4-chlorophenol in water can be achieved by photo catalytic degradation of oxygenated solutions containing suspended TiO2. Th e chemical pathways of this degradation are complex, and in this paper, tha t which begins with hydroquinone is examined. Hydroxylation to form 1,2,4-b enzenetriol is the first step, though a very small amount of cleavage of th e C1-C2 bond is observed. The first major group of acyclic compounds derive s from oxidative cleavage of either the C1-C2 or C3-C4 bond of 1,2,4-benzen etriol. It is argued that this results from single electron oxidation and c apture by superoxide. Many smaller compounds have also been identified, and routes to various ones of them are proposed. Nearly all of the compounds a re verified by use of authentic samples.