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Photocatalytic Degradation of 4-Chlorophenol. 1. The Hydroquinone Pathway

Li, Xiaojing, Cubbage, Jerry W., Tetzlaff, Troy A., Jenks, William S.·1999·The Journal of Organic Chemistry

Abstract

Complete mineralization of 4-chlorophenol in water can be achieved by photocatalytic degradation of oxygenated solutions containing suspended TiO 2 . The chemical pathways of this degradation are complex, and in this paper, that which begins with hydroquinone is examined. Hydroxylation to form 1,2,4-benzenetriol is the first step, though a very small amount of cleavage of the C1−C2 bond is observed. The first major group of acyclic compounds derives from oxidative cleavage of either the C1−C2 or C3−C4 bond of 1,2,4-benzenetriol. It is argued that this results from single electron oxidation and capture by superoxide. Many smaller compounds have also been identified, and routes to various ones of them are proposed. Nearly all of the compounds are verified by use of authentic samples.

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Metadata

Authors
Li, X., Cubbage, J. W., Tetzlaff, T. A., & Jenks, W. S.
Venue
The Journal of Organic Chemistry
Published
1999-10-16
Volume
64
Issue
23
Pages
8509-8524
ISSN
  • 0022-3263 (ISSN-L)
  • 1520-6904
OpenAlex
W1998370686
Cited by
240
References
0
FWCI
15.59
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Photocatalytic Degradation of 4-Chlorophenol. 1. The Hydroquinone Pathway. https://app.cochat.ai/papers/10.1021/jo990820y
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Li, X., Cubbage, J. W., Tetzlaff, T. A., & Jenks, W. S. (1999). Photocatalytic Degradation of 4-Chlorophenol. 1. The Hydroquinone Pathway. The Journal of Organic Chemistry. https://doi.org/10.1021/jo990820y

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.