Photochemical Behaviour of Carbamates Structurally Related to Herbicides in Aqueous Media: Nucleophilic Solvent Trapping versus Radical Reactions

Author:

Passananti Monica1ORCID,Cermola Flavio1,DellaGreca Marina1,Iesce Maria Rosaria1,Previtera Lucio1,Sferruzza Rosalia1,Temussi Fabio1ORCID

Affiliation:

1. UdR Napoli 4 INCA, Dipartimento di Scienze Chimiche, Università di Napoli Federico II, Complesso Universitario Monte S. Angelo, Via Cintia 21, 80126 Napoli, Italy

Abstract

Irradiation ofN-arylO-aryl carbamates has been carried out in H2O/CH3CN (1 : 1 v/v) solutions atλ>290 nm. When chlorine is on theN-aryl ring, halogen-substituted products are found. These photoproducts derive from the trapping of the intermediate radical cation by water and, even, by acetonitrile leading to phenols andN-arylacetamides (photo-Ritter products), respectively. UnsubstitutedN-aryl carbamates slowly undergo photo-Fries reaction.

Publisher

Hindawi Limited

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment,Atomic and Molecular Physics, and Optics,General Chemistry

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Ritter-Type Reaction;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024

2. Mycoremediation of environmental pollutants: a review with special emphasis on mushrooms;Environmental Sustainability;2021-07-14

3. Simultaneous biodegradation of mixture of carbamates by newly isolated Ascochyta sp. CBS 237.37;Ecotoxicology and Environmental Safety;2019-03

4. Photo-Fries Reaction and Related Processes;Arene Chemistry;2015-11-27

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