Formation of halogenated chloroxylenols through chlorination and their photochemical activity.

[1]  Xiangru Zhang,et al.  Occurrence and stability of PCMX in water environments and its removal by municipal wastewater treatment processes. , 2022, Journal of Hazardous Materials.

[2]  J. Chovelon,et al.  Aquatic photolysis of the pharmaceutical ambroxol: The role of 2,4-dibromoaniline chromophore and heavy atom effect of bromine. , 2022, Water research.

[3]  K. Kümmerer,et al.  Transformation products of sulfonamides in aquatic systems: Lessons learned from available environmental fate and behaviour data. , 2022, The Science of the total environment.

[4]  J. Chovelon,et al.  Direct and nitrite-sensitized indirect photolysis of effluent-derived phenolic contaminants under UV254 irradiation. , 2022, Environmental science. Processes & impacts.

[5]  David M. Cwiertny,et al.  Computational Approaches for the Prediction of Environmental Transformation Products: Chlorination of Steroidal Enones , 2021, Environmental science & technology.

[6]  V. Sharma,et al.  Mechanistic Investigation of Enhanced Photoreactivity of Dissolved Organic Matter after Chlorination. , 2021, Environmental science & technology.

[7]  J. Chovelon,et al.  Trace level nitrite sensitized photolysis of the antimicrobial agents parachlormetaxylenol and chlorophene in water. , 2021, Water research.

[8]  Jianhua Tan,et al.  Human exposure and health risk assessment of an increasingly used antibacterial alternative in personal care products: Chloroxylenol. , 2021, The Science of the total environment.

[9]  J. Chovelon,et al.  Aqueous photodecomposition of the emerging brominated flame retardant tetrabromobisphenol S (TBBPS). , 2020, Environmental pollution.

[10]  K. McNeill,et al.  Linking Triclosan's Structural Features to Its Environmental Fate and Photoproducts. , 2020, Environmental science & technology.

[11]  J. Rimoldi,et al.  Novel disinfection byproducts formed from the pharmaceutical gemfibrozil are bioaccumulative and elicit increased toxicity relative to the parent compound in marine polychaetes (Neanthes arenaceodentata). , 2020, Environmental science & technology.

[12]  D. Dionysiou,et al.  Formation and enhanced photodegradation of chlorinated derivatives of bisphenol A in wastewater treatment plant effluent. , 2020, Water research.

[13]  Erdeng Du,et al.  ROS reevaluation for degradation of 4-chloro-3,5-dimethylphenol (PCMX) by UV and UV/persulfate processes in the water: Kinetics, mechanism, DFT studies and toxicity evolution , 2020, Chemical Engineering Journal.

[14]  N. Ortuño,et al.  Photodecomposition properties of brominated flame retardants (BFRs). , 2020, Ecotoxicology and environmental safety.

[15]  D. Sedlak,et al.  Chlorination of Phenols Revisited: Unexpected Formation of α,β-Unsaturated C4-Dicarbonyl Ring Cleavage Products. , 2020, Environmental science & technology.

[16]  K. Kümmerer,et al.  Experimental and in silico assessment of fate and effects of the UV filter 2-phenylbenzimidazole 5-sulfonic acid and its phototransformation products in aquatic solutions. , 2019, Water research.

[17]  Lei Zhou,et al.  New insights into clopyralid degradation by sulfate radical: Pyridine ring cleavage pathways. , 2019, Water research.

[18]  G. Ying,et al.  Occurrence, fate and risk assessment of biocides in wastewater treatment plants and aquatic environments in Thailand. , 2019, The Science of the total environment.

[19]  K. Kümmerer,et al.  Studying the fate of the drug Chlorprothixene and its photo transformation products in the aquatic environment: Identification, assessment and priority setting by application of a combination of experiments and various in silico assessments. , 2019, Water research.

[20]  Yong Chen,et al.  Ultraviolet absorption redshift induced direct photodegradation of halogenated parabens under simulated sunlight. , 2018, Water research.

[21]  Hongbo Ma,et al.  Benzalkonium chloride, benzethonium chloride, and chloroxylenol - Three replacement antimicrobials are more toxic than triclosan and triclocarban in two model organisms. , 2018, Environmental pollution.

[22]  E. Capkin,et al.  Antimicrobial agents, triclosan, chloroxylenol, methylisothiazolinone and borax, used in cleaning had genotoxic and histopathologic effects on rainbow trout. , 2017, Chemosphere.

[23]  H. Cao,et al.  Effect of bromine substituent on optical properties of aryl compounds , 2017 .

[24]  U. von Gunten,et al.  Mechanistic Aspects of the Formation of Adsorbable Organic Bromine during Chlorination of Bromide-containing Synthetic Waters. , 2017, Environmental science & technology.

[25]  Yuefeng F. Xie,et al.  Effect of bromide on the transformation and genotoxicity of octyl-dimethyl-p-aminobenzoic acid during chlorination. , 2017, Journal of Hazardous Materials.

[26]  J. Criquet,et al.  Reaction of bromine and chlorine with phenolic compounds and natural organic matter extracts--Electrophilic aromatic substitution and oxidation. , 2015, Water research.

[27]  Feng Wu,et al.  Wavelength-dependent photochemistry of acetaminophen in aqueous solutions , 2014 .

[28]  B. Legube,et al.  Aqueous chlorination of carbamazepine: kinetic study and transformation product identification. , 2013, Water research.

[29]  A. Kruppa,et al.  A mechanistic study of the photodegradation of herbicide 2,4,5-trichlorophenoxyacetic acid in aqueous solution , 2013, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology.

[30]  W. Arnold,et al.  Quantification of triclosan, chlorinated triclosan derivatives, and their dioxin photoproducts in lacustrine sediment cores. , 2013, Environmental science & technology.

[31]  W. Arnold,et al.  Direct and indirect photolysis of the phytoestrogens genistein and daidzein. , 2012, Environmental science & technology.

[32]  C. Larive,et al.  Analytical and biological characterization of halogenated gemfibrozil produced through chlorination of wastewater. , 2012, Environmental science & technology.

[33]  S. Rayne,et al.  pKa values of the monohydroxylated polychlorinated biphenyls (OH-PCBs), polybrominated biphenyls (OH-PBBs), polychlorinated diphenyl ethers (OH-PCDEs), and polybrominated diphenyl ethers (OH-PBDEs) , 2010, Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering.

[34]  W. Arnold,et al.  Dioxin photoproducts of triclosan and its chlorinated derivatives in sediment cores. , 2010, Environmental science & technology.

[35]  W. Arnold,et al.  Pharmaceuticals and Personal Care Products in the Environment AQUATIC PHOTOCHEMISTRY OF CHLORINATED TRICLOSAN DERIVATIVES: POTENTIAL SOURCE OF POLYCHLORODIBENZO-P-DIOXINS , 2009 .

[36]  L. Eriksson,et al.  Photodegradation mechanism of the common non-steroid anti-inflammatory drug diclofenac and its carbazole photoproduct. , 2009, Physical chemistry chemical physics : PCCP.

[37]  S. Rayne,et al.  Mechanistic aspects regarding the direct aqueous environmental photochemistry of phenol and its simple halogenated derivatives. A review. , 2009, Environment international.

[38]  U. von Gunten,et al.  Transformation of 17alpha-ethinylestradiol during water chlorination: effects of bromide on kinetics, products, and transformation pathways. , 2009, Environmental science & technology.

[39]  S. Canonica,et al.  Phototransformation of selected pharmaceuticals during UV treatment of drinking water. , 2008, Water research.

[40]  N. Negreira,et al.  Formation of halogenated by-products of parabens in chlorinated water. , 2006, Analytica chimica acta.

[41]  W. Maccrehan,et al.  Transformation of acetaminophen by chlorination produces the toxicants 1,4-benzoquinone and N-acetyl-p-benzoquinone imine. , 2006, Environmental science & technology.

[42]  U. von Gunten,et al.  Kinetics and mechanisms of formation of bromophenols during drinking water chlorination: assessment of taste and odor development. , 2005, Water research.

[43]  B. Nicholson,et al.  Bromide levels in natural waters: its relationship to levels of both chloride and total dissolved solids and the implications for water treatment. , 2004, Chemosphere.

[44]  B. Legube,et al.  Aqueous chlorination kinetics of some endocrine disruptors. , 2004, Environmental science & technology.

[45]  S. Itoh,et al.  Contribution of brominated organic disinfection by-products to the mutagenicity of drinking water. , 2004, Water science and technology : a journal of the International Association on Water Pollution Research.

[46]  D. Sedlak,et al.  Transformation of aromatic ether- and amine-containing pharmaceuticals during chlorine disinfection. , 2004, Environmental science & technology.

[47]  S. Richardson,et al.  Tribromopyrrole, brominated acids, and other disinfection byproducts produced by disinfection of drinking water rich in bromide. , 2003, Environmental science & technology.

[48]  B. Legube,et al.  Rate constants of reactions of bromine with phenols in aqueous solution. , 2003, Water research.

[49]  Jianying Hu,et al.  Products of aqueous chlorination of bisphenol A and their estrogenic activity. , 2002, Environmental science & technology.

[50]  H. Gallard,et al.  Chlorination of phenols: kinetics and formation of chloroform. , 2002, Environmental science & technology.

[51]  C. Richard,et al.  Formation and Reactivity of 4-Oxocyclohexa-2,5-dienylidene in the Photolysis of 4-Chlorophenol in Aqueous Solution at Ambient Temperature , 1994 .

[52]  T. Ternes,et al.  Water Analysis: Emerging Contaminants and Current Issues. , 2014, Analytical chemistry.

[53]  J. Criquet,et al.  Oxidative treatment of bromide-containing waters: formation of bromine and its reactions with inorganic and organic compounds--a critical review. , 2014, Water research.

[54]  U. von Gunten,et al.  Reactions of chlorine with inorganic and organic compounds during water treatment-Kinetics and mechanisms: a critical review. , 2008, Water research.

[55]  C. Richard,et al.  Mechanisms of Direct Photolysis of Biocides Based on Halogenated Phenols and Anilines , 2005 .