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Journal articles on the topic 'Halogenated organic compounds'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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1

Yagi, Osami. "Biodegradation of halogenated organic compounds." Japan journal of water pollution research 8, no. 5 (1985): 289–95. http://dx.doi.org/10.2965/jswe1978.8.289.

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2

Chaudhry, G. R., and S. Chapalamadugu. "Biodegradation of halogenated organic compounds." Microbiological Reviews 55, no. 1 (1991): 59–79. http://dx.doi.org/10.1128/mmbr.55.1.59-79.1991.

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3

Chaudhry, G. R., and S. Chapalamadugu. "Biodegradation of halogenated organic compounds." Microbiological Reviews 55, no. 1 (1991): 59–79. http://dx.doi.org/10.1128/mr.55.1.59-79.1991.

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4

Enell, M., and L. Wennberg. "Distribution of Halogenated Organic Compounds (AOX) – Swedish Transport to Surrounding Sea Areas and Mass Balance Studies in Five Drainage Systems." Water Science and Technology 24, no. 3-4 (1991): 385–95. http://dx.doi.org/10.2166/wst.1991.0494.

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In the discussion of environmental pollution problems halogenated organic compounds often play a dominant role because of their properties e.g. persistence and bioaccumulation in organisms. A research project on “Long distance distribution of halogenated organic compounds” was started in 1987 at the Swedish Environmental Research Institute (IVL). The first part of the project focused on the transport of halogenated organic compounds, measured as AOX (adsorbable organic halogens), in Swedish rivers to surrounding sea areas. This work started in October 1987 and was finished in September 1988. W

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5

Windawi, H., and M. Wyatt. "Catalytic Destruction of Halogenated Volatile Organic Compounds." Platinum Metals Review 37, no. 4 (1993): 186–93. http://dx.doi.org/10.1595/003214093x374186193.

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Halogenated volatile organic compounds are associated with a broad range of industrial processes, but when discharged into the atmosphere they constitute a major source of air pollution. Recognition of the potentially damaging effects that these emissions can have on the environment is leading to increasing demands for their control. Catalytic combustion appears to offer advantages over thermal destruction, resulting from lower incineration temperatures and higher destructive efficiencies. While platinum metals catalyst systems are known to be the most effective for the catalytic destruction o

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6

Nielsen, Birthe V., Supattra Maneein, Md Mahmud Al Farid, and John J. Milledge. "The Effects of Halogenated Compounds on the Anaerobic Digestion of Macroalgae." Fermentation 6, no. 3 (2020): 85. http://dx.doi.org/10.3390/fermentation6030085.

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The urgent need to replace fossil fuels has seen macroalgae advancing as a potential feedstock for anaerobic digestion. The natural methane productivity (dry weight per hectare) of seaweeds is greater than in many terrestrial plant systems. As part of their defence systems, seaweeds, unlike terrestrial plants, produce a range of halogenated secondary metabolites, especially chlorinated and brominated compounds. Some orders of brown seaweeds also accumulate iodine, up to 1.2% of their dry weight. Fluorine remains rather unusual within the chemical structure. Halogenated hydrocarbons have modera

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7

Neilson, A. H. "The biodegradation of halogenated organic compounds." Journal of Applied Bacteriology 69, no. 4 (1990): 445–70. http://dx.doi.org/10.1111/j.1365-2672.1990.tb01536.x.

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8

Gouverneur, Véronique, Sophie Boldon, Ida Stenhagen, Jane Moore, and Sajinder Luthra. "Supported Synthesis of Halogenated Organic Compounds." Synthesis 2011, no. 24 (2011): 3929–53. http://dx.doi.org/10.1055/s-0031-1289590.

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9

Horvath, Ari L. "Boiling points of halogenated organic compounds." Chemosphere 44, no. 4 (2001): 897–905. http://dx.doi.org/10.1016/s0045-6535(00)00276-9.

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10

Li, Chao, and Dayong Shi. "Structural and Bioactive Studies of Halogenated Constituents from Sponges." Current Medicinal Chemistry 27, no. 14 (2020): 2335–60. http://dx.doi.org/10.2174/0929867325666181112092159.

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: Marine organisms are abundant sources of bioactive natural products. Among metabolites produced by sponges and their associated microbial communities, halogenated natural compounds accounted for an important part due to their potent biological activities. The present review updates and compiles a total of 258 halogenated organic compounds isolated in the past three decades, especially brominated derivatives derived from 31 genera of marine sponges. These compounds can be classified as the following classes: brominated polyunsaturated lipids, nitrogen compounds, brominated tyrosine derivative

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11

Zakary, sefatullah, Habeebat Oyewusi, and Fahrul Huyop. "Dehalogenases for pollutant degradation in brief: A mini review." Journal of Tropical Life Science 11, no. 1 (2021): 17–24. http://dx.doi.org/10.11594/jtls.11.01.03.

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Dehalogenases are microbial enzyme catalysed the cleavage of carbon-halogen bond of halogenated organic compounds. It has potential use in the area of biotechnology such as bioremediation and chemical industry. Halogenated organic compounds can be found in a considerable amount in the environment due to utilization in agriculture and industry, such as pesticides and herbicides. The presence of halogenated compound in the environment have been implicated on the health and natural ecosystem. Microbial dehalogenation is a significant method to tackle this problem. This review intends to briefly d

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12

Michael, J. V., and S. S. Kumaran. "Thermal Decomposition Studies of Halogenated Organic Compounds." Combustion Science and Technology 134, no. 1-6 (1998): 31–44. http://dx.doi.org/10.1080/00102209808924124.

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13

Teo, Khay Chuan, Yanrong Xu, and Chun Yang. "Sonochemical degradation for toxic halogenated organic compounds." Ultrasonics Sonochemistry 8, no. 3 (2001): 241–46. http://dx.doi.org/10.1016/s1350-4177(01)00083-9.

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14

McGrath, Michael. "Catalytic destruction of halogenated volatile organic compounds." Applied Catalysis B: Environmental 3, no. 2-3 (1994): N12. http://dx.doi.org/10.1016/0926-3373(94)80002-2.

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15

SLAYDEN, S. W., and J. F. LIEBMAN. "ChemInform Abstract: Thermochemistry of Halogenated Organic Compounds." ChemInform 28, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199708298.

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16

Włodarczyk-Makuła, Maria, and Ewa Wiśniowska. "Halogenated Organic Compounds in Water and in Wastewater." Civil and Environmental Engineering Reports 29, no. 4 (2019): 236–47. http://dx.doi.org/10.2478/ceer-2019-0057.

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Abstract Currently, organic halogen compounds (halogen derivatives) are often identified in water. The paper presents the problem of the presence of these newly formed compounds during water treatment processes and their occurrence in sewage. The general indicator determining the content of these compounds in aqueous solutions is the concentration of halogen derivatives of organic compounds adsorbed on activated carbon AOX, which is converted to the concentration of chlorides. The groups of derivatives of halogenated organic compounds containing chlorine and/or bromine in a molecule were chara

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17

Kayser, Margaret M., Jun Zhu, and Donald L. Hooper. "Stabilized haloylides: synthesis and reactivity." Canadian Journal of Chemistry 75, no. 10 (1997): 1315–21. http://dx.doi.org/10.1139/v97-157.

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This paper describes simple and successful methods for the preparation of stabilized halogenated phosphoylides and discusses their stability, reactivity, and utility in organic synthesis. Preparations of several halogenated compounds including pharmaceutically interesting enol lactones are reported. Keywords: halogenated stabilized ylides, preparation, structure, stability, reactivity, applications; vinylic halides, halo enol lactones.

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18

Hodin, Fredrik, Hans Borén, Anders Grimvall, and Susanne Karlsson. "Formation of Chlorophenols and Related Compounds in Natural and Technical Chlorination Processes." Water Science and Technology 24, no. 3-4 (1991): 403–10. http://dx.doi.org/10.2166/wst.1991.0496.

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Surface water was halogenated by the addition of: (i) chloroperoxidase, hydrogen peroxide and chloride; (ii) hydrogen peroxide and chloride or bromide; (iii) hypochlorite. Analysis of adsorbable organic halogen (AOX), halogenated phenols and purgeable organic compounds showed that reactions (i) and (ii) produced almost the same halogenated compounds. It was also shown that active chlorine occurred as an intermedi-ate in reaction (i). Reaction (ii) implied a marked halogenation only after the addition of bromide, and this reaction was enhanced by a low pH. Existing evidence that 2,4,6-trichloro

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19

Schulz, Stefanie, and Hermann H. Hahn. "Generation of halogenated organic compounds in municipal waste water." Water Science and Technology 37, no. 1 (1998): 303–9. http://dx.doi.org/10.2166/wst.1998.0071.

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Cleaning agents and disinfectants from housekeeping, hospitals and canteen kitchens are important sources of adsorbable halogenated organic compounds (AOX) in municipal waste water. They often contain inorganic compounds which are able to release activated chlorine. Together with organic waste water compounds the activated chlorine can generate halogenated organic compounds. Within the scope of this research project the generation of AOX through these active agents is compared. The effects of concentration, pH, time, temperature, presence of other oxidizing or reducing agents and synergetic ef

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20

D'AQUINO, MIGUEL, PILAR SANTINI, and HUMBERTO MUZIO. "Action of Halogenated Compounds on Aspergillus Conidiospores." Journal of Food Protection 49, no. 7 (1986): 537–40. http://dx.doi.org/10.4315/0362-028x-49.7.537.

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The fungicidal activity of two halogenated compounds against conidiospores of four Aspergillus strains (A. flavus and A. sydowi isolated from a poultry farm, A. parasiticus NRRL 2999 and A. niger 29-CCM-A 41) was studied. Accordingly, the sodium salt of a synthetic organic compound derived from trichloroisocyanuric acid and an organic complex of iodine (iodophor) were used at 20°C at their recommended dilution (0.1%). More than 99.9% of the exposed spore population of all strains was inactivated within 30 min of contact with either product. During the first minute of contact, the iodophor solu

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21

Miclea, Manuela, Kerstin Kunze, Joachim Franzke, and Kay Niemax. "Microplasma jet mass spectrometry of halogenated organic compounds." Journal of Analytical Atomic Spectrometry 19, no. 8 (2004): 990. http://dx.doi.org/10.1039/b401319k.

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22

Hung, Hui‐Ming, A. J. Colussi, and M. R. Hoffmann. "Kinetics of halogenated organic compounds degradation by ultrasound." Journal of the Acoustical Society of America 105, no. 2 (1999): 1382. http://dx.doi.org/10.1121/1.426535.

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23

Laturnus, Frank, Christian Wiencke, and Heinz Klöser. "Antarctic macroalgae — Sources of volatile halogenated organic compounds." Marine Environmental Research 41, no. 2 (1996): 169–81. http://dx.doi.org/10.1016/0141-1136(95)00017-8.

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24

Boldon, Sophie, Ida S. R. Stenhagen, Jane E. Moore, Sajinder K. Luthra, and Veronique Gouverneur. "ChemInform Abstract: Supported Synthesis of Halogenated Organic Compounds." ChemInform 43, no. 10 (2012): no. http://dx.doi.org/10.1002/chin.201210250.

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25

Holzinger, R., A. Kasper-Giebl, M. Staudinger, G. Schauer, and T. Röckmann. "Analysis of the chemical composition of organic aerosol at the Mt. Sonnblick observatory using a novel high mass resolution thermal-desorption proton-transfer-reaction mass-spectrometer (hr-TD-PTR-MS)." Atmospheric Chemistry and Physics 10, no. 20 (2010): 10111–28. http://dx.doi.org/10.5194/acp-10-10111-2010.

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Abstract. For the first time a high mass resolution thermal desorption proton transfer reaction mass spectrometer (hr-TD-PTR-MS) was deployed in the field to analyze the composition of the organic fraction of aerosols. We report on measurements from the remote Mt. Sonnblick observatory in the Austrian alps (3108 m a.s.l.) during a 7 week period in summer 2009. A total of 638 mass peaks in the range 18–392 Da were detected and quantified in aerosols. An empirical formula was tentatively attributed to 464 of these compounds by custom-made data analysis routines which consider compounds containin

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26

Holzinger, R., A. Kasper-Giebl, M. Staudinger, G. Schauer, and T. Röckmann. "Analysis of the chemical composition of organic aerosol at the Mt. Sonnblick observatory using a novel high mass resolution thermal-desorption proton-transfer-reaction mass-spectrometer (hr-TD-PTR-MS)." Atmospheric Chemistry and Physics Discussions 10, no. 6 (2010): 13969–4011. http://dx.doi.org/10.5194/acpd-10-13969-2010.

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Abstract. For the first time a high mass resolution thermal desorption proton transfer reaction mass spectrometer (hr-TD-PTR-MS) was deployed in the field to analyze the composition of the organic fraction of aerosols. We report on measurements from the remote Mt. Sonnblick observatory in the Austrian alps (3108 m a.s.l.) during a 7 week period in summer 2009. A total of 638 mass peaks in the range 18–392 Da were detected and quantified in aerosols. An empirical formula was tentatively attributed to 464 of these compounds by custom-made data analysis routines which consider compounds containin

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27

Schlesinger, Danielle R., and Satish C. B. Myneni. "Impact of bromide exposure on natural organochlorine loss from coastal wetland soils in the Winyah Bay, South Carolina." Environmental Science: Processes & Impacts 22, no. 3 (2020): 642–52. http://dx.doi.org/10.1039/c9em00604d.

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28

Youssef-Saliba, Sparta, and Yannick Vallée. "Organo-Halogens and their Possible Involvement in Prebiotic Chemistry." Current Organic Chemistry 24, no. 7 (2020): 774–84. http://dx.doi.org/10.2174/1385272824999200420074204.

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: In this review, we examined the possibility that some halogenated organic derivatives were used in the primitive ocean at the beginning of life on Earth. Firstly, we described the existence of extraterrestrial halogenated molecules, then we studied their nonbiological syntheses on the present Earth, especially in volcanic environments. In order to demonstrate the diversity of today’s halogenated biomolecules, representative examples are given and the biosynthesis of some of them is summarized. Finally, we proposed two aspects of the chemistry of halogenated compounds that may have been usefu

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29

Tratnyek, Paul G., Elizabeth Edwards, Lucy Carpenter, and Sarah Blossom. "Environmental occurrence, fate, effects, and remediation of halogenated (semi)volatile organic compounds." Environmental Science: Processes & Impacts 22, no. 3 (2020): 465–71. http://dx.doi.org/10.1039/d0em90008g.

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Guest editors Elizabeth Edwards, Lucy Carpenter, Sarah Blossom and Paul Tratnyek introduce the Halogenated (semi)volatile organic compounds themed issue of Environmental Science: Processes & Impacts.

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30

Kos, Gregor, Visahini Kanthasami, Nafissa Adechina, and Parisa A. Ariya. "Volatile organic compounds in Arctic snow: concentrations and implications for atmospheric processes." Environ. Sci.: Processes Impacts 16, no. 11 (2014): 2592–603. http://dx.doi.org/10.1039/c4em00410h.

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31

Weidlich, Tomáš. "The Influence of Copper on Halogenation/Dehalogenation Reactions of Aromatic Compounds and Its Role in the Destruction of Polyhalogenated Aromatic Contaminants." Catalysts 11, no. 3 (2021): 378. http://dx.doi.org/10.3390/catal11030378.

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The effect of copper and its compounds on halogenation and dehalogenation of aromatic compounds will be discussed in the proposed article. Cu oxidized to appropriate halides is an effective halogenation catalyst not only for the synthesis of halogenated benzenes or their derivatives as desired organic fine chemicals, but is also an effective catalyst for the undesirable formation of thermodynamically stable and very toxic polychlorinated and polybrominated aromatic compounds such as polychlorinated biphenyls, dibenzo-p-dioxins and dibenzofurans accompanied incineration of waste contaminated wi

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32

Jelsch, Christian, Sarra Soudani, and Cherif Ben Nasr. "Likelihood of atom–atom contacts in crystal structures of halogenated organic compounds." IUCrJ 2, no. 3 (2015): 327–40. http://dx.doi.org/10.1107/s2052252515003255.

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The likelihood of occurrence of intermolecular contacts in crystals of halogenated organic compounds has been analysed statistically using tools based on the Hirshfeld surface. Several families of small halogenated molecules (containing organic F, Cl, Br or I atoms) were analysed, based on chemical composition and aromatic or aliphatic character. The behaviour of crystal contacts was also probed for molecules containing O or N. So-called halogen bonding (a halogen making short interactions with O or N, or a π interaction with C) is generally disfavoured, except when H is scarce on the molecula

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33

HIROSE, YOSHIFUMI, RYUJI MATSUMOTO, SAYURI YAMADA, TOMIO NOZAKA, MASAZO ISHINO, and AKIO TANAKA. "The Determination of Volatile Halogenated Organic Compounds in Drugs." Eisei kagaku 40, no. 3 (1994): 298–301. http://dx.doi.org/10.1248/jhs1956.40.298.

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34

Aalto, Mika M. "Correlation of liquid densities of some halogenated organic compounds." Fluid Phase Equilibria 141, no. 1-2 (1997): 1–11. http://dx.doi.org/10.1016/s0378-3812(97)00192-1.

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35

Bachas-Daunert, Philip G., Zachariah P. Sellers, and Yinan Wei. "Detection of halogenated organic compounds using immobilized thermophilic dehalogenase." Analytical and Bioanalytical Chemistry 395, no. 4 (2009): 1173–78. http://dx.doi.org/10.1007/s00216-009-3057-5.

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36

Schauffler, S. M., L. E. Heidt, W. H. Pollock, et al. "Measurements of halogenated organic compounds near the tropical tropopause." Geophysical Research Letters 20, no. 22 (1993): 2567–70. http://dx.doi.org/10.1029/93gl02840.

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37

Bettoli, M. G., M. Ravanelli, L. Tositti, et al. "Radiation induced decomposition of halogenated organic compounds in water." Radiation Physics and Chemistry 52, no. 1-6 (1998): 327–31. http://dx.doi.org/10.1016/s0969-806x(98)00027-9.

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38

Von Borczyskowski, C. "Optically detected nuclear spin alignment in halogenated organic compounds." Chemical Physics 105, no. 1-2 (1986): 187–98. http://dx.doi.org/10.1016/0301-0104(86)80068-4.

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39

Bouwer, Edward J. "Secondary utilization of trace halogenated organic compounds in biofilms." Environmental Progress 4, no. 1 (1985): 43–45. http://dx.doi.org/10.1002/ep.670040113.

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40

Wang, Cong, Huanyun Lu, Jianzhou Lan, KH Zaman, and Shugeng Cao. "A Review: Halogenated Compounds from Marine Fungi." Molecules 26, no. 2 (2021): 458. http://dx.doi.org/10.3390/molecules26020458.

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Marine fungi produce many halogenated metabolites with a variety of structures, from acyclic entities with a simple linear chain to multifaceted polycyclic molecules. Over the past few decades, their pharmaceutical and medical application have been explored and still the door is kept open due to the need of new drugs from relatively underexplored sources. Biological properties of halogenated compounds such as anticancer, antiviral, antibacterial, anti-inflammatory, antifungal, antifouling, and insecticidal activity have been investigated. This review describes the chemical structures and biolo

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41

Reimann, Stefan, Martin K. Vollmer, Matthias Hill, et al. "Long-term Observations of Atmospheric Halogenated Organic Trace Gases." CHIMIA International Journal for Chemistry 74, no. 3 (2020): 136–41. http://dx.doi.org/10.2533/chimia.2020.136.

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CFCs (chlorofluorocarbons) and other strong ozone-depleting halogenated organic trace gases were used in numerous industrial, household and agriculture applications. First atmospheric measurements of CFCs were performed in the 1970s, well ahead of the detection of the ozone hole in the 1980s. The continuous observation of these ozone-depleting substances (ODSs) is crucial for monitoring their global ban within the Montreal Protocol. In addition, also HFCs (fluorinated hydrocarbons) are measured, which were introduced as substitutes of ODSs and are potent greenhouse gases. Since 2000, Empa cont

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42

Moqadam, Samira, and Mehdi Salami-Kalajahi. "Halogenated sunflower oil as a precursor for synthesis of polysulfide polymer." e-Polymers 16, no. 1 (2016): 33–39. http://dx.doi.org/10.1515/epoly-2015-0152.

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AbstractPolysulfide polymers usually are prepared by the reaction of different dihalide compounds with disodium polysulfides. In this field, dihalides are expensive and produced from halogenation of organic compounds by different methods with harsh conditions. To overcome this problem, in this work, sunflower oil as polyunsaturated oil was used as precursor to produce polyhalide compound. In this field, double bonds of oil were applied as functional groups to halogenate the sunflower via benzoyl peroxide-catalyzed reaction with hydrochloric acid. Also, Na2S3 was synthesized via the reaction be

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43

Shi, Yijun, Xuejing Liu, Ying Han, Peng Yan, Fusheng Bie, and Han Cao. "Synthesis of bi-halogenated spiropolycyclic cage compounds." Tetrahedron Letters 61, no. 15 (2020): 151752. http://dx.doi.org/10.1016/j.tetlet.2020.151752.

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44

Defibaugh, Dana R., and Michael R. Moldover. "Compressed and Saturated Liquid Densities for 18 Halogenated Organic Compounds†." Journal of Chemical & Engineering Data 42, no. 1 (1997): 160–68. http://dx.doi.org/10.1021/je960266e.

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45

Carnimeo, Ivan, Cristina Puzzarini, Nicola Tasinato, et al. "Anharmonic theoretical simulations of infrared spectra of halogenated organic compounds." Journal of Chemical Physics 139, no. 7 (2013): 074310. http://dx.doi.org/10.1063/1.4817401.

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46

Luek, Jenna L., Mourad Harir, Philippe Schmitt-Kopplin, Paula J. Mouser, and Michael Gonsior. "Temporal dynamics of halogenated organic compounds in Marcellus Shale flowback." Water Research 136 (June 2018): 200–206. http://dx.doi.org/10.1016/j.watres.2018.02.055.

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47

Braune, Birgit M., and Mary Simon. "Trace elements and halogenated organic compounds in Canadian Arctic seabirds." Marine Pollution Bulletin 48, no. 9-10 (2004): 986–92. http://dx.doi.org/10.1016/j.marpolbul.2004.02.018.

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48

URANO, K., and T. TAKEMASA. "Formation equation of halogenated organic compounds when water is chlorinated." Water Research 20, no. 12 (1986): 1555–60. http://dx.doi.org/10.1016/0043-1354(86)90120-x.

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49

Murray, H. E., and J. N. Beck. "Halogenated organic compounds found in shrimp from the Calcasieu Setuary." Chemosphere 19, no. 8-9 (1989): 1367–74. http://dx.doi.org/10.1016/0045-6535(89)90084-2.

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50

Demissie, Taye B., Michal Repisky, Stanislav Komorovsky, et al. "Four-component relativistic chemical shift calculations of halogenated organic compounds." Journal of Physical Organic Chemistry 26, no. 8 (2013): 679–87. http://dx.doi.org/10.1002/poc.3157.

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