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Journal articles on the topic 'Iodine monochloride'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

da Forezi, Luana. "Iodine Monochloride." Synlett 2011, no. 04 (2011): 585–86. http://dx.doi.org/10.1055/s-0030-1259532.

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2

Bhargava, Suresh, Pravin Likhar, Vijay Rao та Nedaossadat Mirzadeh. "Highly Selective Approach to α-Iodoketones from Aminoalkynols with Iodine Monochloride". Synthesis 49, № 24 (2017): 5380–86. http://dx.doi.org/10.1055/s-0036-1590897.

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A protocol has been developed to achieve selective and direct synthesis of α-iodoketones under mild condition, from the reaction of aminoalkynols with iodine monochloride. The scope of the reaction was investigated using various aminoalkynols with iodine monochloride and the corresponding α-iodoketones were obtained selectively without forming iodocyclized and/or addition products.

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3

Popov, N. I., A. V. Suvorov, S. A. Michko, et al. "EVALUATION OF THE EFFECTIVENESS OF DISINFECTING ACTION OF MONOCHLORIDE (IODINE CHLORIDE) 2% IN PRODUCTION CONDITIONS." Problems of Veterinary Sanitation, Hygiene and Ecology 1, no. 4 (2019): 400–406. http://dx.doi.org/10.36871/vet.san.hyg.ecol.201904010.

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The results of production tests of the effectiveness of the disinfectant Monochloride (Iodine chloride) 2% for disinfection of objects of veterinary supervision are presented. Test results show that Monochloride (Iodine Chloride) 2% is effective disinfectant and can be recommended for preventive and forced disinfection at the objects of veterinary surveillance while monitoring its quality for the isolation of bacteria of the Escherichia coli group and staphylococci, as well as forced disinfection in infectious bacterial diseases (including tuberculosis) and viral etiology, especially dangerous

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4

Muathen, Hussni A. "Mild and Efficient Iodination of Aromatic Compounds with Pyridine–Iodine Monochloride Complex (PyICI)." Journal of Chemical Research 23, no. 1 (1999): x—xi. http://dx.doi.org/10.1177/174751989902300102.

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5

Bentley, Cameron L., Alan M. Bond, Anthony F. Hollenkamp, Peter J. Mahon, and Jie Zhang. "Electrochemistry of Iodide, Iodine, and Iodine Monochloride in Chloride Containing Nonhaloaluminate Ionic Liquids." Analytical Chemistry 88, no. 3 (2016): 1915–21. http://dx.doi.org/10.1021/acs.analchem.5b04332.

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6

Yencha, Andrew J., M. Cristina A. Lopes, and George C. King. "Threshold photoelectron spectroscopy of iodine monochloride." Chemical Physics Letters 325, no. 5-6 (2000): 559–67. http://dx.doi.org/10.1016/s0009-2614(00)00719-3.

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7

Popov, N. I., A. V. Suvorov, S. M. Lobanov, S. A. Michko, Z. E. Alieva, and G. Sh Shcherbakova. "LABORATORY TESTS OF DISINFECTANT «MONOCHLORIDE (IODINE CHLORIDE) 2%»." Problems of Veterinary Sanitation, Hygiene and Ecology 1, no. 4 (2018): 27–33. http://dx.doi.org/10.36871/vet.san.hyg.ecol.201804004.

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The article describes the results of laboratory tests of the effectiveness of the disinfectant Monochloride (Iodine chloride) 2%. Laboratory studies were carried out on test objects and test surfaces contaminated with test cultures of microorganisms, which included museum cultures of E. coli (E. coli 1257), S. aureus 209-P, mycobacteria (pcs. B5), and spores (B. cereus pieces. 96). Disinfection of test objects was carried out by the method of irrigation at a consumption rate of 0,25...0,3 l/ m2 with disinfection of smooth surfaces and 0,5 l/m2, with disinfection of rough surfaces. The treatmen

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8

Nashashibi, Imad F., Jonathan M. Tumey, Benjamin L. Owens, and Kenneth Turnbull. "Chlorination of 3-Arylsydnones with Iodine Monochloride." Organic Preparations and Procedures International 49, no. 1 (2017): 59–63. http://dx.doi.org/10.1080/00304948.2017.1260398.

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9

Bellina, Fabio, Francesca Colzi, Luisa Mannina, Renzo Rossi, and Stephane Viel. "Reaction of Alkynes with Iodine Monochloride Revisited." Journal of Organic Chemistry 68, no. 26 (2003): 10175–77. http://dx.doi.org/10.1021/jo035372f.

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10

Ameduri, B., B. Boutevin, M. Kharroubi, G. Kostov, and P. Petrova. "Radical addition of iodine monochloride to trifluoroethylene." Journal of Fluorine Chemistry 91, no. 1 (1998): 41–48. http://dx.doi.org/10.1016/s0022-1139(98)00207-3.

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11

Gowda, B. Thimme, and J. Ishwara Bhat. "Mechanism of positive iodine reactions: Kinetics of oxidation of semicarbazide by iodamine-T, iodine monochloride and iodine." Proceedings / Indian Academy of Sciences 100, no. 4 (1988): 275–86. http://dx.doi.org/10.1007/bf02840536.

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12

Kumar, Rakesh, Leonard I. Wiebe, and Edward E. Knaus. "A mild and efficient methodology for the synthesis of 5-halogeno uracil nucleosides that occurs via a 5-halogeno-6-azido-5,6-dihydro intermediate." Canadian Journal of Chemistry 72, no. 9 (1994): 2005–10. http://dx.doi.org/10.1139/v94-256.

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A mild and efficient methodology for the synthesis of 5-halogeno (iodo, bromo, or chloro) uracil nucleosides has been developed. 5-Halo-2′-deoxyuridines 4a–c (84–95%), 5-halouridines 7a–c (45–95%), and 5-haloarabinouridines 8a–c (65–95%) were synthesized in good to excellent yields by the reaction of 2′-deoxyuridine (2), uridine (5), and arabinouridine (6), respectively, with iodine monochloride, or N-bromo (or chloro)succinimide, and sodium azide at 25–45 °C. These C-5 halogenation reactions proceed via a 5-halo-6-azido-5,6-dihydro intermediate (3), from which HN3 is eliminated, to yield the

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13

Chimni, Swapandeep, and Sarbjit Singh. "Recent Advances in Iodine Monochloride Mediated Electrophilic Cyclizations." Synthesis 47, no. 14 (2015): 1961–89. http://dx.doi.org/10.1055/s-0034-1378705.

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14

Marshall, William G., Richard H. Jones, Kevin S. Knight, et al. "Structural organization in the trimethylamine iodine monochloride complex." CrystEngComm 19, no. 35 (2017): 5194–201. http://dx.doi.org/10.1039/c7ce00869d.

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15

Awwadi, Firas F., Deeb Taher, Mohammed H. Kailani, et al. "Halogen Bonding Interactions in Halopyridine–Iodine Monochloride Complexes." Crystal Growth & Design 20, no. 2 (2019): 543–51. http://dx.doi.org/10.1021/acs.cgd.9b00408.

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16

Kharroubi, M., A. Manséri, B. Améduri, and B. Boutevin. "Radical addition of iodine monochloride to vinylidene fluoride." Journal of Fluorine Chemistry 103, no. 2 (2000): 145–53. http://dx.doi.org/10.1016/s0022-1139(99)00308-5.

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17

Rogers, Leon J., Michael N. R. Ashfold, Yutaka Matsumi, Masahiro Kawasaki, and Benjamin J. Whitaker. "The photodissociation of iodine monochloride at 235 nm." Chemical Physics Letters 258, no. 1-2 (1996): 159–63. http://dx.doi.org/10.1016/0009-2614(96)00617-3.

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18

Hedderich, Hartmut G., Peter F. Bernath, and Glenn A. McRae. "The high-resolution infrared spectrum of iodine monochloride." Journal of Molecular Spectroscopy 155, no. 2 (1992): 384–92. http://dx.doi.org/10.1016/0022-2852(92)90527-u.

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19

Hahn, Linlea, Kin‐Chung Wong, and Elmer A. Ogryzlo. "The Etching of Gallium Arsenide with Iodine Monochloride." Journal of The Electrochemical Society 140, no. 1 (1993): 226–29. http://dx.doi.org/10.1149/1.2056093.

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20

Tanner, Dennis D., Jeffrey E. Rowe, and Alan Potter. "Gas-phase atomic halogenation reactions using iodine monochloride." Journal of Organic Chemistry 51, no. 4 (1986): 457–60. http://dx.doi.org/10.1021/jo00354a008.

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21

Ghaffari, M. A., H. Ali, and J. E. Van Lier. "The oxidative cleavage of amines by iodine monochloride." Journal of Labelled Compounds and Radiopharmaceuticals 27, no. 1 (1989): 117–22. http://dx.doi.org/10.1002/jlcr.2580270116.

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22

Boden, Neville, Richard J. Bushby, Andrew N. Cammidge, and Gareth Headdock. "Iodine monochloride can act as a chlorinating agent." Tetrahedron Letters 36, no. 47 (1995): 8685–86. http://dx.doi.org/10.1016/0040-4039(95)01793-h.

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23

Jayanna, B. K., G. Nagendrappa, and Ninge Gowda. "A Facile Spectrophotometric Method for the Determination of Cobalt(II) Using Iodine Monochloride Reagent." E-Journal of Chemistry 7, no. 4 (2010): 1426–34. http://dx.doi.org/10.1155/2010/519391.

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A novel, simple, sensitive spectrophotometric method is proposed for the determination of cobalt(II). Chloromine-T with iodine in acetic acid produces iodine monochloride, which oxidizes promethazine hydrochloride and diphenylamine to absorbing cations. Those would associate later with cobalt complex to form an ion pair, [Ph+] [CoCl4]-and [Dh2+] [CoCl4]-2in acid medium. These appear to provide exceptional color stability to the systems. The results compare favorably with those of reported method. The conditions required for the determination of cobalt(II) are described and related analytical p

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24

Pomogaeva, A. V., A. S. Lisovenko, and A. Y. Timoshkin. "Stability of Molecular Complexes of Iodine and Iodine Monochloride with Nitrogen-Containing Donors." Russian Journal of General Chemistry 94, S1 (2024): S40—S46. http://dx.doi.org/10.1134/s1070363224140068.

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25

Ziegler, Karolin, Konstantin Yu Amsharov, and Martin Jansen. "Synthesis, Separation and Structure Elucidation of a Missing C60 Chloride: C2v-C60Cl8." Zeitschrift für Naturforschung B 67, no. 10 (2012): 1091–97. http://dx.doi.org/10.5560/znb.2012-0190.

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The so far missing chloro analog of the bromofullerene C2v-C60Br8 has been synthesized by reaction of C60 fullerene with iodine monochloride. The title compound has been separated by means of HPLC, and its molecular structure has been unambiguously determined by single-crystal X-ray analysis. A facile synthesis of Cs-C60Cl6 and C2v-C60Cl8 in preparative amounts is presented.

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26

Y., K. Gupta. "Some aspects of a chemical relationship. Kinetics and Analytical Chemistry in the service of each other." Journal of Indian Chemical Society Vol. 83, May 2006 (2006): 468–78. https://doi.org/10.5281/zenodo.5819365.

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Department of Chemistry. University of Rajasthan, Jaipur-302 004, India E-mail : ykgl924@yahoo.com <em>Manuscript received 5 October 2005, accepted 16 January 2006</em> Synopsis (A) Contribution of Kinetics to Analytical Chemistry (1) Trace metal-ion catalysis and its determination kinetically (2) General metal-ion catalysis and its kinetic determination (3) Volumetric methods (4) Fe<sup>II</sup> as a pre-reductor for the determination of H<sub>2</sub>0<sub> 2</sub> with Tl<sup>III</sup> (5) Nature of acid monitoring the reactivity and course of a metal-ion reaction (6) Modification of known m

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27

Day, David P., Nawaf I. Alsenani, and Abdulrahman A. Alsimaree. "Reactivity and Applications of Iodine Monochloride in Synthetic Approaches." European Journal of Organic Chemistry 2021, no. 30 (2021): 4299–307. http://dx.doi.org/10.1002/ejoc.202100554.

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28

Hof, Ferdinand, Anthony Impellizzeri, Emmanuel Picheau, Xiaoyang Che, Alain Pénicaud, and Christopher P. Ewels. "Chainlike Structure Formed in Iodine Monochloride Graphite Intercalation Compounds." Journal of Physical Chemistry C 125, no. 42 (2021): 23383–89. http://dx.doi.org/10.1021/acs.jpcc.1c06303.

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29

Srivastava, P. C., A. Hasan, R. Pratap, and D. S. Bhakuni. "An Unusual Iodine Monochloride Chlorination of an Imidazole Nucleoside." Nucleosides and Nucleotides 8, no. 7 (1989): 1281–85. http://dx.doi.org/10.1080/07328318908054332.

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30

Hatcher, J. A., J. A. Lynch, and E. T. Lane. "Thermometric Titrations of Free Fatty Acids with Iodine Monochloride." Microchemical Journal 47, no. 1-2 (1993): 127–33. http://dx.doi.org/10.1006/mchj.1993.1022.

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31

Samanta, Akash, Nupur Kataria, Kiran Dobhal, et al. "Wijs, Potassium Iodate, and AOCS Official Method to Determine the Iodine Value (IV) of Fat and Oil." Biomedical and Pharmacology Journal 16, no. 2 (2023): 1201–10. http://dx.doi.org/10.13005/bpj/2700.

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Fatty acid, present in edible oil, is a key constituent in our diet. The iodine number is a measure of the amount of unsaturated fatty acid in fat and oil. Iodine is a trace element that is required by humans for normal biological function. The iodine value (IV) of four edible oils was determined in this study: castor oil, peppermint oil, almond oil, and coconut oil. Iodine is a wonderful reagent for converting the unsaturation into the saturation of fat and oil. The purported technique offered a reliable and rapid determination of IV. The Wijs, or iodine monochloride, potassium iodate, and Am

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32

Saab, Marina, Fady Nahra, and Kristof Van Hecke. "Charge-Transfer Adducts of Chalcogenourea Derivatives of N-Heterocyclic Carbenes with Iodine Monochloride." Molbank 2022, no. 1 (2022): M1344. http://dx.doi.org/10.3390/m1344.

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In this communication, we investigate the reaction between seleno- and thiourea, derived from N-heterocyclic carbenes, with the interhalogen iodine monochloride. The formation of all three products was confirmed by NMR spectroscopy, while single-crystal X-ray analyses were able to establish a charge-transfer coordination type, which showed a linear Se/S-I-Cl arrangement, for all adducts formed. Based on a detailed crystallographic analysis, we can deduce the zwitterionic character of these compounds.

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33

Wei, Yu, Bing-Wu Wang, Shao-Wen Hu, et al. "Theoretical study of the iodination of methoxybenzene by iodine monochloride." Journal of Physical Organic Chemistry 18, no. 7 (2005): 625–31. http://dx.doi.org/10.1002/poc.911.

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34

Singh, Sarbjit, and Swapandeep Singh Chimni. "ChemInform Abstract: Recent Advances in Iodine Monochloride Mediated Electrophilic Cyclizations." ChemInform 46, no. 38 (2015): no. http://dx.doi.org/10.1002/chin.201538235.

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35

BODEN, N., R. J. BUSHBY, A. N. CAMMIDGE, and G. HEADDOCK. "ChemInform Abstract: Iodine Monochloride Can Act as a Chlorinating Agent." ChemInform 27, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199612124.

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36

Margerum, Dale W., Peter N. Dickson, Julius C. Nagy, Krishan Kumar, Conrad P. Bowers, and Kimber D. Fogelman. "Kinetics of the iodine monochloride reaction with iodide measured by the pulsed-accelerated-flow method." Inorganic Chemistry 25, no. 27 (1986): 4900–4904. http://dx.doi.org/10.1021/ic00247a025.

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37

Filimonov, V. D., E. A. Krasnokutskaya, and Yu A. Lesina. "Generation of Electrophilic Iodine from Iodine Monochloride in Neutral Media. Iodination and Protodeiodination of Carbazole." Russian Journal of Organic Chemistry 39, no. 6 (2003): 875–80. http://dx.doi.org/10.1023/b:rujo.0000003168.84924.b9.

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38

Boyle, Philip D., Wendy I. Cross, Stephen M. Godfrey, Charles A. McAuliffe, Robin G. Pritchard, and Simon Teat. "The reaction of N-methylbenzothiazole-2-selone with the interhalogens iodine monobromide and iodine monochloride." Journal of the Chemical Society, Dalton Transactions, no. 13 (1999): 2219–24. http://dx.doi.org/10.1039/a902188d.

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39

Andrews, L. J., and R. M. Keefer. "Iodine monochloride and iodine complexes of certain mono- and polyoxygenated ethers and ether aromatic donors." Journal of Organic Chemistry 52, no. 13 (1987): 2690–94. http://dx.doi.org/10.1021/jo00389a011.

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40

Gowtham, Malledevarapura D., Mysore S. Yogendra Kumar, Mahadeshwarabetta A. Sathish, and Giddappa Nagendrappa. "A Novel Spectrophotometric Determination of Some Phenothiazines Involving Iodine monochloride from Chloramine-T with Iodine." Archiv der Pharmazie 337, no. 11 (2004): 605–14. http://dx.doi.org/10.1002/ardp.200200759.

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41

Brandt, N. B., V. A. Kul’bachinskii, O. M. Nikitina, et al. "Supermetal conductivity and the Shubnikov–de Haas effect in the first-stage graphite heterointercalation compound C10CuCl2 · 0.6ICl." Soviet Journal of Low Temperature Physics 13, no. 11 (1987): 685–86. https://doi.org/10.1063/10.0031828.

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The first synthesis of a new type of first-stage graphite intercalation compound, C10CuCl2 · 0.6ICl, is reported, where layers of cupric chloride CuCl2, graphite, and iodine monochloride IC1 alternate in succession. An unexpected phenomenon is observed; The density of holes in the graphite layers and the conductivity are significantly higher (two- or threefold) than in monointercalation compounds of CuCl2, and IC1. The Shubnikov–de Haas effect exhibits two frequencies instead of the usual single frequency for first-state graphite monointercalation compounds.

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42

Tham, Yee Jun, Xu-Cheng He, Qinyi Li, et al. "Direct field evidence of autocatalytic iodine release from atmospheric aerosol." Proceedings of the National Academy of Sciences 118, no. 4 (2021): e2009951118. http://dx.doi.org/10.1073/pnas.2009951118.

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Reactive iodine plays a key role in determining the oxidation capacity, or cleansing capacity, of the atmosphere in addition to being implicated in the formation of new particles in the marine boundary layer. The postulation that heterogeneous cycling of reactive iodine on aerosols may significantly influence the lifetime of ozone in the troposphere not only remains poorly understood but also heretofore has never been observed or quantified in the field. Here, we report direct ambient observations of hypoiodous acid (HOI) and heterogeneous recycling of interhalogen product species (i.e., iodin

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43

Antonucci, Vincent, Richard Osifchin, Ray Alabaster, Simon Johnson, Lisa Wright, and Diane Fienemann. "Development of a Sensitive Indirect Chromatographic Method to Characterize Iodine Monochloride." Journal of Liquid Chromatography & Related Technologies 20, no. 20 (1997): 3401–17. http://dx.doi.org/10.1080/10826079708005840.

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44

Qu, Zan, Naiqiang Yan, Ping Liu, Jinping Jia, and Shijian Yang. "The role of iodine monochloride for the oxidation of elemental mercury." Journal of Hazardous Materials 183, no. 1-3 (2010): 132–37. http://dx.doi.org/10.1016/j.jhazmat.2010.06.126.

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45

Aghabali, Amineh, Sharon Jun, Marilyn M. Olmstead, and Alan L. Balch. "Piperazine-functionalized C60 and diiodine or iodine monochloride as components in forming supramolecular assemblies." Dalton Transactions 46, no. 11 (2017): 3710–15. http://dx.doi.org/10.1039/c7dt00026j.

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Reaction of N(CH<sub>2</sub>CH<sub>2</sub>)<sub>2</sub>NC<sub>60</sub> with iodine monochloride produced two materials: (ClIN(CH<sub>2</sub>CH<sub>2</sub>)<sub>2</sub>NICl)C<sub>60</sub>·2.3(CS<sub>2</sub>)·0.7(CH<sub>2</sub>Cl<sub>2</sub>) with two, nearly linear N–I–Cl units, or the salt, [(N(CH<sub>2</sub>CH<sub>2</sub>)<sub>2</sub>NH)C<sub>60</sub><sup>+</sup>][ICl<sub>2</sub><sup>−</sup>]·CS<sub>2</sub>.

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46

Drepaul, Ian, Veronica Fagundez, Franklin Guiterrez, Eddy Hung Lau, and Jeffrey A. Joens. "Thermochemistry of Molecular Complexes of Iodine Monochloride, Iodine Monobromide, and Bromine with Benzene and Benzene Derivatives." Journal of Organic Chemistry 61, no. 10 (1996): 3571–72. http://dx.doi.org/10.1021/jo960084n.

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47

Oss, Giulia, and Thanh Vinh Nguyen. "Iodonium-Catalyzed Carbonyl–Olefin Metathesis Reactions." Synlett 30, no. 17 (2019): 1966–70. http://dx.doi.org/10.1055/s-0039-1690297.

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The carbonyl–olefin metathesis reaction has become increasingly important in organic synthesis due to its versatility in functional group interconversion chemistry. Recent developments in the field have identified a number of transition-metal and organic Lewis acids as effective catalysts for this reaction. Herein, we report the use of simple organic compounds such as N-iodosuccinimide or iodine monochloride to catalyze the carbonyl–olefin metathesis process under mild reaction conditions. This work broadens the scope of this chemical transformation to include iodonium sources as simple and pr

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48

Brenner, Wolfgang, Jenny Malig, Christian Oelsner, Dirk M. Guldi, and Norbert Jux. "Synthesis and physico-chemical properties of porphycenes." Journal of Porphyrins and Phthalocyanines 16, no. 05n06 (2012): 651–62. http://dx.doi.org/10.1142/s1088424612500563.

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A new and improved synthesis for porphycenes is presented. In particular, treating pyrroles with iodine monochloride results in quantitative yields and easier work up. This key step was employed for the synthesis of different 2,7,12,17-substituted porphycenes (TPrPc, TPPc, TtBPPc). The synthetic part of this project is followed by a global analysis of the physico-chemical properties of three exemplary porphycenes, including absorption, emission, and electrochemistry. In-situ UV-vis/nIR spectroelectrochemistry was used to determine the spectral signatures of the radical anion and cation species

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49

Diamantopoulou, N., A. Kartakoulis, P. Glodic, Theofanis N. Kitsopoulos, and Peter C. Samartzis. "Ultraviolet photodissociation of iodine monochloride (ICl) at 235, 250, and 265 nm." Journal of Chemical Physics 134, no. 19 (2011): 194314. http://dx.doi.org/10.1063/1.3592783.

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50

Tashiro, K., M. Saito, and T. Tsuzuki. "Order-disorder and stage transitions of graphite intercalation compounds with iodine monochloride." Synthetic Metals 12, no. 1-2 (1985): 63–69. http://dx.doi.org/10.1016/0379-6779(85)90088-8.

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