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Relevant bibliographies by topics / Iodine monochloride

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Academic literature on the topic 'Iodine monochloride'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 June 2025

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Journal articles on the topic "Iodine monochloride"

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

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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4

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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5

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 infections (Siberian ulcer and other spore infections).

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6

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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7

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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8

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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9

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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10

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 treatment was performed twice with an interval of 60 minutes. Our work established that the Monochloride (Iodine chloride) 2% has a high disinfectant activity against Escherichia coli, Staphylococcus aureus, mycobacteria and spores. On the basis of the laboratory work, this tool can be recommended for production tests at veterinary surveillance facilities.

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Dissertations / Theses on the topic "Iodine monochloride"

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Kerr, Elinor A. "Kinetic and spectroscopic studies of ion-pair states of iodine monochloride." Thesis, University of Edinburgh, 1989. http://hdl.handle.net/1842/12354.

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2

Liddy, Kyle Jacob. "Synthesis of 4-iodo-3-(2-iodoaryl) and 4-bromo-3-(2-bromoaryl) sydnones and their Reactions with Sodium Sulfite, Sodium Borohydride, and Iodine Monochloride." Wright State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=wright1501499797285277.

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3

Tiwari, Rohit. "COMPUTATIONAL AND SYNTHETIC STUDIES ON ANTIMETABOLITES FOR ANTICANCER-, ANTIVIRAL-,AND ANTIBIOTIC DRUG DISCOVERY." The Ohio State University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=osu1267819591.

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4

HUANG, YUNG-SAN, and 黃云珊. "Per-O-Acetylation of N-Acetylglucosamine and N-Acetylgalactosamine by Iodine Monochloride." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/16002181370243273086.

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碩士<br>中原大學<br>化學研究所<br>103<br>Abstact Acetylation is one of the most common organic reactions so that to develop a low cost, low toxicity and easy acetylation approach is necessary. In this study, the iodine monochloride was utilized as the catalyst for the acetylation of the N-acetylglucosamine, and N-acetylgalactosamine with acetic anhydride. The advantages of this methodology are that there would be no pretreatment on the catalyst, no solvent required, and reduce the reaction time. However, the disadvantage is the low yield for this acetylation. The resule showed that the reaction time for the D-glucose, N-acetyl-D-glucosamine, and N-acetyl-D-galactosamine is 14 min, 3h, and 1h, respectively, as the 0.8 eq of ICl was used.

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5

Lin, Ming-Feng, and 林明峰. "Reaction of iodine monobromide and iodine monochloride with molybdenum complexes derivatives of pyrazol-and pyridyl-derived nitrogen bidentate." Thesis, 1990. http://ndltd.ncl.edu.tw/handle/49770539429641679400.

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Wang, Shixin. "The electric dipole moment in the B ³Π₀₊ state of molecular iodine monochloride". Thesis, 1993. http://hdl.handle.net/2429/1532.

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The laser-induced fluorescence spectrum in ICl of the electronic system B ³Π₀₊ ← X ¹Σ₀₊ for the (2-0) vibrational band has been measured as a function of the electric field strength up to 32.5 kV/cm. From the Stark shift measurements, the dipole moment in vibrational level v' = 2 of the B ³Π₀₊ state, not previously measured experimentally, has been found to equal 1.122(25) D for I³⁵Cl and 1.116(35) D for I³⁷Cl . Intensity measurements of the (2-0) Q(0) and Q(1) of I³⁵Cl have shown that these normally forbidden lines become allowed through the mixing of rotational levels generated by the interaction of the dipole moment with the externally applied electric field. The Stark shift measurement of the magnitude of the dipole moment was confirmed and the sign of the dipole moment was shown to be the same as that in the ground X ¹Σ₀₊ state.

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7

吳欣樺. "Comparison of Atomic Selectivity during the Abstractive Reactions of Iodine Monochloride on Si(100) and Ge(100)." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/89878328778649958364.

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8

Su, Kuan-Yu, and 蘇冠宇. "Studies on the Development of A Facile and Efficient Method for Per-O-Acetylation of Carbohydrates by Iodine Monochloride." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/07777155908945624211.

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碩士<br>中原大學<br>化學研究所<br>103<br>The primary concern of this study is to research in the acetylation reactions in organic synthesis, planning to use acetic anhydride as a reagent, iodine chloride (ICl) as a catalyst for the G-1, G-3, G-5, G-7 and G-9 to react per-O-acetylation reaction of carbohydrates, this reaction has the advantage that without the pre-treatment before use catalyst, none of additional solvents, and also can achieve the same effect, effectively reducing the organic synthesis process, improved acetylation reaction efficiency. In addition, the reaction yield of the resulting product. From the experiment results that, G-1 and G-3 using 0.01 equivalents of iodine monochloride as catalyst, the reaction time is 1 minute, the yield was 100%, while the G-7 and G-9 using 0.01 equivalents of iodine monochloride as catalyst, because of its large steric hindrance, the reaction time is 180 minutes, the yield was 86 to 88%.

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Books on the topic "Iodine monochloride"

1

Gaier, James R. Stability of bromine, iodine monochloride, copper (II) chloride, and nickel (II) chloride intercalated pitch-based graphite fibers. National Aeronautics and Space Administration, 1987.

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2

Turner, Dean. Electrophilic halogenation of aromatic compounds by iodine monochloride ; Additive rearrangement of 1,1-diphenylethylene by iodine and silver bifluoride. 1987.

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Book chapters on the topic "Iodine monochloride"

1

Cornog, J., R. A. Karges, and L. A. Test. "Iodine Monochloride." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132326.ch56.

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Conference papers on the topic "Iodine monochloride"

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Hughey, Kendall D., Ashley Bradley, Heather M. Felmy, et al. "Quantitative far-infrared band strengths of iodine monochloride (ICl), a molten salt off-gas product." In Chemical, Biological, Radiological, Nuclear, and Explosives (CBRNE) Sensing XXI, edited by Jason A. Guicheteau and Chris R. Howle. SPIE, 2020. http://dx.doi.org/10.1117/12.2557555.

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