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Journal articles on the topic 'Hydriolic acid'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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1

Liu, Zhengchun, Alessandro Granata, Xinhua Shen, and Arthur S. Perlin. "Reactions of hydriodic acid with aldonolactones and n-alkanolactones. Interconversions between lactones and iodocarboxylic acids." Canadian Journal of Chemistry 70, no. 7 (July 1, 1992): 2081–88. http://dx.doi.org/10.1139/v92-264.

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Aldonolactones containing from four to eight carbon atoms, and lactones of the related monohydroxy-n-alkanoic acids, were subjected to reaction with 57% hydriodic acid at 125 °C. As in the classical studies of Kiliani, the reduction of D-glycero-D-ido-heptono-1,4-lactone yielded mainly γ-heptanolactone. Analogously, the corresponding γ-alkanolactones were obtained as major products from the 1,4-lactones of the D-xylono-, D-allono-, and D-erythro-L-talo-octono configuration. Monoiodo-n-alkanoic acids were also formed in admixture with the lactones in all of these reactions. D-Erythrono-1,4-lactone was unique among the aldonolactones in that it led only to an acid, i.e., 3-iodo-n-butanoic acid. The latter was also the product of the non-reductive reaction of hydriodic acid with β-butyrolactone whereas, by contrast, γ-butyrolactone afforded 4-iodobutanoic acid. Among compounds in the five to eight carbon series, it was found that under conditions close to equilibrium the ratio of lactone to iodoacid decreased progressively with the length of the carbon chain; e.g., in the 4 h reactions of γ-valero-, γ-capro-, γ-heptano-, and γ-octanolactone, the ratios were 2.4, 1.2, 0.2, and 0.1, respectively. An accompanying characteristic of these reactions is a progression in the number of isomeric iodoacids formed. Whereas γ-valerolactone was accompanied by 4-iodopentanoic acid, there were two isomers (4- and 5-) of iodohexanoic acid, three monoiodo- (including 6-iodo-) heptanoic acids, and four (including 7-iodo-) octanoic acids. In all instances, the isomer substituted at the penultimate carbon was major. An interplay of several individual reactions, including ring-opening displacements, eliminations–additions, and rearrangements, as well as a probable influence of entropy changes on the lactone-acid equilibria, appear to account largely for these observations.

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2

Oksuz, Melik, and H. Yildirim Erbil. "Wet-spun graphene filaments: effect of temperature of coagulation bath and type of reducing agents on mechanical & electrical properties." RSC Advances 8, no. 31 (2018): 17443–52. http://dx.doi.org/10.1039/c8ra02325e.

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3

Greenberg, Fred H. "Reaction of Dibenzoylethylene with Hydriodic Acid." Journal of Chemical Education 77, no. 4 (April 2000): 505. http://dx.doi.org/10.1021/ed077p505.

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4

Ardo, Shane, Sang Hee Park, Emily L. Warren, and Nathan S. Lewis. "Unassisted solar-driven photoelectrosynthetic HI splitting using membrane-embedded Si microwire arrays." Energy & Environmental Science 8, no. 5 (2015): 1484–92. http://dx.doi.org/10.1039/c5ee00227c.

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5

HODOTSUKA, Masatoshi, Xiaoyong YANG, and Hiroyuki OKUDA. "ICONE15-10169 STUDY ON VAPOR-LIQUID EQUILIBRIUM OF HYDRIODIC ACID FOR THERMOCHEMICAL HYDROGEN PRODUCTION IS PROCESS." Proceedings of the International Conference on Nuclear Engineering (ICONE) 2007.15 (2007): _ICONE1510. http://dx.doi.org/10.1299/jsmeicone.2007.15._icone1510_71.

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6

Dobmeier, Michael, Josef M. Herrmann, Dieter Lenoir, and Burkhard König. "Reduction of benzylic alcohols and α-hydroxycarbonyl compounds by hydriodic acid in a biphasic reaction medium." Beilstein Journal of Organic Chemistry 8 (March 2, 2012): 330–36. http://dx.doi.org/10.3762/bjoc.8.36.

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The synthetic protocol for the reduction of alcohols to hydrocarbons by using hydriodic acid, first described by Kiliani more than 140 years ago, was improved to be more applicable to organic synthesis. Instead of a strongly acidic, aqueous solution, a biphasic toluene–water reaction medium was used, which allowed the conversion of primary, secondary and tertiary benzylic alcohols, in good yields and short reaction times, into the corresponding hydrocarbons. Red phosphorous was used as the stoichiometric reducing agent. Keto, ester, amide or ether groups are tolerated, and catalytic amounts of hydriodic acid (0.2 equiv) in the presence of 0.6 equiv phosphorous are sufficient to achieve conversion.

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7

Zhu, Weiguang, Guoqing Xin, Yiping Wang, Xin Min, Tiankai Yao, Wenqian Xu, Minghao Fang, Sufei Shi, Jian Shi, and Jie Lian. "Tunable optical properties and stability of lead free all inorganic perovskites (Cs2SnIxCl6−x)." Journal of Materials Chemistry A 6, no. 6 (2018): 2577–84. http://dx.doi.org/10.1039/c7ta10040j.

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Cs₂SnI_xCl_6−x perovskites were synthesized using hydriodic acid as an iodine source, and the color scheme displays a tunable band gap with varying I⁻/Cl⁻ ratios.

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8

Onuki, Kaoru, Gab-Jin Hwang, and Saburo Shimizu. "Electrodialysis of hydriodic acid in the presence of iodine." Journal of Membrane Science 175, no. 2 (August 2000): 171–79. http://dx.doi.org/10.1016/s0376-7388(00)00415-4.

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9

Lionelli, G. T., E. J. Pickus, J. G. Bray, W. T. Lawrence, and R. A. Korentager. "Myoglobinuria and Hypocalcemia After a Superficial Hydriodic Acid Burn." Journal of Burn Care & Rehabilitation 22, no. 5 (September 2001): 341–45. http://dx.doi.org/10.1097/00004630-200109000-00009.

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10

Miethchen, Ralf, Andreas Schmidt, Katharina Neitzel, Manfred Michalik, Thomas Pundt, and Wolfgang Ruth. "Concentrated hydriodic acid in simultaneous deprotections of multifunctional inositols." Carbohydrate Research 340, no. 4 (March 2005): 741–48. http://dx.doi.org/10.1016/j.carres.2004.11.031.

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11

Williamson, Peter R., Kazumasa Wakamatsu, and Shosuke Ito. "Melanin Biosynthesis in Cryptococcus neoformans." Journal of Bacteriology 180, no. 6 (March 15, 1998): 1570–72. http://dx.doi.org/10.1128/jb.180.6.1570-1572.1998.

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ABSTRACT Pigment production by Cryptococcus neoformans is virulence associated. Dopamine- and 3,4-dihydroxyphenylalanine–melanin products were identified after acidic permanganate oxidation, alkaline hydrogen peroxide oxidation, or hydrolysis with hydriodic acid. These data provide direct chemical evidence for the formation of eumelanin polymers by catecholamine oxidation by laccase alone followed by oxidative coupling of dihydroxyindole.

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12

Granata, Alessandro, and Arthur S. Perlin. "Formation of isomeric monohalo-n-alkanoic acids in the reactions of γ- and δ-n-alkanolactones with hydrogen halides." Canadian Journal of Chemistry 71, no. 6 (June 1, 1993): 864–71. http://dx.doi.org/10.1139/v93-115.

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In 57% hydriodic acid or 48% hydrobromic acid, under reflux, n-alkanoic γ- or δ-lactones of from 5 to 18 carbon atoms undergo facile ring opening to monohalo-n-alkanoic acids. With both reagents the ratio of acid to lactone at equilibrium varies widely, ranging from about 1:3 for γ-valerolactone (C5) to 3:1 or more for γ-octanolactone and the larger members of the series. Extensive scrambling of the halogen atoms accompanies the formation of the haloacids, whereby mixtures of monohalo isomers substituted at all positions from C-4 to the penultimate carbon are found. In an 18 h reaction with HBr, for example, γ-caprolactone was converted into a 1:3 mixture of 4- and 5-bromohexanoic acids, and γ-decanolactone into a 1:1.4:1.4:1.4:2.3:2.3 mixture of 4-, 5-, 6-, 7-, 8-, and 9-bromodecanoic acids. By contrast, the γ-lactones containing 14 or 16 carbon atoms gave only 10:1 mixtures of the 4- and 5-bromoacids, and at the level of 18 carbon atoms rearrangement was no longer evident; i.e., γ-octadecanolactone afforded only 4-bromooctadecanoic acid. Similar isomer distributions were obtained for the iodoacid homologs. Hydrochloric acid (37%) was far less effective in opening the lactone rings, and also in inducing rearrangement of the chlorine atoms introduced. Differences in entropy and in solvation appear to be the main factors contributing to the variations observed among isomeric lactones.

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13

Li, Teng, Shengqin Liu, Bing Wang, Jingen Long, Jun Jiang, Ping Jin, Yao Fu, Haizhu Yu, and Weiran Yang. "Highly selective conversion of glyceric acid to 3-iodopropionic acid by hydriodic acid mediated hydrogenation." Green Chemistry 21, no. 16 (2019): 4434–42. http://dx.doi.org/10.1039/c9gc01084j.

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14

Andrés, José M., Ana C. Ferrando, and Pedro Ferrer. "Liquefaction of Low-Rank Coals with Hydriodic Acid and Microwaves." Energy & Fuels 12, no. 3 (May 1998): 563–69. http://dx.doi.org/10.1021/ef9701807.

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15

Skinner, Harry F. "Methamphetamine synthesis via hydriodic acid/red phosphorus reduction of ephedrine." Forensic Science International 48, no. 2 (December 1990): 123–34. http://dx.doi.org/10.1016/0379-0738(90)90104-7.

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16

Ito, S., T. Kato, K. Maruta, K. Jimbow, and K. Fujita. ""Total" acidic metabolites of catecholamines in urine as determined by hydrolysis with hydriodic acid and liquid chromatography: application to patients with neuroblastoma and melanoma." Clinical Chemistry 31, no. 7 (July 1, 1985): 1185–88. http://dx.doi.org/10.1093/clinchem/31.7.1185.

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Abstract We describe a method for determining the "total" excretion of acidic metabolites of catecholamines by measuring 3,4-dihydroxyphenylacetic acid (DOPAC) formed by hydriodic acid hydrolysis of 4-hydroxy-3-methoxyphenylacetic acid (HVA), 4-hydroxy-3-methoxymandelic acid (VMA), and their conjugates. The DOPAC in the diluted hydrolysate is measured directly by liquid chromatography with electrochemical detection. Normal values, expressed in relation to excretion of creatinine, vary as a function of age. For healthy subjects, the mean DOPAC value after hydrolysis was 1.15 times that for unconjugated HVA, VMA, and DOPAC combined. Preliminary results for patients with neuroblastoma and melanoma indicate the potential usefulness of the method for diagnosis and prognosis of patients with neural crest tumors that produce dopa or catecholamines.

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17

Klein, Suzane M., Cungen Zhang, and Yu Lin Jiang. "Simple synthesis of fresh alkyl iodides using alcohols and hydriodic acid." Tetrahedron Letters 49, no. 16 (April 2008): 2638–41. http://dx.doi.org/10.1016/j.tetlet.2008.02.106.

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18

Sow, Pradeep Kumar, Sonal Sant, and Anupam Shukla. "EIS studies on electro-electrodialysis cell for concentration of hydriodic acid." International Journal of Hydrogen Energy 35, no. 17 (September 2010): 8868–75. http://dx.doi.org/10.1016/j.ijhydene.2010.06.031.

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19

LIU, Z., A. GRANATA, X. SHEN, and A. S. PERLIN. "ChemInform Abstract: Reactions of Hydriodic Acid with Aldonolactones and n-Alkanolactones. Interconversions Between Lactones and Iodocarboxylic Acids." ChemInform 24, no. 11 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199311114.

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20

Robinson, J. Michael, Paul T. Herndon, Preston L. Holland, and Laura D. Marrufo. "Regeneration and Recovery of Hydriodic Acid after Reduction of Polyols to Fuels1." Organic Process Research & Development 3, no. 5 (September 1999): 352–56. http://dx.doi.org/10.1021/op990181t.

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21

Gavrilov, V. I., A. A. Karavanov, R. R. Musin, F. R. Garieva, and R. Z. Musin. "Reaction of 10-Methyl(phenyl)-5,10-dihydrophenarsazine 10-Oxides with Hydriodic Acid." Chemistry of Heterocyclic Compounds 40, no. 9 (September 2004): 1212–15. http://dx.doi.org/10.1023/b:cohc.0000048297.35826.d3.

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22

Goto, Hitoshi, Keiichi Koda, Guolin Tong, Yuji Matsumoto, and Gyosuke Meshitsuka. "Formation of methyl iodide from methoxyl-free compounds by hydriodic acid treatment." Journal of Wood Science 51, no. 3 (June 25, 2005): 312–14. http://dx.doi.org/10.1007/s10086-005-0709-8.

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23

van der Stelt, C., P. S. Hofman, C. van der Vlies, and F. Bickelhaupt. "The Reaction of 4,4-dimethyl-1-phenylisochroman with hydriodic acid and phosphorus." Recueil des Travaux Chimiques des Pays-Bas 86, no. 12 (September 2, 2010): 1316–19. http://dx.doi.org/10.1002/recl.19670861207.

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24

Onuki, K. "Electro-electrodialysis of hydriodic acid in the presence of iodine at elevated temperature." Journal of Membrane Science 192, no. 1-2 (October 15, 2001): 193–99. http://dx.doi.org/10.1016/s0376-7388(01)00500-2.

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25

ONUKI, K., S. SHIMIZU, H. NAKAJIMA, Y. IKEZOE, and S. SATO. "Reaction of methanol with hydriodic acid as a step of the CIS process." International Journal of Hydrogen Energy 15, no. 2 (1990): 93–97. http://dx.doi.org/10.1016/0360-3199(90)90030-3.

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26

Kobayashi, Kazuhiro, Kazuaki Shikata, Yuri Fujii, Shuhei Fukamachi, Miyuki Tanmatsu, and Hisatoshi Konishi. "Convenient Synthesis of 1,3-Dihydroisobenzofurans by Hydriodic Acid-Catalyzed Cyclization of 2-Vinylbenzyl Alcohols." HETEROCYCLES 81, no. 6 (2010): 1459. http://dx.doi.org/10.3987/com-10-11947.

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27

Orme, Christopher J., and Frederick F. Stewart. "Pervaporation of water from aqueous hydriodic acid and iodine mixtures using Nafion® membranes." Journal of Membrane Science 304, no. 1-2 (November 2007): 156–62. http://dx.doi.org/10.1016/j.memsci.2007.07.028.

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28

Kowalenko, C. G. "A modified apparatus for quick and versatile sulphate sulphur analysis using hydriodic acid reduction." Communications in Soil Science and Plant Analysis 16, no. 3 (March 1985): 289–300. http://dx.doi.org/10.1080/00103628509367603.

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29

Xu, Shaojie, Yong He, Biyi Huang, Yanwei Zhang, Zhihua Wang, and Kefa Cen. "Decomposition of hydriodic acid by electrolysis in the thermochemical water sulfur–iodine splitting cycle." International Journal of Hydrogen Energy 43, no. 7 (February 2018): 3597–604. http://dx.doi.org/10.1016/j.ijhydene.2017.12.177.

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30

BAI, Ying, Ping ZHANG, Hanfei GUO, Songzhe CHEN, Laijun WANG, and Jingming XU. "Purification of Sulfuric and Hydriodic Acids Phases in the Iodine-sulfur Process." Chinese Journal of Chemical Engineering 17, no. 1 (February 2009): 160–66. http://dx.doi.org/10.1016/s1004-9541(09)60049-5.

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31

�linson, M. N., S. K. Fedukovich, and G. I. Nikishin. "Electrochemical oxidation of malonic esters in the presence of catalyst carriers ? salts of hydriodic acid." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 11 (November 1988): 2285–89. http://dx.doi.org/10.1007/bf00959879.

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32

Shan, Xiao-quan, and Bin Chen. "Determination of carbon-bonded sulfur in soils by hydriodic acid reduction and hydrogen peroxide oxidation." Fresenius' Journal of Analytical Chemistry 351, no. 8 (1995): 762–67. http://dx.doi.org/10.1007/bf00323633.

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33

Caputo, Giampaolo, Irena Balog, Alberto Giaconia, Salvatore Sau, and Alfonso Pozio. "Experimental Study for HIx Concentration by Electro-Electrodialysis (EED) Cells in the Water Splitting Sulfur-Iodine Thermochemical Cycle." ChemEngineering 3, no. 2 (May 12, 2019): 50. http://dx.doi.org/10.3390/chemengineering3020050.

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The efficiency of HI concentration/separation from a HIx solution, (mixture of HI/H2O/I2) represents a crucial factor in the sulfur-iodine thermochemical water splitting process for hydrogen production. In this paper, an experimental study on HI cathodic concentration in HIx solution using stacked electro-electrodialysis (EED) cells was carried out under the conditions of 1 atm and at three different temperature (25, 55 and 85 °C) and using a current density of 0.10 A/cm2. Results showed that an increase in HI concentration can be obtained under certain conditions. The apparent transport number (t+) in all the experiments was very close to 1, and the electro-osmosis coefficient (β) changed in a range of 1.08–1.16. The tests showed a detectable, though slow, increase in both the anodic iodine and cathodic hydriodic acid concentrations.

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34

Kumar, J. S. Dileep, ManKit M. Ho, and Tatsushi Toyokuni. "Simple and chemoselective reduction of aromatic nitro compounds to aromatic amines: reduction with hydriodic acid revisited." Tetrahedron Letters 42, no. 33 (August 2001): 5601–3. http://dx.doi.org/10.1016/s0040-4039(01)01083-8.

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35

Arifal, Gab-Jin Hwang, and Kaoru Onuki. "Electro-electrodialysis of hydriodic acid using the cation exchange membrane cross-linked by accelerated electron radiation." Journal of Membrane Science 210, no. 1 (December 2002): 39–44. http://dx.doi.org/10.1016/s0376-7388(02)00372-1.

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36

Kobayashi, Kazuhiro, Kazuaki Shikata, Yuri Fujii, Shuhei Fukamachi, Miyuki Tanmatsu, and Hisatoshi Konishi. "ChemInform Abstract: Convenient Synthesis of 1,3-Dihydroisobenzofurans by Hydriodic Acid-Catalyzed Cyclization of 2-Vinylbenzyl Alcohols." ChemInform 41, no. 43 (September 30, 2010): no. http://dx.doi.org/10.1002/chin.201043102.

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37

Jones, R. L., and H. D. Chandler. "Strength loss in E-glass fibres after exposure to hydrochloric, hydrobromic and hydriodic acids." Journal of Materials Science 20, no. 9 (September 1985): 3320–24. http://dx.doi.org/10.1007/bf00545201.

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38

David, Gabrielle E., D. Brynn Hibbert, Russell D. Frew, and Alan R. Hayman. "Significant Determinants of Isotope Composition During HI/Pred Synthesis of Methamphetamine." Australian Journal of Chemistry 63, no. 1 (2010): 22. http://dx.doi.org/10.1071/ch09429.

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Methamphetamine HCl was synthesized using three variations of the hydriodic acid/red phosphorus (HI/Pred) synthetic route. A Plackett-Burman experimental design was used to determine how reaction parameters affected the isotopic composition of the product. Isotope ratio mass spectrometry results showed only the source of precursor 13C was significant in determining product δ 13C; the manufacturer, reaction temperature, time, scale, and source of HI were not significant. The precursor was also the main determinant of product δ 2H, with smaller contributions from the HI source for one method. From precursor to product, large δ 2H depletion occurred for most samples. Deuterium nuclear magnetic resonance spectroscopy (2H NMR) was used to investigate the specific site of this. Significant fraction of deuterium was observed only at the benzylic position, the site of hydrogen addition during synthesis. Methamphetamine synthesized from ephedrine was shown to be depleted in this position.

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39

Liu, Lide, Kazumasa Wakamatsu, Shosuke Ito, and Peter R. Williamson. "Catecholamine Oxidative Products, but Not Melanin, Are Produced by Cryptococcus neoformans during Neuropathogenesis in Mice." Infection and Immunity 67, no. 1 (January 1, 1999): 108–12. http://dx.doi.org/10.1128/iai.67.1.108-112.1999.

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ABSTRACT Melanin has been proposed as a virulence factor inCryptococcus neoformans, but its presence has not been shown unambiguously in vivo. Validated methods used previously to show production of cryptococcal eumelanin pigment in vitro (P. R. Williamson, K. Wakamatsu, and S. Ito, J. Bacteriol. 180:1570–1572, 1998) were used to assess for production of laccase-derived products in mouse brain of the Lacc+ strains, 2E-TUC, H99 (serotype A), and ATCC 34873 (serotype D), and the Lacc− strain, 2E-TU. Pyrrole-2,3,5-tricarboxylic and pyrrole-2,3-dicarboxylic acid, specific degradation products of catecholamine derivatives such as melanin, were found in all Lacc+ strains, but not in the Lacc− strain, 2E-TU. However, the presence of melanin pigment itself could not be demonstrated in the same cells. Lack of the specific degradation products aminohydroxyphenylalanine and aminohydroxyphenylethylamine in Lacc+ strains upon hydriodic acid hydrolysis showed that pheomelanin was also not produced by the fungus in vivo. These are the first data to support the generation of catecholamine oxidation products by C. neoformans in vivo, but they do not support postenzymatic polymerization of these products to form typical eumelanin, as previously proposed.

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40

Mohanakrishnan, Arasambattu, and Settu Rafiq. "Synthesis of Annulated Arenes and Heteroarenes by Hydriodic Acid and Red Phosphorus Mediated Reductive Cyclization of 2-(Hetero)aroylbenzoic Acids or 3-(Hetero)arylphthalides." Synlett 28, no. 03 (October 17, 2016): 362–70. http://dx.doi.org/10.1055/s-0036-1588337.

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41

Yang, Weiran, Matthew R. Grochowski, and Ayusman Sen. "Selective Reduction of Biomass by Hydriodic Acid and Its In Situ Regeneration from Iodine by Metal/Hydrogen." ChemSusChem 5, no. 7 (April 11, 2012): 1218–22. http://dx.doi.org/10.1002/cssc.201100669.

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42

Kobayashi, Kazuhiro, Seiki Fujita, and Hisatoshi Konishi. "Synthesis of 1(3H)-Iminobenzo[c]thiophene Derivatives by Hydriodic Acid-mediated Cyclization of 2-(Vinyl)thiobenzamide Derivatives." HETEROCYCLES 75, no. 10 (2008): 2555. http://dx.doi.org/10.3987/com-08-11425.

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43

Kobayashi, Kazuhiro, Kazuaki Shikata, Hiroki Maegawa, Shuhei Fukamachi, Miyuki Tanmatsu, and Hisatoshi Konishi. "Synthesis of Isochromans by Hydriodic Acid or Iodine Mediated Cyclization Reactions of 1-(2-Vinylphenyl)propan-2-ols." HETEROCYCLES 81, no. 10 (2010): 2361. http://dx.doi.org/10.3987/com-10-12021.

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44

Robinson, J. Michael, Eric J. Mechalke, Teresa E. Rogers, Preston L. Holland, and Wendell C. Barber. "Electrohydrolysis recycling of waste iodide salts into hydriodic acid for the chemical conversion of biomass into liquid hydrocarbons." Journal of Membrane Science 179, no. 1-2 (November 2000): 109–25. http://dx.doi.org/10.1016/s0376-7388(00)00499-3.

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45

Schulze, Matthias, David E. Scott, Alexander Scherer, Frank Hampel, Robin J. Hamilton, Murray R. Gray, Rik R. Tykwinski, and Jeffrey M. Stryker. "Steroid-Derived Naphthoquinoline Asphaltene Model Compounds: Hydriodic Acid Is the Active Catalyst in I2-Promoted Multicomponent Cyclocondensation Reactions." Organic Letters 17, no. 23 (November 20, 2015): 5930–33. http://dx.doi.org/10.1021/acs.orglett.5b03193.

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46

Dileep Kumar, J. S., ManKit M. Ho, and Tatsushi Toyokuni. "ChemInform Abstract: Simple and Chemoselective Reduction of Aromatic Nitro Compounds to Aromatic Amines: Reduction with Hydriodic Acid Revisited." ChemInform 33, no. 5 (May 22, 2010): no. http://dx.doi.org/10.1002/chin.200205084.

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47

Windahl, K. L., M. J. McTigue, J. R. Pearson, S. J. Pratt, J. E. Rowe, and E. M. Sear. "Investigation of the impurities found in methamphetamine synthesised from pseudoephedrine by reduction with hydriodic acid and red phosphorus." Forensic Science International 76, no. 2 (December 1995): 97–114. http://dx.doi.org/10.1016/0379-0738(95)01803-4.

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48

Herrington, Thelma M., Alan D. Pethybridge, and Michael G. Roffey. "Densities of hydrochloric, hydrobromic, hydriodic, and perchloric acids from 25 to 75.degree.C at 1 atm." Journal of Chemical & Engineering Data 30, no. 3 (July 1985): 264–67. http://dx.doi.org/10.1021/je00041a008.

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49

Kobayashi, Kazuhiro, Shuhei Fukamachi, and Hisatoshi Konishi. "Synthesis of 1,4-Dihydro-2H-3,1-benzoxazin-2-ones by Hydriodic Acid Mediated Cyclization of tert-Butyl 2-Vinylphenylcarbamates." HETEROCYCLES 75, no. 9 (2008): 2301. http://dx.doi.org/10.3987/com-08-11399.

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Alayande, Abayomi Babatunde, Hee‐Deung Park, Johannes S. Vrouwenvelder, and In S. Kim. "Implications of Chemical Reduction Using Hydriodic Acid on the Antimicrobial Properties of Graphene Oxide and Reduced Graphene Oxide Membranes." Small 15, no. 28 (May 30, 2019): 1901023. http://dx.doi.org/10.1002/smll.201901023.

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