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Journal articles on the topic 'Potassium Cyanide, chemistry'

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Published: 4 June 2021
Last updated: 28 July 2025

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1

Young, Jay A. "Potassium Cyanide." Journal of Chemical Education 80, no. 9 (2003): 998. http://dx.doi.org/10.1021/ed080p998.

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2

Connors, Richard, Elisabeth Tran, and Tony Durst. "Acyl cyanides as carbonyl heterodienophiles: application to the synthesis of naphthols, isoquinolones, and isocoumarins." Canadian Journal of Chemistry 74, no. 2 (1996): 221–26. http://dx.doi.org/10.1139/v96-024.

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Irradiation of 2-methylbenzoyl cyanide (3a) in acetonitrile solution results in the formation of its dimer, which upon loss of HCN gives rise to the cycloadduct 7a. The dimerization also proceeds efficiently with derivatives of 3a giving adducts 7b and 7c. When 2-methylaroyl cyanides are photolyzed in the presence of a more reactive acyl cyanide the mixed adducts 8a–e are obtained in excellent yields. The cycloadducts 7a–c and 8a–e react with carbon and nitrogen nucleophiles by a tandem addition–cyclization sequence furnishing substituted naphthols (10a and 10b) and isoquinolones (11a–d), resp
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3

BOUZIDA, SAMIRA, EL BACHIR BENAMAR, MANALE BATTAS, et al. "EFFECT OF POTASSIUM CYANIDE ETCHING ON STRUCTURAL, OPTICAL AND ELECTRICAL PROPERTIES OF Cu2ZnSnS4 THIN FILMS DEPOSITED BY A MODIFIED SPRAY PROCESS." Surface Review and Letters 26, no. 09 (2019): 1950053. http://dx.doi.org/10.1142/s0218625x19500537.

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We report the effect of potassium cyanide etching treatment on structural, optical and electrical properties of Cu2ZnSnS4 thin films prepared by a spray-assisted chemical vapor deposition process. Raman spectroscopy and X-ray diffraction measurements before and after potassium cyanide etching have confirmed the kesterite structure of Cu2ZnSnS4 films. Potassium cyanide treatment led to the elimination of [Formula: see text]S secondary phase. Optical measurements showed that the band gap value was about 1.52[Formula: see text]eV. The best electrical resistivity and Hall mobility values were reac
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4

Maranna, Manjunatha Chinnaiahnapalya, Lalgudy Mahadevan Saikrishnan, Tarur Konikkaledom Dinesh, and Kamal Kumar Tyagi. "Determination of Hydrogen Cyanide in Cigarette Smoke by Continuous Flow Analysis Method Using Safer Chemistry." Beiträge zur Tabakforschung International/Contributions to Tobacco Research 28, no. 4 (2018): 191–202. http://dx.doi.org/10.2478/cttr-2018-0018.

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SummaryA new safe and sensitive method to determine hydrogen cyanide (HCN) in cigarette smoke using continuous flow analyser (CFA) has been developed and validated. The use of highly toxic potassium cyanide (KCN) as a standard necessitates the development of a safer method for the determination of HCN in cigarette smoke. In this described method KCN is replaced by less toxic potassium tetracyanozincate (Lethal Dose LD50 oral is 7.49 mg/kg for KCN and 2000 mg/kg for potassium tetracyanozincate). Furthermore, the new method uses isonicotinic acid-barbituric acid (coupling reagent) instead of pyr
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5

Cao, Yu-Qing, Yun-Fei Du, and Ji-Tai Li. "A Practical and Improved Method for the Preparation of Trimethylsilyl Cyanide Catalysed by PEG400 and Zinc Iodide." Journal of Chemical Research 2003, no. 8 (2003): 500–501. http://dx.doi.org/10.3184/030823403103174704.

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The useful synthetic reagent trimethylsilyl cyanide was readily prepared in high yield by the cyanation of trimethylchlorosilane with potassium cyanide in the presence of PEG400 and zinc iodide under stirring at room temperature or ultrasonic radiation.
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6

Nay, Bastien, Valérie Arnaudinaud, Jean-François Peyrat, et al. "13C-Labelled (±±)-Catechin From Potassium [13C]Cyanide." European Journal of Organic Chemistry 2000, no. 7 (2000): 1279–83. http://dx.doi.org/10.1002/1099-0690(200004)2000:7<1279::aid-ejoc1279>3.0.co;2-d.

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7

Bhagyalakshmi, Kamasala, and Nanguneri V. Nanda Kumar. "Simple, Rapid, and Portable Chromatographic Tetrazolium Reduction Method for Detection of Potassium Cyanide in Medicinal Drugs and Confectionery." Journal of AOAC INTERNATIONAL 72, no. 3 (1989): 429–31. http://dx.doi.org/10.1093/jaoac/72.3.429.

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Abstract A simple, rapid, and portable paper chromatographic method for detection of potassium cyanide in medicinal drugs and a few confectionery samples is described. Potassium cyanide is extracted in methanol and concentrated. Acetone-water-1.5% EDTA (4 + 5.5 + 0.5) mixture is used as the solvent system for paper chromatography. The KCN chromatograms appear as pink spots on paper due to reduction of the chromogenic salt 2-(4-iodophenyl)-3-(4-nitrophenyl)-5- phenyl tetrazolium chloride; phenazonium methosulfate is a catalyst. Microgram amounts of KCN can be separated and detected in the labor
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8

Mallah, Eyad, Qutaiba Abu-Salem, Kamal Sweidan, et al. "Imidazolium Dicyanoargentates." Zeitschrift für Naturforschung B 66, no. 5 (2011): 545–48. http://dx.doi.org/10.1515/znb-2011-0517.

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New imidazolium dicyanoargentate salts were synthesized by treatment of 2-chloro-1,3-diisopropyl-4,5-dimethylimidazolium chloride (2a) with an excess of silver cyanide in acetonitrile to afford 2-chloro-1,3-diisopropyl-4,5-dimethylimidazolium dicyanoargentate (3) and its conversion into the corresponding 2-cyano-1,3-diisopropyl-4,5-dimethylimidazolium dicyanoargentate (4) by reaction with an excess amount of potassium cyanide. The crystal structures of 3 and 4 are reported
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9

Grundke, Caroline, and Till Opatz. "Strecker reactions with hexacyanoferrates as non-toxic cyanide sources." Green Chemistry 21, no. 9 (2019): 2362–66. http://dx.doi.org/10.1039/c9gc00720b.

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10

Li, Zheng, and Jun Xu. "Solvent-Free Synthesis of Arylsulfonyl Cyanides Using Potassium Hexacyanoferrate(II) as An Ecofriendly Cyanide Source." Phosphorus, Sulfur, and Silicon and the Related Elements 189, no. 3 (2014): 374–78. http://dx.doi.org/10.1080/10426507.2013.819870.

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11

Clark, James H., and Catherine V. A. Duke. "Supported cyanides: the interaction of potassium cyanide with high surface area inorganic support materials and the development of highly reactive cyanide reagents." Journal of Organic Chemistry 50, no. 8 (1985): 1330–32. http://dx.doi.org/10.1021/jo00208a046.

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12

Jarring, K., B. Holmberg, and L. Bengtsson. "Coordination of silver(I) by thiocyanate, cyanide, and iodide in molten potassium, thiocyanate-potassium cyanide, and potassium thiocyanate-potassium iodide mixtures at 185.degree.C. An x-ray scattering and emf study." Inorganic Chemistry 27, no. 14 (1988): 2445–49. http://dx.doi.org/10.1021/ic00287a015.

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13

Ohmatsu, Kohsuke, Yusuke Morita, Mari Kiyokawa, Kimihiro Hoshino, and Takashi Ooi. "Catalytic Asymmetric Strecker Reaction of Ketoimines with Potassium Cyanide." Asian Journal of Organic Chemistry 10, no. 12 (2021): 3237–40. http://dx.doi.org/10.1002/ajoc.202100608.

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14

Jacquot-Rousseau, Sandrine, Gérard Schmitt, Bernard Laude, Marek M. Kubicki, and Olivier Blacque. "Nucleophilic Additions of the Cyanide Anion to 4,4-Dichloro-1,1-Diphenyl-2-Azabuta-1,3-Diene." Journal of Chemical Research 2002, no. 4 (2002): 151–52. http://dx.doi.org/10.3184/030823402103171681.

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The unexpected formation of a 2H-pyrrole by reaction of potassium cyanide with 4,4-dichloro-1,1-diphenyl-2-azabuta-1,3-diene and the mechanism of this reaction are described and the structures of the product and a trapped intermediate confirmed by X-ray crystallographic studies.
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15

Hemmen, R., M. E. Kordesch, P. Hollins, and H. Conrad. "Potassium cyanide production from the dissociative adsorption cyanogen and potassium on palladium(100)." Journal of Physical Chemistry 92, no. 17 (1988): 4829–31. http://dx.doi.org/10.1021/j100328a005.

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16

Yasumatsu, Hisato, Tamotsu Kondow, and Kaoru Suzuki. "Vibrational distributions of the cyanogen(B2.SIGMA.+) produced in the dissociative excitation of potassium cyanide and sodium cyanide with argon metastable atoms: bimodal vibrational distribution from potassium cyanide." Journal of Physical Chemistry 97, no. 26 (1993): 6788–92. http://dx.doi.org/10.1021/j100128a007.

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17

Salama, Tarek A., Saad S. Elmorsy, Abdel‐Galel M. Khalil, Margret M. Girges, and Abdel‐Aziz S. El‐Ahl. "Novel Uncatalyzed Hydrocyanation of Ketones utlizing Tetrachlorosilane–Potassium Cyanide Reagent." Synthetic Communications 37, no. 8 (2007): 1313–19. http://dx.doi.org/10.1080/00397910701226897.

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18

Numazawa, Mitsuteru, Mutsumi Satoh, Satoshi Satoh, Masao Nagaoka, and Yoshio Osawa. "Reaction of 16-bromo-17-oxo steroids with potassium cyanide." Journal of Organic Chemistry 51, no. 8 (1986): 1360–62. http://dx.doi.org/10.1021/jo00358a040.

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19

Naeimi, Hossein, та Mohsen Moradian. "Metal(II) Schiff base complexes as catalysts for the high-regioselective conversion of epoxides to β-hydroxy nitriles in glycol solvents". Canadian Journal of Chemistry 84, № 11 (2006): 1575–79. http://dx.doi.org/10.1139/v06-158.

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A facile preparation of 3-hydroxy propanenitrile derivatives is described involving ring opening of epoxides with potassium cyanide in glycol solvents in the presence of Schiff base complexes as catalysts. This method occurs under neutral and mild conditions with high yields and high regioselectivity. Thus, several β-Hydroxy nitriles, useful intermediates toward biologically-active molecules, are easily obtained at room temperature.Key words: β-hydroxy nitrile, Schiff base, epoxide, glycol, catalyst.
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20

Li, Zheng, Yan Du, Hao Lu, Aizhen Yang, and Jingya Yang. "Hydrocyanation of 2-arylmethyleneindan-1,3-diones using potassium hexacyanoferrate(II) as a nontoxic cyanating agent." Green Processing and Synthesis 8, no. 1 (2019): 93–99. http://dx.doi.org/10.1515/gps-2018-0017.

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Abstract The hydrocyanation of 2-arylmethyleneindan-1,3-diones with potassium hexacyanoferrate(II) as a nontoxic cyanating agent to synthesize 2-(1,3-dioxoindan-2-yl)-2-arylacetonitriles in the presence of benzoyl chloride as a promoter and potassium carbonate as a base by a one-pot procedure is described. The use of nontoxic and inexpensive cyanide source, high yield and simple workup procedures are the advantages of this protocol.
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21

Deubner, H. Lars, and Florian Kraus. "A spatially separated [KBr6]5− anion in the cyanido-bridged uranium(IV) compound [U2(CN)3(NH3)14]5+[KBr6]5−·NH3." Zeitschrift für Naturforschung B 75, no. 1-2 (2020): 111–16. http://dx.doi.org/10.1515/znb-2019-0161.

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AbstractThe reaction of uranium tetrabromide with potassium cyanide in anhydrous liquid ammonia at room temperature leads to the formation of brown crystals of [U2(CN)3(NH3)14]5+ [KBr6]5− · NH3. We determined the crystal structure of the compound by single crystal X-ray diffraction. To the best of our knowledge it contains the unprecedented spatially separated [KBr6]5− anion and presents the first uranium(IV) cyanide compound which forms a layer structure. The compound crystallizes in the trigonal space group P3̅m1 (No. 164) with a = 10.3246(13), c = 8.4255(17) Å, V = 777.8(3) Å3, Z = 1 at T =
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22

Nasseri, Mohammad Ali, Seyyedeh Ameneh Alavi, Boshra Mahmoudi, and Milad Kazemnejadi. "A Facile Approach to Catalyst-Free Cyanation and Azidation of ­Organic Compounds and a One-Pot Preparation of 5-Substituted 1H-Tetrazoles by Using a Dimethyl Sulfoxide–Nitric Acid Combination." Synlett 30, no. 20 (2019): 2290–94. http://dx.doi.org/10.1055/s-0039-1690742.

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In this study, cyanations or azidations of imines were performed by using hydroxy(dimethyl)-λ4-sulfanecarbonitrile or azido(dimethyl)-λ4-sulfanol, respectively, prepared in situ by treatment of potassium cyanide or sodium azide with a dimethyl sulfoxide–nitric acid combination. Furthermore, a one-pot preparation of 5-substituted 1H-tetrazole derivatives was carried out by using this reagent combination in the presence of an aldehyde, hydroxylamine hydrochloride, and sodium azide under mild conditions.
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23

Ogbonnaya, Nwokoro. "Linamarase production by some microbial isolates and a comparison of the rate of degradation of cassava cyanide by microbial and cassava linamarases." Chemical Industry 70, no. 2 (2016): 129–36. http://dx.doi.org/10.2298/hemind141028021o.

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Production of linamarase and the effects of media composition on enzyme production were studied. A total of eight linamarase-producing bacteria were isolated from fermenting cassava tubers and soil samples. Selection of the isolates was based on their high growth in media containing 800 mg/L potassium cyanide solution. Eight of the isolates which showed very high growth in the growth medium as demonstrated by increase in their optical density readings to at least 0.6 in the cyanide containing media were selected for further studies. The isolates were identified as Lactobacillus plantarum, Lact
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24

Sukata, Kazuaki. "A Convenient Method for the Synthesis of Alkylsilyl Cyanides Using Potassium or Sodium Cyanide Impregnated on Amberlite XAD Resin." Bulletin of the Chemical Society of Japan 60, no. 6 (1987): 2257–58. http://dx.doi.org/10.1246/bcsj.60.2257.

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25

Johnson, J. D., and G. E. Isom. "Quantification of Expired Metabolites Following Potassium Cyanide Administration: A New Method." Journal of Analytical Toxicology 9, no. 3 (1985): 112–15. http://dx.doi.org/10.1093/jat/9.3.112.

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26

Avdalovic, Jelena, Tatjana Solevic-Knudsen, Biljana Dojcinovic, et al. "Bioleaching of copper, zinc and gold from a polymetallic ore flotation concentrate from the Coka Marin deposit (Serbia)." Journal of the Serbian Chemical Society, no. 00 (2021): 16. http://dx.doi.org/10.2298/jsc210127016a.

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The aim of this study was to investigate the possibility of applying Acidithiobacillus sp. B2 to copper, zinc and gold recovery from a polymetallic ore flotation concentrate. The study was designed in two phases. The first phase was a classic biooxidation process in which the microorganisms oxidize sulfides, leaching copper and zinc while simultaneously concentrating gold in the ore. In the second phase, after elimination of the sulfide substrate, the rate of gold leaching by potassium cyanide was analyzed. The leaching was conducted using the shake flask testing technique during a period of 2
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27

Milentijević, Goran, Milena Milošević, Svetomir Milojević, et al. "One-Pot Syntheses of PET-Based Plasticizer and Tetramethyl Thiuram Monosulfide (TMTS) as Vulcanization Accelerator for Rubber Production." Processes 11, no. 4 (2023): 1033. http://dx.doi.org/10.3390/pr11041033.

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Styrene-butadiene (SBR) and acrylonitrile-butadiene (NBR) rubber blends with tetramethyl thiuram disulfide (TMTD) and tetramethyl thiuram monosulfide (TMTS) accelerators and environmentally friendly plasticizers, obtained from PET recycling and biobased resources (LA/PG/PET/EG/LA), were prepared. The mechanical properties of the obtained rubber products were tested and compared with those of commercial dioctyl terephthalate (DOTP). TMTS was prepared by simple and efficient one-pot synthesis from dimethylamine, carbon disulfide, potassium cyanide, and ammonium chloride as catalysts in recycled
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28

Tandon, Santokh S., and C. Robert Lucas. "Metal-induced facile synthesis of a tricyclic system — 10-Methyl-12-thia-2,9-diaza-tricyclo[8.3.1.03,8]tetradeca-3,5,7-triene-1-carbonitrile. Formation of an intramolecular carbon–carbon bond." Canadian Journal of Chemistry 86, no. 9 (2008): 912–17. http://dx.doi.org/10.1139/v08-100.

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The reaction between 4-thiaheptane-2,6-dione and 1,2-diaminobenzene in the presence of nickel(II) perchlorate results in the formation of a nickel(II) complex of a novel new heterotricyclic system: 1-methoxy-10-methyl-12-thia-2,9-diaza-tricyclo[8.3.1.03,8]tetradeca-3,5,7-triene, which on treatment with potassium cyanide gives 10-methy-12-thia-2,9-diaza-tricyclo[8.3.1.03,8]tetradeca-3,5,7-triene-1-carbonitrile, a case of metal-induced carbon–carbon bond formation.Key words: nickel-induced carbon–carbon bond formation, intramolecular cyclization, tricyclic formation.
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29

Liu, Hui, Xue-Bin Shao, Mu-Xin Jia, Xi-Kui Jiang, Zhan-Ting Li, and Guang-Ju Chen. "Selective recognition of sodium cyanide and potassium cyanide by diaza-crown ether-capped Zn-porphyrin receptors in polar solvents." Tetrahedron 61, no. 34 (2005): 8095–100. http://dx.doi.org/10.1016/j.tet.2005.06.058.

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30

Kuzmič, Petr, and Milan Souček. "Photocyanation of 3,4-dimethoxy-1-nitrobenzene. A quantitative study." Collection of Czechoslovak Chemical Communications 51, no. 2 (1986): 358–67. http://dx.doi.org/10.1135/cccc19860358.

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UV photolysis (365 nm) of 3,4-dimethoxy-1-nitrobenzene in the presence of potassium cyanide leading to 3-cyano-4-methoxy-1-nitrobenzene was subjected to a quantitative photokinetic study. The reaction exhibits a second order kinetics with respect to the nucleophile and is effectively quenched by molecular oxygen as well as 2,4-hexadienoic acid. The excited triplet lifetime of 0.9 microseconds was determined on the basis of the dependence of quantum yield on the nucleophile and quencher concentrations in 50% aqueous tert-butanol. The quantum yield of intersystem crossing is at least 0.38 in the
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31

Sassaman, Mark B., G. K. Surya Prakash, and George A. Olah. "Synthetic methods and reactions. 144. Regiospecific and chemoselective ring opening of epoxides with trimethylsilyl cyanide-potassium cyanide/18-crown-6 complex." Journal of Organic Chemistry 55, no. 7 (1990): 2016–18. http://dx.doi.org/10.1021/jo00294a012.

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32

Popp, Frank D., and Frederick F. Duarte. "HETEROGENEOUS SYNTHESIS OF REISSERT COMPOUNDS UTILIZING POTASSIUM CYANIDE ADSORBED ON AMBERLITE XAD RESINS." Organic Preparations and Procedures International 21, no. 3 (1989): 366–68. http://dx.doi.org/10.1080/00304948909356400.

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33

Adachi, Atsuko, Sachiko Nojima, Yukiko Hagiwaras, Makoto Hamamoto, and Tadashi Kobayashi. "Studies on the oxidative decomposition of cyanide ion by potassium permanganate." Environmental Technology 12, no. 1 (1991): 93–96. http://dx.doi.org/10.1080/09593339109384986.

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34

El-shenawy, Hamdy A., and Conrad Schuerch. "Potassium Cyanide as Catalyst for Deesterification of Acid- and Base-Sensitive D-Galactopyranosides." Journal of Carbohydrate Chemistry 4, no. 2 (1985): 215–25. http://dx.doi.org/10.1080/07328308508058833.

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35

Ohmatsu, Kohsuke, Yusuke Morita, Mari Kiyokawa, and Takashi Ooi. "Catalytic Asymmetric Cyanoalkylation of Electron-Deficient Olefins with Potassium Cyanide and Alkyl Halides." Journal of the American Chemical Society 143, no. 29 (2021): 11218–24. http://dx.doi.org/10.1021/jacs.1c05380.

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36

Sukata, Kazuaki. "Reaction of Aromatic Acyl Chlorides with Potassium or Sodium Cyanide Impregnated onto Amberlite XAD Resins. Efficient Synthesis of Aromatic Acyl Cyanides." Bulletin of the Chemical Society of Japan 60, no. 3 (1987): 1085–89. http://dx.doi.org/10.1246/bcsj.60.1085.

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37

Sunil, K., Merla Arjuna Rajendra, Ayyiliath Meleveetil Sajith, Muthipeedika Nibin Joy, Vasiliy A. Bakulev, and Karickal Raman Haridas. "Palladium-Catalyzed Cyanation under Mild Conditions: A Case Study to Discover Appropriate Substrates among Halides and Pseudohalides." Synlett 31, no. 16 (2020): 1629–33. http://dx.doi.org/10.1055/s-0040-1707218.

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A case study has been effectively carried out to identify a suitable substrate among halides and pseudohalides for the palladium-catalyzed cyanation reactions under mild conditions. Among the various substrates considered for evaluation, aryl pentafluorobenzenesulfonates and nonaflates were identified to be the best substrates when compared to corresponding halides and pseudohalides. The substoichiometric use of nontoxic, environmentally benign potassium hexacyanoferrate as a cyanide source and exceptionally milder conditions further highlights the significance of the protocol developed. A wid
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38

Rodriguez-Ramos, I., A. Guerrero-Ruiz, J. L. G. Fierro, P. Ramirez de la Piscina, and N. Homs. "CO hydrogenation over potassium promoted iron, cobalt, and nickel Catalysts Prepared from Cyanide Complexes." Zeitschrift f�r anorganische und allgemeine Chemie 582, no. 1 (1990): 197–210. http://dx.doi.org/10.1002/zaac.19905820124.

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39

López-Ruiz, Heraclio, Horacio Briseño-Ortega, Susana Rojas-Lima, Rosa Santillán, and Norberto Farfán. "An efficient potassium cyanide-promoted synthesis of 2-arylbenzoxazoles from [4.3.0]boron heterobicycles." Tetrahedron Letters 51, no. 19 (2010): 2633–35. http://dx.doi.org/10.1016/j.tetlet.2010.03.027.

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40

Slyvka, Nataliia, Lesya Saliyeva, Mariia Litvinchuk, Svitlana Shishkina, and Mykhailo Vovk. "Features of (Benzo)Imidazo[2,1-b][1,3]thiazine Mezylates Reaction with Nucleophilic Reagents." Chemistry & Chemical Technology 17, no. 3 (2023): 542–48. http://dx.doi.org/10.23939/chcht17.03.542.

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Peculiarities of the course of the methanesulfo-derivatives of (benzo)imidazo[2,1-b][1,3]thiazines reac-tions with a number of nucleophilic reagents were studied. It was determined that they react nonselectively with potassium thiocyanate to form a mixture of thio- and isothiocyanate derivatives. When interacting with sodium azide, nucleophilic substitution competes with an elimination reaction. The latter is dominant in the reaction with sodium cyanide. The spatial structure of one of the isomer elimination products, 4H-benzo[4,5]imidazo[2,1-b][1,3] thiazine, was established by X-ray structur
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41

Lewis, Laurent J., and Michael L. Klein. "Quadrupolar freezing in potassium bromide cyanide ((KBr)1-x(KCN)x) mixed crystals." Journal of Physical Chemistry 91, no. 19 (1987): 4990–94. http://dx.doi.org/10.1021/j100303a018.

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42

Ge, Hoon, Gary N. Oman, and Frank J. Ebert. "On-Line Generation of Cyanogen Chloride in Semiautomated Determination of Niacin and Niacinamide in Food Products." Journal of AOAC INTERNATIONAL 69, no. 3 (1986): 560–62. http://dx.doi.org/10.1093/jaoac/69.3.560.

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Abstract The current AOAC procedure for semiautomated determination of niacin specifies the use of externally generated cyanogen bromide. Because of the safety concerns in handling this material, we investigated the use of an alternative system of generating cyanogen chloride in situ, using chloramine-T and potassium cyanide. Recovery studies conducted on 9 different food products yielded average recoveries of 101 %. A repeatability study resulted in a measured coefficient of variation of 2.9%. The AOAC niacin method was compared with this semiautomated method; 115 paired analyses on 8 differe
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43

Yang, Jingya, Baohua Zhan, Ben Ma, Xiancheng Xiang, Yunfen Bao та Zheng Li. "Me3SiCl-Promoted Conjugate Hydrocyanation ofα,β-Unsaturated Ketones Using Potassium Hexacyanoferrate(II) as Cyanide Source". Chinese Journal of Organic Chemistry 35, № 6 (2015): 1286. http://dx.doi.org/10.6023/cjoc201501019.

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44

Okada, Tetsuo, and Tooru Kuwamoto. "Potassium hydroxide eluent for nonsuppressed anion chromatography of cyanide, sulfide, arsenite, and other weak acids." Analytical Chemistry 57, no. 4 (1985): 829–33. http://dx.doi.org/10.1021/ac00281a013.

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45

Redeker, Frenio A., Helmut Beckers, and Sebastian Riedel. "IR‐Laser Ablation of Potassium Cyanide: A Surprisingly Simple Route to Polynitrogen and Polycarbon Species." Chemistry – A European Journal 26, no. 8 (2020): 1763–67. http://dx.doi.org/10.1002/chem.201905103.

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46

Bourne, John R., Peter Dell'Ava, Othmar Dossenbach, and Thomas Post. "Densities, viscosities, and diffusivities in aqueous sodium hydroxide-potassium ferri- and ferro-cyanide solutions." Journal of Chemical & Engineering Data 30, no. 2 (1985): 160–63. http://dx.doi.org/10.1021/je00040a008.

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47

Park, Sung, Hong-Sick Kim, Ju-Hyeon Lee, Youn Cheol Kim, Jae Chun Lee, and Yun-Joong Chung. "Photoreaction of gold ions from potassium gold cyanide wastewater using solution-combusted ZnO nanopowders." Journal of the European Ceramic Society 30, no. 2 (2010): 177–80. http://dx.doi.org/10.1016/j.jeurceramsoc.2009.09.001.

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48

Bräu, Michael F., and Arno Pfitzner. "[Cu(CN)en2]I – Copper Amine Propellers." Zeitschrift für Naturforschung B 61, no. 7 (2006): 775–78. http://dx.doi.org/10.1515/znb-2006-0701.

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Abstract:
Light blue [Cu(CN)en2]I was prepared by reaction of copper iodide with ethylenediamine (en) and potassium cyanide in acetonitrile in air. It crystallizes in the space group C2 (No. 5) with a = 11.082(6), b = 7.155(2), c = 9.017(3) Å , β = 127.00(3)°, and Z = 2. The structure was refined from 1069 unique reflections and 90 parameters. The refinement converged to R1=0.018 and wR2=0.041 (all reflections). Copper has a trigonal bi-pyramidal environment formed by two en molecules and one CN− anion. The iodine anion shows no direct contact to the Cu2+ center. The propeller shaped complexes [Cu(CN)en
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49

Ali, Syed Shahed. "Potassium ferro-cyanide trihydrate complex catalyzed one-pot synthesis of 2-phenylimidazo [4,5-f] [1,10] phenanthroline." Chinese Chemical Letters 22, no. 7 (2011): 793–96. http://dx.doi.org/10.1016/j.cclet.2011.01.017.

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50

S., Pradhan, S. Dhundhel R., K. Rai M., and K. Rai J. "A new sensitive method for the determination of deltamethrine in environmental, agricultural and biological samples." Journal of Indian Chemical Society Vol. 84, Nov 2007 (2007): 1176–78. https://doi.org/10.5281/zenodo.5824815.

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School of Studies in Chemistry, Chhattisgarh Council of Science &amp; Technology Pt. Ravishankar Shukla University, Raipur-492 010, Chhattisgarh, India <em>E-mail</em> : rakeshsingh _109I @rediffmail.com <em>Manuscript received 8 August 2007, accepted 10 August 2007</em> A new sensitive method for the determination of deltamethrine pesticide in ppm level is described. The method is based on the hydrolysis of deltamethrine to produce cyanide ion which reacts with bromine water to form cyanogen bromide. To this solution on adding potassium iodide solution to remove excess of bromine which react
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