Academic literature on the topic '1-Nitroso-2-naphthol'

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Journal articles on the topic "1-Nitroso-2-naphthol"

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Didukh-Shadrina, Svetlana L., Vladimir N. Losev, Alexandr Samoilo, Anatoliy К. Trofimchuk, and Pavel N. Nesterenko. "Determination of Metals in Natural Waters by Inductively Coupled Plasma Optical Emission Spectroscopy after Preconcentration on Silica Sequentially Coated with Layers of Polyhexamethylene Guanidinium and Sulphonated Nitrosonaphthols." International Journal of Analytical Chemistry 2019 (July 1, 2019): 1–13. http://dx.doi.org/10.1155/2019/1467631.

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A series of complexing adsorbents is prepared by coating silica particles with linear polyhexamethylene guanidinium (PHMG) chloride followed by saturation with a number of sulphonated nitrosonaphthols reagents electrostatically retained by positively charged polymer layer. PHMG coated silica is hydrolytically stable even during treatment with 6 M HCl heated up to 50 °C. The adsorption of 1-nitroso-2-naphthol-3,6-disulfonic acid (nitroso-R-salt), 2-nitroso-1-naphthol-4-sulfonic acid (nitroso-N-salt), and 2-nitroso-1-naphthol-3,6-disulfonic acid (nitroso-K-salt) on PHMG modified silica was studi
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Foretić, B., N. Burger, and V. Hankonyi. "Reactions of the aquapentacyanoferrate(II) ion with 2-nitroso-1-naphthol and 2-nitroso-1-naphthol-4-sulphonic acid." Polyhedron 14, no. 5 (1995): 605–9. http://dx.doi.org/10.1016/0277-5387(94)00280-r.

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A., Sheela, та L. Harikumaran Nair M. "Dioxotungsten(VI) complexes of α-nitroso-β-naphthol and β-nitroso-α-naphthol". Journal of Indian Chemical Society Vol. 89, Apr 2012 (2012): 445–54. https://doi.org/10.5281/zenodo.5760383.

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Department of Chemistry, M. S. M. College, Kayamkulam-690 502, Kerala, India Department of Chemistry, University College, Thiruvarianthapuram-695 034, Kerala, India <em>E-mail</em> : drmlhnair@gmail.com <em>Manuscript received 27 July 2010, revised 30 June 2011, accepted 21 July 2011</em> Some novel dioxotungsten(VI) complexes of &alpha;-nitroso-&beta;-naphthol and &beta;-nitroso-&alpha;-naphthol having the compositions [WO<sub>2</sub>L<sub>2</sub>ClX] (where X = Cl, N0<sub>3</sub>, NCS or Cl0<sub>4</sub> and L = &alpha;-nitroso-&beta;-naphthol or &beta;-nitroso-&alpha;-naphthol) have been syn
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Singh, Ratnesh Kumar, Anju Kumari Gupta, Sachin Prakash, and D. Prakash. "Mixed Ligand Complexes of Al(III) with Chelating Organic Acids and Ethylenediamine." Oriental Journal Of Chemistry 36, no. 6 (2020): 1225–28. http://dx.doi.org/10.13005/ojc/360630.

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Mixed ligand complexes of Al(III) with o-Nitrophenol, 1-Nitroso-2-naphthol, 2,4-Dinitrophenol, 8-Hydroxyquinoline, 2,4,6-Trinitrophenol or o-Nitrobenzoic acid and Ethylenediamine were prepared and studied by elemental analyses, conductometric measurements, FTIR and UV-Vis measurements. These studies indicates the coordination of aluminium metal with o-Nitrophenol, 1-Nitroso-2-naphthol, 2,4-Dinitrophenol, 8-Hydroxyquinoline, 2,4,6-Trinitrophenol or o-Nitrobenzoic acid through oxygen or/and nitrogen atom and with Ethylenediamine through nitrogen atom.
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Efimenko, Zarina M., Anton V. Rozhkov, Vitalii V. Suslonov, Maxim L. Kuznetsov, Vadim Yu Kukushkin, and Nadezhda A. Bokach. "Copper(II)-Mediated Iodination of 1-Nitroso-2-naphthol." Molecules 26, no. 18 (2021): 5708. http://dx.doi.org/10.3390/molecules26185708.

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The 3-Iodo-1-nitrosonaphthalene-2-ol (I-NON) was obtained by the copper(II)-mediated iodination of 1-nitroso-2-naphthol (NON). The suitable reactants and optimized reaction conditions, providing 94% NMR yield of I-NON, included the usage of Cu(OAc)2·H2O and 1:2:8 CuII/NON/I2 molar ratio between the reactants. The obtained I-NON was characterized by elemental analyses (C, H, N), high-resolution ESI+-MS, 1H and 13C{1H} NMR, FTIR, UV-vis spectroscopy, TGA, and X-ray crystallography (XRD). The copper(II) complexes bearing deprotonated I-NON were prepared as follows: cis-[Cu(I-NON–H)(I-NON)](I3) (1
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Sir�n, Heli, and Marja-Liisa Riekkola. "Separation and determination of metals as complexes of 1-nitroso-2-naphthol-6-sulphonic and 2-nitroso-1-naphthol-6-sulphonic acids." Mikrochimica Acta 90, no. 3-4 (1986): 159–73. http://dx.doi.org/10.1007/bf01364298.

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antoniadou, S., A. D. Jannakoudakis, P. Karabinas, and E. Theodoridou. "Electromodification of carbon-fibre electrodes by 2-nitroso-1-naphthol." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 207, no. 1-2 (1986): 203–11. http://dx.doi.org/10.1016/0022-0728(86)87072-3.

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A., K. BANERJEE, K. GHOSH MONOJIT, K. SINHA SAILENDRA, and K. ROY S. "Alkali Metal Complexes. Binuclear Alkali Metal Complexes with Magnesium(II) and Zinc(II) Acetylacetonates." Journal of Indian Chemical Society Vol. 62, Apr 1985 (1985): 272–74. https://doi.org/10.5281/zenodo.6324541.

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Chemistry Department, Patna University, Patna-800 005 <em>Manuscript received 16 June 1983, accepted 30 April 1985</em> Heterobinuclear alkali metal complexes have been synthesised by treating metal chelates of magnesium and zinc acetylacetonates with alkali metal salts of 1-nitroso&shy;-2-naphthol and 8-hydroxyquinoline in ethanol/benzene-ethanol mixture. The general formula of the complex has been established as [M<sub>&alpha;&nbsp;</sub>(acac)<sub>2</sub>&nbsp;M<sub>b</sub>L], where M<sub>&alpha;</sub>&nbsp;-magnesium or zinc, acac<em>- </em>acetylacetonate, and M<sub>b</sub>L -Li, Na and K
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Aljaar, N., S. M. Fraihat, A. Alothman, and N. A. Khalaf. "Microwave-assisted Synthesis of 2-Substituted Naphtho[1,2-d][1,3]oxazoles by Reacting 1-Nitroso-2-naphthol with Allyl Bromides and Benzyl Bromides using FeCl3 as Catalyst." Asian Journal of Chemistry 32, no. 8 (2020): 2038–42. http://dx.doi.org/10.14233/ajchem.2020.22745.

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Efficient and improved preparation of 2-substituted[1,2-d][1,3]oxazoles by the reaction of 1-nitroso-2-naphthol and allyl bromides, benzyl bromides under microwave condition utilizing FeCl3 as a catalyst with yield ranging from 32% to 72%. Reaction with bromo acetonitrile yields the corresponding 2-cyanonaphthoxazole with 58% yield.
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Sirén, H. M. M., and M. M. Shapi. "Thermal behavior and ir absorption spectra of the sodium salts of 1-nitroso-2-naphthol-6-sulfonic acid and 2-nitroso-1-naphthol-6-sulfonic acid." Thermochimica Acta 102 (June 1986): 239–44. http://dx.doi.org/10.1016/0040-6031(86)85330-8.

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Books on the topic "1-Nitroso-2-naphthol"

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Turner, Richard. Iron complexes of 1-Nitroso-2-Naphthol-3,6-Disulphonic Acid Disodium Salt. 1986.

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Book chapters on the topic "1-Nitroso-2-naphthol"

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Ulrich, H. "From Phenols and 1-Nitroso-2-naphthol." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00134.

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Urleb, U., and S. Gobec. "From Benzene-1,2-diamine and 1-Nitroso-2-naphthol." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-01130.

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Kumar, Chandan. "The Synthesis, Spectral and Antimicrobial Study of Heterobinuclear Complexes of Copper (II) Schiff Base with Alkali Metals Salts." In Progress in Chemical and Biological Science. Lincoln University College, Malaysia, 2023. http://dx.doi.org/10.31674/book.2023pcbs004.

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The condensation reaction of a primary amine with carbonyl compounds results in a Schiff base, which is effectively incorporated in the preparation of metal complexes. Herein, a series of hetero binuclear complexes have been synthesized of the general formula CuPS.ML, where PS = Schiff base prepared by condensation of salicylaldehyde and propylene diamine; ML = Li, Na or K salts of 2-nitrophenol; 2,4-dinitrophenol; 2,4,6- trinitrophenol &amp; 1-nitroso-2-naphthol. The compounds are generally soluble in most of the organic solvents but insoluble in water. These complexes have been characterized
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