Works matching DE "NITROSYL chloride"
Results: 32
Intensification of Opening a Thrust Alloy Based on Platinum and Rhodium.
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- Inorganic Materials, 2024, v. 60, n. 1, p. 78, doi. 10.1134/S0020168524700110
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Modulation of Uptake and Reactivity of Nitrogen Dioxide in Metal‐Organic Framework Materials.
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- Angewandte Chemie, 2023, v. 135, n. 28, p. 1, doi. 10.1002/ange.202302602
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XRD and EXAFS study of nitrato ammine complexes of nitrosyl ruthenium.
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- Journal of Structural Chemistry, 2010, v. 51, p. 73, doi. 10.1007/s10947-010-0192-y
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Synthesis and crystal structure of nitrosoruthenium aquadiammine complex, [Ru(NO)(NH<sub>3</sub>)<sub>2</sub>Cl<sub>2</sub>(H<sub>2</sub>O)]Cl·H<sub>2</sub>O.
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- Journal of Structural Chemistry, 2006, v. 47, n. 2, p. 380, doi. 10.1007/s10947-006-0311-y
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Electronic structures of tetragonal nitrido and nitrosyl metal complexes.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2008, v. 119, n. 1-3, p. 35, doi. 10.1007/s00214-006-0236-8
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Mechanochemistry of the 5f-element compounds.
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- Journal of Radioanalytical & Nuclear Chemistry, 2007, v. 274, n. 3, p. 473, doi. 10.1007/s10967-006-6926-9
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S-nitrosylation of NADPH oxidase regulates cell death in plant immunity.
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- Nature, 2011, v. 478, n. 7368, p. 264, doi. 10.1038/nature10427
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Synthesis and Characterization of Nitrosyl[tris(3,5dimethylpyrazolyl)borato]molybdenum Complexes Containing Aryloxo, Arylamido and Arylcyano Ligands.
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- Turkish Journal of Chemistry, 2005, v. 29, n. 3, p. 225
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Theoretical Comparison of the Bonding in CpCr(CO) 2 (N X ) [ X = O, S, Se, Te].
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- Journal of Coordination Chemistry, 2002, v. 55, n. 6, p. 627, doi. 10.1080/00958970290027480
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Novel azo dyes derived from phthalimide. Part 1: Synthesis and spectroscopic properties.
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- Coloration Technology, 2008, v. 124, n. 2, p. 92, doi. 10.1111/j.1478-4408.2008.00127.x
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Structural analysis of 5-[thiazol-2-yldiazenyl]pyrimidine-2,4,6(1 H,3 H,5 H)-trione in both solid state and solution.
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- Coloration Technology, 2008, v. 124, n. 2, p. 111, doi. 10.1111/j.1478-4408.2008.00130.x
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Metastable States of Ruthenium Nitrosyl Complexes. Density Functional Quantum-Chemical Calculations.
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- Russian Journal of General Chemistry, 2004, v. 74, n. 3, p. 317, doi. 10.1023/B:RUGC.0000030383.74873.1f
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A Novel Route to One-step Formation of ɛ-caprolactam from Cyclohexane and Nitrosyl Sulfuric Acid Catalyzed by VPO Composites.
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- Catalysis Letters, 2007, v. 118, n. 1/2, p. 129, doi. 10.1007/s10562-007-9168-8
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Design of Highly Efficient and Selective Transfer Reaction of Nitrosyl Group to dC and d M C Resulting in Specific Deamination.
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- Nucleosides, Nucleotides & Nucleic Acids, 2005, v. 24, n. 5-7, p. 721, doi. 10.1081/NCN-200060312
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Nitric Oxide and Mitochondrial Complex IV.
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- IUBMB Life, 2003, v. 55, n. 10/11, p. 605, doi. 10.1080/15216540310001628726
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Anhydrous Dinitrogen Trioxide Solutions for Brønsted Acid Free Nitrous Acid Chemistry.
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- European Journal of Inorganic Chemistry, 2017, v. 2017, n. 46, p. 5461, doi. 10.1002/ejic.201701091
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Double Photoionization of Nitrosyl Chloride by Synchrotron Radiation in the 24–70 eV Photon Energy Range.
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- Molecules, 2023, v. 28, n. 13, p. 5218, doi. 10.3390/molecules28135218
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A compact, high-purity source of HONO validated by Fourier Transform Infrared and Thermal Dissociation Cavity Ring-down Spectroscopy.
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- Atmospheric Measurement Techniques Discussions, 2020, p. 1, doi. 10.5194/amt-2020-92
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A compact, high-purity source of HONO validated by Fourier transform infrared and thermal-dissociation cavity ring-down spectroscopy.
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- Atmospheric Measurement Techniques, 2020, v. 13, n. 8, p. 4159, doi. 10.5194/amt-13-4159-2020
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Density functional theory of the iron–nitrosyl (S = 3/2) complex.
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- International Journal of Quantum Chemistry, 2005, v. 105, n. 5, p. 511, doi. 10.1002/qua.20734
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Ab initio and DFT modeling of stereoselective deamination of aziridines by nitrosyl chloride.
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- International Journal of Quantum Chemistry, 2005, v. 102, n. 2, p. 139, doi. 10.1002/qua.20364
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Homoleptic Gold Acetonitrile Complexes with Medium to Very Weakly Coordinating Counterions: Effect on Aurophilicity?
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- Chemistry - A European Journal, 2016, v. 22, n. 42, p. 15085, doi. 10.1002/chem.201602797
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Nitrosochlorination of 2-alkylideneadamantanes.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 3, p. 325, doi. 10.1134/S1070428015030069
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Transformations of gem-dichloroarylcyclopropanes in the reaction with NOCl·2SO. Synthesis of 3-aryl-5-chloroisoxazoles.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 2, p. 186, doi. 10.1134/S1070428013020024
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Δ<sup>2</sup>-isoxazolines from arylcyclopropanes: III. Phenylcyclopropanes substituted in three-membered ring in reaction with nitrosyl chloride activated with oxides of sulfur(IV, VI).
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- Russian Journal of Organic Chemistry, 2009, v. 45, n. 2, p. 218, doi. 10.1134/S1070428009020110
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2-isoxazolines from arylcyclopropanes: I. Monoarylcyclopropanes in a reaction with nitrosyl chloride activated by sulfur(IV) oxide.
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- Russian Journal of Organic Chemistry, 2006, v. 42, n. 2, p. 249, doi. 10.1134/S1070428002120163
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Synthesis of 4,5-Dihydroisoxazoles from Arylcyclopropanes and Nitrosyl Chloride.
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- Russian Journal of Organic Chemistry, 2003, v. 39, n. 7, p. 1021, doi. 10.1023/B:RUJO.0000003196.89457.a4
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In vitro and in vivo antiproliferative and trypanocidal activities of ruthenium NO donors.
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- British Journal of Pharmacology, 2007, v. 152, n. 1, p. 112, doi. 10.1038/sj.bjp.0707363
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Paramagnetic nitrosyliron adducts in pentasilic zeolites: an EPR study.
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- Research on Chemical Intermediates, 2003, v. 29, n. 7-9, p. 805, doi. 10.1163/156856703322601816
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Deactivation of Ru/Al<sub>2</sub>O<sub>3</sub> Catalyst for Preferential CO Oxidation in the Presence of Low-concentration NH<sub>3</sub> by Nitrosyl Species.
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- Chemistry Letters, 2006, v. 35, n. 7, p. 13, doi. 10.1246/cl.2006.734
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One-Step Synthesis of the Vicinal Dinitroguaianolides Achillin and Grossmisin.
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- Chemistry of Natural Compounds, 2003, v. 39, n. 4, p. 362, doi. 10.1023/B:CONC.0000003417.79920.8d
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ELECTRON IMPACT DISSOCIATIVE IONIZATION OF NITROSYL CHLORIDE.
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- Modern Physics Letters B, 2012, v. 26, n. 11, p. 1250065-1, doi. 10.1142/S0217984912500650
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