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1

Larin, Vasil’, and Serghiy Shapovalov. "Association of Complex Ferrumcyanide Anions with Pinacyanol Cation in Aqueous Solution." Chemistry & Chemical Technology 6, no. 1 (2012): 25–29. http://dx.doi.org/10.23939/chcht06.01.025.

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2

Zhang, Jixi. "The Theoretical Calculation of the Cu Isotope Fractionation Effect in Solution/Hydrothermal Solution Systems." Molecules 29, no. 11 (2024): 2582. http://dx.doi.org/10.3390/molecules29112582.

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Abstract: Copper (Cu) is an important transition metal, and its isotopes have important applications in geology, environmental science, soil science, and other fields. Cu isotope fractionation can occur in many natural processes. However, the mechanism of Cu isotope fractionation in solution/hydrothermal solution systems is not very clear. In this study, the fractionation effects of complexes of Cu(I) and Cu(II) in solution/hydrothermal solution systems were systematically studied by means of an ab initio method based on first principles. In the simulation of an aqueous solution system, the th
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3

Safarmamadov, Safarmamad M., Dilovar Ch Mirzokhonov, and Kimyo S. Mabatkadamzoda. "The COMPLEX FORMATION OF CADMIUM (II) WITH 2-METHYLIMIDAZOLE IN AQUEOUS AND AQUEOS-ALCOHOL SOLUTIONS." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 63, no. 10 (2020): 36–45. http://dx.doi.org/10.6060/ivkkt.20206310.6201.

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Using potentiometric titration data, titration curves of the protonated form of 2-methylimidazole [H2-MI]+ in water and water-alcohol solutions were constructed. Forms of formation curves correspond to weak monobasic acids. The value of the formation function () for the studied systems varies between 0.45-0.87, which corresponds to the formation of one protonated form of 2-methylimidazole in aqueous and aqueous - alcoholic solutions. The acid dissociation constant (pKa) of 2-methylimidazole at 298 K was determined by the pH - metric method in aqueous and aqueous - methanol (ethanol) solutions
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4

Jacobsen, Frank, Jerzy Holcman, and Knud Sehested. "Manganese(II)−Superoxide Complex in Aqueous Solution." Journal of Physical Chemistry A 101, no. 7 (1997): 1324–28. http://dx.doi.org/10.1021/jp962867i.

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5

Miladinova, Elisaveta. "Molecular dynamic study of the stability of oxytocin - divalent zinc complex in aqueous solution." SDRP Journal of Computational Chemistry & Molecular Modelling 3, no. 1 (2019): 1–10. http://dx.doi.org/10.25177/jccmm.3.1.sc.494.

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6

Rajamohan, Rajaram, Sundarajulu Kothai Nayaki та Meenakshisundaram Swaminathan. "Spectrofluorimetric Study on Inclusion Complexation of 2-Amino-6-fluorobenzothiazole with β-Cyclodextrin". Collection of Czechoslovak Chemical Communications 73, № 2 (2008): 147–60. http://dx.doi.org/10.1135/cccc20080147.

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The interaction between 2-amino-6-fluorobenzothiazole (AFBT) and β-cyclodextrin (β-CDx) has been investigated in aqueous solution and in the solid state. The stoichiometry and binding constant of the complex between AFBT and β-CDx in solution were determined by steady-state and time-resolved fluorescence spectroscopy. The FT-IR spectral data and SEM images of the solid complex confirmed the formation of inclusion complex. The proton transfer behaviour of AFBT has been investigated in aqueous and β-CDx solutions.
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7

Zhang, Jixi. "Gallium Isotope Effect of Ga-Si Complex Solutions in Water: Theoretical Study Based on Density Functional Theory." Water 16, no. 12 (2024): 1680. http://dx.doi.org/10.3390/w16121680.

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A Ga isotope is a new proxy for different geochemical processes such as a weathering process, solution process, etc. Si (Si(OH)4) is ubiquitous in natural water bodies. However, studies on the Ga isotope effect about a Ga3+ aqueous solution reacting with Si (Si(OH)4) are lacking. In this study, the Ga isotope effect of this process will be studied using a theoretical calculation method based on first principles. The results show that the heavy Ga (71Ga) isotope enrichment ability of different Ga-Si complex solutions is different. The 1000lnβ (‰) sequence of different Ga-Si complex solutions is
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8

Chatziefthimiou, Spyros D., Mario Inclán, Petros Giastas, Athanasios Papakyriakou, Konstantina Yannakopoulou та Irene M. Mavridis. "Molecular recognition of N-acetyltryptophan enantiomers by β-cyclodextrin". Beilstein Journal of Organic Chemistry 13 (9 серпня 2017): 1572–82. http://dx.doi.org/10.3762/bjoc.13.157.

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The enantioselectivity of β-cyclodextrin (β-CD) towards L- and D-N-acetyltryptophan (NAcTrp) has been studied in aqueous solution and the crystalline state. NMR studies in solution show that β-CD forms complexes of very similar but not identical geometry with both L- and D-NAcTrp and exhibits stronger binding with L-NAcTrp. In the crystalline state, only β-CD–L-NAcTrp crystallizes readily from aqueous solutions as a dimeric complex (two hosts enclosing two guest molecules). In contrast, crystals of the complex β-CD–D-NAcTrp were never obtained, although numerous conditions were tried. In aqueo
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9

Gasparyan, F. V., L. F. Gasparyan, and V. V. Simonyan. "Dynamics of Charged Complex Molecules in Aqueous Solution." Journal of Contemporary Physics (Armenian Academy of Sciences) 57, no. 1 (2022): 98–103. http://dx.doi.org/10.3103/s1068337222010091.

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10

Webster, Lee, Malcolm B. Huglin, and Ian D. Robb. "Complex formation between polyelectrolytes in dilute aqueous solution." Polymer 38, no. 6 (1997): 1373–80. http://dx.doi.org/10.1016/s0032-3861(96)00650-7.

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11

Rodriguez, Jason, and Joseph Kremer. "Probing Chemical Environment Using Polymeric Reverse Micellar Solutions Which Sequester Inorganic Coordination Complex Fluorophores." Journal of the Pennsylvania Academy of Science 90, no. 1 (2016): 1–6. http://dx.doi.org/10.5325/jpennacadscie.90.1.0001.

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ABSTRACT A series of tris(bipyridine)ruthenium(II) chloride ([Ru(bpy)3]Cl2)-sequestered reverse micellar solutions of variable surfactant concentration were examined using fluorescence spectroscopy before and after thermal radical polymerization of the nonpolar phase. The [Ru(bpy)3]Cl2 emission spectra simulated aqueous solution chemical environments irrespective whether the nonpolar phase is liquid or polymerized into a solid. A range of surfactant concentrations were examined. Emission maxima of the reverse micelle solution-sequestered [Ru(bpy)3]Cl2 species are red-shifted with respect to aq
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12

Korchak, Sergey, Wolfgang Kilian, and Lorenz Mitschang. "Degeneracy in cryptophane–xenon complex formation in aqueous solution." Chemical Communications 51, no. 9 (2015): 1721–24. http://dx.doi.org/10.1039/c4cc08601e.

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13

Tyunina, Elena Yu, Valentin G. Badelin, and Valentina S. Egorkina. "INTERACTION OF NICOTINIC ACID WITH L-PHENYLALANINE IN BUFFER SOLUTIONS: HEAT CAPACITY AND VOLUME PROPERTIES STUDY." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 60, no. 4 (2017): 33. http://dx.doi.org/10.6060/tcct.2017604.5548.

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Thermodynamic and physicochemical properties of multicomponent aqueous solutions containing biologically active solutes are important in various areas of applied chemistry and are essential for understanding the chemistry of biological systems. Interactions between nicotinic acid (NA) and L-phenylalanine (Phe) were studied in aqueous phosphate buffer solutions (pH=7.35) by differential scanning calorimetry and volume methods. Heat capacities and densities of nicotinic acid-buffer, L-phenylalanine-buffer, and nicotinic acid-L-phenylalanine-buffer mixtures were determined at T=(288.15, 298.15, 3
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14

Kutsyk, A. M., O. O. Ilchenko, Ya M. Yuzvenko, V. V. Obukhovsky, and V. V. Nikonova. "Vibration Spectroscopy of Complex Formation in Aqueous Solutions of Isopropanol." Ukrainian Journal of Physics 63, no. 6 (2018): 506. http://dx.doi.org/10.15407/ujpe63.6.506.

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The formation of molecular complexes in isopropanol-water solutions is studied by means of vibrational spectroscopy techniques. The ATR FTIR spectra of solutions with different mixing ratios are detected. The multivariate curve resolution of the experimental data set shows that the investigated solution could be treated as a four-component mixture, which contains pure isopropanol, pure water, and two molecular complexes.
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15

Pham, Thu Thao, and Shin-ichi Yusa. "Thermo-Responsive Polyion Complex of Polysulfobetaine and a Cationic Surfactant in Water." Polymers 14, no. 15 (2022): 3171. http://dx.doi.org/10.3390/polym14153171.

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Poly(4-((3-methacrylamidopropyl)dimethylammonium)butane-1-sulfonate) (PSBP) was prepared via controlled radical polymerization. PSBP showed upper critical solution temperature (UCST) behavior in aqueous solutions, which could be controlled by adjusting the polymer and NaCl concentrations. Owing to its pendant sulfonate anions, PSBP exhibited a negative zeta potential of −7.99 mV and formed a water-soluble ion complex with the cationic surfactant cetyltrimethylammonium bromide (CTAB) via attractive electrostatic interaction. A neutral PSBP/CTAB complex was formed under equimolar concentrations
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16

Ding, Yuan Rong, Zhi Wei Li, He Qun Su, and Yang Ding. "Study on Viscosity of Poly(Acrylic Acid-Co-Acrylamide) Concentrated Solution with Different Potential Crosslinking Agent." Advanced Materials Research 311-313 (August 2011): 1157–60. http://dx.doi.org/10.4028/www.scientific.net/amr.311-313.1157.

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Poly(acrylic acid-co-acrylamide) has large number of ionic and nonionic hydrophilic groups, such making the rheological behavior of its solution complex. In this research, four different potential crosslinking agents which contains activating hydroxyl group and unsaturated bond were introduced into the poly(acrylic acid-co-acrylamide) polymer during aqueous solution radical polymerizations. Rotary viscosimeter was chosen to characterize the apparent viscosity of poly(acrylic acid-co-acrylamide) concentrated solutions. Temperature, concentration of the aqueous concentrated solutions and proport
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17

Fateev, A. I., S. I. Krivosheev, V. A. Kvitsinnsky, and T. G. Shendrik. "METHODS FOR THE DETERMINATION OF SODIUM IN THE PROCESS OF WATER WASHING OF SALTY COAL." Energy Technologies & Resource Saving, no. 1 (March 20, 2020): 19–26. http://dx.doi.org/10.33070/etars.1.2020.2.

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Coal with high content of alkaline and alkaline earth metals (salty coal) occupies its definite place in an energy reserve of the country. Standard methods to assess the dynamics of the release of salts (mainly sodium chloride) into the aqueous solution during the desalting of salty coal were used. The advantages and disadvantages of existing methods for determining the sodium content in aqueous solutions are considered. The principle of operation of the upgraded spectral complex KSVU-5 based on the determination of the content of alkali metals in aqueous solutions by the method of atomic emis
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18

Driscoll, Darren M., Frankie D. White, Subhamay Pramanik, et al. "Observation of a promethium complex in solution." Nature 629, no. 8013 (2024): 819–23. http://dx.doi.org/10.1038/s41586-024-07267-6.

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AbstractLanthanide rare-earth metals are ubiquitous in modern technologies1–5, but we know little about chemistry of the 61st element, promethium (Pm)6, a lanthanide that is highly radioactive and inaccessible. Despite its importance7,8, Pm has been conspicuously absent from the experimental studies of lanthanides, impeding our full comprehension of the so-called lanthanide contraction phenomenon: a fundamental aspect of the periodic table that is quoted in general chemistry textbooks. Here we demonstrate a stable chelation of the 147Pm radionuclide (half-life of 2.62 years) in aqueous solutio
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19

J, PRASAD, SRIVASTAVA KRISHNA, SRIVASTAVA DIVYA, J. UKPONG E., and B. PANDEYA KRISHNA. "Cyclic Voltammetric Studies of Mixed-valence Copper(I,II) D-Penicillamine Complexes in Aqueous Medium." Journal of Indian Chemical Society Vol. 70, Nov-Dec 1993 (1993): 973–76. https://doi.org/10.5281/zenodo.5948169.

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Department of Chemistry, University of Allahabad, Allahabad-211 002 Department of Chemistry, A. P. S. University, Rewa-486 003 <em>Manuscript received 29 August 1993</em> The cyclic voltammetric studies of complex species formed in aqueous solutions between copper(II) and D-penicillamine under different experimental conditions have been made. The cyclic votammograms for the yellow copper(I)-D-penicillamine and red-violel mixed-valence copper-D-penicillamine complex are quite different from each other. The cyclic voltammetric parameters are calculated and the results are discussed.
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20

Leung, Bonnie O., Farideh Jalilehvand, and Vicky Mah. "Mercury(ii) penicillamine complex formation in alkaline aqueous solution." Dalton Transactions, no. 41 (2007): 4666. http://dx.doi.org/10.1039/b711436b.

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21

Ting-Chia, Huang, and Lin Yih-Kung. "Ion-exchange equilibria involving complex formation in aqueous solution." Journal of Membrane Science 34, no. 2 (1987): 127–39. http://dx.doi.org/10.1016/s0376-7388(00)80027-7.

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22

Jalilehvand, Farideh, Zahra Amini, Karnjit Parmar, and Eun Young Kang. "Cadmium(ii) N-acetylcysteine complex formation in aqueous solution." Dalton Transactions 40, no. 47 (2011): 12771. http://dx.doi.org/10.1039/c1dt11705j.

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23

Connors, Kenneth A. "Population Characteristics of Cyclodextrin Complex Stabilities in Aqueous Solution." Journal of Pharmaceutical Sciences 84, no. 7 (1995): 843–48. http://dx.doi.org/10.1002/jps.2600840712.

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24

Kuter, David, Victor Streltsov, Natalia Davydova, Gerhard Venter, Kevin Naidoo, and Timothy Egan. "Characterization of Chloroquine-Ferriheme Solution Structure Using EXAFS and MD." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C721. http://dx.doi.org/10.1107/s205327331409278x.

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The complex formed between the antimalarial drug chloroquine (CQ) and its target iron(III)protoporphyrin IX (ferriheme) in aqueous solution is of considerable importance in understanding its mechanism of antimalarial activity. Recently, convincing evidence showed that CQ induces the μ-oxo dimeric form of ferriheme in aqueous solution, but the structure of this complex in solution is uncertain.[1] Molecular dynamics (MD) simulations in aqueous solution were used to model the structure of μ-oxo ferriheme and two possible conformations of the CQ-ferriheme complex, one in which CQ π-stacked with t
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25

Jia, Xiang Feng, Xing Wang Shi, and Yong Shan Ma. "The Organic-Inorganic Complex Material Formed by {Mo154} and TTABr." Advanced Materials Research 236-238 (May 2011): 2032–35. http://dx.doi.org/10.4028/www.scientific.net/amr.236-238.2032.

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The formation of inorganic/organic Complex Material from giant polyoxomolybdate (POM) macro-anions in solutions mixed a positively charged surfactant tetradecyltrimethylammonium bromide (TTA+Br-1) was described.surfactant tetradecyltrimethylammonium bromide (TTA+Br-1) was described. The complex can further dissolve in aqueous solution with the excess TTABr and the larger hydrophilicaggregations formed. TEM and Dynamic Light Scattering (DLS) investigations were applied to analyze the aggregations in the simple-phase solution.
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26

Md., Munsur Rahman. "Mechanistic studies on the reactions of iodopentaammineruthenium(III) complex cation and thiocyanate ion in aqueous solution." Journal of Indian Chemical Society Vol. 76, Apr 1999 (1999): 188–90. https://doi.org/10.5281/zenodo.5848183.

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Department of Chemistry, University of Kalyani, Kalyani-741 235, India <em>Manuscript received 14 July 1998, accepted 8 December 1998</em> The substitution of iodide ion by thiocyanate ion in the iodopentaammineruthenium(III) complex cation in aqueous solution has been investigated at 35-50&ordm;. Rate increases linearly with thiocyanate ion concentration having a positive intercept on the rate axis. The intercept gives the aquation rate constant of the iodo complex, and the slope represents thiocyanate anation rate. The rate was compared with the thiocyanate anation rate of the aqua complex b
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27

Smolko, Vitaly, and Elizaveta Antoshkina. "Measurement of Complex Dielectric Permittivity of Quartz Systems." Materials Science Forum 946 (February 2019): 129–33. http://dx.doi.org/10.4028/www.scientific.net/msf.946.129.

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The article describes the problem of the experimental determination of complex dielectric permittivity for natural, activated, and modified quartz systems. The results of determination of specific surface, complex dielectric permittivity, sands porosity are presented in this article. The authors obtained the empirical equation of complex dielectric permittivity calculation for natural, activated, and modified quartz sands, taking into account the effect of moisture, specific surface, porosity, impurities content into consideration. The modification of the sand surface by means of mechanical be
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28

Prostomolotov, Anatoly I., Nataliya A. Verezub, Natalia A. Vasilyeva, and Alexey E. Voloshin. "Hydrodynamics and Mass Transfer during the Solution Growth of the K2(Co,Ni)(SO4)2•6H2O Mixed Crystals in the Shapers." Crystals 10, no. 11 (2020): 982. http://dx.doi.org/10.3390/cryst10110982.

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Mathematical models of the hydrodynamics and mass transfer processes during the mixed crystal growth from low-temperature aqueous solutions have been analyzed. The features of these processes are caused by complex design of the crystallizer with a shaper. Two models of the solution flowing into the shaper have been considered. In the first model, the solution is fed to the central part of the crystal. The second model presents a peripheral solution supply along the shaper perimeter, which allows us to create a swirling flow. The calculation models correspond to laminar and turbulent regimes of
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29

Sunada, Satoshi, Masaru Kawagishi, and Kazuhiko Majima. "Corrosion Behavior of Pure Titanium Produced by MIM Process under SSRT Condition." Materials Science Forum 561-565 (October 2007): 2139–42. http://dx.doi.org/10.4028/www.scientific.net/msf.561-565.2139.

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Metal injection molding (MIM) process has the advantage of better formability of three dimensional complex shape products with high density and high performance properties compared to the ingot metallurgy (I/M) process. Two kinds of pure titanium specimens, i.e., the first one is prepared by the I/M process and the second one is prepared by MIM process are used in this experiment, and their corrosion behavior under stress has been investigated in several aqueous solutions by Slow Strain Rate Tensile (SSRT) test. Both I/M and MIM specimens showed good corrosion resistance in the aqueous solutio
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30

Yao, Takeshi. "Synthesis of functional ceramic materials from aqueous solutions." Journal of Materials Research 13, no. 5 (1998): 1091–98. http://dx.doi.org/10.1557/jmr.1998.0150.

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Methods for synthesizing ceramic materials from aqueous solutions at ordinary temperature and pressure are advantageous because of the applicability to making films with wide areas and/or complicated shapes with no requirement of vacuum or high temperature, and because of lower cost. Powder of ZrO2 or LnMeO3 (Ln = La, Nd; Me = Cr, Mn, Fe, Co) perovskite was dissolved in hydrofluoric acid and a solution of fluoro-complex ions was obtained. Boric acid was added to the solution, the fluoride ions were consumed by the formation of BF4-, and then the fluoro-complex ions were hydrolyzed to ZrO2 or L
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31

Petrovic, Goran, Blaga Stojceva-Radovanovic та O. Jovanovic. "Characterization of pesticide-β-cyclodextrin inclusion complexes in aqueous solution". Facta universitatis - series: Physics, Chemistry and Technology 3, № 2 (2005): 151–55. http://dx.doi.org/10.2298/fupct0502151p.

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The solubility of four different pesticides, "dimethoate", "simazine" "linuron" and "thiram", poorly soluble or non-soluble in water, were measured in water and in aqueous solution of ?-cyclodextrin by ultraviolet spectrophotometry. Standard water solutions of pesticides were prepared in the range of concentrations up to the maximum solubility of each pesticide in water. Concentrations of the pesticides were determined as absorbance on the absorption maximum. The obtained results show that the aqueous solution of ?-cyclodextrin was a powerful solubilizer of investigated pesticides due to the f
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32

Eriksson, Gunnar, and Erich Königsberger. "FactSage and ChemApp: Two tools for the prediction of multiphase chemical equilibria in solutions." Pure and Applied Chemistry 80, no. 6 (2008): 1293–302. http://dx.doi.org/10.1351/pac200880061293.

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The integrated thermochemical databank system FactSage enables the user to calculate equilibria and thermodynamic properties for a wide variety of multicomponent, multiphase systems and reactions. The Gibbs energy models and databases for condensed, gaseous, and aqueous solutions presently implemented in FactSage are of interest to chemical and physical metallurgy, chemical and corrosion engineering, inorganic and solution chemistry, geochemistry, environmental science, etc. Models for the aqueous phase include the Pitzer and Helgeson formalisms, but data and subroutines for concentrated aqueo
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33

M., UPADHYAY, GANGOPADHYAY S., and BANERJEA D. "Kinetics and Mechanism of Dissociation and Electroreduction (at DME) of the Copper(ll) and Nickel(II) Complexes of the Macrocyclic Ligand 1,3,6,9,11,14- Hexa-azacyclohexadecane ([16]-ane-N6) in Aqueous Solution." Journal of Indian Chemical Society Vol. 62, Dec 1985 (1985): 1029–32. https://doi.org/10.5281/zenodo.6326745.

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Department of Chemistry, Inorganic Chemistry Division, University College of Science, 92 Acharya P. C. Road, Calcutta-700 009 Acid catalysed dissociation of the title complexes have been studied spectrophoto&shy;metrically in aqueous perchlorate media. Both the complexes dissociate quite slowly ; the observed rate <em>for </em>the copper(II) complex corresponds to k<sub>obs</sub>&nbsp;= k<sub>o</sub> + KH[H<sup>+</sup>], but in the nickel(II) complex the acid dependent path is absent. The polarographic behaviour of the two complexes has also been studied using DME. In 0.1 <em>M </em>KCI soluti
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34

Samadov, Abdurasul Saidovich, Igor Georgievich Gorichev, Erkin Fathulloevich Faizulloev, and Vasilevich Kuzin Alexander. "COMPLEX FORMATION OF SILVER (I) WITH THIOSEMICARBAZIDE IN AQUEOUS SOLUTION." Вестник Таджикского национального университета. Серия естественных наук, no. 1 (2020): 200–207. http://dx.doi.org/10.51884/2413-452x_2020_1_200.

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35

Samadov, Abdurasul Saidovich, Igor Georgievich Gorichev, Erkin Fathulloevich Faizulloev, and Alexander Vasilevich Kuzin. "COMPLEX FORMATION OF SILVER (I) WITH THIOSEMICARBAZIDE IN AQUEOUS SOLUTION." Вестник Таджикского национального университета. Серия естественных наук, no. 1 (2020): 200–207. http://dx.doi.org/10.51884/2413-452x_2020_4_130.

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36

Chen, Xiao-ming. "Inclusion Complex of β-cyclodextrin with CTAB in Aqueous Solution". Chinese Journal of Chemical Physics 24, № 4 (2011): 484–88. http://dx.doi.org/10.1088/1674-0068/24/04/484-488.

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37

Jalilehvand, Farideh, Natalie S. Sisombath, Adam C. Schell, and Glenn A. Facey. "Lead(II) Complex Formation with l-Cysteine in Aqueous Solution." Inorganic Chemistry 54, no. 5 (2015): 2160–70. http://dx.doi.org/10.1021/ic5025668.

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38

Demicheli, Cynthia, Frédéric Frézard, Marc Lecouvey, and Arlette Garnier-Suillerot. "Antimony(V) complex formation with adenine nucleosides in aqueous solution." Biochimica et Biophysica Acta (BBA) - General Subjects 1570, no. 3 (2002): 192–98. http://dx.doi.org/10.1016/s0304-4165(02)00198-8.

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39

Bühl, Michael. "Molecular Dynamics of a Vanadate−Dipeptide Complex in Aqueous Solution†." Inorganic Chemistry 44, no. 18 (2005): 6277–83. http://dx.doi.org/10.1021/ic050694i.

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40

WEBSTER, LEE, and MALCOLM B. HUGLIN. "OBSERVATIONS ON COMPLEX FORMATION BETWEEN POLYELECTROLYTES IN DILUTE AQUEOUS SOLUTION." European Polymer Journal 33, no. 7 (1997): 1173–77. http://dx.doi.org/10.1016/s0014-3057(96)00295-9.

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41

Lopes-da-Silva, José A. "Thermorheological complex behaviour of maltosyl-chitosan derivatives in aqueous solution." Reactive and Functional Polymers 72, no. 9 (2012): 657–66. http://dx.doi.org/10.1016/j.reactfunctpolym.2012.06.011.

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42

Zeng, Birong, Xiongbin Zhu, Suihui Cai, and Zhong Chen. "Interactions between diperoxovanadate complex and amide ligands in aqueous solution." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 67, no. 1 (2007): 202–7. http://dx.doi.org/10.1016/j.saa.2006.07.003.

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43

Mah, Vicky, and Farideh Jalilehvand. "Mercury(II) complex formation with glutathione in alkaline aqueous solution." JBIC Journal of Biological Inorganic Chemistry 13, no. 4 (2008): 541–53. http://dx.doi.org/10.1007/s00775-008-0342-2.

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Chun, Myung-Kwan, and Hoo-Kyun Choi. "Preparation and characterization of enrofloxacin/carbopol complex in aqueous solution." Archives of Pharmacal Research 27, no. 6 (2004): 670–75. http://dx.doi.org/10.1007/bf02980168.

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Di Bernardo, Plinio, Giuliana Tomat, Pierluigi Zanonato, Roberto Portanova, and Marilena Tolazzi. "Thermodynamics of vanadyl(IV)—carboxylate complex formation in aqueous solution." Inorganica Chimica Acta 145, no. 2 (1988): 285–88. http://dx.doi.org/10.1016/s0020-1693(00)83971-7.

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Toma, Henrique E., and Eduardo Stadler. "Electrochemical behaviour of a heme model complex in aqueous solution." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 235, no. 1-2 (1987): 179–87. http://dx.doi.org/10.1016/0022-0728(87)85206-3.

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Hu, Qili, Nan Chen, Chuanping Feng, and WeiWu Hu. "Nitrate adsorption from aqueous solution using granular chitosan-Fe3+ complex." Applied Surface Science 347 (August 2015): 1–9. http://dx.doi.org/10.1016/j.apsusc.2015.04.049.

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Branca, M. "Oxovanadium(IV) complex formation by simple sugars in aqueous solution." Journal of Inorganic Biochemistry 45, no. 3 (1992): 169–77. http://dx.doi.org/10.1016/0162-0134(92)80042-t.

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Abate, Lorenzo, Alessandro De Robertis, and Carmelo Rigano. "Complex formation between imidazole and carboxylate ligands in aqueous solution." Journal of Solution Chemistry 22, no. 4 (1993): 339–49. http://dx.doi.org/10.1007/bf00647206.

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Michaelis, Esther, Kazuteru Nonomura, Derck Schlettwein, Tsukasa Yoshida, Hideki Minoura, and Dieter Wöhrle. "Hybrid thin films of ZnO with porphyrins and phthalocyanines prepared by one-step electrodeposition." Journal of Porphyrins and Phthalocyanines 08, no. 12 (2004): 1366–75. http://dx.doi.org/10.1142/s1088424604000726.

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Abstract:
Hybrid thin films of crystalline zinc oxide and the zinc complex of 5,10,15,20-tetrakis-(4-sulfonatophenyl)porphyrin (ZnTPPS) have been prepared by cathodic electrodeposition from different aqueous zinc salt solutions. Films from a solution containing zinc nitrate and the porphyrin derivate show a rough surface and porosity, whereas films prepared from an oxygen-saturated zinc chloride solution were very smooth. The presence of the porphyrin derivative in the deposition solution has a clear influence on the morphology of the hybrid films compared with pure zinc oxide films. In aqueous zinc nit
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