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Hydrogen selenide in biological systems: from synthetic donors to fluorescent probes. [PDF]
Chem SciZhou Y +4 more
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Generating, visualizing and tuning π-π interactions in metal-induced supramolecular assembly.
CrystEngCommLe-Hoang G, Guénée L, Piguet C.
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Individual extraction constants of some organic cations in the two-phase water–nitrobenzene system
Journal of Radioanalytical and Nuclear Chemistry, 2010From extraction experiments and c-activity measurements, the exchange extraction constants corre- sponding to the general equilibrium C ? (aq) ? Cs ? (nb) , C ? (nb) ? Cs ? (aq) taking part in the two-phase water- nitrobenzene system (C ? = organic cation; aq = aqueous phase, nb = nitrobenzene phase) were evaluated.
E. Makrlík +3 more
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Collection of Czechoslovak Chemical Communications, 1984 The stability constants for the ML + complex species, where M + is an alkali metal cation and L is dibenzo-18-crown-6, in nitrobenzene saturated with water were calculated by employing published equilibrium data.
Emanuel Makrlík +2 more
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Zeitschrift für Physikalische Chemie, 2006
From extraction experiments and γ-activity measurements, the exchange extraction constants corresponding to the general equilibrium M+(aq) + NaL+(nb) ⇔ ML+(nb) + Na+(aq) taking place in the two–phase water–nitrobenzene system (M+ = Li+, K+, Rb+, Cs+; L = benzo-18-crown-6; aq = aqueous phase, nb = nitrobenzene phase) were evaluated.
E. Makrlík, P. Vaňura
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From extraction experiments and γ-activity measurements, the exchange extraction constants corresponding to the general equilibrium M+(aq) + NaL+(nb) ⇔ ML+(nb) + Na+(aq) taking place in the two–phase water–nitrobenzene system (M+ = Li+, K+, Rb+, Cs+; L = benzo-18-crown-6; aq = aqueous phase, nb = nitrobenzene phase) were evaluated.
E. Makrlík, P. Vaňura
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Journal of Radioanalytical and Nuclear Chemistry, 2010
From extraction experiments and c-activity measurements, the exchange extraction constants corresponding to the general equilibrium M(aq) ? Sr(nb) ¢ M(nb) ? Sr(aq) taking part in the two-phase water– nitrobenzene system (M = Mg, Ca, Ba, Cu, Zn, Cd, Pb, UO2þ 2 , Mn , Fe, Co, Ni; aq = aqueous phase, nb = nitrobenzene phase) were evaluated.
E. Makrlík, P. Vaňura
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From extraction experiments and c-activity measurements, the exchange extraction constants corresponding to the general equilibrium M(aq) ? Sr(nb) ¢ M(nb) ? Sr(aq) taking part in the two-phase water– nitrobenzene system (M = Mg, Ca, Ba, Cu, Zn, Cd, Pb, UO2þ 2 , Mn , Fe, Co, Ni; aq = aqueous phase, nb = nitrobenzene phase) were evaluated.
E. Makrlík, P. Vaňura
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Colloids and Surfaces A: Physicochemical and Engineering Aspects, 1997
Abstract General relationships were formulated among thermodynamic parameters characterizing complex-formation equilibria in both phases of a two-phase water-nitrobenzene extraction system and ion transfers across the interface of this system. Using these relationships and known parameters, the stability constants of Ni2+ with ethylenediamine and ...
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Abstract General relationships were formulated among thermodynamic parameters characterizing complex-formation equilibria in both phases of a two-phase water-nitrobenzene extraction system and ion transfers across the interface of this system. Using these relationships and known parameters, the stability constants of Ni2+ with ethylenediamine and ...
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Journal of Radioanalytical and Nuclear Chemistry, 1999
E. Makrlík, P. Vaňura, M. Daňková
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E. Makrlík, P. Vaňura, M. Daňková
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Journal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1983
Abstract The dynamic condenser method has been used for determination of Volta potentials in water-nitrobenzene partition systems, δ nw wn ψ (MX), as well as determining the difference between surface potentials Δ nw wn χ of both solvents. Values of Δ nw wn ψ o for several electrolytes have been measured and mutual consistency of these date ...
Zbigniew Koczorowski, Irwina Zagórska
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Abstract The dynamic condenser method has been used for determination of Volta potentials in water-nitrobenzene partition systems, δ nw wn ψ (MX), as well as determining the difference between surface potentials Δ nw wn χ of both solvents. Values of Δ nw wn ψ o for several electrolytes have been measured and mutual consistency of these date ...
Zbigniew Koczorowski, Irwina Zagórska
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