Thermodynamics of hydroxo complex formation of dialkyltin(IV) ions in aqueous solution

1989 ◽  
pp. 773 ◽  
Author(s):  
Giuseppe Arena ◽  
Roberto Purrello ◽  
Enrico Rizzarelli ◽  
Antonio Gianguzza ◽  
Lorenzo Pellerito
Keyword(s):  
Aqueous Solution ◽  
Complex Formation ◽  
Hydroxo Complex

scholarly journals Insertion of Unsaturated C–C Bonds into the O–H Bond of an Iridium(III)-Hydroxo Complex: Formation of Phosphorescent Emitters with an Asymmetrical β-Diketonate Ligand

2020 ◽  
Vol 59 (21) ◽  
pp. 15877-15887
Author(s):  
Pierre-Luc T. Boudreault ◽  
Miguel A. Esteruelas ◽  
Ana M. López ◽  
Enrique Oñate ◽  
Esther Raga ◽  
...  
Keyword(s):  
Complex Formation ◽  
Hydroxo Complex

Schiff base equilibria. II. Beryllium complexes of N-n-butylsalicylideneimine and the hydrolysis of the Be2+ ion

1965 ◽  
Vol 18 (5) ◽  
pp. 651 ◽  
Author(s):  
RW Green ◽  
PW Alexander
Keyword(s):  
Aqueous Solution ◽  
Schiff Base ◽  
Complex Formation ◽  
Distribution Coefficient ◽  
Dilute Aqueous Solution ◽  
The Stability ◽  
Ph Range ◽  
Hydrolysis Of ◽  
Beryllium Complexes ◽  
Equilibria In Aqueous Solution

The Schiff base, N-n-butylsalicylideneimine, extracts more than 99.8% beryllium into toluene from dilute aqueous solution. The distribution of beryllium has been studied in the pH range 5-13 and is discussed in terms of the several complex equilibria in aqueous solution. The stability constants of the complexes formed between beryllium and the Schiff base are log β1 11.1 and log β2 20.4, and the distribution coefficient of the bis complex is 550. Over most of the pH range, hydrolysis of the Be2+ ion competes with complex formation and provides a means of measuring the hydrolysis constants. They are for the reactions: Be(H2O)42+ ↔ 2H+ + Be(H2O)2(OH)2, log*β2 - 13.65; Be(H2O)42+ ↔ 3H+ + Be(H2O)(OH)3-, log*β3 -24.11.

Complex Formation in the Ternary System Tl(III)−CN-−Cl-in Aqueous Solution. A205Tl NMR Study

1996 ◽  
Vol 35 (24) ◽  
pp. 7074-7081 ◽  
Author(s):  
Katja E. Berg ◽  
Johan Blixt ◽  
Julius Glaser
Keyword(s):  
Aqueous Solution ◽  
Complex Formation ◽  
Ternary System ◽  
Nmr Study

scholarly journals Chemical Properties of Element 105 in Aqueous Solution: Halide Complex Formation and Anion Exchange into Triisoctyl Amine

1989 ◽  
Vol 48 (3-4) ◽  
Author(s):  
J. V. Kratz ◽  
H. P. Zimmermann ◽  
U. W. Scherer ◽  
M. Schädel ◽  
W. Brüchle ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Complex Formation ◽  
Anion Exchange ◽  
Chemical Properties ◽  
Halide Complex

Uranyl(VI) complexes with alpha-substituted carboxylic acids in aqueous solution

2003 ◽  
Vol 91 (1) ◽  
Author(s):  
H. Moll ◽  
G. Geipel ◽  
T. Reich ◽  
G. Bernhard ◽  
Th. Fanghänel ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Complex Formation ◽  
Carboxylic Acids

SummaryThe complex formation in the binary uranium(VI)-glycolate, -

Ferricyanide Oxidation of Butanol Homogeneously Catalysed by Chlororuthenium Complexes

1979 ◽  
Vol 32 (9) ◽  
pp. 1905 ◽  
Author(s):  
AF Godfrey ◽  
JK Beattie
Keyword(s):  
Aqueous Solution ◽  
Complex Formation ◽  
Linear Dependence ◽  
Rate Constants ◽  
Homogeneous Catalyst ◽  
Basic Solution ◽  
Rate Law ◽  
Kinetics Of ◽  
Solution Estimates ◽  
Butanol Concentration

The oxidation of butan-1-ol by ferricyanide ion in alkaline aqueous solution is catalysed by solutions of ruthenium trichloride hydrate. The kinetics of the reaction has been reinvestigated and the data are consistent with the rate law -d[FeIII]/dt = [Ru](2k1k2 [BuOH] [FeIII])/(2k1 [BuOH]+k2 [FeIII]) This rate law is interpreted by a mechanism involving oxidation of butanol by the catalyst (k1) followed by reoxidation of the catalyst by ferricyanide (k2). The non-linear dependence of the rate on the butanol concentration is ascribed to the rate-determining, butanol-independent reoxidation of the catalyst, rather than to the saturation of complex formation between butanol and the catalyst as previously claimed. Absolute values of the rate constants could not be determined, because some of the ruthenium precipitates from basic solution. With K3RuCl6 as the source of a homogeneous catalyst solution, estimates were obtained at 30�0�C of k1 = 191. mol-1 s-1 and k2 = 1�4 × 103 l. mol-1 s-1.

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