Kinetics of the Exchange Reaction between Carbon-14-labeled Carbonate and Carbonato-bis-(trimethylenediamine)-Cobalt(III) Complex in Aqueous Solution. Effect of Steric Hindrance in a Ligand Substitution Process

1958 ◽  
Vol 80 (4) ◽  
pp. 782-786 ◽  
Author(s):  
James E. Boyle ◽  
G. M. Harris
Keyword(s):  
Aqueous Solution ◽  
Exchange Reaction ◽  
Steric Hindrance ◽  
Ligand Substitution ◽  
Carbon 14 ◽  
Substitution Process ◽  
Kinetics Of

Kinetics of ligand exchange reaction of Cu(II)-ammine complex with poly(vinyl alcohol) in aqueous solution

Polymer ◽  
1983 ◽  
Vol 24 (3) ◽  
pp. 335-338 ◽  
Author(s):  
Tsuneo Suzuki ◽  
Hirofusa Shirai ◽  
Sonoko Tokutake ◽  
Nobumasa Hojo
Keyword(s):  
Aqueous Solution ◽  
Exchange Reaction ◽  
Ligand Exchange ◽  
Vinyl Alcohol ◽  
Poly Vinyl Alcohol ◽  
Ligand Exchange Reaction ◽  
Ammine Complex ◽  
Kinetics Of

scholarly journals Kinetics of the Reaction between Ni(tetren)2+and Bipyridine

2012 ◽  
Vol 1 (2) ◽  
pp. 39-45
Author(s):  
Lawrence Hugh Kolopajlo ◽  
Nekuma Korey Hollis ◽  
Ian Pendelton
Keyword(s):  
Aqueous Solution ◽  
Rate Constants ◽  
Substitution Reaction ◽  
Ternary Complex ◽  
Ligand Substitution ◽  
Hydrogen Ion ◽  
Rate Law ◽  
Kinetics Of ◽  
Ligand Substitution Reaction

We report a rate law, rate constants and a mechanism for the ligand substitution reaction between Ni(tetren)2+ and 2, 2'-bipyridine in aqueous solution at 25.0 0C. The rate law is: R = k [Ni(tetren2+)] [bipy]. The data supports a mechanism involving a hydrogen ion assisted pathway in which a ternary complex is not formed.

Kinetics and mechanism of the reaction of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione

1990 ◽  
Vol 55 (8) ◽  
pp. 1984-1990 ◽  
Author(s):  
José M. Hernando ◽  
Olimpio Montero ◽  
Carlos Blanco
Keyword(s):  
Aqueous Solution ◽  
Metal Ion ◽  
Activation Parameters ◽  
Enol Form ◽  
Kinetics And Mechanism ◽  
Kinetic Constants ◽  
Steric Factors ◽  
Kinetics Of ◽  
Mechanism Of The Reaction

The kinetics of the reactions of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione to form the corresponding monocomplexes have been studied spectrophotometrically in the range 5 °C to 16 °C at I 25 mol l-1 in aqueous solution. In the proposed mechanism for the two complexes, the enol form reacts with the metal ion by parallel acid-independent and inverse-acid paths. The kinetic constants for both pathways have been calculated at five temperatures. Activation parameters have also been calculated. The results are consistent with an associative activation for Fe(H2O)63+ and dissociative activation for Fe(H2O)5(OH)2+. The differences in the results for the complexes of heptanediones studied are interpreted in terms of steric factors.

Temperature Effect on the Two-Dimensional Phase Transition Kinetics of Adenine Adsorbed at the Hg Electrode/Aqueous Solution Interface

2003 ◽  
Vol 68 (8) ◽  
pp. 1407-1419 ◽  
Author(s):  
Claudio Fontanesi ◽  
Roberto Andreoli ◽  
Luca Benedetti ◽  
Roberto Giovanardi ◽  
Paolo Ferrarini
Keyword(s):  
Phase Transition ◽  
Aqueous Solution ◽  
Phase Change ◽  
Temperature Effect ◽  
Transition Rate ◽  
Effect Of Temperature ◽  
Two Dimensional ◽  
Solution Interface ◽  
Phase Transition Kinetics ◽  
Kinetics Of

The kinetics of the liquid-like → solid-like 2D phase transition of adenine adsorbed at the Hg/aqueous solution interface is studied. Attention is focused on the effect of temperature on the rate of phase change; an increase in temperature is found to cause a decrease of transition rate.

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