The Kinetics of Formation of Some Divalent Transition Metal-Dye Complexes, Studied by the Temperature-Jump Relaxation Method

1964 ◽  
Vol 3 (4) ◽  
pp. 520-522 ◽  
Author(s):  
R. G. Wilkins
1987 ◽  
Vol 41 (3) ◽  
pp. 402-407 ◽  
Author(s):  
Wan Peter Hsu ◽  
Ramesh C. Patel ◽  
Egon Matijevic

A calibration method based on absolute intensities of scattered light from colloidal silica was developed to standardize the stopped-flow temperature jump spectrophotometer (SFTJ). The need for such calibration was exemplified by the study of the temperature effect on the Rayleigh ratio changes during the formation of solid iron (hydrous) oxides.


1990 ◽  
Vol 68 (2) ◽  
pp. 278-281 ◽  
Author(s):  
M. A. Zon ◽  
H. Fernandez ◽  
L. Sereno ◽  
J. J. Silber

The kinetics of the Electron Donor–Acceptor (EDA) complex between N,N,N′,N′-tetramethyl-p-phenylenediamine and m-dinitrobenzene in acetonitrile has been studied by the temperature-jump technique. The magnitude of the rate constants of association and dissociation, although relatively large, is well below the diffusion control values. The calculated rates closely coincide with those obtained by chronoamperometry. An entropy control is suggested for this reaction. The results obtained in this work are useful to demonstrate that the concept about EDA complexes being formed by diffusion-controlled reactions should not be generalized. Keywords: electron donor–acceptor complexes, m-dinitrobenzene, N,N,N′,N′-tetramethyl-p-phenylenediamine, T-jump, kinetics.


1976 ◽  
Vol 54 (11) ◽  
pp. 1820-1826 ◽  
Author(s):  
Brian B. Hasinoff

The volumes of activation for the kinetics of the reaction of Cl− with Fe3+ and FeOH2+ have been determined by a laser temperature jump relaxation method at pressures up to 2.76 kbar. The results indicate that the two species, FeOH2+ and Fe3+, react with Cl− by different mechanisms. The activation volume for the binding of Cl− to FeOH2+ is positive (7.8 ± 1.0 cm3 mol−1), which is consistent with a dissociative interchange mechanism. The activation volume for the binding of Cl−1 to Fe3+ is negative (–4.5 ± 1.1 cm3 mol−1), which is consistent with an associative interchange mechanism.


1979 ◽  
Vol 44 (3) ◽  
pp. 912-917 ◽  
Author(s):  
Vladimír Macháček ◽  
Said A. El-bahai ◽  
Vojeslav Štěrba

Kinetics of formation of 2-imino-4-thiazolidone from S-ethoxycarbonylmethylisothiouronium chloride has been studied in aqueous buffers and dilute hydrochloric acid. The reaction is subject to general base catalysis, the β value being 0.65. Its rate limiting step consists in acid-catalyzed splitting off of ethoxide ion from dipolar tetrahedral intermediate. At pH < 2 formation of this intermediate becomes rate-limiting; rate constant of its formation is 2 . 104 s-1.


1986 ◽  
Vol 51 (12) ◽  
pp. 2786-2797
Author(s):  
František Grambal ◽  
Jan Lasovský

Kinetics of formation of 1,2,4-oxadiazoles from 24 substitution derivatives of O-benzoylbenzamidoxime have been studied in sulphuric acid and aqueous ethanol media. It has been found that this medium requires introduction of the Hammett H0 function instead of the pH scale beginning as low as from 0.1% solutions of mineral acids. Effects of the acid concentration, ionic strength, and temperature on the reaction rate and on the kinetic isotope effect have been followed. From these dependences and from polar effects of substituents it was concluded that along with the cyclization to 1,2,4-oxadiazoles there proceeds hydrolysis to benzamidoxime and benzoic acid. The reaction is thermodynamically controlled by the acid-base equilibrium of the O-benzylated benzamidoximes.


2021 ◽  
Vol 329 ◽  
pp. 115537
Author(s):  
Nazia Iqbal ◽  
S.M. Shakeel Iqubal ◽  
Aejaz Abdullatif Khan ◽  
Tasneem Mohammed ◽  
Ali Mohamed Alshabi ◽  
...  

2014 ◽  
Vol 16 (6) ◽  
pp. 2297-2304 ◽  
Author(s):  
Koffi P. C. Yao ◽  
Yi-Chun Lu ◽  
Chibueze V. Amanchukwu ◽  
David G. Kwabi ◽  
Marcel Risch ◽  
...  

Polyhedron ◽  
1995 ◽  
Vol 14 (10) ◽  
pp. 1299-1306 ◽  
Author(s):  
Ki-Young Choi ◽  
Dong Won Kim ◽  
Choon Pyo Hong

2021 ◽  
pp. 130612
Author(s):  
Eliara Acipreste Hudson ◽  
Hauster Maximiler Campos de Paula ◽  
Yara Luiza Coelho ◽  
Nícolas Glanzmann ◽  
Adilson David da Silva ◽  
...  

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