Solvent effect on the relative nucleofugalities of pyridines and phenoxide ions: Broensted-type plots in the pyridinolysis of 2,4-dinitrophenyl methyl carbonate and 2,4-dinitrophenyl acetate in aqueous ethanol

1986 ◽  
Vol 51 (26) ◽  
pp. 5072-5077 ◽  
Author(s):  
Enrique A. Castro ◽  
Maria T. Borquez ◽  
Paulina M. Parada
1965 ◽  
Vol 43 (6) ◽  
pp. 1770-1777 ◽  
Author(s):  
R. Anantaraman ◽  
K. Saramma

The rates of mercuric chloride catalyzed solvolysis of some alkyl chlorides in aqueous acetone and ethanol solvents have been compared. It is found that the increase in rate on changing from the acetone to the ethanol solvent is less in the catalyzed than in the normal reaction. On the basis that the electrophilic activity of the catalyst is less in aqueous ethanol than in aqueous acetone an explanation for the anomaly has been suggested. The effect, on the rates of solvolysis, of added chloride ions is in accord with the suggested explanation.


2004 ◽  
Vol 59 (11-12) ◽  
pp. 1600-1604 ◽  
Author(s):  
Jesús Pitarch López ◽  
Frank W. Heinemann ◽  
Andreas Grohmann

In the context of derivatisation studies of the pentaamine ligand 2,6-C5H3N[CMe(CH2NH2)2]2 (2-(6-(1,3-diamino-2-methylpropan-2-yl)pyridin-2-yl)-2-methylpropane-1,3-diamine, 1), we explored its zinc(II) coordination chemistry. With ZnBr2 in hot aqueous ethanol, in the absence of Lewis acid, the aqua complex [Zn(1)(H2O)]Br2 (2) is obtained, in which the pentaamine ligand acts as a square-pyramidal coordination cap. Single crystal structure data for the dihydrate of 2 are reported. In methanol solution, the complex is reactive towards carbon dioxide, and spectroscopic data (IR, 13C NMR) indicate the reversible formation of the dinuclear methyl carbonate complex [(Zn(1))2(μ2-(η1-O,η1-O)O2COCH3)]Br3.


2017 ◽  
Author(s):  
Belinda Slakman ◽  
Richard West

<div> <div> <div> <p>This article reviews prior work studying reaction kinetics in solution, with the goal of using this information to improve detailed kinetic modeling in the solvent phase. Both experimental and computational methods for calculating reaction rates in liquids are reviewed. Previous studies, which used such methods to determine solvent effects, are then analyzed based on reaction family. Many of these studies correlate kinetic solvent effect with one or more solvent parameters or properties of reacting species, but it is not always possible, and investigations are usually done on too few reactions and solvents to truly generalize. From these studies, we present suggestions on how best to use data to generalize solvent effects for many different reaction types in a high throughput manner. </p> </div> </div> </div>


2018 ◽  
Vol 25 (3) ◽  
pp. 253-259 ◽  
Author(s):  
Phanindra B. Kasi ◽  
Marta Kotorman ◽  
Attila Borics ◽  
Beata G. Hervay ◽  
Kinga Molnar ◽  
...  

1978 ◽  
Vol 43 (7) ◽  
pp. 1832-1837
Author(s):  
Rostislav Kudláček ◽  
Josef Cabicar ◽  
Milan Buňata
Keyword(s):  

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