Studies of catalysis in fluoride solutions

Measurements are reported of the catalytic effect of aqueous hydrogen fluoride and fluoride buffer solutions in the following eight reactions: the hydrolysis of diethyl acetal, the depoly­merization of paraldehyde, the decomposition of nitramide, the bromination of ethyl acetoacetate and of ethyl cyclo pentanone-2-carboxylate, the iodination of acetonylacetone and of acetone, and the dehydration of acetaldehyde hydrate. In the first two, which are specifically catalyzed by hydrogen ions, the catalytic effect of the fluoride systems corre­sponds to the calculated hydrogen-ion concentrations, and it is suggested that under some conditions fluoride buffer solutions may be particularly useful for controlling pH. In the remaining six reactions there is also general acid-base catalysis by hydrogen fluoride mole­cules, or by fluoride ions, or by both. The catalytic effects of these two species are close to those predicted by relations previously established for carboxylic acids and their anions. The bifluoride ion has approximately the same effect as hydrogen fluoride in acid catalysis but has no detectable catalytic effect as a base. These findings are discussed in terms of the structures and thermodynamic properties of the species concerned.

1980 ◽  
Vol 58 (2) ◽  
pp. 124-129 ◽  
Author(s):  
Y. Chiang ◽  
W. K. Chwang ◽  
A. J. Kresge ◽  
S. Szilagyi

Rates of hydrolysis of 1-ethoxy-3,3,5,5-tetramethylcyclopentene and 1-methoxy-2,3,3,5,5-pentamethylcyclopentene measured in mineral acid and formic and acetic acid buffer solutions show general acid catalysis and give large kinetic isotope effects in the normal direction (kH/kD > 1). This indicates that these reactions proceed by the conventional mechanism for vinyl ether hydrolysis in which proton transfer from the catalyzing acid to the substrate is rate-determining, and that the I-strain in these substrates is insufficiently great to shift the reaction mechanism to rapidly reversible substrate protonation followed by rate-determining hydration of the ensuing cationic intermediate.


1971 ◽  
Vol 124 (1) ◽  
pp. 117-122 ◽  
Author(s):  
G. Lowe ◽  
Y. Yuthavong

The pH-dependence of the Michaelis–Menten parameters for the papain-catalysed hydrolysis of N-acetyl-l-phenylalanylglycine p-nitroanilide was determined. The equilibrium binding constant, Ks, is independent of pH between 3.7 and 9.3, whereas the acylation constant, k+2, shows bell-shaped pH-dependence with apparent pKa values of 4.2 and 8.2. The effect of substituents in the leaving group on the acylation constant of the papain-catalysed hydrolysis of hippuryl anilides and N-acetyl-l-phenylalanylglycine anilides gives rise in both series to a Hammett ρ value of -1.04. This indicates that the enzyme provides electrophilic, probably general-acid, catalysis, as well as the nucleophilic or general-base catalysis previously found. A mechanism involving a tetrahedral intermediate whose formation is general-base-catalysed and whose breakdown is general-acid-catalysed seems most likely. The similarity of the Hammett ρ values appears to exclude facilitated proton transfer as a means through which the specificity of papain is expressed.


1990 ◽  
Vol 55 (1) ◽  
pp. 202-222 ◽  
Author(s):  
Jaromír Kaválek ◽  
Ulrika Králíková ◽  
Vladimír Macháček ◽  
Miloš Sedlák ◽  
Vojeslav Štěrba

The methanolysis and hydrolysis kinetics have been studied with the following sulfuric diamide derivatives: N-methyl-N-phenyl- (IIIa), N-methyl-N-(4-methoxycarbonylphenyl)- (IIIb), N-(4-methoxycarbonylphenyl)- (IIIc), N-methyl-N-(2-methoxycarbonylphenyl)- (IIId), N-(2-methoxycarbonylphenyl)- (IIIe), and N-methyl-N-(2,4-dibromophenyl)- (IIIf). The solvolyses of the neutral substrates IIIa and IIIb proceed by the addition-elimination mechanism. In the presence of the solvent lyate ions the solvolyses go by the E1cb mechanism. The solvolyses of the conjugated bases of compounds IIIa and IIIb are subject to general acid catalysis, the effects of the ring substituents being opposite to those in the addition-elimination mechanism. The solvolyses of compounds IIId and IIIf exhibit a distinct catalytic effect of neighbouring group; the reaction goes via a reactive intermediate, the transformation of the intermediate into the solvolysis product being subject to general acid and base catalysis.


1992 ◽  
Vol 20 (4) ◽  
pp. 296-312 ◽  
Author(s):  
Michael W. Washabaugh ◽  
Charles C. Yang ◽  
James T. Stivers ◽  
Kyung-Sang Lee

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 373 ◽  
Author(s):  
Satoshi Inaba

We have performed a number of quantum chemical simulations to examine the reduction process of methanol in hot water. Methanol is converted into a methane by capturing a hydrogen molecule and leaving a water molecule behind. The required energy for the reduction is too high to proceed in the gas phase. The energy barrier for the reduction of methanol is reduced by the catalytic effect of water molecules when we consider the reduction in aqueous solution. However, the calculated reduction rate is still much slower than that found experimentally. The ion product of water tends to increase in hot water, even though it eventually decreases at the high temperature of supercritical water. It is valuable to consider the acid–base catalytic effects on the reduction of methanol in hot water. The significant reduction of the energy barrier is accomplished by the acid–base catalytic effects due to hydronium or hydroxyde. Mean collision time between a hydronium and a methanol in hot water is shorter than the reduction time, during which a methanol is converted into a methane. The calculated reduction rate with the acid–base catalytic effects agrees well with that determined by laboratory experiments. The present study reveals a crucial role of the acid–base catalytic effects on reactions in hot water.


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