Ultrasonic Examination of Proton‐Transfer Reactions at the α‐Amino and Side‐Chain Groups of Arginine and Lysine in Aqueous Solution

1971 ◽  
Vol 49 (6B) ◽  
pp. 1907-1908 ◽  
Author(s):  
Matthew Hussey ◽  
Peter D. Edmonds
2012 ◽  
Vol 134 (50) ◽  
pp. 20421-20432 ◽  
Author(s):  
Richard S. Massey ◽  
Christopher J. Collett ◽  
Anita G. Lindsay ◽  
Andrew D. Smith ◽  
AnnMarie C. O’Donoghue

1994 ◽  
Vol 84 (1) ◽  
pp. 227-235
Author(s):  
Elena Morales ◽  
M. Rosa Gómez-Antón ◽  
Inés F. Piérola

1976 ◽  
Vol 31 (5-6) ◽  
pp. 219-224 ◽  
Author(s):  
P. Schuster ◽  
K. Tortschanoff ◽  
H. Winkler

Proton transfer in aqueous solutions of 3-hydroxypyridin (3HP) has been studied by tempera­ture jump relaxation and ultrasound absorption techniques. Two chemical relaxations have been observed. In the range pK1<pH<pK2 the slower of the two processes corresponds to proton transfer between the N and O atoms. A mechanism is proposed which describes the pH and con­centration dependence of the relaxation time measured. Proton transfer involves two types of pro­cesses which operate in parallel: I. pseudomonomolecular, by consecutive diffusion-controlled protonation and deprotonation steps, and 2. bimolecular by diffusion-controlled proton transfer between the neutral 3HP molecule and its corresponding cation or anion. There is no evidence for direct monomolecular proton transfer within the hydration shell of the molecule (k→ ~ k← < 2 × 1O3 sec-1).


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