Reactions of Muonium with simple biochemical solutes in water and micelles

1991 ◽  
Vol 69 (8) ◽  
pp. 1252-1258 ◽  
Author(s):  
Mary V. Barnabas ◽  
David C. Walker

Rate constants are reported for the reaction of muonium atoms in water with some 36 organic compounds, many of interest in biology. These kM values range from < l05 to 7 × 1010 M−1 s−1, according to the type of reaction involved, with the sugar–phosphate backbones of nucleic acids being at the low end and their bases at the high end. They are compared with corresponding published H-atom data (kH), where possible, and show kinetic-isotope-effects ranging over five orders of magnitude. Since all kH data were obtained at pH = 1, while kM values refer to pH ~ 7 of the natural state, the pH-dependence of kM was examined in representative cases. The changes found result from protonation of the solute rather than a changed reactivity of Mu on being converted to MuH+. On localizing the solutes in the hydrophobic phase of dilute micelles, the reactivity of Mu was again measured (kM(mic)). The resulting "enhancement" factor was considered in terms of: the reaction mechanism, its dependence on microenvironment (solvation), and the concentrating effect of mutual confinement to small sections of a biphasal system. Key words: kinetic isotope effects, muonium, biochemicals, micelles.

2006 ◽  
Vol 128 (51) ◽  
pp. 16851-16863 ◽  
Author(s):  
Silvia Ferrer ◽  
Iñaki Tuñón ◽  
Sergio Martí ◽  
Vicente Moliner ◽  
Mireia Garcia-Viloca ◽  
...  

2002 ◽  
Vol 360 (1-2) ◽  
pp. 59-64 ◽  
Author(s):  
Emilio Martı́nez-Núñez ◽  
Antonio Fernández-Ramos ◽  
Saulo A Vázquez ◽  
Miguel A Rı́os

2003 ◽  
Vol 118 (14) ◽  
pp. 6280-6288 ◽  
Author(s):  
A. Fernández-Ramos ◽  
E. Martı́nez-Núñez ◽  
J. M. C. Marques ◽  
S. A. Vázquez

Rate constants in aqueous solutions are reported for proton and deuteron abstraction by a variety of bases from tricarbomethoxymethane, the propan-2-one-1-sulphonate ion, 2-acetylcyclohexanone and ethyl nitroacetate. The rates of ionization were measured by using bromine or iodine as scavengers to remove the anions, and, for ethyl nitroacetate by direct observation of the rate of appearance of the anion. The kinetic isotope effects vary from k H / k D = 2.5 to k H / k D = 10.3, and confirm the regularities previously found (Bell & Crooks 1965; Bell & Goodall 1966). In particular, the results for the reaction of ethyl nitro-acetate with nine bases show clearly that with increasing basic strength the isotope effect passes through a well-marked maximum. Sterically hindered pyridine bases give rise to abnormally high isotope effects, probably attributable to increased tunnel corrections.


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