Reactivity of Ru(bpy) + 3 towards the radicals originating from the scavenging of hydrogen atoms and hydroxyl radicals by methanol, ethanol, propan-2-ol, tert-butyl alcohol and formate ions in aqueous solution: a pulse radiolytic study

1991 ◽  
Vol 87 (14) ◽  
pp. 2179 ◽  
Author(s):  
Quinto G. Mulazzani ◽  
Mila D'Angelantonio ◽  
Nadia Camaioni ◽  
Margherita Venturi
Keyword(s):  
Aqueous Solution ◽  
Hydroxyl Radicals ◽  
Butyl Alcohol ◽  
Hydrogen Atoms ◽  
Tert Butyl ◽  
Tert Butyl Alcohol

scholarly journals Mechanism of protection of adenosine from tert-butoxyl radicals and repair of adenosine radicals by α-tocopherol in aqueous solution

2014 ◽  
Vol 7 (1) ◽  
Author(s):  
G. Vijayalakshmmi ◽  
M. Adinarayanna ◽  
P. Jayaprrakash Rao
Keyword(s):  
Aqueous Solution ◽  
Rate Constant ◽  
Butyl Alcohol ◽  
Quantum Yields ◽  
Oh Radicals ◽  
Butyl Hydroperoxide ◽  
Tert Butyl ◽  
Tert Butyl Hydroperoxide ◽  
Tert Butyl Alcohol

The rates of oxidation of adenosine and α-tocopherol by tert-butoxyl radicals (t-BuO•) were studied spectrophotometrically. Radicals (t-BuO•) were generated by the photolysis of tert-butyl hydroperoxide (t-BuOOH) in presence of tert-butyl alcohol to scavenge •OH radicals. The rates and the quantum yields () of oxidation of α-tocopherol by t-BuO• radicals were determined in the absence and presence of varying concentrations of adenosine. An increase in the concentration of adenosine was found to decrease the rate of oxidation of α-tocopherol, suggesting that adenosine and α-tocopherol competed for t-BuO• radicals. From competition kinetics, the rate constant of α-tocopherol reaction with t-BuO• was calculated to be 7.29 x 108 dm3 mol-1 s-1. The quantum yields expt and cal values suggested that α-tocopherol not only protected adenosine from t-BuO• radicals, but also repaired adenosine radicals, formed by the reaction of adenosine with t-BuO• radicals.

Sonolysis of tert-butyl alcohol in aqueous solution

1999 ◽  
pp. 1129-1136 ◽  
Author(s):  
Armin Tauber ◽  
Gertraud Mark ◽  
Heinz-Peter Schuchmann ◽  
Clemens von Sonntag
Keyword(s):  
Aqueous Solution ◽  
Butyl Alcohol ◽  
Tert Butyl ◽  
Tert Butyl Alcohol

Thermodynamic and Kinetic Investigation of the Solvent Effect on the Oxidation of [Co(en)2SCH2COO]+ with S2O82- In Water-Methanol and Water-tert-Butyl Alcohol Mixtures

1993 ◽  
Vol 58 (5) ◽  
pp. 1001-1006 ◽  
Author(s):  
Oľga Vollárová ◽  
Ján Benko
Keyword(s):  
Transfer Functions ◽  
Activation Parameters ◽  
Butyl Alcohol ◽  
Oxidation Of Co ◽  
Kinetics Of Oxidation ◽  
Tert Butyl ◽  
Tert Butyl Alcohol ◽  
Alcohol Mixtures ◽  
Kinetics Of

The kinetics of oxidation of [Co(en)2SCH2COO]+ with S2O82- was studied in water-methanol and water-tert-butyl alcohol mixtures. Changes in the reaction activation parameters ∆H≠ and ∆S≠ with varying concentration of the co-solvent depend on the kind of the latter, which points to a significant role of salvation effects. The solvation effect on the reaction is discussed based on a comparison of the transfer functions ∆Ht0, ∆St0 and ∆Gt0 for the initial and transition states with the changes in the activation parameters accompanying changes in the CO-solvent concentration. The transfer enthalpies of the reactant were obtained from calorimetric measurements.

scholarly journals Impacts of Sn(II) doping on the Keggin heteropolyacid-catalyzed etherification of glycerol with tert-butyl alcohol

2021 ◽  
pp. 116913
Author(s):  
Márcio José da Silva ◽  
Diego Morais Chaves ◽  
Sukarno Olavo ferreira ◽  
Rene Chagas da Silva ◽  
Jose Balena Gabriel Filho ◽  
...  
Keyword(s):  
Butyl Alcohol ◽  
Tert Butyl ◽  
Tert Butyl Alcohol
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