Photochemical Hydroxylation of Salicylic Acid with Hydrogen Peroxide; Mechanistic Study of Substrate Sensitized Reaction

1996 ◽  
Vol 61 (12) ◽  
pp. 1729-1737 ◽  
Author(s):  
Kamil Lang ◽  
Jiřina Brodilová ◽  
Stanislav Luňák
Keyword(s):  
Hydrogen Peroxide ◽  
Salicylic Acid ◽  
Quantum Yields ◽  
Mechanistic Study ◽  
Isomer Ratio ◽  
Dihydroxybenzoic Acid ◽  
Effect Of Ph ◽  
Product Ratio

The photochemical hydroxylation of salicylic acid (SA) by hydrogen peroxide proceeds via the same intermediate independently of the excited reactant (i.e. SA or H2O2). This conclusion is supported by the similar effect of pH on the quantum yields and on the isomer ratio of formed products: 2,3-dihydroxybenzoic acid (2,3-DHB) and 2,5-dihydroxybenzoic acid (2,5-DHB). The product ratio ([2,3-DHB]/[2,5-DHB]) is not affected by H2O2 concentration.

Cooxidation reactions of ascorbic acid

1979 ◽  
Vol 44 (10) ◽  
pp. 2893-2903 ◽  
Author(s):  
Eva Schwertnerová ◽  
Dana M. Wagnerová ◽  
Josef Vepřek-Šiška
Keyword(s):  
Hydrogen Peroxide ◽  
Ascorbic Acid ◽  
Salicylic Acid ◽  
Catalytic Oxidation ◽  
Molecular Oxygen ◽  
Catalytic Effect ◽  
Metal Chelates ◽  
Dihydroxybenzoic Acid ◽  
Reaction Intermediate ◽  
Kinetics Of

Catalytic oxidation of salicylic acid by molecular oxygen, induced by the oxidation of ascorbic acid, leads to the formation of a mixture of isomers of dihydroxybenzoic acid. The reaction is catalyzed by a series of metal chelates, especially Fe(II) and Co(II), the most marked catalytic effect having been found in the case of tetrasulphophthalocyanine of cobalt (CoTSP). The kinetics of the oxidation of ascorbic acid in the presence of salicylic acid was followed, and the formation of hydrogen peroxide as reaction intermediate was proved.

scholarly journals Mechanistic Study on the Reaction of pinB-BMes2 with Alkynes Based on Experimental Investigation and DFT Calculations: Gradual Change of Mechanism Depending on the Substituent

2021 ◽  
Author(s):  
Linlin Wu ◽  
Chiemi Kojima ◽  
Ka Ho Lee ◽  
Shogo Morisako ◽  
Zhenyang Lin ◽  
...  
Keyword(s):  
Experimental Investigation ◽  
Transition Metal ◽  
Dft Calculations ◽  
Kinetic Analysis ◽  
Reaction Rate ◽  
Mechanistic Study ◽  
Isomer Ratio ◽  
Gradual Change ◽  
Isomeric Mixture ◽  
Metal Free

Transition-metal free direct and base-catalyzed 1,2-diborations of arylacetylenes using pinB-BMes2 provided syn/anti-isomeric mixture of diborylalkenes. The kinetic analysis showed that the reaction rate and isomer ratio were affected by reaction...

scholarly journals Impact of Advanced Oxidation Products on Nanofiltration Efficiency

Water ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 541 ◽  
Author(s):  
Renata Żyłła ◽  
Rafał Milala ◽  
Irena Kamińska ◽  
Marcin Kudzin ◽  
Marta Gmurek ◽  
...  
Keyword(s):  
Salicylic Acid ◽  
Membrane Filtration ◽  
Main Product ◽  
Membrane Separation ◽  
Negative Impact ◽  
Microscopic Analysis ◽  
Contact Angles ◽  
Oxidation Products ◽  
Acid Oxidation ◽  
Dihydroxybenzoic Acid

The aim of the work was to determine the influence of salicylic acid (SA) oxidation products on the effectiveness of their further removal in the membrane filtration process. Two commercial polyamide-based polymer membranes, HL (GE Osmonics) and TS80 (TriSepTM), were used and characterized by SEM microscopic analysis, contact angles, and free surface energy. The products of salicylic acid oxidation, 2,3- and 2,5-dihydroxybenzoic acid and catechol, were determined and their impact on the removal of unreacted salicylic acid in the nanofiltration process was investigated. It was also checked to what extent and why they were retained or not by the membranes. The results of the research have shown that the main product of salicylic acid oxidation, 2,3-dihydroxybenzoic acid, has a negative impact on the retention of salicylic acid in the nanofiltration stage, while the other product, catechol, improves SA retention. The determined values of contact angles correlate well with solubility (S) of the tested compounds, which increases in the following order SSA < S2,3-DHBA < SCAT, while the contact angle of the membrane decreases. Nevertheless, it has been shown that some oxidation products can penetrate the environment due to poorer membrane separation properties of these products.

scholarly journals Mechanistic Study of the Conversion of Superoxide to Oxygen and Hydrogen Peroxide in Carbon Nanoparticles

2016 ◽  
Vol 8 (24) ◽  
pp. 15086-15092 ◽  
Author(s):  
Almaz S. Jalilov ◽  
Chenhao Zhang ◽  
Errol L. G. Samuel ◽  
William K. A. Sikkema ◽  
Gang Wu ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Carbon Nanoparticles ◽  
Mechanistic Study

Solvent and substituent effects on rearrangement of 4-(4-X-phenyl)-2,7-dioxa-3-azabicyclo[3,3,0]oct-3-enes

1985 ◽  
Vol 50 (9) ◽  
pp. 1971-1981 ◽  
Author(s):  
Lubor Fišera ◽  
Marta Konopíková ◽  
Ladislav Štibrányi ◽  
Hans-Joachim Timpe
Keyword(s):  
Substituent Effects ◽  
Quantum Yields ◽  
Polar Solvents ◽  
Aromatic Residue ◽  
Product Ratio ◽  
Oxazoline Derivatives ◽  
Oxazine Derivatives

Preparation of the title compounds V is described. They give, on irradiation, the 2,3-dihydro-6H-1,3-oxazine derivatives VI as the main products besides the tetrahydrofuro[3,4-d]oxazoline derivatives VII. The VI to VII product ratio depends on the substituent bound to the aromatic residue. Polar solvents favour formation of the VI derivatives in the order Cl >H > CH3. In non-polar solvents the proportion of VII is increased. The quantum yields of the photoreaction vary within the limits from 0.006 to 0.04 (H >F > Cl > CH3 > OCH3).

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