Table 1.
|
|
Yield (%)e |
||||
---|---|---|---|---|---|---|
Entry | Porphyrins | Aqueous solution | Decanoic acidf | Dodecaneg | Mesityleneh | 5-comp. mixturei |
1 | etiob | 1.4 | 6.0 | 1.1 | 1.0 | 3.6 |
2 | coproc | 7.1 | 7.6 | 7.6 | naj | na |
3 | urod | 1.5 | 1.2 | 1.4 | na | na |
The pairwise reactions (30 mM for each reactant) were carried out for 24 h at 60°C in aqueous solution (pH 7) in the presence or absence of organic constituents (“oil slick”).
Etio denotes etioporphyrins from the reaction of 1-Me + 2-Et.
Copro denotes coproporphyrins from the reaction of 1-Me + 2-PrOH.
Uro denotes uroporphyrins from the reaction of 1-AcOH + 2-PrOH.
Porphyrin yields upon chemical oxidation (with I2).
Aqueous solution containing 0.1 M decanoic acid.
Aqueous solution (0.4 mL) and dodecane (0.1 mL).
Aqueous solution (0.4 mL) and mesitylene (0.1 mL).
Aqueous solution (0.4 mL) and the five-component organic mixture (0.1 mL).
Not available.