Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1305019 | Inorganic Chemistry Communications | 2006 | 4 Pages |
Kinetics of oxidation of catechol (H2cat) to benzoquinone (BQ) and, ascorbate (HA−) to dehydroascorbic acid (A) by [RuIII(tpy)(pic)(OH)]+ (1) (tpy = 2,2’6’,2”-terpyridine; pic− = picolinate) have been studied as function of [H2cat] (or [HA−]), ionic strength (0.01 − 0.25 M), temperature (10–30 °C) at a constant pH = 3.2, using stopped-flow and rapid-scan diode array spetrophotometric techniques. The rate of reaction of 1 with HA− was found to be very fast as compared to that of with H2cat. The kinetic data and activation parameters are interpreted in terms of an associative interchange mechanism. Analysis of spectral and kinetic data revealed that the reaction of 1 with catechol proceeds by a straightforward outer-sphere electron transfer pathway, whereas, reduction of 1 with HA− involves ion-pair formation.
Graphical abstractThe Kinetics of reduction of [RuIII(tpy)(pic)OH]+ (1) by catechol and ascorbic acid is studied by following the growth of characteristic peak of [RuII(tpy)(pic)H2O]+ (2) at 500 nm.Figure optionsDownload full-size imageDownload as PowerPoint slide