posted on 2018-10-29, 16:25authored byJill E. Crossley
The kinetics of electron transfer between the radical cations of a series of
anthracene derivatives and a variety of amine electron donors were studied on the
surface of silica gel. The anthracene derivatives were excited with 355 nm radiation
and formed radical cations by multi-photon ionisation. The radical cation
absorption decay was measured by diffuse reflectance laser flash photolysis at
wavelengths between 680 and 780 nm, depending upon the identity of the
substituent of the anthracene.
The decay kinetics of the radical cations were complex and non-exponential.
The addition to the surface of a co-adsorbed electron donor, with an
oxidation potential below that of the anthracene derivative resulted in an increase in
the rate of the radical cation decay because of the electron transfer from the donor
species. The kinetics of electron transfer were fitted with using the dispersive
model of Albery. [Continues.]
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Publication date
2000
Notes
A Doctoral Thesis. Submitted in partial fulfilment of the requirements for the award of Doctor of Philosophy at Loughborough University.