Transient absorption signal delayed by a magnitude of 100 μs with respect to the exciting laser shot is observed
after UV laser flash photolysis of degassed benzene, acetone, and acetonitrile solutions of an interface probe
complex, i.e., gold(I) complex [{Au[P(C6H4OMe-p)3]}2-(μ-C≡C)] ([μ-ethynylene-bis{tris(4-methoxyphenyl)phosphine}gold]). Chemical reactions leading to the transient absorbance change are confirmed to be occurring
at the solid−liquid interface, and the delay time is believed to arise from the photogenerated intermediate
species in the bulk solution crossing the diffusion layer, which ultimately undergo interfacial reactions resulting
in the observed transient absorbance change. The delay time is suggested as a direct measure for the thickness
of the diffusion layer. The thickness of the diffusion layer around 0.2 μm, estimated by this method, is
comparable to that from the sonovoltammetric study. Oscillations in transient absorbance kinetics are also
observed, which can be attributed to the coupling between the interfacial chemical reactions and a photoacoustic
effect; oscillation due to a single physical process arising from the schlieren effect under certain condition is
also discussed. Similar transient phenomena are observed in another luminescent complex, i.e., a hexanuclear
Cu(I) cluster Cu6(t-NS)6 (t-NS = 4-tert-butylpyridine-2-thiolate). The characterization of the photochemical
reaction processes of the Cu(I) complex by means of transient absorbance difference spectra reveals that a
consecutive biphotonic ionization process occurs after the laser flash. The intermediate species with a lifetime
of 65 μs responsible for the interfacial reaction is tentatively assigned as a charge separation pair. A reaction
scheme involving surface-assisted ionization of the charge separation pair is proposed to account for the
coupling between the interfacial chemical reaction and the photoacoustic effect.