TY - JOUR AU - Vauthey, E. TI - Investigation of the Photoinduced Electron Transfer Rection between 9,10-Dicyanoanthracene and 1-Methylnaphthalene in Acetonitrile using Picosecond Transient Grating Spectroscopy PY - 1997 JF - Journal of Physical Chemistry A JA - J. Phys. Chem. A SN - 1089-5639 VL - 101 IS - 9 SP - 1635 EP - 1639 L1 - http://pubs.acs.org/doi/pdf/10.1021/jp961853%2B L2 - http://pubs.acs.org/doi/full/10.1021/jp961853%2B L3 - http://pubs.acs.org/doi/abs/10.1021/jp961853%2B M3 - 10.1021/jp961853+ UR - http://dx.doi.org/10.1021/jp961853+ N2 - A spectroscopic and kinetic study of the photoinduced electron transfer (ET) reaction between 9,10-dicyanoanthracene (DCA) and 1-methylnaphthalene (MNA) in acetonitrile using the transient grating technique is reported. Apart from the bands assigned to 1DCA* and DCA•-, the transient spectrum exhibits a band located at 580 nm and ascribed to MNA2•+. This species is generated upon reaction of a second donor molecule with a 1:1 complex to form a 1:2 complex (DCA•-·MNA2•+). Using chloranil as electron acceptor, the rate constant of this reaction has been measured to be 6.8 × 109 M-1 s-1. From the donor concentration dependence of the kinetics of DCA•- diffraction intensity and of the free ion yield, the rates of back ET to the ground state within the 1:1 and the 1:2 complexes have been determined to be equal to 1.8 × 108 and 16.9 × 108 s-1, respectively, while their rate constants of separation into free ions are 1.6 × 108 and 1.1 × 108 s-1, respectively. These values have been obtained assuming a reaction scheme in which both forward and backward ET essentially take place at contact distance. In the case of the 1:1 complex, however, charge recombination within a loose ion pair cannot be ruled out. ID - 103 ER -