Ultrafast intermolecular electron transfer (ET) from orthomethoxyaniline (orthoanisidine, ANS) to a number of excited (S-1) 4-trifluoromethyl-1,2-benzopyrones (coumarins) having differently substituted 7-amino group has been investigated by femtosecond fluorescence up-conversion technique. The ET dynamics in the present systems are nonsingle-exponential and occur faster than the diffusive solvation dynamics. The ET rates are largely dependent on the nature of the substituents at the 7-amino group of the coumarins. This dependence is well correlated with the free energy changes (Delta G(0)) for the ET reactions. The ET dynamics become slower on using deuterated ANS as the donor, where the amino group hydrogens of ANS are substituted by deuterium. The deuterium isotope effect, however, gradually reduces as the ET dynamics becomes faster. Conventional ET theories can not explain all the observations. The results are explained on the basis of the two-dimensional ET model, which considers the solvent coordinate and the intramolecular coordinate separately to depict the ET process. It is seen that in coumarin-ANS systems the ET occurs much faster than the coumarin-aniline systems. It is indicated that the electronic coupling matrix element, a parameter which determines the extent of interaction between the reactant and the product states in the ET process, is much larger in the present systems than for the coumarin-aniline systems. The deuterium isotope effect on the ET dynamics is explained in terms of the changes in the Delta G(0) values on isotopic substitution of the solvent donors.