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Radical ion pairs generated by electron transfer from photo-excited aromatic hydrocarbons to maleo- and fumaronitrile (cis- and trans-1,2-dicyanoethylene, 1) undergo back electron transfer from singlet and triplet pairs. The pair energies relative to the reactant ground states and to the triplet state, respectively, determine the competition between the recombination pathways. Cross sections through the potential surfaces of the radical anion and the triplet state of 1 have been examined by density functional theory calculations. The radical anion surface has minima in which the carbon and nitrogen skeleton is essentially planar; the central C-C bond is lengthened (weakened), but the barrier to geometric isomerization is still sizeable (31.2 kcal mol(-1)). The triplet energy surface has a minimum at a bisected geometry (plus its enantiomer); rotation of the H-C-CN segments of the triplet yields a syn-periplanar and an anti-periplanar point 9.3 kcal mol(-1) and 8.2 kcal mol(-1) above the minimum, respectively.

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304ChemInform Abstract The substituted 6-amino-3H-xanthen-3-ones (III) and the thio analogue (V) are synthesized from the resorcinols (II) or thioresorcinol (IV) as outlined in the reaction scheme. An approach to the systematic design of absorption and fluorescence band shapes of the compounds synthesized is developed, beginning with considerations of the solvatochromism and electronic perturbation of unsymmetrical chromophores. Predicted spectral shifting and line broadening are demonstrated.