Static and time-resolved photocrystallographic studies in supramolecular solids

Abstract

Abstract The supramolecular solid state is a medium par excellence for photochemical studies of molecules in a well-defined environment. If the photoactive molecule is embedded within a strong photochemically-inert framework, reactions can proceed without breakdown of the crystal lattice. A number of examples of trans-cis and cis-trans reactions are presented. A variable temperature study of Zn-coordinated tiglic acid shows that the reaction is energy-controlled with a small activation energy of approx. 2 kJ/mol, dependent on the size of the cavity in which the molecule is located. Time-resolved studies of the instantaneous dimer-formation of an organic and an inorganic species are presented. The Cu(I)(NH3)2 cation forms a dimeric species with a contracted Cu(I)—Cu(I) distance through promotion of an electron from an antibonding to a weakly bonding orbital, whereas xanthone forms an excimer with decrease interplanar spacing. The concept of the photodifference map is defined and used thoughout the article.