Polymorph crystal packing effects on charge transfer emission in the solid state

Condensation of 1,8-naphthalic anhydride with , -(dimethylamino)aniline produced the donor-acceptor compound , which crystallised from a chloroform-diethyl ether mixture to afford two different coloured crystal polymorphs. Crystals for one polymorph are small and green, whereas the other crystals are orange and needle-like. X-ray crystal structures for both polymorphs were determined. The donor , -dimethylaniline and acceptor naphthalimide groups are twisted with respect to each other; the degree of twist is marginally different for the two structures. The orange crystal polymorph crystallises in the monoclinic space group 2/ and contains two slightly different molecular conformers in the unit cell (calculated density is 1.410 g cm ). The green crystal polymorph crystallises in the triclinic space group 1 and contains only one type of molecule in the unit cell (calculated density is 1.401 g cm ). The crystal packing motifs for the two polymorphs are subtly different, explaining the small variance in the observed densities. Very weak room temperature emission was observed for in a CHCl solution, but crystals deposited on a glass slide glowed when irradiated at 488 nm using a fluorescence microscope. Disparate solid-state emission spectra and lifetimes for the two polymorphic crystal forms are observed for the dyad. The emission is assigned to charge recombination fluorescence from a charge transfer state.