Abstract
The steric interference of proximal dialkyl amino and acyl groups at the peri (1,8) positions of naphthalene affects the intramolecular charge transfer fluorescence. Previous studies indicate that acyl and freely rotating dimethyl amino groups twist toward coplanarity with the naphthalene ring in the excited state. The present study examines the effect of constraining the amino group in a ring. The photophysical properties of 2,2-dimethyl-1-(1-methyl-1,2,3,4-tetrahydrobenzo[h]quinolin-10-yl)propan-1-one (4), ethyl 1-methyl-1,2,3,4-tetrahydrobenzo[h]quinoline-10-carboxylate (5), and 1-methyl-1,2,3,4-tetrahydrobenzo[h]quinoline-10-carbaldehyde (6) are compared with the dimethyl amino derivatives 2 and 3. Crystal structures of 4-6 show that the amine ring adopts a chair conformation, where the N-methyl group is axial. Computational results suggest that the pyramidal amino group planarizes and twists together with the acyl toward coplanarity in the excited state. The ring structure does not thwart the formation of a planar intramolecular charge transfer (PICT) state.