Intramolecular excimer formation in short- and long-chainlength di(9-anthryl) bichromophoric compounds and relation to ground state properties

Abstract

The ground state conformational, UV absorption and fluorescence spectral as well as decay time data for a series of polymethylene- and one polyoxyethylene-linked di(9-anthracenes) in solution are compared, for chainlengths varying from n=0 (directly linked system A0A, 9,9′-bianthryl) to n=∞ (A∞, reference system 9-decylanthracene). ¹H NMR spectroscopy of A2A to A11A shows that there is no clearly preferred ground state conformation of the anthracene moieties. The crystal structure of A2A was solved and the anti conformation of the anthracene units was established. The UV spectra show a redshift interpreted within the Förster exciton model (predominance of extended conformations). Fluorescence spectra for (CH₂)_n-bridged systems show no clear excimer band for short-chain systems but redshifted excimer emission for A4A to A9A. Loss of structure and fluorescence band shape changes as well as biexponential decay times allow the conclusion that excimer formation occurs in all chained systems. For a related polyoxyethylene-chained system, the excimer band is substantial, probably a consequence of the increased flexibility of the chain and moderate photoreactivity. Solvent polarity changes are strong for A0A [formation of a twisted intramolecular charge transfer (TICT) state] but also significant in the systems A1A and A2A. This is rationalized by the possiblity for competitive formation of an excimer-type (parallel but tilted chromophore arrangement) and a TICT-type (near perpendicular) conformation. For AnA (n>2) the solvent polarity was found to have virtually no influence.