Bent naphthodithiophenes: synthesis and characterization of isomeric fluorophores.

Thiophene-containing heteroarenes are one of the most well-known classes of π-conjugated building blocks for photoactive molecules. Isomeric naphthodithiophenes (NDTs) are at the forefront of this research area due to their straightforward synthesis and derivatization. Notably, NDT geometries that are bent - such as naphtho[2,1- b :3,4- b ']dithiophene (α-NDT) and naphtho[1,2- b :4,3- b ']dithiophene (β-NDT) - are seldom employed as photoactive small molecules. This report investigates how remote substituents impact the photophysical properties of isomeric α- and β-NDTs. The orientation of the thiophene units plays a critical role in the emission: in the α(OHex)R 2 series conjugation from the end-caps to the NDT core is apparent, while in the β(O i -Pent)R 2 series minimal change is observed unless strong electron acceptors, such as β(O i -Pent)(PhCF 3 ) 2 , are employed. This push-pull acceptor-donor-acceptor (A-D-A) fluorophore exhibits positive fluorosolvatochromism that correlates with increasing solvent polarity parameter, E T (30). In total, these results highlight how remote substituents are able to modulate the emission of isomeric bent NDTs.