Alpha,omega-bis(thioacetyl)oligophenylenevinylene chromophores from thioanisol precursors

The selective cleavage of arylmethyl thioethers provides a convenient protocol for the synthesis of all-E isomers of alpha, omega-bis(thioacetyl)oligophenyenevinylene molecules (OPVs). The S-methyl group is tolerant of Wittig-type and Heck-type reactions for forming OPV structures and can be converted to the S-acetyl group by treatment with sodium thiomethoxide and acetyl chloride. The thermal conditions of the deprotection/reprotection step concurrently isomerize the conjugated chromophore to the all-E isomer, regardless of the stereochemistry of the starting olefins. This approach is demonstrated for a variety of linear and [2.2]paracyclophane containing OPVs, which have been characterized by electrochemical and spectroscopic techniques. Additionally, these S-acetyl-terminated OPVs self-assemble on gold surfaces. Monolayers containing these molecules were characterized by water contact angle measurements, ellipsometry, and X-ray photoelectron spectroscopy.