It was recently reported that the most popular electron-accepting units introduced to π-conjugated oligomers studied for organic photovoltaic applications are susceptible to unwanted and even destructive photochemical reactions. The consequences of / photoisomerization of the popular 2-(1,1-dicyanomethylene)rhodanine (RCN) unit on the optical and morphological properties of a homologous series of RCN-functionalized oligothiophenes are studied here. Oligomers consisting of one, two, or three thiophene units were studied as pure isomers and with isomer compositions of 25, 53, and 45%, respectively, for / mixtures.
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