Functionalization of sexithiophene with electron‐donating methylsulphanyl groups
Source abstract
Abstract
Novel soluble sexithiophenes (6Ts) β‐functionalized with electron‐donating methylsulphanyl groups are reported. The resulting processable sexithiophenes, two examples of which are shown in the Figure, have optical gaps that can be finely tuned around the value for unsubstituted α‐6T. The observed liquid‐crystal behavior described here indicates a high degree of molecular organization in the solid in at least one case. magnified image
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Research context
OpenAlex topics: Molecular Junctions and Nanostructures · Synthesis and properties of polymers · Liquid Crystal Research Advancements
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