Publication | Closed Access
Synthesis and Cofacial π-Stacked Packing Arrangement of 6,13-Bis(alkylthio)pentacene
85
Citations
24
References
2006
Year
Materials ScienceOrganic Charge-transfer CompoundOrganic Material ChemistryEngineeringOrganic ElectronicsOrganic Field-effect TransistorsOrganic SemiconductorOrganic ChemistryX-ray Crystallographic AnalysisChemistryPentacene RevealsHeterocycle ChemistryBiomolecular EngineeringPolymers
[reaction: see text] 6,13-Bis(alkylthio)pentacenes directed toward organic field-effect transistors (OFETs) were synthesized by the ZnI(2)-mediated reaction of trans-6,13-dihydroxy-6,13-dihydropentacene with alkylthiols, followed by the dehydrogenative aromatization of the resulting trans-6,13-bis(alkylthio)-6,13-dihydropentacenes with p-chloranil. The X-ray crystallographic analysis of 6,13-bis(methylthio)pentacene reveals that this compound is arranged as a result of cofacial pi-stacking with S-S and S-pi interactions.
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