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2,8- and 2,9-Diboryltetracenes as Useful Building Blocks for Extended π-Conjugated Tetracenes
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2009
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Organic Charge-transfer CompoundChemical EngineeringNovel OrganocatalystsThiophene-tetracene-anthracene-tetracene-thiophene Pi-systemsEngineeringHeterocyclicOrganic ElectronicsOrganic SemiconductorOrganic ChemistryPi-conjugated TetracenesExtended π-Conjugated TetracenesChemistryHeterocycle ChemistryIr-catalyzed Direct DiborylationUseful Building BlocksBiomolecular Engineering
Ir-catalyzed direct diborylation of tetracene gave a 1:1 mixture of 2,8- and 2,9-bis[(pinacolato)boryl]tetracenes, which were separated by recrystallization. These diboryltetracenes are useful building blocks for the regiospecific synthesis of extended pi-conjugated tetracenes directed to semiconductors for organic field-effect transistors (OFETs). Syntheses of thiophene-tetracene-thiophene, thiophene-tetracene-bithiophene-tetracene-thiophene, and thiophene-tetracene-anthracene-tetracene-thiophene pi-systems have been achieved on the basis of the 2,8- and 2,9-diboryltetracenes.