Organic light emitting device

The heterocyclic compound of claim 1, wherein R1 is selected from the group consisting ofnunsubstituted monocyclic to tetracyclic aryl groups selected from the group consisting of phenyl groups, naphthyl groups, biphenyl groups, terphenyl groups, anthracenyl groups, fluorenyl groups, carbazolyl groups, and pyrenyl groups;unsubstituted C4-C60 heteroaryl groups;substituted monocyclic to tetracyclic aryl groups selected from the group consisting of phenyl groups, naphthyl groups, biphenyl groups, terphenyl groups, anthracenyl groups, fluorenyl groups, carbazolyl groups, and pyrenyl groups substituted with at least one substituent selected from the group consisting of C1-C5 alkyl groups, C1-C5 alkoxy groups, cyano groups, amine groups, phenoxy groups, phenyl groups, and halogen groups; andsubstituted C4-C60 heteroaryl groups substituted with at least one substituent selected from the group consisting of C1-C5 alkyl groups, C1-C5 alkoxy groups, cyano groups, amine groups, phenoxy groups, phenyl groups, and halogen groups.

The heterocyclic compound of claim 1, wherein each of R2 and R3 is independently selected from the group consisting of methyl groups and phenyl groups.

The heterocyclic compound of claim 1, wherein the compound represented by Formula 1 is selected from the group consisting of Compounds 3, 13, 19 and 29:

An organic light-emitting device comprising:na first electrode;a second electrode; andan organic layer between the first electrode and the second electrode,wherein the organic layer comprises the heterocyclic compound of claim 1.

An organic light-emitting device comprising:na first electrode;a second electrode; andan organic layer between the first electrode and the second electrode,wherein the organic layer comprises at least one layer comprising the heterocyclic compound of claim 1, the at least one layer being formed using a wet process.