“…Coupling of 2,7-dibromo-9,9-dioctyl-9 H -fl uorene in excess carbazole under ( ∼ 65 ° C for TPD and ∼ 100 ° C for NPB), ease of crystallization and unsatisfactory morphological stability. [ 5,6 ] Recently, AHTMs with high T g such as dendritic carbazole molecules with a fl uorene core, [ 7,8 ] 1,4-bis( N-carbazolyl)benzene as a central unit and different numbers of diphenylamine moieties as the peripheral group, [ 9 ] 1,3,5-tris(2-(9-ethylcarbazolyl-3)ethylene)benzene, [ 10 ] 4,4 ′ ,4 ′ ′ -tri( N -dibenzocarbazolyl)triphenylamine [ 11 ] and monodisperse carbazole-based oligomers, [ 12 ] have been reported.…”