Citation:
ZHAO Xiang-Hua, LI Xiao-Sheng, ZHOU Li, WU Na-Na, YANG Xing-Kun, YUAN Shun-Dong, DING Dong-Xue, XU Hui. A Novel Molecule Based on 2,2'-Dipyridylamine Functionalized 9,9-Diarylfluorene with Steric Hindance: Design, Synthesis and Electro-Optical Property Research[J]. Acta Physico-Chimica Sinica,
;2015, 31(10): 1971-1976.
doi:
10.3866/PKU.WHXB201509011
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The bipolar molecule N-(4-(9-phenyl-fluoren-9-yl)phenyl)-2,2'-bipydylamine (PFPhDPy) with bulky steric hindrance was synthesized successfully by substituting 9-(4-anilino)-9-phenyl-fluorene with 2-bromopyridine via Ullmann reaction, which is expected to possess od thermal stability, stable morphology, high triplet energy (ET), and od bipolar characteristics because of the bulky steric hindrance, excellent bipolar transporting characteristics of fluorene, interrupted conjugation, andelectrondeficient pyridine group. Thermo gravimetric analysis (TGA) indicates a decomposition transition temperature of 336 ℃ with 5% weight loss. Differential scanning calorimetry (DSC) curve reveals no crystallization and melting phenomena by heating to 190 ℃, which indicates the high morphological stability of the compound. The separation of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO), calculated by density functional theory (DFT), indicates that a bipolar molecule was obtained and high triplet energy (ET, 3.0 eV) was calculated from the phosphorescence spectrum. The UV-Vis spectrum is independent of solvent effects with three absorption peaks at about 276, 298, and 308 nm, respectively. The fluorescence emission spectra show blue shift as the solvents' polarity increasing with emission peaks from 390 to 363 nm in the solvents of dichloromethane, ethyl acetate, ethanol, and acetonitrile. In addition, the structure of the compound was characterized by matrix-assisted laser desorption ionization time of flight mass spectrometer (MALDI-TOF MS), hydrogen nuclear magnetic resonance (1H NMR), and carbon nuclear magnetic resonance (13C NMR) spectra, respectively.
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