This article describes the synthesis and OTFT characteristics of anthracene and dibenzothiophene derivatives.
The OTFT materials were synthesized by well knowen reaction, bromination, Suzuki coupling, Yamamoto reaction, etc.
Monomers, polymers, and ol...
This article describes the synthesis and OTFT characteristics of anthracene and dibenzothiophene derivatives.
The OTFT materials were synthesized by well knowen reaction, bromination, Suzuki coupling, Yamamoto reaction, etc.
Monomers, polymers, and oligomers were characterized by the spectroscopic methods such as UV-visible, FT-IR, and 1H-NMR spectroscopies.
The resulting polymers were soluble in common organic solvents such as toluene, xylene, chlorobenzene, etc. The oligomers were well soluble in hot aromatic solvent, toluene, xylene, chlorobenzene.
The obtained polymers and oligomers showed high thermal stabilities with high Td's(Td : 298 oC - 441 oC), which were characterized by TGA.
Optical properties of these polymers and oligomer were characterized by UV-visible and photoluminescence (PL) spectra, which were measured in solution and film, respectively. The polymers and oligomers were red shift solution to film in UV-visible and photoluminescence (PL) spectra. The materials were good orderness and stacking, respectively.
The thin-film transistor (TFT) performances of dibenzothiophene derivatives are examined. Through studied of the thin film morphology using X-ray diffraction (XRD) and atomic force microscopy. Due to the extended π-conjugation and efficient hole injection, the devices exhibited hole mobility of up to 0.026 cm2/Vs. The devices showed very low subthreshold-slope of 0.4 V/dec.