TY - JOUR
T1 - Oligothiophene-functionalized truxene
T2 - Star-shaped compounds for organic field-effect transistors
AU - Sun, Yanming
AU - Xiao, Kai
AU - Liu, Yunqi
AU - Wang, Jinliang
AU - Pei, Jian
AU - Yu, Gui
AU - Zhu, Daoben
PY - 2005/5
Y1 - 2005/5
N2 - Organic field-effect transistors (OFETs) based on oligothiophene- functionalized truxene derivatives have been fabricated for use as novel star-shaped organic semiconductors in solution-processible organic electronics. The electronic and optical properties of compounds 1-3, with increasing numbers of thiophene rings at each of the three branches, have been investigated using scanning electron microscopy (SEM), X-ray diffraction measurements, and ultraviolet-visible (UV-vis) and photoluminescence spectroscopies. The results show that with a stepwise increase of the thiophene rings at every branch, a transition from a polycrystalline to an amorphous state is observed. The characteristics of compounds 1, 2, and 3 used for OFETs exhibit a significant difference. The mobility depends greatly on the morphology in the solid state, and decreases in going from 1 to 3. Mobilities up to 1.03 × 10 -3 cm2 V-1 s-1 and an on/off ratio of about 103 for compound 1 have been achieved; these are the highest values for star-shaped organic semiconductors used for OFETs so far. All the results demonstrate that the truxene core of the oligothiophene-functionalized truxene derivatives not only extends the π-delocalized system, but also leads to high mobilities for the compounds.
AB - Organic field-effect transistors (OFETs) based on oligothiophene- functionalized truxene derivatives have been fabricated for use as novel star-shaped organic semiconductors in solution-processible organic electronics. The electronic and optical properties of compounds 1-3, with increasing numbers of thiophene rings at each of the three branches, have been investigated using scanning electron microscopy (SEM), X-ray diffraction measurements, and ultraviolet-visible (UV-vis) and photoluminescence spectroscopies. The results show that with a stepwise increase of the thiophene rings at every branch, a transition from a polycrystalline to an amorphous state is observed. The characteristics of compounds 1, 2, and 3 used for OFETs exhibit a significant difference. The mobility depends greatly on the morphology in the solid state, and decreases in going from 1 to 3. Mobilities up to 1.03 × 10 -3 cm2 V-1 s-1 and an on/off ratio of about 103 for compound 1 have been achieved; these are the highest values for star-shaped organic semiconductors used for OFETs so far. All the results demonstrate that the truxene core of the oligothiophene-functionalized truxene derivatives not only extends the π-delocalized system, but also leads to high mobilities for the compounds.
UR - http://www.scopus.com/inward/record.url?scp=18744373924&partnerID=8YFLogxK
U2 - 10.1002/adfm.200400380
DO - 10.1002/adfm.200400380
M3 - Article
AN - SCOPUS:18744373924
SN - 1616-301X
VL - 15
SP - 818
EP - 822
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 5
ER -