4402-40-8Relevant academic research and scientific papers
Microwave-assisted synthesis of 2,5-diarylthiazolo[5,4-d]thiazoles from benzaldehydes and dithiooxamide
Papernaya,Shatrova,Sterkhova,Levkovskaya,Rozentsveig
, p. 373 - 377 (2015/05/04)
One-pot condensation of dithiooxamide with aromatic aldehydes and subsequent oxidation of intermediate 2,5-dihydro[1,3]thiazolo[5,4-d][1,3]thiazoles with selenium dioxide afforded 2,6-diaryl[1,3]thiazolo-[5,4-d][1,3]thiazoles which were characterized by
Synthesis, physical properties and field-effect transistors of novel thiazolothiazole-phenylene co-oligomers
Ando, Shinji,Kumaki, Daisuke,Nishida, Jun-Ichi,Tada, Hirokazu,Inoue, Youji,Tokito, Shizuo,Yamashita, Yoshiro
, p. 553 - 558 (2008/02/05)
A series of thiazolothiazole-phenylene co-oligomers was synthesized and their properties, particularly as semiconductors for OFETs, were investigated. The naphthyl and biphenyl- substituted derivatives showed p-type semiconducting behavior with hole mobilities ranging from 10-2 to 10-1 cm2 V-1 s-1. The hole mobility and on/off ratio were enhanced to 0.12 cm2 V-1 s-1 and 10 6 on the HMDS treated substrate. The introduction of phenyl groups as end substituents was found to be favorable for charge transport and air-stability. The Royal Society of Chemistry 2007.
