School of Science, MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, Xi'an Jiao Tong University, Xi'an 710049, P. R. China.
Department of Chemistry, Key Lab of Environment-Friendly Chemistry and Application in the Ministry of Education, Xiangtan University, Xiangtan 411105, P. R. China.
Phys Chem Chem Phys. 2018 May 16;20(19):13171-13177. doi: 10.1039/c7cp08567b.
Isomeric TF1 and TF2 with highly fused thiophene cores were designed and synthesized here, in which a highly planar molecular structure was obtained for TF1 with the face-to-face sulfur atoms in the lateral region and a twisted molecular backbone was observed for TF2 with the back-to-back sulfur atoms. It is worth noting that different intermolecular interactions dominated in TF1 and TF2 caused by their isomeric thiophene cores, in which strong π-π stacking was achieved for TF1, whereas sulphur-involved nonbonding intermolecular interactions dominated in TF2, leading to the different fluorescence behaviors and also the altered liquid crystalline phases. Finally, typical P-type charge transport behaviors were achieved in both TF1- and TF2-based solution-processed OFETs. Also owing to the much ordered molecular packing in TF1, a higher charge carrier mobility of 3.7 × 10-3 cm2 V-1 s-1 was achieved for TF1-based OFETs compared to TF2-based OFETs.
这里设计并合成了具有高度稠合噻吩核的同分异构 TF1 和 TF2,其中 TF1 的侧基中面对面的硫原子具有高度平面的分子结构,而 TF2 的背靠背硫原子则观察到扭曲的分子骨架。值得注意的是,由于它们的同分异构噻吩核,TF1 和 TF2 中存在不同的分子间相互作用,其中 TF1 实现了强的π-π堆积,而在 TF2 中则主要存在涉及硫的非键分子间相互作用,导致了不同的荧光行为和改变的液晶相。最后,在基于 TF1 和 TF2 的溶液处理 OFET 中都实现了典型的 P 型电荷输运行为。也由于 TF1 中分子排列更加有序,基于 TF1 的 OFET 的电荷载流子迁移率达到了 3.7×10-3cm2V-1s-1,高于基于 TF2 的 OFET。