594838-61-6Relevant articles and documents
Substitution site effect of naphthyl substituted anthracene derivatives and their applications in organic optoelectronics
Chen, Mingxi,Dang, Yangyang,Dong, Huanli,Hu, Wenping,Hu, Yongxu,Ji, Deyang,Li, Jie,Li, Liqiang,Liu, Jinyu,Qin, Zhengsheng,Sun, Yajing,Zhen, Yonggang
, p. 15597 - 15602 (2020/12/03)
By introducing the naphthyl group into the 2,6-positions of anthracene, two different anthracene derivatives, 2,6-di(2-naphthyl)anthracene (2,6-di(2-Na)Ant) and 2,6-di(1-naphthyl)anthracene (2,6-di(1-Na)Ant) were synthesized. The tiny change in the substitution site of the naphthyl group leads to a significant difference in the molecular packing and further exerts a great impact on their optoelectronic properties. Thin film field-effect transistors for 2,6-di(2-Na)Ant show charge transport mobility up to 2.1 cm2 V-1 s-1, while 2,6-di(1-Na)Ant demonstrates no mobility. Moreover, thin film phototransistors of 2,6-di(2-Na)Ant show a photoresponsivity of 6.9 × 103 A W-1, a high photosensitivity of 2.6 × 106 and an excellent detectivity of 3.4 × 1016 Jones, which is one of the highest performances of thin film organic phototransistors reported to date. This journal is
A new asymmetric anthracene derivative with high mobility
Yu, Xixia,Zheng, Lei,Li, Jinfeng,Wang, Lu,Han, Jiangli,Chen, Huayi,Zhang, Xiaotao,Hu, Wenping
, p. 251 - 255 (2019/01/14)
An asymmetric anthracene derivative (4-HDPA) was designed and synthesized. With the optimization of proper scenario of fabrication process, top-contact thin film devices based on 4-HDPA exhibit mobility as high as 3.59 cm2 V–1 s
π-Extended Indenofluorenes
Rao, M. Rajeswara,Desmecht, Antonin,Perepichka, Dmitrii F.
, p. 6193 - 6201 (2015/04/14)
A series of π-extended aromatic indenofluorene (IF) analogues with naphthalene and anthracene cores have been synthesized through acid-catalyzed intramolecular cyclization. The regioselectivity of the reaction is controlled by a combination of steric and
