Other grades of this product :
| Product Name: | ITIC-TH | | Synonyms: | ITIC-TH;S6677;3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone))-5,5,11,11-tetrakis(5-hexylthienyl)-dithieno[2,3-d:2’,3’-d’]-s-indaceno[1,2-b:5,6-b’]dithiophene;ITIC-Th (n-type acceptor) | | CAS: | 1889344-13-1 | | MF: | C86H74N4O2S8 | | MW: | 1452.04 | | EINECS: | | Product Categories: | ITIC | | Mol File: | 1889344-13-1.mol |
| ITIC-TH Chemical Properties |
| solubility | Chloroform, chlorobenzene, dichlorobenzene |
| ITIC-TH Usage And Synthesis |
| Classification | NFAs, Organic semiconducting materials, Low band-gap small molecule, Small molecular acceptor, Organic photovoltaics, Polymer solar cells, NF-PSCs. | | Applications | When compared with ITIC, instead of having phenyl side-chains, ITIC-Th has hexylthienyl side chains which promotes intermolecular interaction - thus the electron mobility induced by sulfur–sulfur interaction.
ITIC-Th also shows lower energy levels (HOMO = −5.66 eV, LUMO = −3.93 eV) than ITIC due to the effect of thienyl side-chains. With even deeper energy levels,it can potentially match the energy levels of most of the high-performance narrow, medium, to wide band-gap polymer semiconductor donors.
| | Description | When compared with ITIC, instead of having phenyl side-chains, ITIC-Th has hexylthienyl side chains which promotes intermolecular interaction - thus the electron mobility induced by sulfur–sulfur interaction. |
| ITIC-TH Preparation Products And Raw materials |
|
日本语
한국어
Français
Deutsch
España
Türkiye