| Literature DB >> 26443499 |
Shohei Kato1, Yuma Serizawa1, Daisuke Sakamaki2, Shu Seki2, Yoshihiro Miyake1, Hiroshi Shinokubo1.
Abstract
We have succeeded in the diversity-oriented synthesis of tetrathia[8]circulenes by sequential C-H borylation and annulation from cyclic tetrathiophene, and time-resolved microwave conductivity studies have proved that the intrinsic hole mobilities of tetrathia[8]circulenes are dependent on the chain length of the alkyl substituents at the peripheral positions.Entities:
Year: 2015 PMID： 26443499 DOI： 10.1039/c5cc06921a
Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222