| Literature DB >> 30496630 |
Kiyonori Kuroda1, Kohei Yazaki2, Yuya Tanaka1, Munetaka Akita1, Hayato Sakai3, Taku Hasobe3, Nikolai V Tkachenko4, Michito Yoshizawa1.
Abstract
Unlike previously well-studied, acyclic pentacene oligomers, the first synthesis of a cyclic pentacene trimer with a fixed tubular conformation is reported. A short-step synthesis starting from common pentacenequinone yielded the target molecule with a 1.5 nanometer length and a subnanometer pore. Steady-state spectroscopic analyses revealed that the close proximity of the non-conjugated, three pentacene chromophores allows the nanotube to display stepwise electrochemical/chemical oxidation characteristics. Furthermore, time-resolved transient absorption measurements elucidated the generation of an excited triplet state of the nanotube, with high quantum yield reaching about 180 % through intramolecular singlet fission and a very long triplet lifetime.Entities:
Keywords: macrocycles; nanotubes; pentacene; singlet fission; triplet states
Year: 2018 PMID: 30496630 DOI: 10.1002/anie.201812976
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336