Abstrakti
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.
Alkuperäiskieli | Englanti |
---|---|
Sivut | 1115-1119 |
Julkaisu | Angewandte Chemie - International Edition |
Vuosikerta | 58 |
Numero | 4 |
Varhainen verkossa julkaisun päivämäärä | 2018 |
DOI - pysyväislinkit | |
Tila | Julkaistu - tammik. 2019 |
OKM-julkaisutyyppi | A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä |
Julkaisufoorumi-taso
- Jufo-taso 3
!!ASJC Scopus subject areas
- Catalysis
- Chemistry(all)