Paper
1 November 1997 Photoinduced electron transfer in fullerenes containing donor-bridge-acceptor dyads
Dirk M. Guldi, Michele Maggini, Simonetta Mondini, Gianfranco Scorrano, Maurizio Prato
Author Affiliations +
Abstract
Excited states properties of supramolecular fullerene donor- bridge-acceptor dyads were studied under various conditions. The steady-state emission yields of C60-Fc and Ru-C60 dyads are noticeably quenched relative to ruthenium and fullerene model compounds, respectively. This indicates that intramolecular electron-energy transfer plays a predominant contribution in the deactivation of the photoexcited chromophores, e.g. the singlet excited state of the fullerene core and ruthenium excited MLCT state. Picosecond and nanosecond resolved photolysis show that the photoexcited C60-Fc and Ru-C60 dyads transform rapidly into charge separated states. Characteristic NIR absorption of the fullerene (pi) -radical anions were complimented by a detailed UV/vis analysis and confirm the existence of long-lived radical pairs. The structure, length, and nature of the bridging spacer separating the two reactive centers had a significant impact on the lifetime nd stabilization of the charge separated states.
© (1997) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Dirk M. Guldi, Michele Maggini, Simonetta Mondini, Gianfranco Scorrano, and Maurizio Prato "Photoinduced electron transfer in fullerenes containing donor-bridge-acceptor dyads", Proc. SPIE 3142, Fullerenes and Photonics IV, (1 November 1997); https://doi.org/10.1117/12.283756
Lens.org Logo
CITATIONS
Cited by 2 scholarly publications.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Fullerenes

Ruthenium

Absorption

Luminescence

Photolysis

Dielectrics

Chromophores

Back to Top