Synthesis and Photoinduced Electron Transfer Studies of a Tri(Phenothiazine)–Subphthalocyanine–Fullerene Pentad
Organic Letters2013Vol. 15(17), pp. 4612–4615
Citations Over TimeTop 11% of 2013 papers
Abstract
A novel donor-acceptor pentad featuring subphthalocyanine and fullerene as the primary electron donor and acceptor, and three phenothiazine entities as secondary hole transferring agents, have been newly synthesized and characterized as an photosynthetic reaction center model compound. Occurrences of ultrafast photoinduced electron transfer (PET) and slower charge recombination are witnessed in the pentad from the femtosecond and nanosecond transient absorption studies.
Related Papers
- → A novel platform to study the photoinduced electron transfer at a dye-sensitized solid/liquid interface(2012)7 cited
- → Evolution of the Reaction Mechanism during Ultrafast Photoinduced Electron Transfer(2008)11 cited
- → Photoinduced electron-transfer reactions in a host-guest assembly of mono-6-p-nitrobenzoyl-β-cyclodextrin with N-(1-naphthylacetyl)-1-adamantanamine(2003)3 cited
- Photoinduced electron transfer reactions : inorganic substrates and applications(1988)
- → Catalysis of Photoinduced Electron Transfer Reactions(1999)19 cited