Abstract
A highly stable porphyrin-fullerene conjugate with defined distance and orientation, was formed using a newly developed 'two-point' binding strategy involving axial-coordination and cation-crown ether complexation; photochemical studies performed in benzonitrile revealed efficient charge separation and slow charge-recombination in the supramolecular complex.
Original language | English |
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Pages (from-to) | 1279-1281 |
Number of pages | 3 |
Journal | Chemical Communications |
Issue number | 10 |
DOIs | |
Publication status | Published - 2005 Mar 14 |
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Chemistry(all)
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry