Abstract
A series of silylene-spaced alternating [(donor-SiMe2) n=1-3-(acceptor-SiMe2)] copolymers 4-6 was synthesized by rhodium-catalyzed hydrosilylation of bisalkynes with bissilyl hydrides. Monomeric reference compounds 7-10 with similar chromophore components were prepared for comparison. The ratio of donor to acceptor groups is well-controlled by the precise regiochemistry and nature of the repeat units. The silylene moieties serve as insulating spacers between chromophores. The polymers exhibit light-harvesting abilities, for which the intensity of the emission enhanced with larger donor-to-acceptor ratios. No emission originating from the donors was observed in fluorescence spectra, illustrating that intrachain energy transfer is highly efficient along the polymer chain.
Original language | English |
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Pages (from-to) | 5361-5368 |
Number of pages | 8 |
Journal | Chemistry - A European Journal |
Volume | 10 |
Issue number | 21 |
DOIs | |
State | Published - 25 Oct 2004 |
Keywords
- Chromophores
- Energy transfer
- Hydrosilylation
- Inorganic polymers
- Light harvesting