The synthesis and optical properties of the first quinone-linked porphyrin dimer
β Scribed by Jonathan L. Sessler; Scott Piering
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 226 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The quinone-linked porphyrin dimer 2 was prepared by the coupling of dipyrrolic intermediates.
Compound 2, as a dilute solution in toluene, shows no detectable fluorescence when irradiated at 407 nm.
Complex photosynthetic models containing two or more porphyrins with covalently attached acceptors1-3 are of current interest since X-ray
π SIMILAR VOLUMES
A new linear switchable diporphyrin array has been the host-guest complexes promotes a change of the geometry of the system toward a topology in which the two synthesized in good yield by a Williamson coupling of 5-(4Πhydroxyphenyl)-10,15,20-triphenylporphyrin with tetraethyl-tetrapyrrolic macrocycl