Abstract
This paper describes the preparation of a bis free-base porphyrin and a bis-zinc porphyrin system in which the two 5,10,15-tris(3,5-ditertbutylphenyl)porphyrinyl units are connected in meso position by a tetraenic chain. The preparation of the dyad relies on the Wittig-Horner-Emmons reaction between diethyl 3-[5-[10,15,20-tris(3,5-ditert-butyl-phenyl)-porphyrinyl]] prop-2-enyl phosphonate and the aldehyde-1,3-diene[5-[10,15,20-tris(3,5-ditert-butyl-phenyl)-porphyrinyl]]. The two latter porphyrin derivatives were obtained via a Stille cross-coupling reaction between the corresponding tributyltin derivatives and the 5-iodo-10,15,20-tris(3,5-ditert-butyl-phenyl)-porphyrin. The UV-visible absorption and fluorescence spectra of the bis-porphyrin systems are measured and indicate that both the energy level and the lifetime of the porphyrin singlet excited state are reduced upon the attachment of the polyene chain to the porphyrin unit.
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