82040-65-1Relevant articles and documents
Synthesis of zinc chlorophyll homo/hetero-dyads and their folded conformers with porphyrin, chlorin, and bacteriochlorin π-systems
Tamiaki, Hitoshi,Fukai, Kazuhiro,Shimazu, Hideki,Shoji, Sunao
, p. 121 - 128 (2014/01/23)
Zinc complex of pyropheophorbide-b, a derivative of chlorophyll-b, was covalently dimerized through ethylene glycol diester. The synthetic homo-dyad was axially ligated with two methanol molecules from the β-face and both the diastereomerically coordinating methanol species were hydrogen bonded with the keto-carbonyl groups of the neighboring chlorin in a complex. The resulting folded conformer in a solution was confirmed by visible, 1H NMR and IR spectra. All the synthetic zinc chlorin homo- and hetero-dyads consisting of pyropheophorbides-a, b and/or d took the above methanol-locked and π-π stacked supramolecules in 1% (v/v) methanol and benzene to give redmost (Qy) electronic absorption band(s) at longer wavelengths than those of the corresponding monomeric chlorin composites. The other zinc chlorin and bacteriochlorin homo-dyads completely formed similar folded conformers in the same solution, while zinc inverse chlorin and porphyrin homo-dyads partially took such supramolecules. The J-type aggregation to folded conformers and the redshift values of composite Qy bands were dependent on the electronic and steric factors of porphyrinoid moieties in dyads. Synthetic zinc chlorophyll dyads were intramolecularly folded with two methanol molecules to form their supramolecules by doubly coordinating and hydrogen-bonding. The resulting π-π stacked J-aggregates gave red-shifted Qy bands in a solution.
