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Synthesis of Zinc Chlorophyll Homo/Hetero‐Dyads and their Folded Conformers with Porphyrin, Chlorin, and Bacteriochlorin π ‐Systems
Author(s) -
Tamiaki Hitoshi,
Fukai Kazuhiro,
Shimazu Hideki,
Shoji Sunao
Publication year - 2013
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/php.12173
Subject(s) - chlorin , chemistry , photochemistry , porphyrin , conformational isomerism , zinc , bacteriochlorophyll , monomer , molecule , crystallography , organic chemistry , pigment , polymer
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, 1 H 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.