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ABC–ABC‐Type Directly meso – meso Linked Porphyrin Dimers
Author(s) -
Higashino Tomohiro,
Kurumisawa Yuma,
Iiyama Hitomi,
Imahori Hiroshi
Publication year - 2019
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201805405
Subject(s) - porphyrin , chemistry , type (biology) , photochemistry , biology , ecology
Covalently linked porphyrin oligomers are attractive because of their extended π‐conjugated systems. Among various porphyrin oligomers, directly meso – meso linked porphyrin oligomers exhibit unique photophysical properties due to their strong exciton couplings derived from the alternative orthogonal geometry of the porphyrins. Although their structural and electronic properties can be greatly altered by substituents at meso positions, it is still difficult to introduce different substituents at the meso positions. Thus, it is a challenge to develop general synthetic methodologies for functional porphyrin dimers and oligomers with different substituents at the meso positions. Herein, a general synthetic strategy for ABC–ABC‐type directly meso – meso linked porphyrin dimers by stepwise functionalization starting from 10,15,20‐ meso ‐free 5‐substituted porphyrin as building block is established. A meso ‐ABC–ABC‐type meso – meso ‐linked donor–π‐acceptor‐type porphyrin dimer was prepared and exhibited the highest power conversion efficiency (7.91 %) ever reported for dye‐sensitized solar cells based on dimeric orthogonal donor–π‐acceptor‐type organic sensitizers. This synthetic strategy will provide useful guidance for the rational design of functional porphyrin dimers and oligomers for diverse applications.