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Self‐organized monolayer assemblies of octopusporphyrins: photoinduced electron transfer and O 2 coordination in aqueous media
Author(s) -
Tsuchida Eishun,
Komatsu Teruyuki,
Fuhrhop JürgenHinrich
Publication year - 1998
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/(sici)1099-1581(199809)9:9<569::aid-pat814>3.0.co;2-c
Subject(s) - porphyrin , photoinduced electron transfer , electron transfer , materials science , photochemistry , quenching (fluorescence) , aqueous solution , stacking , micelle , crystallography , fluorescence , chemistry , organic chemistry , physics , quantum mechanics
Bolaamphiphilic tetraresorcinolporphyrins with eight long side chains (octopusporphyrins) and their metal complexes form monolayered assemblies in bulk aqueous solution. The nano‐structure, the photoinduced electron transfers and the O 2 coordination of these octopusporphyrin assemblies are described. In the micellar fibers of 1a and 1b, a unique spherical arrangement of eight methyl groups on both sides of the porphyrin ring plane provides hydrophobic porphyrin centers which align in a string of pearls. Exciton calculations indicated a tilt stacking porphyrins arrangement with a separation of 11 Å. These fibers fluoresced strongly; electron transfer reaction was therefore observed between the porphyrin center and hydrophobic quenchers as well as hydrophilic quenchers. The fibers were also active as photocatalysts in the reduction of dimethylviologen by triethanolamine. Octopusporphyrins with different metal centers can also produce fibrous aggregates, for example, H 2 P/Zn(II)P and Zn(II)P/Fe(III)P couples. The fluorescence quenching of Zn(II)P in the Zn(II)P/Fe(III)P hybrid fibers can be ascribed to the intermolecular electron transfer within the fibers. In H 2 P/Zn(II)P couple, excitation energy transfer from excited Zn 1 *P to H 2 P occurred after photoexcitation. Octopusporphyrin with four dialkylglycerophosphocholine groups on both sides of the ring plane ( 2b ) forms spherical unilamellar vesicles. Based on cryomicroscopy, a white line was observed with a diameter of 15 Å in the middle of the membrane which are obviously a porphyrin layer with low molecular packing. The octopusheme ( 2c ) vesicles prepared in a similar manner with 20‐fold excess molar coexistence of 1‐dodecyl‐2‐methylimidazole (DMIm) can bind and release oxygen reversibly at 25°C. Moreover, water‐soluble octopusporphyrin ( 3a ) produced fluorescent and non‐fluorescent monolayer assemblies by anion exchange of the head groups, e.g. 3a with sodium perchlorate showed planar sheets. An exciton calculation is consistent with a two‐dimensional arrangement with porphyrin separations of 25.6 and 17.4 Å in the x‐ and y‐directions, respectively. External addition of negatively charged electron acceptors, naphtoquinone sulfonate and anthraquinone sulfonate, led to partial quenching of the fluorescence of the central porphyrin layer. The results have been evaluated using equations derived for this special quenching. © 1998 John Wiley & Sons, Ltd.