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Aiko Nakano

Researcher at Kyoto University

Publications -  14
Citations -  578

Aiko Nakano is an academic researcher from Kyoto University. The author has contributed to research in topics: Porphyrin & Electron transfer. The author has an hindex of 9, co-authored 14 publications receiving 565 citations. Previous affiliations of Aiko Nakano include Kyoto Institute of Technology.

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Windmill-Like Porphyrin Arrays as Potent Light-Harvesting Antenna Complexes.

TL;DR: Up to 14 porphyrin rings are present in the title compounds 1, which are readily available with high regioselectivity from linear nickel-zinc porphyrs, and upon irradiation with light a rapid energy transfer from the peripheral porphirin rings to the diporphyrIn core takes place.
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Doubly meso‐β‐Linked Diporphyrins from Oxidation of 5,10,15‐Triaryl‐Substituted NiII– and PdII – Porphyrins

TL;DR: In this paper, lower oxidation potentials than for the monomeric starting materials are displayed by diporphyrins obtained by one-electron oxidation with tris(4-bromophenyl)ammonium hexachloroantimonate.
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Modified Windmill Porphyrin Arrays: Coupled Light‐Harvesting and Charge Separation, Conformational Relaxation in the S1 State, and S2–S2 Energy Transfer

TL;DR: The architecture of windmill hexameric zinc(II) -porphyrin array 1 is attractive as a light-harvesting functional unit in view of its three-dimensionally extended geometry that is favorable for a large cross-section of incident light as well as for a suitable energy gradient from the peripheral porphyrins to the meso-meso-linked diporphyrin core.
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Three-dimensionally arranged windmill and grid porphyrin arrays by AgI-promoted meso-meso block oligomerization

TL;DR: Competitive experiments with three linear porphyrin trimers bearing different peripheral metalloporphyrins (ZnII, NiII, and Cull) suggested that an initial one-electron oxidation of the easily oxidizable peripheral ZnII beta-octaalkylporphyrin with an AgI ion and a subsequent endothermic hole transfer assist the generation of the radical cation at the central Zn II beta-free porphyrsin.
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Facile regioselective meso-iodination of porphyrins

TL;DR: In this paper, a mixture of CHCl 3 and pyridine (60:1) resulted in meso-iodination of porphyrins with high regioselectivity.