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Coordination Programming of Photofunctional Molecules
AbstractOur recent achievements relating to photofunctional molecules are addressed. Section 1 discloses a new concept of photoisomerization. Pyridylpyrimidine-copper complexes undergo a ring inversion that can be modulated by the redox state of the copper center. In combination with an intermolecular photoelectron transfer (PET) initiated by the metal-to-ligand charge transfer (MLCT) transition of the Cu(I) state, we realize photonic regulation of the ring inversion. Section 2 reports on the first examples of heteroleptic bis(dipyrrinato)zinc(II) complexes. Conventional homoleptic bis(dipyrrinato)zinc(II) complexes suffered from low fluorescence quantum yields, whereas the heteroleptic ones feature bright fluorescence even in polar solvents. Section 3 describes our new findings on Pechmann dye, which was first synthesized in 1882. New synthetic procedures for Pechmann dye using dimethyl bis(arylethynyl)fumarate as a starting material gives rise to its new structural isomer. We also demonstrate potentiality of a donor-acceptor-donor type of Pechmann dye in organic electronics.
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Sakamoto, R.; Kusaka, S.; Hayashi, M.; Nishikawa, M.; Nishihara, H. Coordination Programming of Photofunctional Molecules. Molecules 2013, 18, 4091-4119.View more citation formats
Sakamoto R, Kusaka S, Hayashi M, Nishikawa M, Nishihara H. Coordination Programming of Photofunctional Molecules. Molecules. 2013; 18(4):4091-4119.Chicago/Turabian Style
Sakamoto, Ryota; Kusaka, Shinpei; Hayashi, Mikihiro; Nishikawa, Michihiro; Nishihara, Hiroshi. 2013. "Coordination Programming of Photofunctional Molecules." Molecules 18, no. 4: 4091-4119.
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