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2009年–2003年
Axial Ligand Exchange Reactions of meso-Aryl Subporphyrins - Axially Fluoro-Substituted Subporphyrin and a μ-Oxo Dimer and Trimer Of Subporphyrins
Axial Ligand Exchange Reactions of meso-Aryl Subporphyrins - Axially Fluoro-Substituted Subporphyrin and a μ-Oxo Dimer and Trimer Of Subporphyrins
Shimizu S.; Matsuda A.; Kobayashi N.
Inorg. Chem., 2009, 48, 7885–7890.
Effect of peripheral fused ring substitution on the optical spectroscopy and electronic structure of metal phthalocyanine complexes
Effect of peripheral fused ring substitution on the optical spectroscopy and electronic structure of metal phthalocyanine complexes
Chidawanyika W.; MacK J.; Shimizu S.; Kobayashi N.; Nyokong T.
J. Porphyrins Phthalocyanines, 2009, 13, 1053–1062.
Conformational Changes of meso-Aryl Substituted Expanded Porphyrins upon Protonation: Effects on Photophysical Properties and Aromaticity
Conformational Changes of meso-Aryl Substituted Expanded Porphyrins upon Protonation: Effects on Photophysical Properties and Aromaticity
Shin J. Y.; Lim J. M.; Yoon Z. S.; Kim K. S.; Yoon M. C.; Hiroto S.; Shinokubo H.; Shimizu S.; Osuka A.; Kim D.
J. Phys. Chem. B, 2009, 113, 5794–5802.
meso-Aryl Substituted Rubyrin and Its Higher Homologues: Structural Characterization and Chemical Properties
meso-Aryl Substituted Rubyrin and Its Higher Homologues: Structural Characterization and Chemical Properties
Shimizu S.; Cho W. S.; Sessler J. L.; Shinokubo H.; Osuka A.
Chem. –Eur. J., 2008, 14, 2668–2678.
meso-Aryl tribenzosubporphyrin - a totally substituted subporphyrin species
meso-Aryl tribenzosubporphyrin - a totally substituted subporphyrin species
Makarova E. A.; Shimizu S.; Matsuda A.; Luk'yanets E. A.; Kobayashi N.
Chem. Commun., 2008, 2109–2111.
Group 12 Metal Complexes Of [26]Hexaphyrin(1.1.1.1.1.1)
Group 12 Metal Complexes Of [26]Hexaphyrin(1.1.1.1.1.1)
Mori S.; Shimizu S.; Shin J.-Y.; Osuka A.
Inorg. Chem., 2007, 46, 4374–4376.
[40]Nonaphyrin(1.1.1.1.1.1.1.1.1) and Its Heterometallic Complexes with Palladium-Carbon Bonds
[40]Nonaphyrin(1.1.1.1.1.1.1.1.1) and Its Heterometallic Complexes with Palladium-Carbon Bonds
Kamimura Y.; Shimizu S.; Osuka A.
Chem. Eur. J., 2007, 13, 1620–1628.
Nonlinear Optical Properties and Excited-State Dynamics of Highly Symmetric Expanded Porphyrins
Nonlinear Optical Properties and Excited-State Dynamics of Highly Symmetric Expanded Porphyrins
Yoon Z. S.; Kwon J. H.; Yoon M. C.; Koh M. K.; Noh S. B.; Sessler J. L.; Lee J. T.; Seidel D.; Aguilar A.; Shimizu S.; Suzuki M.; Osuka A.; Kim D.
J. Am. Chem. Soc., 2006, 128, 14128–14134.
meso-Trifluoromethyl-Substituted Expanded Porphyrins
meso-Trifluoromethyl-Substituted Expanded Porphyrins
Shimizu S.; Aratani N.; Osuka A.
Chem. –Eur. J., 2006, 12, 4909–4918.
meso-Aryl-Substituted [26]Hexaphyrin(1.1.0.1.1.0) and [38]Nonaphyrin(1.1.0. 1.1.0.1.1.0) from Oxidative Coupling of a Tripyrrane
meso-Aryl-Substituted [26]Hexaphyrin(1.1.0.1.1.0) and [38]Nonaphyrin(1.1.0. 1.1.0.1.1.0) from Oxidative Coupling of a Tripyrrane
Shimizu S.; Taniguchi R.; Osuka A.
Angew. Chem. Int. Ed., 2005, 44, 2225–2229.
Dicopper and Disilver Complexes of Octaphyrin(1.1.1.1.1.1.1.1): Reversible Hydrolytic Cleavage of the Pyrrolic Ring to a Keto-Imine
Dicopper and Disilver Complexes of Octaphyrin(1.1.1.1.1.1.1.1): Reversible Hydrolytic Cleavage of the Pyrrolic Ring to a Keto-Imine
Shimizu S.; Tanaka Y.; Youfu K.; Osuka A.
Angew. Chem. Int. Ed., 2005, 44, 3726–3729.
N-Fused Pentaphyrins and Their Rhodium Complexes: Oxidation-Induced Rhodium Rearrangement
N-Fused Pentaphyrins and Their Rhodium Complexes: Oxidation-Induced Rhodium Rearrangement
Mori S.; Shin J.-Y.; Shimizu S.; Ishikawa F.; Furuta H.; Osuka A.
Chem. Eur. J., 2005, 11, 2417–2425.
Group 10 Metal Complexes of meso-Aryl-Substituted [26]Hexaphyrins with a Metal-Carbon Bond
Group 10 Metal Complexes of meso-Aryl-Substituted [26]Hexaphyrins with a Metal-Carbon Bond
Mori S.; Shimizu S.; Taniguchi R.; Osuka A.
Inorg. Chem., 2005, 44, 4127–4129.
Internally 1,4-Phenylene-Bridged meso Aryl-Substituted Expanded Porphyrins: The Decaphyrin and Octaphyrin Cases
Internally 1,4-Phenylene-Bridged meso Aryl-Substituted Expanded Porphyrins: The Decaphyrin and Octaphyrin Cases
Anand V. G.; Saito S.; Shimizu S.; Osuka A.
Angew. Chem. Int. Ed., 2005, 44, 7244–7248.
Comparative Photophysics of [26]- and [28]Hexaphyrins(1.1.1.1.1.1): Large Two-Photon Absorption Cross Section of Aromatic [26]Hexaphyrins(1.1.1.1.1.1)
Comparative Photophysics of [26]- and [28]Hexaphyrins(1.1.1.1.1.1): Large Two-Photon Absorption Cross Section of Aromatic [26]Hexaphyrins(1.1.1.1.1.1)
Ahn T. K.; Kwon J. H.; Kim D. Y.; Cho D. W.; Jeong D. H.; Kim S. K.; Suzuki M.; Shimizu S.; Osuka A.; Kim D.
J. Am. Chem. Soc., 2005, 127, 12856–12861.
Thermal Splitting of Bis-Cu(II) Octaphyrin(1.1.1.1.1.1.1.1) into Two Cu(II) Porphyrins
Thermal Splitting of Bis-Cu(II) Octaphyrin(1.1.1.1.1.1.1.1) into Two Cu(II) Porphyrins
Tanaka Y.; Hoshino W.; Shimizu S.; Youfu K.; Aratani N.; Maruyama N.; Fujita S.; Osuka A.
J. Am. Chem. Soc., 2004, 126, 3046–3047.
Biscopper Complexes of meso-Aryl-Substituted Hexaphyrin: Gable Structures and Varying Antiferromagnetic Coupling
Biscopper Complexes of meso-Aryl-Substituted Hexaphyrin: Gable Structures and Varying Antiferromagnetic Coupling
Shimizu S.; Anand V. G.; Taniguchi R.; Furukawa K.; Kato T.; Yokoyama T.; Osuka A.
J. Am. Chem. Soc., 2004, 126, 12280–12281.
Ring size selective synthesis of meso-aryl expanded porphyrins
Ring size selective synthesis of meso-aryl expanded porphyrins
Taniguchi R.; Shimizu S.; Suzuki M.; Shin J.-Y.; Furuta H.; Osuka A.
Tetrahedron Letters, 2003, 44, 2505–2507.
Regioselective nucleophilic substitution reaction of meso-hexakis(pentafluorophenyl) substituted [26]hexaphyrin
Regioselective nucleophilic substitution reaction of meso-hexakis(pentafluorophenyl) substituted [26]hexaphyrin
Suzuki M.; Shimizu S.; Shin J.-Y.; Osuka A.
Tetrahedron Letters, 2003, 44, 4597–4601.
Perfluorinated meso-Aryl-Substituted Expanded Porphyrins
Perfluorinated meso-Aryl-Substituted Expanded Porphyrins
Shimizu S.; Shin J.-Y.; Furuta H.; Ismael R.; Osuka A.
Angew. Chem. Int. Ed., 2003, 42, 78–82.
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