Atsuhiro Osuka
Researcher Next ID · RN-036073
Researcher · Chemistry
Changsha, China
- Works count
- 2,536
- Citation count
- 50,071
- H-index
- 105
- i10-index
- 846
Research interests
Publications
Chemistry of meso -Aryl-Substituted Expanded Porphyrins: Aromaticity and Molecular Twist
Chemical Reviews · 2016 · 10.1021/acs.chemrev.6b00371
Conjugated porphyrin arrays: synthesis, properties and applications for functional materials
Chemical Society Reviews · 2014 · 10.1039/c3cs60443h
Kinetically Blocked Stable Heptazethrene and Octazethrene: Closed-Shell or Open-Shell in the Ground State?
Journal of the American Chemical Society · 2012 · https://doi.org/10.1021/ja304618v
Expanded porphyrins and aromaticity
Chemical Communications · 2011 · 10.1039/c1cc10534e
Expanded Porphyrins: Intriguing Structures, Electronic Properties, and Reactivities
Angewandte Chemie International Edition · 2011 · 10.1002/anie.201003909
Aromaticity and photophysical properties of various topology-controlled expanded porphyrins
Chemical Society Reviews · 2010 · 10.1039/b925417j
Möbius aromaticity and antiaromaticity in expanded porphyrins
Nature Chemistry · 2009 · 10.1038/nchem.172
Discrete Cyclic Porphyrin Arrays as Artificial Light-Harvesting Antenna
Accounts of Chemical Research · 2009 · 10.1021/ar9001697
Unambiguous Identification of Möbius Aromaticity formeso-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1)
Journal of the American Chemical Society · 2008 · 10.1021/ja801983d
Metalation of Expanded Porphyrins: A Chemical Trigger Used To Produce Molecular Twisting and Möbius Aromaticity
Angewandte Chemie International Edition · 2007 · 10.1002/anie.200704407
Cyclic porphyrin arrays as artificial photosynthetic antenna: synthesis and excitation energy transfer
Chemical Society Reviews · 2007 · 10.1039/b618854k
Optically active single-walled carbon nanotubes
Nature Nanotechnology · 2007 · 10.1038/nnano.2007.142
A Quadruply Azulene‐Fused Porphyrin with Intense Near‐IR Absorption and a Large Two‐Photon Absorption Cross Section
Angewandte Chemie International Edition · 2006 · 10.1002/anie.200600892
A Directly Fused Tetrameric Porphyrin Sheet and Its Anomalous Electronic Properties That Arise from the Planar Cyclooctatetraene Core
Journal of the American Chemical Society · 2006 · 10.1021/ja057812l
Tribenzosubporphines: Synthesis and Characterization
Angewandte Chemie International Edition · 2006 · 10.1002/anie.200503426
Directly Linked Porphyrin Arrays with Tunable Excitonic Interactions
Accounts of Chemical Research · 2004 · 10.1021/ar030242e
Confusion, inversion, and creation—a new spring from porphyrin chemistry
Chemical Communications · 2002 · 10.1039/b200525p
Photophysical Properties of Porphyrin Tapes
Journal of the American Chemical Society · 2002 · 10.1021/ja020826w
meso-Aryl-Substituted Expanded Porphyrins
Journal of the American Chemical Society · 2001 · 10.1021/ja0106624
Syntheses, Structural Characterizations, and Optical and Electrochemical Properties of Directly Fused Diporphyrins
Journal of the American Chemical Society · 2001 · 10.1021/ja0110933
Fully Conjugated Porphyrin Tapes with Electronic Absorption Bands That Reach into Infrared
Science · 2001 · 10.1126/science.1059552
Doubly N-Confused Porphyrin: A New Complexing Agent Capable of Stabilizing Higher Oxidation States
Journal of the American Chemical Society · 2000 · 10.1021/ja992679g
Extremely Long, Discrete meso – meso-Coupled Porphyrin Arrays
Angewandte Chemie International Edition · 2000 · 10.1002/(sici)1521-3773(20000417)39:8<1458::aid-anie1458>3.0.co;2-e
meso, meso ‐Linked Porphyrin Arrays
Angewandte Chemie International Edition in English · 1997 · 10.1002/anie.199701351
Synthesis of naphthalene-bridged porphyrin dimers and their orientation-dependent exciton coupling
Journal of the American Chemical Society · 1988 · 10.1021/ja00221a079
Current projects
No projects listed.