Hiroshi Nishihara (西原寛, Nishihara Hiroshi), born 21 March 1955, is a Japanese chemist and Professor of Chemistry at The University of Tokyo in Japan. Currently heading the department of Chemistry and Inorganic Chemistry Laboratory in The University of Tokyo, he is a distinguished professor, researcher and pioneer in the field of synthesis and electrochemistry of conductive metal complex polymers.

Hiroshi Nishihara
西原寛
Hiroshi Nishihara celebrating his 60th birthday. (March 21, 2015)
Born21 March 1955
NationalityJapanese
Scientific career
InstitutionsUniversity of Tokyo

His research is focused on creation of new electro- and photo-functional materials comprising both transition metals and π-conjugated chains, and invention of unidirectional electron transfer systems utilizing molecular layer interfaces. He is presently a Vice President of The Electrochemical Society of Japan, and the regional representative of Japan for International Society of Electrochemistry (ISE).

Education and professional experiences

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  • 1977 B.Sc. (Chemistry), The University of Tokyo
  • 1982 D.Sc. (Chemistry), The University of Tokyo (Professor Yukiyoshi Sasaki)
  • 1982-1990 Research Associate, Faculty of Science and Technology, Keio University (Professor Kunitsugu Aramaki)
  • 1987-1989 Visiting Research Associate, The University of North Carolina at Chapel Hill (Professor Royce W. Murray)
  • 1990 Lecturer, Faculty of Science and Technology, Keio University
  • 1992 Associate Professor, Faculty of Science and Technology, Keio University (Interface Chemistry)
  • 1993-1996 Researcher, PRESTO, Japan Science and Technology Agency (Research Supervisor: Prof. K. Honda)
  • 1996–Present Professor, Department of Chemistry, School of Science, The University of Tokyo (Inorganic Chemistry)

Research interests

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Coordination Chemistry, Organometallic Chemistry, Electrochemistry, Photochemistry, Nanomaterials

Awards and honours

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Reviews

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  • Kurihara, M.; Nishihara, H. (2002). "Azo-and quinone-conjugated redox complexes—photo-and proton-coupled intramolecular reactions based on d–π interaction". Coordination Chemistry Reviews. 226 (1): 125–135. doi:10.1016/s0010-8545(01)00421-0.
  • Nishihara, H (2005). "Combination of redox-and photochemistry of azo-conjugated metal complexes". Coordination Chemistry Reviews. 249 (13): 1468–1475. doi:10.1016/j.ccr.2004.11.009.
  • Nishihara, H.; Kanaizuka, K.; Nishimori, Y.; Yamanoi, Y. (2007). "Construction of redox-and photo-functional molecular systems on electrode surface for application to molecular devices". Coordination Chemistry Reviews. 251 (21): 2674–2687. doi:10.1016/j.ccr.2007.04.002.
  • Allakhverdiev, S. I.; Thavasi, V.; Kreslavski, V. D.; Zharmukhamedov, S. K.; Klimov, V. V.; Ramakrishna, S.; Losa, D. A.; Mimurod, M.; Nishiharae, H.; Carpentierf, R. (2010). "Photosynthetic hydrogen production". Journal of Photochemistry and Photobiology C: Photochemistry Reviews. 11 (2): 101–113. doi:10.1016/j.jphotochemrev.2010.07.002.
  • Sakamoto, R.; Rao, K. P.; Nishihara, H. (2011). "Arylethynylanthraquinone and Bis (arylethynyl) anthraquinone: Strong Donor-Acceptor Interaction and Proton-induced Cyclization to Form Pyrylium and Dipyrylium Salts". Chemistry Letters. 40 (12): 1316–1326. doi:10.1246/cl.2011.1316.
  • Sakamoto, R.; Katagiri, S.; Maeda, H.; Nishihara, H. (2013). "Bis (terpyridine) metal complex wires: Excellent long-range electron transfer ability and controllable intrawire redox conduction on silicon electrode". Coordination Chemistry Reviews. 257 (9): 1493–1506. doi:10.1016/j.ccr.2012.08.025.
  • Nishihara, H (2014). "Coordination Programming-A Concept for the Creation of Multifunctional Molecular Systems". Chem. Lett. 43 (4): 388–395. doi:10.1246/cl.140010.
  • Sakamoto, R.; Wu, K. H.; Matsuoka, R.; Maeda, H.; Nishihara, H. (2015). "π-Conjugated bis (terpyridine) metal complex molecular wires". Chemical Society Reviews. 44 (21): 7698–7714. doi:10.1039/C5CS00081E. PMID 25864838.
  • Guldi, D. M.; Nishihara, H.; Venkataraman, L. (2015). "Molecular wires". Chemical Society Reviews. 44 (4): 842–844. doi:10.1039/c5cs90010g. PMID 25636152.

References

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