Curriculum Vitaes

Tomohiro AGOU

  (吾郷 友宏)

Profile Information

Affiliation
Professor, Department of Material Science, Graduate School of Science, University of Hyogo
Degree
Doctor of Science(Mar, 2007, The University of Tokyo)

Researcher number
90466798
J-GLOBAL ID
201401019521697610
researchmap Member ID
7000008827

External link

2006年4月−2007年3月
日本学術振興会 特別研究員(DC2)
2007年4月−2007年10月
日本学術振興会 特別研究員(PD)
2007年11月−2008年4月
東京大学大学院理学系研究科化学専攻 GCOE特任助教
2008年5月−2009年7月
東京大学大学院理学系研究科化学専攻 助教
2009年8月−2011年3月
京都大学次世代開拓研究ユニット 特定助教
2011年4月−2016年3月
京都大学化学研究所 助教
2016年4月-
茨城大学大学院理工学研究科 准教授

Major Papers

 108

Misc.

 10
  • 吾郷 友宏
    月刊 機能材料, 42(8) 11-18, Aug 7, 2022  Invited
  • Organometallic News (OM News), (3) 89-89, Aug 1, 2022  Peer-reviewedInvited
  • 吾郷友宏, 時任宣博
    有機合成化学協会誌, 75 723-734, Jul 25, 2017  Peer-reviewedInvitedLead author
  • Tomohiro Agou, Norihiro Tokitoh
    JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 75(7) 723-734, Jul, 2017  
    Organoaluminum compounds have been widely utilized in synthetic organic chemistry as nucleophiles, reducing reagents, and Lewis acids. Most of the organoaluminum compounds contain trivalent aluminum atoms with the formula of AIR(3). In contrast, the properties of low-oxidation state aluminum species, Al (II) and Al (I), have not been investigated thoroughly to date. The low-oxidation state aluminum species are generally highly reactive and thus have been proposed only as short-lived, elusive intermediates in several organic reactions. Recent development in main group element chemistry, however, have made its possible to isolate highly reactive low-valent organoaluminum species as bottlable compounds and investigate their reactivity in detail. We report here the reactivity of organoaluminum species bearing Al-Al bonding towards various unsaturated compounds and dihydrogen. Structure and reactivity of formally anti-aromatic aluminacyclopentadienes (alumoles) are also described.
  • Tomohiro Agou, Takayuki Kawashima
    Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 71(4) 330-340, Apr 1, 2013  Peer-reviewedLead author
    From the viewpoint of the improvement of organic optoelectronic devices, including organic electroluminescence devices, organic solar cells, and organic field effect transistors, development of novel π-conjugated molecules with unique structures and properties should be of great importance. In the course of our study on functional π-systems by taking advantage of characteristics of main group elements, we have synthesized dibenzoheteraborin-based hetero-n-conjugated molecules. Rigid and planar π-backbones of the dibenzoheteraborin derivatives have been shown to enhance synergetic interactions between the main group elements. In this paper, syntheses and properties of the dibenzoheteraborin derivatives involving various main group elements, such as nitrogen, oxygen, phosphorus, sulfur, and selenium, are described.
  • Tomohiro Agou, Takayuki Kawashima
    JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 71(4) 330-340, Apr, 2013  
    From the viewpoint of the improvement of organic optoelectronic devices, including organic electroluminescence devices, organic solar cells, and organic field effect transistors, development of novel pi-conjugated molecules with unique structures and properties should be of great importance. In the course of our study on functional pi-systems by taking advantage of characteristics of main group elements, we have synthesized dibenzoheteraborin-based hetero-pi-conjugated molecules. Rigid and planar pi-backbones of the dibenzoheteraborin derivatives have been shown to enhance synergetic interactions between the main group elements. In this paper, syntheses and properties of the dibenzoheteraborin derivatives involving various main group elements, such as nitrogen, oxygen, phosphorus, sulfur, and selenium, are described.
  • Tomohiro Agou
    JOURNAL OF SYNTHETIC ORGANIC CHEMISTRY JAPAN, 64(9) 971-972, Sep, 2006  
    This short review describes syntheses and properties of several pi-conjugated polymers bearing boron atoms in the main chains. These polymers exhibit interesting optical and electronic properties including strong luminescence because of conjugation between pi* orbitals of the unsaturated hydrocarbon units and vacant 2p orbitals of the boron atoms. Boron-containing pi-conjugate polymers are potentially applicable for novel organic functional materials.
  • 吾郷 友宏
    有機合成化学協会誌 : JOURNAL OF Synthetic Organic Chemistry JAPAN, 64(9) 971-972, Sep 1, 2006  Peer-reviewed
    This short review describes syntheses and properties of several π-conjugated polymers bearing boron atoms in the main chains. These polymers exhibit interesting optical and electronic properties including strong luminescence because of conjugation between π* orbitals of the unsaturated hydrocarbon units and vacant 2p orbitals of the boron atoms. Boron-containing π-conjugate polymers are potentially applicable for novel organic functional materials.
  • J Kobayashi, T Agou, T Kawashima
    PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 179(4-5) 959-960, Apr, 2004  

Books and Other Publications

 1

Presentations

 52

Teaching Experience

 11

Research Projects

 13

Industrial Property Rights

 38

Media Coverage

 2