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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Yoshihiro Yamaguchi

Department of Chemistry

Faculty of Science and Engineering

Kinki University

3-4-1 Kowakae

Japan

[email]@*.kindai.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Chemistry, Faculty of Science and Engineering, Kinki University, 3-4-1 Kowakae, Japan. 2003 - 2008

References

  1. Photophysical properties of oligophenylene ethynylenes modified by donor and/or acceptor groups. Yamaguchi, Y., Shimoi, Y., Ochi, T., Wakamiya, T., Matsubara, Y., Yoshida, Z. J. Phys. Chem. A (2008) [Pubmed]
  2. How the pi conjugation length affects the fluorescence emission efficiency. Yamaguchi, Y., Matsubara, Y., Ochi, T., Wakamiya, T., Yoshida, Z. J. Am. Chem. Soc. (2008) [Pubmed]
  3. New fluorophores with rod-shaped polycyano pi-conjugated structures: synthesis and photophysical properties. Yamaguchi, Y., Ochi, T., Wakamiya, T., Matsubara, Y., Yoshida, Z. Org. Lett. (2006) [Pubmed]
  4. Rigid molecular architectures that comprise a 1,3,5-trisubstituted benzene core and three oligoaryleneethynylene arms: light-emitting characteristics and pi conjugation between the arms. Yamaguchi, Y., Ochi, T., Miyamura, S., Tanaka, T., Kobayashi, S., Wakamiya, T., Matsubara, Y., Yoshida, Z. J. Am. Chem. Soc. (2006) [Pubmed]
  5. Light-emitting efficiency tuning of rod-shaped pi conjugated systems by donor and acceptor groups. Yamaguchi, Y., Tanaka, T., Kobayashi, S., Wakamiya, T., Matsubara, Y., Yoshida, Z. J. Am. Chem. Soc. (2005) [Pubmed]
  6. Banana-shaped oligo(aryleneethynylene)s: synthesis and light-emitting characteristics. Yamaguchi, Y., Kobayashi, S., Wakamiya, T., Matsubara, Y., Yoshida, Z. Angew. Chem. Int. Ed. Engl. (2005) [Pubmed]
  7. Synthesis and light-emitting characteristics of doughnut-shaped pi-electron systems. Yamaguchi, Y., Kobayashi, S., Miyamura, S., Okamoto, Y., Wakamiya, T., Matsubara, Y., Yoshida, Z. Angew. Chem. Int. Ed. Engl. (2004) [Pubmed]
  8. Shape-persistency and molecular function in heteromacrocycles: creation of heteroarenecyclynes and arene-azaarenecyclynes. Yamaguchi, Y., Yoshida, Z. Chemistry (2003) [Pubmed]
 
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