Synthesis, structures, and properties of new organic conductors based on tellurocycle-fused TTF donor molecules

Advanced Materials

Volumn 11, Issue 18, 1999, Pages 1527-1530

  Ojima, Emiko ^a   Fujiwara, Hideki ^a   Kobayashi, Hayao ^a   Kobayashi, Akiko ^b  

^a INSTITUTE FOR MOLECULAR SCIENCE   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ELECTROCHEMISTRY; MOLECULAR STRUCTURE; OXIDATION; SULFUR COMPOUNDS; SYNTHESIS (CHEMICAL); TELLURIUM;

TETRATHIAFULVALENE;

ORGANIC CONDUCTORS;

EID: 0033327749     PISSN: 09359648     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-4095(199912)11:18<1527::AID-ADMA1527>3.0.CO;2-X     Document Type: Article

References (17)

1. a) D. O. Cowan, A. M. Kini, in The Chemistry of Organic Selenium and Tellurium Compounds, Vol. II (Ed: S. Patai), Wiley, Chichester 1987.
2. b) M. R. Bryce, Chem. Soc. Rev. 1991, 20, 355.
3. c) J. M. Williams, J. R. Ferraro, R. J. Thorn, K. D. Carlson, U. Geiser, H. H. Wang, A. M. Kini, M.-H. Whangbo, Organic Superconductors (Including Fullerenes), Prentice Hall, Englewood Cliffs, NJ 1992.
4. a) M. Nakata, A. Kobayashi, T. Saito, H. Kobayashi, K. Takimiya, T. Otsubo, F. Ogura, Chem. Commun. 1997, 593.
5. b) E. Arai, H. Fujiwara, H. Kobayashi, A. Kobayashi, K. Takimiya, T. Olsubo, F. Ogura, Inorg. Chem. 1997, 37, 2850.
6. a) E. Aharon-Shalom, J. Y. Becker, J. Bernstein, S. Bittner, S. Shaik, Tetrahedron Lett. 1985, 26, 2783.
7. b) N. Okada, H. Yamochi, F. Shinozaki, K. Oshima, G. Saito, Chem. Lett. 1986, 1861.
8. V. Y. Khodorkovsky, C. Wang, J. Y. Becker, A. Ellen, L. Shapiro, J. Bernstein, Adv. Mater. 1994, 6, 656.
9. a) H. Inokuchi, K. Imaeda, T. Enoki, T. Mori, Y. Maruyama, G. Saito, N. Okada, H. Yamochi, K. Seki, Y. Higuchi, N. Yasuoka, Nature 1987, 329, 39.
10. b) K. Imaeda, T. Enoki, Z. Shi, P. Wu, N. Okada, H. Yamochi, G. Saito, H. Inokuchi, Bull. Chem. Soc. Jpn. 1987, 60, 3163.
11. K. Tsutsui, K. Takimiya, Y. Aso, T. Otsubo, Tetrahedron Lett. 1997, 38, 7569.
12. K. Lerstrup, I. Johannsen, M. Jørgensen, Synth. Met. 1988, 27, B9.
13. H. Kobayashi, A. Kobayashi, Y. Sasaki, G. Saito, H. Inokuchi, Bull. Chem. Soc. Jpn. 1986, 59, 301.
14. C. Wang, A. Ellen, J. Y. Becker, J. Bernstein, Tetrahedron Lett. 1994, 35, 8489.
15. C. Wang, A. Ellen, V. Khodorkovsky, J. Y. Becker, J. Bernstein, J. Chem. Soc., Chem. Commun. 1994, 2115.
16. Slater type atomic orbitals were used for the calculation of molecular orbitals. The exponent ζ and the ionization potential [eV] are (respectively): Te 5s, 2.112, -20.00; Te 5p, 1.827, -11.00; Te 5d, 1.500, -6.80; C 2s, 1.625, -21.4; C 2p, 1.625, -11.4; H 1s, 1.0, -13.6.
17. E. Herr, M. D. Mays, R. D. McCullough, A. B. Bailey, D. O. Cowan, J. Org. Chem. 1996, 61, 7006.