Bis-substituted tetrathiapentalenes - Novel building blocks for extended tetrathiafulvalenes and conducting polymers

Tetrahedron Letters

Volumn 38, Issue 18, 1997, Pages 3215-3218

  Müller, Harald ^a   Salhi, Fouad ^a   Divisia Blohorn, B ^b  

^a EUROPEAN SYNCHROTRON RADIATION FACILITY   (France)

^b CEA GRENOBLE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TETRATHIAFULVALENE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; IN VITRO STUDY; REACTION ANALYSIS;

STAPHYLOCOCCUS PHAGE 3A;

EID: 0043115527     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00581-9     Document Type: Article

References (13)

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2. For a recent review see: Proc. Int. Conf. Science and Technol. Synth. Metals (ICSM '94); Elsevier: Seoul, Korea, 1994, A.J. Heeger (Ed.), Synth. Met., 1995, 69-71, 1-2308.
3. Misaki, Y., Yamabe, T., Higuchi, N., Fujiwara, H., Mori, T., Mori, H., Tanaka, S., Angew. Chem. Int. Ed. Engl., 1995, 34, 1222-1225.
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8. Schumaker, R. R., Engler, E. M., J. Am. Chem. Soc., 1977, 99, 5521-5522.
9. Müller, H. Thesis, Technical University of Munich, 1991. A detailed discussion of the electrochemical properties will be published elsewhere.
10. Tatemitsu, H., Nishikawa, E., Sakata, Y., Misumi, S., J. Chem. Soc. Chem. Comm., 1985, 106-107.
11. Hapiot, P., Lorcy, D., Tallec, A., Charlier, R., Robert, A., J. Phys. Chem., 1996, 100, 14823-14827.
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13. 8: 709.9487, found: 709.9481. For the CT-complexes 7-11 satisfactory elemental analyses were obtained (C + 0.39, H + 0.17).