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IBM Thomas J. Watson Research Center; (b). IBM Research Laboratory
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a). IBM Thomas J. Watson Research Center; (b). IBM Research Laboratory.
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Some recent TCNQ modifications
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Some recent TCNQ modifications: R. C. Wheland and E. L. Martin, J. Org. Chem., 40, 3101 (1975).;
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0001244459
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Alternate syntheses of TSeF and DSeDTF have appeared
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Alternate syntheses of TSeF and DSeDTF have appeared: M. V. Lakshmikanthan and M. P. Cava, J. Org. Chem., 41, 882 (1976).;
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Reviews: A. F. Garito and A. J. Heeger, Acc. Chem. Res., 7, 232 (1974).;
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Garito, A.F.1
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K. Masuda and M. Silver, Ed.
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A. N. Bloch, D. O. Cowan, and T. O. Poehler in “Energy and Charge Transfer in Organic Semiconductors”, K. Masuda and M. Silver, Ed., Plenum Press, New York, N. Y., 1974;
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Bloch, A.N.1
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Low Dimensional Cooperative Phenomena
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H. J. Keller, Ed.
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A. J. Heeger and A. F. Garito in “Low Dimensional Cooperative Phenomena”, H. J. Keller, Ed., Plenum Press, New York, N. Y., 1975.
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Perlstein, J.H.1
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0343573125
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Recently, a bipyridinium TCNQ salt was reported to be metallic to <1 K. See London
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Recently, a bipyridinium TCNQ salt was reported to be metallic to <1 K. See G. J. Ashwell, D. D. Eley, and M. R. Willis, Nature (London). 259, 201 (1976).;
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G. J., Ashwell, D. D. Eley, M. R. Willis, and J. Woodward, Phys. Status Solidi B, 79, 629 (1977).
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31
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0017490970
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However, these results have been disputed
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However, these results have been disputed: R. B. Somorno, V. Hadek, S. P. S. Yen, A. Rembaum, C. Hsu, R. J. Deck, T. Datta, and A. M. Hermann, J. Woodward, Phys. Status Solidi B, 81, 281 (1977).
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E. M. Engler, B. A. Scott, S. Etemad, T. Penney, and V. V. Patel, J. Am. Chem. Soc., 99, 5909 (1977).;
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S. Etemad, E. M. Engler, T. Penney, B. A. Scott, and T. D. Schultz, Phys. Rev. Sect. B, 17, 513 (1978).
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Y. Tomkiewicz, E. M. Engler, and T. D. Schultz, Phys. Rev. Lett., 35, 456 (1975).
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T. E. Phillips, T. J. Kristenmacher, A. N. Bloch, and D. O. Cowan, J. Chem. Soc., Chem. Commun., 334 (1976).
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J. R. Cooper, M. Weger, D. Jerome, D. Lefur, K. Bechgaard, A. N. Bloch, and D. O. Cowan, Solid State Commun., 19, 749 (1976).
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Phys., to be published
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R. H. Friend, D. Jerome, J. M. Fabre, L. Giral, and K. Bechgaard, J. Phys., to be published.
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0004551273
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Other syntheses of HMTTF
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Other syntheses of HMTTF: E. Fanghänel, L. van Hink, and G. Schukat, Z. Chem., 16, 317, 360 (1976).;
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85022986799
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P. Delhaes, S. Flandrois, J. Amiell, G. Keryer, E. Toreilles, J. M. Fabre, L. Giral, C. S. Jacobsen, and K. Bechgaard, J. Phys., 233 (1977).
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41
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30244555720
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For earlier references on this cyclization see E. Campaigne
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Hamilton
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For earlier references on this cyclization see E. Campaigne, R. D. Hamilton, and N. W. Jacobsen, J. Org. Chem., 29, 1708 (1964).;
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49849129367
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A convenient, high-yield synthesis of 1,2,3-selenadiazoles has been discovered by
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A convenient, high-yield synthesis of 1,2,3-selenadiazoles has been discovered by I. Lalezari, A. Shafiee, and M. Yalpani, Tetrahedron Lett., 5105 (1969).;
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Abstracts, 167th National Meeting of the American Chemical Society, Los Angeles, Calif., March No. ORGN-12.
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0001680542
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For the preparation of less dangerous hexafluorophosphate salts see L. R. Melby, H. D. Hartzler, and W. A. Sheppard, J. Org. Chem
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For the preparation of less dangerous hexafluorophosphate salts see L. R. Melby, H. D. Hartzler, and W. A. Sheppard, J. Org. Chem., 39, 2456 (1974).
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85023152832
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For an overview of some of these techniques see J. R. Andersen, E. M. Engler, and K. Bechgaard in the Proceedings of the New York Academy of Sciences “Conference on Synthesis and Properties of Low Dimensional Materials
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New York, N. Y.
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For an overview of some of these techniques see J. R. Andersen, E. M. Engler, and K. Bechgaard in the Proceedings of the New York Academy of Sciences “Conference on Synthesis and Properties of Low Dimensional Materials”, New York, N. Y., June 13-16, 1977, to be published.
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70
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0016540122
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For information on this technique see L. B. Coleman, Rev. Sci. Instrum
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For information on this technique see L. B. Coleman, Rev. Sci. Instrum., 46, 1125 (1975).
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