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Volumn 8, Issue 6, 1998, Pages 1361-1372

Aryl ester dendrimers incorporating tetrathiafulvalene units: Convergent synthesis, electrochemistry and charge-transfer properties

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EID: 0000187995     PISSN: 09599428     EISSN: None     Source Type: Journal    
DOI: 10.1039/a800225h     Document Type: Article
Times cited : (40)

References (84)
  • 20
    • 0001344580 scopus 로고    scopus 로고
    • ed. G. R. Newkome, JAI Press, London
    • For a review of redox-active dendrimers see: M. R. Bryce and W. Devonport, in Advances in Dendritic Macromolecules, ed. G. R. Newkome, JAI Press, London, 1996, vol. 3, p. 115.
    • (1996) Advances in Dendritic Macromolecules , vol.3 , pp. 115
    • Bryce, M.R.1    Devonport, W.2
  • 52
    • 37049077991 scopus 로고
    • 16a,22 However, it has subsequently been shown that this is not always the case: T. Ozturk, C. R. Rice and J. D. Wallis, J. Mater. Chem., 1995, 5, 1553.
    • (1995) J. Mater. Chem. , vol.5 , pp. 1553
    • Ozturk, T.1    Rice, C.R.2    Wallis, J.D.3
  • 55
    • 0001009088 scopus 로고
    • For a review of TTF synthesis see: A. Krief, Tetrahedron, 1986, 42, 1209.
    • (1986) Tetrahedron , vol.42 , pp. 1209
    • Krief, A.1
  • 56
    • 84987240897 scopus 로고
    • By analogy with 4,5-(2-hydroxypropane-1,3-diyldithio)tetrathiafulvalene (ref. 22 and P. R. Ashton, R. A. Bissel, N. Spencer, J. F. Stoddart and M. S. Tolley, Synlett., 1992, 923) compound 20 may serve as a useful building block in other areas of TTF chemistry. The alcohol group of 20 has been transformed into a range of substituents, e.g., mesylate, tosylate, chloride, azide, nitrile and phthalimide
    • (1992) Synlett. , pp. 923
    • Ashton, P.R.1    Bissel, R.A.2    Spencer, N.3    Stoddart, J.F.4    Tolley, M.S.5
  • 57
    • 27844554173 scopus 로고
    • Ph.D. Thesis, University of Durham
    • (G. J. Marshallsay, Ph.D. Thesis, University of Durham, 1994).
    • (1994)
    • Marshallsay, G.J.1
  • 66
    • 27844553197 scopus 로고    scopus 로고
    • note
    • Data obtained in our laboratory and at the Université d'Angers, in collaboration with Professor M. Jubault, showed close agreement.
  • 69
    • 0003154758 scopus 로고
    • ed. A. J. Bard, Marcel Dekker, New York
    • (a) A. T. Hubbard and F. C. Anson, in Electroanalytical Chemistry, ed. A. J. Bard, vol. 4, pp. 129-210, Marcel Dekker, New York, 1970;
    • (1970) Electroanalytical Chemistry , vol.4 , pp. 129-210
    • Hubbard, A.T.1    Anson, F.C.2
  • 84
    • 0030950056 scopus 로고    scopus 로고
    • For the synthesis of TTF, the precursor of 1, see: A. J. Moore and M. R. Bryce, Synthesis, 1997, 407.
    • (1997) Synthesis , pp. 407
    • Moore, A.J.1    Bryce, M.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.