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Volumn 8, Issue 1, 1996, Pages 63-65

Synthesis and aggregation of a phthalocyanine symmetrical-functionalized with eight tetrathiafulvalene units

Author keywords

[No Author keywords available]

Indexed keywords

AGGLOMERATION; CHARACTERIZATION; CHARGE TRANSFER; CYCLIC VOLTAMMETRY; DERIVATIVES; ELECTROCHEMISTRY; MOLECULES; REDOX REACTIONS; SPECTROSCOPY; SYNTHESIS (CHEMICAL);

EID: 0029778030     PISSN: 09359648     EISSN: None     Source Type: Journal    
DOI: 10.1002/adma.19960080112     Document Type: Article
Times cited : (52)

References (33)
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    • VCH, New York
    • Reviews: a) C. C.Leznoff, A. B. P.Lever (Eds.) Phthalocyanines, Properties and Applications, Vols. 1-3, VCH, New York 1989-1993. b) H. Schultz, H. Lehmann, M. Rein, M. Hanack, Struct. Bonding (Berlin) 1990, 74, 41. c) M. Hanack, M. Lang, Adv. Mater. 1994, 6, 819.
    • (1989) Phthalocyanines, Properties and Applications , vol.1-3
    • Leznoff, C.C.1    Lever, A.B.P.2
  • 7
    • 0002261892 scopus 로고
    • Reviews: a) C. C.Leznoff, A. B. P.Lever (Eds.) Phthalocyanines, Properties and Applications, Vols. 1-3, VCH, New York 1989-1993. b) H. Schultz, H. Lehmann, M. Rein, M. Hanack, Struct. Bonding (Berlin) 1990, 74, 41. c) M. Hanack, M. Lang, Adv. Mater. 1994, 6, 819.
    • (1990) Struct. Bonding (Berlin) , vol.74 , pp. 41
    • Schultz, H.1    Lehmann, H.2    Rein, M.3    Hanack, M.4
  • 8
    • 0028550634 scopus 로고
    • Reviews: a) C. C.Leznoff, A. B. P.Lever (Eds.) Phthalocyanines, Properties and Applications, Vols. 1-3, VCH, New York 1989-1993. b) H. Schultz, H. Lehmann, M. Rein, M. Hanack, Struct. Bonding (Berlin) 1990, 74, 41. c) M. Hanack, M. Lang, Adv. Mater. 1994, 6, 819.
    • (1994) Adv. Mater. , vol.6 , pp. 819
    • Hanack, M.1    Lang, M.2
  • 9
    • 4243111668 scopus 로고
    • [4a]
    • Review: C. C.Leznoff in [4a], 1989, Vol. 1, 1.
    • (1989) , vol.1 , pp. 1
    • Leznoff, C.C.1
  • 18
    • 0343990211 scopus 로고
    • For specific examples of funetionalized TTF derivatives where π-π stacking has been established by X-ray crystal structures see: a) C. Nakano, K. Imaeda, T. Mori, Y. Muruyama, H. Inokuchi, N. Iwasawa, G. Saito, J. Mater. Chem. 1991, 1, 37. b) J. Garín, J. Orduna, S. Uriel, A. J. Moore, M. R. Bryce, S. Wegener, D. S. Yufit, J. A. K. Howard, Synthesis 1994, 489. c) A. S. Batsanov, N. Svenstrup, J. Lau, J. Becher, M. R. Bryce, J. A. K. Howard, J. Chem. Soc., Chem. Commun. 1995, 1201.
    • (1991) J. Mater. Chem. , vol.1 , pp. 37
    • Nakano, C.1    Imaeda, K.2    Mori, T.3    Muruyama, Y.4    Inokuchi, H.5    Iwasawa, N.6    Saito, G.7
  • 19
    • 0028302223 scopus 로고
    • For specific examples of funetionalized TTF derivatives where π-π stacking has been established by X-ray crystal structures see: a) C. Nakano, K. Imaeda, T. Mori, Y. Muruyama, H. Inokuchi, N. Iwasawa, G. Saito, J. Mater. Chem. 1991, 1, 37. b) J. Garín, J. Orduna, S. Uriel, A. J. Moore, M. R. Bryce, S. Wegener, D. S. Yufit, J. A. K. Howard, Synthesis 1994, 489. c) A. S. Batsanov, N. Svenstrup, J. Lau, J. Becher, M. R. Bryce, J. A. K. Howard, J. Chem. Soc., Chem. Commun. 1995, 1201.
    • (1994) Synthesis , pp. 489
    • Garín, J.1    Orduna, J.2    Uriel, S.3    Moore, A.J.4    Bryce, M.R.5    Wegener, S.6    Yufit, D.S.7    Howard, J.A.K.8
  • 20
    • 0141795148 scopus 로고
    • For specific examples of funetionalized TTF derivatives where π-π stacking has been established by X-ray crystal structures see: a) C. Nakano, K. Imaeda, T. Mori, Y. Muruyama, H. Inokuchi, N. Iwasawa, G. Saito, J. Mater. Chem. 1991, 1, 37. b) J. Garín, J. Orduna, S. Uriel, A. J. Moore, M. R. Bryce, S. Wegener, D. S. Yufit, J. A. K. Howard, Synthesis 1994, 489. c) A. S. Batsanov, N. Svenstrup, J. Lau, J. Becher, M. R. Bryce, J. A. K. Howard, J. Chem. Soc., Chem. Commun. 1995, 1201.
    • (1995) J. Chem. Soc., Chem. Commun. , pp. 1201
    • Batsanov, A.S.1    Svenstrup, N.2    Lau, J.3    Becher, J.4    Bryce, M.R.5    Howard, J.A.K.6
  • 24
    • 4243066158 scopus 로고    scopus 로고
    • note
    • max [DMF, 25 °C (ε)] 272 (56,500), 336 (27,900), 647 (13,400) and 677 (13,300); (DMF, 0 °C) 330 (shoulder) (15,500) 638 (8,589) and 670 (8.645); (DMF, 25 °C, after addition of an excess of iodine) 646 (11,754), 676 (11,800) and 880 (2,725) nm.
  • 26
    • 4243134774 scopus 로고    scopus 로고
    • note
    • Compound 6, a brown solid, m.p. 195 °C (from hexane) was prepared in 34 % yield by reaction of compound 1 with 4-nitrophthalonitrile in DMF in the presence of potassium carbonate (60-70 °C, 3 days).


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