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Topological implications of Y-conjugation for electronic transitions of cyanine dyes

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Abstract

To understand connections between electronic transitions of dyes having related conjugated systems, topological arguments from graph theory are often helpful. Using the Chebyshev expansion of the characteristic polynomials of cyanines, it is shown that the two possible structures of tribranched cyanines, i.e., a strongly out-of-plane orientation of one of the conjugated branches or a Y-conjugation of the entire unsaturated system, are both consistent with the similarities between visible absorption of these compounds and of simple chains. To choose between these two structures, evidence from other sources should be added.

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References

  1. See Pullman B, Pullman A (1952) In: Les théories électroniques de la chimie organique, chap VI and VII. Masson, Paris

    Google Scholar 

  2. Gund P (1972) J Chem Educ 49:100

    Google Scholar 

  3. Reichardt C, Mormann W (1972) Chem Ber 105:1815; (for nomenclature, see this paper, p 1832)

    Google Scholar 

  4. Grahn W, Reichardt C (1976) Tetrahedron 32:125; Grahn W (1976) Tetrahedron 32:1931

    Google Scholar 

  5. Allmann R, Grahn W, Knecht J, Kucharczyk D, Reichardt C (1985) Chem Ber 118:1295

    Google Scholar 

  6. Reichardt C, Knecht J, Mrozek W, Plaas D, Allmann R, Kucharczyk D (1983) Chem Ber 116:1982

    Google Scholar 

  7. Niaz Khan M, Fleury JP, Baumlin P, Hubschwerlein C (1985) Tetrahedron 41:5341

    Google Scholar 

  8. See Graovac A, Gutman I, Trinajstic N (1977) In: Topological approach to the chemistry of conjugated molecules. Lect Notes Chem 4. Springer, Berlin Heidelberg New York

    Google Scholar 

  9. Günthard HH, Primas H (1956) Helv Chim Acta 39:1645

    Google Scholar 

  10. Ruedenberg K (1954) J Chem Phys 22:1878

    Google Scholar 

  11. Polansky OE, (1975) MATCH 1:183

    Google Scholar 

  12. See Trinajstic N (1977) In: Segal GA (ed) Modern theoretical chemistry—Semi-empirical method. Plenum Press, New York

    Google Scholar 

  13. Balasubramian K, Randic M (1982) Theor Chim Acta 61:307

    Google Scholar 

  14. Balasubramian K (1982) Int J Quantum Chem 21:581; (1984) Theor Chim Acta 65:49

    Google Scholar 

  15. Mayot M, Berthier G, Pullman B (1951) J Phys Radium 12:652, 717; (1953) J Chim Phys 50:170, 176

    Google Scholar 

  16. Hosoya H, Randic M (1983) Theor Chim Acta 63:473; Randic M, Baker B, Kleiner AF (1985) Int J Quantum Chem Symp 19:107

    Google Scholar 

  17. Heilbronner E (1953) Helv Chim Acta 36:170

    Google Scholar 

Download references

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Grajcar, L., Berthier, G., Faure, J. et al. Topological implications of Y-conjugation for electronic transitions of cyanine dyes. Theoret. Chim. Acta 71, 299–304 (1987). https://doi.org/10.1007/BF00529101

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