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Part of the book series: NATO ASI Series ((ASHT,volume 52))

Abstract

Structure-property relationships of conjugated organic compounds are governed by three fundamental principles, the triad principle, the energy principle, and the bonding principle, which enable chemists to design new substances with given properties. Especially color and constitution relationships are understood by five basic color rules which states that polymethine-like compounds absorb at much longer wavelengths than aromatic or polyene-like compounds of the same size. Further strong red-shift necessitates perturbation of the unique alternation of the n-electron densities in polymethines. As the intended red-shifts are compensated through aromatization and polyene formation such effects have to be excluded in molecular engineering of NIR dyes.

More quantitative estimations of structure-property relationships are achieved through long polymethine chain approximation (LPCA) which is a topological approach involving effective parameters of polymethine chain end groups, namely, the electron donor ability, the effective length, and their derivatives with respect to energy.

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References

  1. Dyadyusha, G. G. and Kachkovskii, A. D. (1975) Wavelength of first electronic transitions of symmetric cyanine dyes, Ukr. Khim. Zh. 41, 1176–1181 [Soy. Progr. Chem. 41 (11), 52–57];

    Google Scholar 

  2. Dyadyusha, G. G. and Kachkovskii, A. D. (1978) Basicity of heterocyclic nuclei and coefficients of molecular orbitals of symmetric cyanine dyes,Ukr. Khim. Zh. 44, 948–953 [Soy. Progr. Chem. 44(9), 50–55];

    Google Scholar 

  3. Dyadyusha, G. G. and Ushomirskii, M. N. (1985) Effective additive parameters of fragments of two-nucleus polymethine dyes, Teor. Eksp. Khim. 21, 268–279 [Theor. Exp. Chem. 21, 257–268];

    Google Scholar 

  4. Dyadyusha, G. G., Komilov, M. Yu., and Dekhtyar, M. L. (1988) On the application of the inverse adjacency matrix in HMO method, J. Inf. Recording Materials 16, 275–283;

    CAS  Google Scholar 

  5. Kachkovskii, A. D. (1989) Constitution and Colour ofPolymethine Dyes, Naukova Dumka, Kiev.

    Google Scholar 

  6. Fabian, J. and Zahradnik, R. (1989) The Search for Strongly Colored Organic Compounds, Angew. Chem. 101, 693–710;Angew. Chem. Intern. Ed. Engl. 28, 677–694;

    Google Scholar 

  7. Fabian, J. (1991)Polymethinfarbstoffe mit Lichtabsorption im Nahen Infrarot, J. prakt. Chem. 333, 197–222;

    Article  CAS  Google Scholar 

  8. Fabian, J., Nakazumi, H., and Matsuoka, M. (1992) Near-Infrared Absorbing Dyes, Chem. Rev. 92, 1197–1226;

    Article  Google Scholar 

  9. Atzrodt, J, Brandenbureg, J., Kaepplinger, C., Heckert, R., Guenther, W., Goerls, H., and Fabian, J. (1997) Fuenfring-Cycloamidine — Neue farbige Heterocyclen mit ungewoehnlichen Eigenschaften. I. Synthese und spektrale Besonderheiten, J.prakt. Chem. 339, 729–734;

    Article  CAS  Google Scholar 

  10. Fabian, J., Goerls, H., Heckert, R., und Atzrodt, J. (1997) Fuenfring-Cycloamidine — Neue farbige Heterocyclen mit ungewoehnlichen Eigenschaften. II. Molekuel-und Elektronenstruktur, J. prakt. Chem. 339, 735–741.

    Article  CAS  Google Scholar 

  11. Daehne, S. (1978) Color and Constitution: one Hundred Years of Research, Science [Washington) 199, 1163–1167;

    Article  CAS  Google Scholar 

  12. Daehne, S. and Moldenhauer, F. (1985) Structural Principles of Unsaturated Organic Compounds: Evidence by Quantum Chemical Calculations, Progr. Phys. Org. Chem. 15 (1985) 1–130;

    Article  CAS  Google Scholar 

  13. Daehne, S. and Hoffmann, K. (1990) Free Energy Relationships in Strongly Conjugated Substituents: The Polymethine Approach., Progr. Phys. Org. Chem. 18, 1–64;

    Article  CAS  Google Scholar 

  14. Daehne, S. (1992) Struktur-FarbeBeziehungen im Wandel der Zeit, in C. Memel and H. Scholz (eds.), Die Allianz von Wissenschaft und Industrie: A. W. Hofmann (1818–1892), VCH Verlagsges., Weinheim, pp. 257–268;

    Google Scholar 

  15. Bach, G. and Daehne, S. (1997) Cyanine Dyes and Related Compounds, in M. Sainsbury (ed.), RODD ‘s Chemistry of Carbon Compounds, 2nd Suppl., 2nd Ed., Vol. IVB, Elsevier Sci. Publ., Amsterdam, pp. 383–481.

    Google Scholar 

  16. Daehne, S. (1984) Das Polymethinmodell der Indigoide, Part 1, J. Signal. Aufzeichnungsmaterialien 12, 75–95; dito (1982) Part 2, J. Inf. Recording Materials 14, 3–20; dito (1991) Part 3, J. Inf. Recording Materials 19, 73–104.

    Google Scholar 

  17. Dyadyusha, G. G., Rozenbaum, V. M., and Dekhtyar, M. L. (1991) Perturbation of the quasi-continuous spectrum by locally attached fragments, Zh. Eksp.Teor. Fiz. 100, 1051–1060 [Sov. Phys. JETP 73, 581–586];

    Google Scholar 

  18. Dekhtyar, M. L. (1995) Application of the quasi-long chain approximation to structural perturbations in polymethine dyes, Dyes Pigm. 28, 261–274.

    Article  CAS  Google Scholar 

  19. Dyadyusha, G. G. (1964) Electronic spectra and structure of symmetric organic compounds, Ukr. Khim. Zh. 30, 929–934; 1186–1194.

    Google Scholar 

  20. Longuet-Higgins, H. C. (1950) A molecular orbital theory, J. Chem. Phys. 18, 265–287.

    Article  CAS  Google Scholar 

  21. Dekhtyar, M. L. and Rozenbaum, V. M. (1995) The origin ofnonmonotonic dependence of the first electronic hyperpolarizability of polymethine compounds on the donor-acceptor strength of their end groups, J. Phys. Chem. 99, 11656–11658;

    Article  CAS  Google Scholar 

  22. Dekhtyar, M. L. and Rozenbaum, V. M. (1997) Simple topological estimation of the first electronic hyperpolarizability of polymethine compounds, J. Phys. Chem. 101, 809–812.

    Article  CAS  Google Scholar 

  23. Oudar, J. L. and Chemla, D. S. (1977) Hyperpolarizabilities of the nitroanilines and their relations to the excited state dipole moment, J. Chem. Phys. 66, 2664–2668;

    Article  CAS  Google Scholar 

  24. Oudar, J. L. (1977) Optical nonlinearities of conjugated molecules. Stilbene derivatives and highly polar aromatic compounds, J. Chem. Phys. 67, 446–457.

    Article  CAS  Google Scholar 

  25. Marder, S.R., Gorman, C. B., Meyers, F., Perry, J. V., Bourhill, G., Brédas, J.-L., and Pierce, B. M. (1994) A unified description of linear and nonlinear polarization in organic polymethine dyes, Science [Washington] 265, 632–635.

    Article  CAS  Google Scholar 

  26. Cheng, L.-T., Tam, W., Stevenson, S. H., Marder, S. R., Stiegman, A. E., Rikken, G., and Spangler, C. V. (1991) Experimental investigations of organic molecular nonlinear optical polarizabilities. 2. A study of conjugation dependences, J. Chem. Phys. 95, 10643–10652;

    Article  Google Scholar 

  27. Tiemann, B. G., Cheng, L.-T., and Marder, S. R. (1993) The effect of varying ground-state aromaticity on the first molecule electronic hyperpolarizabilities of Organic donor-acceptor molecules. J. Chem. Soc., Chem. Commun.N 9, 735–737;

    Article  Google Scholar 

  28. Mostovnikov, V. A., Rubinov, A. N., Al’perovich, M. A. et al.(1974) Dependence of luminescent and generation properties of solutions of polymethine dyes on their structure, Zh. Prikl. Spektrosk. 20, 42–47;

    CAS  Google Scholar 

  29. Dyadyusha, G. G., Al’perovich, M. A., Tyurin, V. S., and Kachkovskii, A. D. (1985) First excited states of unsymmetric polymethine dyes, Ukr. Khim. Zh. 51, 298–302.

    CAS  Google Scholar 

  30. Misurkin, I. A. and Ovchinnikov, A. A. (1966) Electron structure of long molecules with conjugated bonds, Pis ‘ma Zh. Eksp. Teor. Fiz 4, 248–252 [JETP Leu. 4, 167–171].

    Google Scholar 

  31. Tyutyulkov, N., Fabian, J., Mehlhorn, A., Dietz, F., and Tadjer, A. (1991)PolymethineDyes: Structure and Properties, St. Kliment Univ. Press, Sofia.

    Google Scholar 

  32. Dyadyusha, G. G. and Ushomirskii, M. N. (1987) Energy structure and electronic transition wavelength for three-nucleus polymethine dyes. Teor. Eksp. Khim. 23, 10–21 [Theor. Exp. Chem. 23, 10–21

    Google Scholar 

  33. Dyadyusha, G. G. and Ushomirskii, M. N. (1987) Study of the energy structure of linear pi-conjugated molecules by the method of effective additive parameters, Zh. Strukt. Khim.. 28, 17–26.

    Google Scholar 

  34. Dekhtyar, M. L. and Rozenbaum, V. M. (1998) Symmetric polymethine dyes with a centrally disposed conjugated bridge:a topological analysis of frontier energy levels, J. Phys. Chem. (in press).

    Google Scholar 

  35. Yasui, S., Matsuoka, M., and Kitao, T. (1988) Syntheses and some properties of some infrared-absorbing croconium and related dyes, Dyes and Pigm. 10, 13–22.

    Article  CAS  Google Scholar 

  36. Kurdyukov, V. V., Kudinova, M. A, and Tohnachev, A. I. (1996) Pyrylocyanines. 35. Squarylium dyes derived from tert-butyl-substituted pyrylium and thiopyrylium salts, Khim. Geterotsikl. Soed. N 8, 1038–1044.

    Google Scholar 

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Daehne, S., Dekhtyar, M.L. (1998). Molecular Engineering of NIR Dyes. In: Daehne, S., Resch-Genger, U., Wolfbeis, O.S. (eds) Near-Infrared Dyes for High Technology Applications. NATO ASI Series, vol 52. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-5102-3_17

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  • DOI: https://doi.org/10.1007/978-94-011-5102-3_17

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-6143-8

  • Online ISBN: 978-94-011-5102-3

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