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Patterns of Counter-Rotating Ring Currents in TwoValence Isomers of Corazulene

Języki publikacji
EN
Abstrakty
EN
Current-density maps computed in the ipsocentric approach are presented for two isomeric polycyclic systems: corazulene (1) in which four azulene units are fused around a central square, and cornaphthalene (2) in which the azulene units of 1 are replaced by naphthalenes. Both show a strong central paratropic current on the square. Whereas 1 presents concentric counter-rotating rim-and-hub currents, 2 shows a ‘Clar-like’ structure of diatropic currents on the four outer hexagonal rings. Partition of the total current into orbital contributions, both canonical and localized, gives a clear rationale for the appearance of the maps.
Słowa kluczowe
Rocznik
Strony
653--662
Opis fizyczny
Bibliogr. 21 poz., rys.
Twórcy
autor
autor
Bibliografia
  • 1. See, e.g., Thematic Issue on Aromaticity (Guest Editor, Schleyer P.v.R.), Chem. Rev., 101, 1119-1566 (2001).
  • 2. Minkin V.L, Glukhovtsev M.N. and Simkin B.V. Aromaticity and Antiaromaticity, John Wiley & Sons:New York, 1994.
  • 3. London F., J. Phys. Radium, 8, 397 (1937).
  • 4. Pauling L., Chem. Phys., 4, 673 (1936).
  • 5. Dauben H. J., Wilson J.D. and Laity J.L., in: J.P. Snyder (Ed.), Non-Benzenoid Aromatics, 2, Academic Press, New York, 1971.
  • 6. Pople J.A.,J. Chem. Phys., 24, 1111 (1956).
  • 7. Schleyer P.v.R., Maerker C., Dransfeld A., Jiao H. and van Eikema Hommes N.J.R., J. Am. Chem. Soc.,118,6317(1996).
  • 8. Fallah-Bagher-Shaidaei H., Wannere C.S., Corminboeuf C., Puchta R. and Schleyer P.v.R., Org. Lett., 8, 863 (2006).
  • 9. Keith T.A. and Bader R.F.W., J. Chem. Phys., 99, 3669 (1993).
  • 10. Coriani S., Lazzeretti P., Malagoli M. and Zanasi R., Theor. Chim. Acta, 89, 181 (1994).
  • 11. Steiner E. and Fowler P.W, J. Phys. Chem. A, 105, 9553 (2001).
  • 12. Steiner E. and Fowler P.W., Chem. Commun., 2220 (2001).
  • 13. Steiner E., Fowler P.W. and Jenneskens L.W., Angew. Chem. Int. Ed., 40, 362 (2001).
  • 14. Acocella A., Havenith R.W.A., Steiner E., Fowler P.W. and Jenneskens L.W., Chem. Phys. Letters, 363, 64 (2002).
  • 15. Diudea M.V., Phys. Chem. Chem. Phys., 7, 3626 (2005).
  • 16. Coulson C.A. and Rushbrooke G.S., Proc. Cambridge Phil. Soc., 36, 193 (1940).
  • 17. Frisch M. J., Trucks G.W., Schlegel H.B., Scuseria G. E., Robb M.A., Cheeseman J.R., Zakrzewski V.G.,Montgomery J.A., Stratmann R.E., Burant J.C., Dapprich S., Millam J.M., Daniels A.D., Kudin K.N.,Strain M.C., Farkas O., Tomasi J., Barone V., Cossi M., Cammi R., Mennucci B., Pomelli C., Adamo C.,Clifford S., Ochterski J., Petersson G.A., Ayala P. V., Cui Q., Morokuma K., Malick D.K., Rabuck A.D.,Raghavachari K., Foresman J.B., Cioslowski J., Ortiz J.V., Stefanov B.B., Liu G., Liashenko A., Piskorz P, Komaromi L, Gomperts R., Martin R.L., Fox D.J., Keith T., Al-Laham M.A., Peng C.Y,Nanayakkara A., Gonzalez C., Challacombe M., Gili P.M.W., Johnson B.G., Chen W., Wong M.W.,Andres J.L., Head-Gordon M., Replogle E.S. and Pople J.A., Gaussian 98, revision A.7; Gaussian, Inc. Pittsburgh, PA, 1998.
  • 18. Lazzeretti P. and Zanasi R., SYSMO package (University of Modena), 1980 (Additional routines by E. Steiner, P.W. Fowler and R.W.A. Havenith).
  • 19. Steiner E., Fowler P.W. and Havenith R.W.A., J. Phys. Chem. A, 106, 7048 (2002).
  • 20. Pipek J. and Mezey P.G., J. Chem. Phys., 90, 4916 (1989).
  • 21. Soncini A., Steiner E., Fowler P.W., Havenith R.W.A. and Jenneskens L.W., Chem. Eur. J., 9, 2974 (2003).
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bwmeta1.element.baztech-article-BUJ5-0014-0031