SEARCH

SEARCH BY CITATION

References

  • 1
    Bandy, T. J., A. Brewer, J. R. Burns, G. Marth, T. Nguyen and E. Stulz (2011) DNA as supramolecular scaffold for functional molecules: Progress in DNA nanotechnology. Chem. Soc. Rev. 40, 138148.
  • 2
    Ruiz-Carretero, A., P. G. A. Janssen, A. Kaeser and A. P. H. J. Schenning (2011) DNA-templated assembly of dyes and extended pi-conjugated systems. Chem. Commun. 47, 43404347.
  • 3
    Su, W., V. Bonnard and G. A. Burley (2011) DNA-templated photonic arrays and assemblies: Design principles and future opportunities. Chem. Eur. J. 17, 79827991.
  • 4
    Chen, W., G. Guler, E. Kuruvilla, G. B. Schuster, H. C. Chiu and E. Riedo (2010) Development of self-organizing, self-directing molecular nanowires: Synthesis and characterization of conjoined DNA-2,5-Bis(2-thienyl)pyrrole oligomers. Macromolecules 43, 40324040.
  • 5
    Malinovskii, V. L., D. Wenger and R. Haner (2010) Nucleic acid-guided assembly of aromatic chromophores. Chem. Soc. Rev. 39, 410422.
  • 6
    Schwartz, E., S. Le Gac, J. J. L. M. Cornelissen, R. J. M. Nolte and A. E. Rowan (2010) Macromolecular multi-chromophoric scaffolding. Chem. Soc. Rev. 39, 15761599.
  • 7
    Kashida, H., T. Takatsu, K. Sekiguchi and H. Asanuma (2010) An efficient fluorescence resonance energy transfer (FRET) between pyrene and perylene assembled in a DNA duplex and its potential for discriminating single-base changes. Chem. Eur. J. 16, 24792486.
  • 8
    Varghese, R. and H. A. Wagenknecht (2009) DNA as a supramolecular framework for the helical arrangements of chromophores: Towards photoactive DNA-based nanomaterials. Chem. Commun., 261, 52624.
  • 9
    Ostergaard, M. E. and P. J. Hrdlicka (2011) Pyrene-functionalized oligonucleotides and locked nucleic acids (LNAs): Tools for fundamental research, diagnostics, and nanotechnology. Chem. Soc. Rev. 40, 57715788.
  • 10
    Dale, T. J. and J. Rebek (2006) Fluorescent sensors for organophosphorus nerve agent mimics. J. Am. Chem. Soc. 128, 45004501.
  • 11
    Brouwer, A. M. (2011) Standards for photoluminescence quantum yield measurements in solution (IUPAC Technical Report). Pure Appl. Chem. 83, 22132228.
  • 12
    Friedel, R. A. and M. Orchin (1951) Ultraviolet Spectra of Aromatic Compounds. Wiley, NY.
  • 13
    Macmillan, A. M. and G. L. Verdine (1990) Synthesis of functionally tethered oligodeoxynucleotides by the convertible nucleoside approach. J. Org. Chem. 55, 59315933.
  • 14
    Macmillan, A. M. and G. L. Verdine (1991) Engineering tethered DNA-molecules by the convertible nucleoside approach. Tetrahedron 47, 26032616.
  • 15
    Xu, Y. Z., Q. G. Zheng and P. F. Swann (1992) Synthesis of DNA containing modified bases by postsynthetic substitution - synthesis of oligomers containing 4-substituted thymine - O4-alkylthymine, 5-methylcytosine, N4-(dimethylamino)-5-methylcytosine, and 4-thiothymine. J. Org. Chem. 57, 38393845.
  • 16
    Long, E. C. and J. K. Barton (1990) On demonstrating DNA intercalation. Acc. Chem. Res. 23, 273279.
  • 17
    Kumar, C. V. and E. H. Asuncion (1993) DNA-binding studies and site-selective fluorescence sensitization of an anthryl probe. J. Am. Chem. Soc. 115, 85478553.
  • 18
    Nakamura, M., Y. Fukunaga, K. Sasa, Y. Ohtoshi, K. Kanaori, H. Hayashi, H. Nakano and K. Yamana (2005) Pyrene is highly emissive when attached to the RNA duplex but not to the DNA duplex: The structural basis of this difference. Nucleic Acids Res. 33, 58875895.
  • 19
    Kepinska, D., G. J. Blanchard, P. Krysinski, J. Stolarski, K. Kijewska and M. Mazur (2011) Pyrene-loaded polypyrrole microvessels. Langmuir 27, 1272012729.
  • 20
    Filichev, V. V. and E. B. Pederson (2009) DNA-conjugated organic chromophores in DNA stacking interactions. Wiley Encyclopedia Chem. Biol. 1, 493524.
  • 21
    Matray, T. J. and E. T. Kool (1998) Selective and stable base pairing without hydrogen bonds. J. Am. Chem. Soc. 120, 61916192.
  • 22
    Mann, J. S., Y. Shibata and T. Meehan (1992) Synthesis and properties of an oligodeoxynucleotide modified with a pyrene derivative at the 5′-phosphate. Bioconjug. Chem. 3, 554558.
  • 23
    Duff, M. R., V. K. Mudhivarthi and C. V. Kumar (2009) Rational design of anthracene-based DNA binders. J. Phys. Chem. B 113, 17101721.