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Search for "fluorophore" in Full Text gives 52 result(s) in Beilstein Journal of Nanotechnology.

Towards multiple readout application of plasmonic arrays

  • Dana Cialla,
  • Karina Weber,
  • René Böhme,
  • Uwe Hübner,
  • Henrik Schneidewind,
  • Matthias Zeisberger,
  • Roland Mattheis,
  • Robert Möller and
  • Jürgen Popp

Beilstein J. Nanotechnol. 2011, 2, 501–508, doi:10.3762/bjnano.2.54

Graphical Abstract
  • to its complementary capture sequence. Thus, the formation of the DNA double helix was indicated by the fluorescence signal of the Cy3.5 label. The absorption and emission spectra of the fluorophore Cy3.5 and moreover the plasmonic profiles of the used gold nanorhomb arrays are depicted in Figure 5A
  • to the spectral overlap of the plasmonic profile with the absorption spectrum of the dye, an enhanced excitation rate may be reached. Thus the fluorescence intensity is enhanced because the fluorophore is excited more often [32]. This mechanism may be the explanation for the signal increase seen with
  • sample 1 and 2 for fluorescence measurements of Cy3.5. A further contribution to SEF is described as an enhanced decay rate that improves the quantum yield of the fluorophore and decreases the lifetime, which should allow the fluorophore to undergo more excitation–de-excitation cycles before
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Letter
Published 30 Aug 2011

Novel acridone-modified MCM-41 type silica: Synthesis, characterization and fluorescence tuning

  • Maximilian Hemgesberg,
  • Gunder Dörr,
  • Yvonne Schmitt,
  • Andreas Seifert,
  • Zhou Zhou,
  • Robin Klupp Taylor,
  • Sarah Bay,
  • Stefan Ernst,
  • Markus Gerhards,
  • Thomas J. J. Müller and
  • Werner R. Thiel

Beilstein J. Nanotechnol. 2011, 2, 284–292, doi:10.3762/bjnano.2.33

Graphical Abstract
  • bearing polycyclic aromatic compounds as terminal groups, Ar–(CH2)n–Si(OR)3 (n = 3, R = Me, Et), which may lead to interesting optical or electronic properties [4][5][6]. Acridone, being a well-known fluorophore used, e.g., for chemosensors [7], has previously been reported to be suitable for the pKa
  • fluorescence intensity. Conclusion We have presented a novel fluorescent organosilane bearing an acridone fluorophore and its successful transformation into a MCM-41 type material via co-condensation with TEOS. As predicted, the hybrid material shows a change in its fluorescence properties when non-covalently
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Full Research Paper
Published 09 Jun 2011
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