Beilstein J. Nanotechnol.2011,2, 501–508, doi:10.3762/bjnano.2.54
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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Figure 1:
Schematic illustration of gold nanorhombs as plasmonic substrate. (A) The SEM image shows the perio...
Beilstein J. Nanotechnol.2011,2, 284–292, doi:10.3762/bjnano.2.33
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