2009
DOI: 10.1016/j.saa.2007.05.067
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Concentration-dependent energy transfer studies in ternary dye mixture of Stilbene-420, Coumarin-540 and Nile Blue

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Cited by 9 publications
(5 citation statements)
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“…Such structures were produced with a laser power of 36 mW (0.15 GW/cm 2 ) and scanning speed of 20 µm/s. The fluorescence spectrum of these microstructures, displayed in Figure 7b, shows that the emission peak is located at 420 nm, which is in good agreement with the ones reported in the literature for Stilbene in several solvents 34 . Our results indicate that the fluorescent dye was not degraded during the microfabrication process, and that it is retained in the microstructures after the washing process.…”
Section: Microstructures Fabricated Using Two-photon Absorption Polymsupporting
confidence: 89%
See 1 more Smart Citation
“…Such structures were produced with a laser power of 36 mW (0.15 GW/cm 2 ) and scanning speed of 20 µm/s. The fluorescence spectrum of these microstructures, displayed in Figure 7b, shows that the emission peak is located at 420 nm, which is in good agreement with the ones reported in the literature for Stilbene in several solvents 34 . Our results indicate that the fluorescent dye was not degraded during the microfabrication process, and that it is retained in the microstructures after the washing process.…”
Section: Microstructures Fabricated Using Two-photon Absorption Polymsupporting
confidence: 89%
“…Afterwards, the mixtures were left resting for solvent evaporation. In this work, we fabricated microstructures doped with Rhodamine B 32,33 and Stilbene 420 34 . To fabricate polymeric microstructures, a Ti: sapphire (KMLabs, 86 MHz, 780 nm, 100 fs) laser oscillator was employed.…”
Section: Femtosecond Laser Microfabrication In Polymers: Two-photon Amentioning
confidence: 99%
“…2). By the addition of (TAIPDI) n , the featureless absorption band of BSSBP starts to decrease with a small shift to 346 nm, 17 while the broad and red-shifted absorption of the TAIPDI stacks appears at 507 nm, which is seen at 501 nm in the absence of BSSBP. 14,18 Isosbestic points and drastic variations in absorption characteristics indicate an electronic interaction between the components mainly through p-p interactions.…”
Section: Resultsmentioning
confidence: 99%
“…These limitations have precluded them from being extensively evaluated in vivo. [29][30][31][32] Another class of compounds centers on the cyclic oxobutanal ring and is referred to as squaraine or squaric acid fluorophores. 33 The extreme electrophilicity of this cyclic butane ring is susceptible to nucleophilic attack, which irreversibly diminishes the optical properties of the compound, unless the core is protected by one of several methods including rotaxane encapsulation 34 which reduces the overall applicability in small molecule bioimaging.…”
Section: Classes Of Nir Fluorophoresmentioning
confidence: 99%