@article{LopezdeGuerenuBastianWessigetal.2019,
  author    = {L{\´o}pez de Guere{\~n}u, Anna and Bastian, Philipp and Wessig, Pablo and John, Leonard and Kumke, Michael Uwe},
  title     = {Energy Transfer between Tm-Doped Upconverting Nanoparticles and a Small Organic Dye with Large Stokes Shift},
  series = {Biosensors : open access journal},
  volume    = {9},
  journal   = {Biosensors : open access journal},
  number    = {1},
  publisher = {MDPI},
  address   = {Basel},
  issn      = {2079-6374},
  doi       = {10.3390/bios9010009},
  pages     = {17},
  year      = {2019},
  abstract  = {Lanthanide-doped upconverting nanoparticles (UCNP) are being extensively studied for bioapplications due to their unique photoluminescence properties and low toxicity. Interest in RET applications involving UCNP is also increasing, but due to factors such as large sizes, ion emission distributions within the particles, and complicated energy transfer processes within the UCNP, there are still many questions to be answered. In this study, four types of core and core-shell NaYF4-based UCNP co-doped with Yb3+ and Tm3+ as sensitizer and activator, respectively, were investigated as donors for the Methyl 5-(8-decanoylbenzo[1,2-d:4,5-d ']bis([1,3]dioxole)-4-yl)-5-oxopentanoate (DBD-6) dye. The possibility of resonance energy transfer (RET) between UCNP and the DBD-6 attached to their surface was demonstrated based on the comparison of luminescence intensities, band ratios, and decay kinetics. The architecture of UCNP influenced both the luminescence properties and the energy transfer to the dye: UCNP with an inert shell were the brightest, but their RET efficiency was the lowest (17\%). Nanoparticles with Tm3+ only in the shell have revealed the highest RET efficiencies (up to 51\%) despite the compromised luminescence due to surface quenching.},
  language  = {en}
}
@article{InalKoelschChiappisietal.2013,
  author    = {Inal, Sahika and Koelsch, Jonas D. and Chiappisi, Leonardo and Kraft, Mario and Gutacker, Andrea and Janietz, Dietmar and Scherf, Ullrich and Gradzielski, Michael and Laschewsky, Andr{\´e} and Neher, Dieter},
  title     = {Temperature-Regulated Fluorescence Characteristics of Supramolecular Assemblies Formed By a Smart Polymer and a Conjugated Polyelectrolyte},
  series = {MACROMOLECULAR CHEMISTRY AND PHYSICS},
  volume    = {214},
  journal   = {MACROMOLECULAR CHEMISTRY AND PHYSICS},
  number    = {4},
  publisher = {WILEY-V C H VERLAG GMBH},
  address   = {WEINHEIM},
  issn      = {1022-1352},
  doi       = {10.1002/macp.201200493},
  pages     = {435 -- 445},
  year      = {2013},
  abstract  = {Aqueous mixtures of a coumarin-labeled non-ionic thermoresponsive copolymer and a cationic polythiophene exhibit marked changes in their fluorescence properties upon heating. At room temperature, emission from the label is significantly quenched due to energy transfer to the conjugated polyelectrolyte. Heating the mixture reduces the energy-transfer efficiency markedly, resulting in a clearly visible change of the emission color. Although the two macromolecules associate strongly at room temperature, the number of interacting sites is largely reduced upon the phase transition. Crucially, the intermolecular association does not suppress the responsiveness of the smart polymer, meaning that this concept should be applicable to chemo- or bioresponsive polymers with optical read-out, for example, as a sensor device.},
  language  = {en}
}