TY - JOUR A1 - Maisuls, I. A1 - Wang, Cui A1 - Gutierrez Suburu, M. E. A1 - Wilde, S. A1 - Daniliuc, C.-G. A1 - Brunink, D. A1 - Doltsinis, N. L. A1 - Ostendorp, S. A1 - Kösters, J. A1 - Resch-Genger, Ute A1 - Strassert, C. A. T1 - Ligand-controlled and nanoconfinement-boosted luminescence employing Pt(II) and Pd(II) complexes: from color-tunable aggregation-enhanced dual emitters towards self-referenced oxygen reporters N2 - In this work, we describe the synthesis, structural and photophysical characterization of four novel Pd(II) and Pt(II) complexes bearing tetradentate luminophoric ligands with high photoluminescence quantum yields (FL) and long excited state lifetimes (s) at room temperature, where the results were interpreted by means of DFT calculations. Incorporation of fluorine atoms into the tetradentate ligand favors aggregation and thereby, a shortened average distance between the metal centers, which provides accessibility to metal–metal-to-ligand charge-transfer (3MMLCT) excimers acting as red-shifted Energy traps if compared with the monomeric entities. This supramolecular approach provides an elegant way to enable room-temperature phosphorescence from Pd(II) complexes, which are otherwise quenched by a thermal population of dissociative states due to a lower ligand field splitting. Encapsulation of These complexes in 100 nm-sized aminated polystyrene nanoparticles enables concentration-controlled aggregation-enhanced dual emission. This phenomenon facilitates the tunability of the absorption and emission colors while providing a rigidified environment supporting an enhanced FL up to about 80% and extended s exceeding 100 ms. Additionally, these nanoarrays constitute rare examples for selfreferenced oxygen reporters, since the phosphorescence of the aggregates is insensitive to external influences, whereas the monomeric species drop in luminescence lifetime and intensity with increasing triplet molecular dioxygen concentrations (diffusion-controlled quenching). KW - Fluorescence KW - Multiplexing KW - Lifetime KW - Bead KW - Particle KW - Dye KW - Barcoding KW - Encoding KW - Quantum yield KW - Label KW - Reporter KW - Pd(II) KW - Pt(II) KW - Complex KW - NMR KW - X-ray KW - Sythesis KW - Aggregation KW - Monomer KW - Color PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-525288 DO - https://doi.org/10.1039/d0sc06126c VL - 12 IS - 9 SP - 3270 EP - 3281 PB - Royal Society of Chemistry AN - OPUS4-52528 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lezhnina, M.M. A1 - Kätker, H. A1 - Kaiser, Martin A1 - Stegemann, L. A1 - Voss, E. A1 - Resch-Genger, Ute A1 - Strassert, C. A1 - Kynast, U. T1 - Chemical behavior and spectroscopic properties of rare earth borates in glazes N2 - Efficient Near UV excited materials (350<λ<400 nm) responding with green line emission are sparse in comparison to higher energy UV excited emitters (λ<350 nm), while corresponding red line emitters are more abundant, albeit typically also restricted to excitation wavelengths below 400 nm. This situation is disadvantageous for several important actual and potential applications. Among these, excitation with high power UV-LEDs and laser diodes are of particular interest. Here we present results on green emitting YBO3:Ce, Tb, which can be excited with 370–380 nm radiation at quantum efficiencies of up to 60% and decay times in excess of 2 ms. Moreover, as powderous phosphors typically require stable matrices to be hosted in, we investigated low melting, lead- and fluoride-free glasses for their capability to accommodate the phosphor and yet retain its optical properties. In these, we even observed an increase of the quantum efficiencies of up to 70% at decay times approaching 3 ms. Finally, we characterized the thermal quenching behavior, which showed a clear advantage of the phosphors in glassy matrices. KW - Rare earth phosphors KW - Energy transfer KW - Luminescent glasses and glazes PY - 2016 DO - https://doi.org/10.1016/j.jlumin.2015.05.005 SN - 0022-2313 SN - 1872-7883 VL - 170 SP - 387 EP - 394 PB - Elsevier B.V. CY - Amsterdam AN - OPUS4-35131 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rex, Tobias A1 - Vilela, Raquel R. C. A1 - Bauer, Nadine A1 - Hepp, Alexander A1 - de Camargo, Andrea S. S. A1 - Kiefer, Friedemann A1 - Strassert, Cristian A. T1 - Host–Guest Nanoparticles Incorporating a Fluorophore-Conjugated Pt(II) Complex: A Ratiometric Dual Emitter Performing as a Self-Referenced Oxygen Reporter N2 - Ratiometric optical sensors, which provide real-time measurements by comparing the intensities of two spectrally separated emission bands, are highly effective for monitoring oxygen levels. By combining oxygen-independent and oxygensensitive emission characteristics, they offer accurate quantification, distinguishing them from other sensor types. In this work, we designed a ratiometric optical sensor concept based on a biscyclometalated platinum(II) complex coupled with an organic naphthalonitrile-based fluorophore and incorporated it into mesoporous silica nanoparticles. This encapsulation strategy significantly improved the stability and water-dispersibility of the otherwise hydrophobic coordination compound while preventing aggregation and enhancing its photophysical properties. Both the free molecule and its nanoparticle-encapsulated form were characterized, revealing high sensitivity to oxygen variations with the unique feature of self-referenced ratiometric readout. The sensor’s response was effectively measured at the single-particle level using photoluminescence microscopy, providing temporally and spatially resolved oxygen readouts. The versatility of the system was demonstrated across different experimental setups, including suspensions, solids, and agarose-embedded forms, highlighting is adaptability to a wide range of applications. This system holds significant promise for advanced oxygen monitoring, offering a reliable tool for high-resolution detection in complex environments with multiple orthogonal readouts. KW - Oxygen sensing KW - Ratiometric luminescence KW - Platinum (II) complex KW - Dual emitter probe KW - Mesoporous silica nanoprticles PY - 2026 DO - https://doi.org/10.1021/acsaom.5c00262 SN - 2771-9855 VL - 4 IS - 2 SP - 332 EP - 342 PB - American Chemical Society (ACS) AN - OPUS4-65689 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -