TY - JOUR A1 - Würth, Christian A1 - Lochmann, Cornelia A1 - Spieles, Monika A1 - Pauli, Jutta A1 - Hoffmann, Katrin A1 - Schüttrigkeit, T. A1 - Franzl, T. A1 - Resch-Genger, Ute T1 - Evaluation of a commercial integrating sphere setup for the determination of absolute photoluminescence quantum yields of dilute dye solutions N2 - The commercial availability of stand-alone setups for the determination of absolute photoluminescence quantum yields (φf) in conjunction with the increasing use of integrating sphere accessories for spectrofluorometers is expected to have a considerable influence not only on the characterization of chromophore systems for use in optical and opto-electronic devices, but also on the determination of this key parameter for (bio)analytically relevant dyes and functional luminophores. Despite the huge potential of systems measuring absolute φf values and the renewed interest in dependable data, evaluated protocols for even the most elementary case, the determination of the fluorescence quantum yield of transparent dilute solutions of small organic dyes with integrating sphere methods, are still missing. This encouraged us to evaluate the performance and sources of uncertainty of a simple commercial integrating sphere setup with dilute solutions of two of the best characterized fluorescence quantum yield standards, quinine sulfate dihydrate and rhodamine 101, strongly differing in spectral overlap between absorption and emission. Special attention is dedicated to illustrate common pitfalls of this approach, thereby deriving simple procedures to minimize measurement uncertainties and improve the comparability of data for the broad community of users of fluorescence techniques. KW - Lifetime KW - Fluorescence KW - Luminescence KW - Quantum yield KW - Quantum efficiency KW - Integrating sphere KW - Reabsorption KW - Rhodamine 101 KW - Quinine sulfate dihydrate KW - Method KW - Photoluminescence KW - Standard KW - Emission KW - Spectral correction KW - Excitation KW - Anisotropy PY - 2010 DO - https://doi.org/10.1366/000370210791666390 SN - 0003-7028 SN - 1943-3530 VL - 64 IS - 7 SP - 733 EP - 741 PB - Society for Applied Spectroscopy CY - Frederick, Md. AN - OPUS4-22089 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta A1 - Spieles, Monika A1 - Schneider, Thomas A1 - Binder, Denny A1 - Güttler, Arne A1 - Resch-Genger, Ute T1 - Entwicklung von Fluoreszenzquantenausbeutestandards N2 - Lumineszenzmethoden und funktionelle Chromophore erlangten in den letzten Jahren breite Anwendungen in den Material- und Lebenswissenschaften wie z.B. in der medizinischen Diagnostik, der Beleuchtungs- und Displaytechnologie, der Photovoltaik oder im Sicherheitsbereich für die Echtheitskodierung. Entscheidend für eine hohe Effizienz und Nachweisempfindlichkeit funktioneller Chromophore ist eine große Helligkeit bzw. Brillanz. Brillante Stoffe zeichnen sich durch eine hohe Absorption des anregenden Lichtes (messbar über den molaren Extinktionskoeffizienten) aus sowie durch eine effiziente Umwandlung des absorbierten Lichtes in Lumineszenzlicht bzw. durch eine große Photolumineszenzquantenausbeute aus. Die Bestimmung der Schlüsselgröße Fluoreszenzquantenausbeute erfolgt i.a. relativ zu einem Farbstoff bekannter Fluoreszenzquantenausbeute über einen Vergleich der absorptionsgewichteten integralen Fluoreszenzspektren von Probe und Standard. Hierfür werden Referenzmaterialien mit zertifizierten Fluoreszenzquantenausbeuten benötigt, die bislang nicht verfügbar sind. Im folgenden werden die laufenden Forschungsarbeiten an einer Serie an Fluoreszenzquantenausbeutestandard vorgestellt, die im Spektralbereich von 350 nm – 1050 nm emittieren. Diese Materialien können auch zur Überprüfung von Ulbrichtkugelmessplätzen eingesetzt werden. T2 - Colloquium Optical Spectrometry (COSP) CY - Berlin, Germany DA - 27.11.2017 KW - Fluoreszenz KW - Referenzmaterial KW - Quantenausbeute PY - 2017 AN - OPUS4-44095 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Jäger, Christian A1 - Pauli, Jutta A1 - Berger, Georg A1 - Spitzer, Andrea T1 - Entwicklung neuartiger Knochenersatzwerkstoffe und strukturelle Charakterisierung mittels der 31P-NMR-Spektroskopie T2 - Tagung "Tag der Chemie" CY - Berlin, Deutschland DA - 2002-12-04 PY - 2002 AN - OPUS4-1900 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta A1 - Brehm, Robert A1 - Grabolle, Markus A1 - Behnke, Thomas A1 - Mathejczyk, J. A1 - Hamann, F. A1 - Alves, F. A1 - Hilger, I. A1 - Resch-Genger, Ute ED - Achilefu, S. ED - Raghavachari, R. T1 - Dye-biomolecule conjugates and NIR-fluorescent particles for targeting of disease-related biomarkers N2 - Indispensable for fluorescence imaging are highly specific and sensitive molecular probes that absorb and emit in the near infrared (NIR) spectral region and respond to or target molecular species or processes. Here, we present approaches to targeted fluorescent probes for in vivo imaging in the intensity and lifetime domain exploiting NIR dyes. Screening schemes for the fast identification of suitable fluorophores are derived and design criteria for highly emissive optical probes. In addition, as a signal amplification strategy that enables also the use of hydrophobic NIR fluorophores as fluorescent reporters, first steps towards versatile strategies for the preparation of NIR-fluorescent polymeric particles are presented that can be utilized also for the design of targeted and analyte-responsive probes. KW - Fluorescence KW - Fluorescence lifetime imaging KW - Near-infrared KW - NIR KW - Cyanine dye KW - Cancer KW - In vivo imaging KW - Aggregation KW - Nanoparticle PY - 2011 DO - https://doi.org/10.1117/12.876828 SN - 1605-7422 N1 - Serientitel: Proceedings of SPIE – Series title: Proceedings of SPIE IS - 7910 SP - 791014-1 EP - 791014-15 AN - OPUS4-24353 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta A1 - Würth, Christian A1 - Güttler, Arne A1 - Schneider, Thomas A1 - Resch-Genger, Ute T1 - Determination of the Uncertainty Budgets of the Fluorescence Quantum Yield Values of Certified Standards as New Optical Reference Materials N2 - Luminescence techniques are amongst the most commonly used analytical methods in the life and material sciences due to their high sensitivity and their nondestructive and multiparametric character. Photoluminescence signals are, however, affected by wavelength-, polarization- and time-dependent instrument specific effects. This hampers the comparability of fluorescence measurements and calls for simple tools for instrument characterization and the quantification of measured fluorescence intensities. Well characterized fluorescence standards for instrument calibration and performance validation (IPV) can be used also to reference fluorescence signals. Of special importance is the reliable and accurate determination of photoluminescence quantum yields (Ф f), that equals the number of emitted per absorbed photons and presents the key performance parameter for emitter efficiency and the comparison of different luminophores. The determination of Ф f is typically done with the aid of so-called quantum yield standards with well-known Ф f values. These standards can also be applied to evaluate integrating sphere setups, which are increasingly being used for absolute measurements of Ф f values. In this respect, division biophotonics of BAM has certificated a set of Ф f standards, which absorb and fluorescence in the wavelength range from 350 to 1100 nm. In the following, the route to Ф f standards with reliable and traceable Ф f values with a complete uncertainty budget will be presented. T2 - Eurachem-Workshop „Uncertainty from sampling and analysis for accredited laboratories CY - Berlin, Germany DA - 19.11.2019 KW - Uncertainty KW - Fluorescence KW - Quantum yield standard KW - Reference Material PY - 2019 AN - OPUS4-49661 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Grabolle, Markus A1 - Brehm, Robert A1 - Pauli, Jutta A1 - Dees, F.M. A1 - Hilger, I. A1 - Resch-Genger, Ute T1 - Determination of the labeling density of fluorophore-biomolecule conjugates with absorption spectroscopy N2 - Dye–biomolecule conjugation is frequently accompanied by considerable spectral changes of the dye’s absorption spectrum that limit the use of the common photometrical method for the determination of labeling densities. Here, we describe an improvement of this method using the integral absorbance of the dye instead of its absorbance at the long wavelength maximum to determine the concentration of the biomolecule-coupled dye. This approach is illustrated for three different cyanine dyes conjugated to the antibody IgG. KW - Fluorescent dye KW - Aggregation KW - Dimerization KW - Fluorophore-labeled antibodies KW - Labeling density KW - Dye-to-protein ratio KW - Absorption PY - 2012 DO - https://doi.org/10.1021/bc2003428 SN - 1043-1802 SN - 1520-4812 VL - 23 IS - 2 SP - 287 EP - 292 CY - Washington, DC AN - OPUS4-25527 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta A1 - Spieles, Monika A1 - Licha, K. A1 - Resch-Genger, Ute T1 - Design of Highly Fluorescent Conjugates T2 - MOBI 2013 CY - Heidelberg, Germany DA - 2013-10-28 PY - 2013 AN - OPUS4-29577 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Pauli, Jutta A1 - Resch-Genger, Ute A1 - Lisy, M.-R. A1 - Thomas, C. A1 - Kaiser, W. A1 - Hilger, I. T1 - Design and characterization of a new contrast agent for the specific and sensitive detection of tumor via in vivo fluorescence imaging T2 - Method and Application of Fluerescence (MAF10) CY - Salzburg, Austria DA - 2007-09-09 PY - 2007 AN - OPUS4-16406 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ramirez Caro, Alejandra A1 - Pauli, Jutta A1 - Mota, Berta A1 - Simon, Sebastian A1 - Schmidt, Wolfram A1 - Resch-Genger, Ute T1 - C⁠3A passivation with gypsum and hemihydrate monitored by optical spectroscopy N2 - Tricalcium aluminate (C⁠3A) is found with less than 10% wt. of the total composition; however, during hydration, C⁠3A plays an important role in the early hydration of cement in the presence of gypsum as a set retarder. The aim of this investigation is to assess the suitability of optical spectroscopy and a dye-based optical probe to monitor early hydration of C⁠3A in the presence of gypsum and hemihydrate. Optical evaluation was performed using steady-state fluorescence and diffuses reflectance spectroscopy (UV-VisDR). Phase characterization during hydration was done with in-situ X-ray diffraction. UV-VisDR with a cyanine dye probe was used to monitor the formation of metastable phases and was employed together with fluorescence spectroscopy, to follow the Aggregation and disaggregation of the dye during hydration. In conclusion, for the first time, a cyanine dye was identified as a feasible and stable probe to monitor C⁠3A hydration changes in the presence of calcium sulfate. KW - Dye KW - Photoluminescence KW - Fluorescence KW - Reflection spectroscopy KW - Cement KW - Hydration KW - Method development PY - 2020 DO - https://doi.org/10.1016/j.cemconres.2020.106082 VL - 133 SP - 106082 PB - Elsevier Ltd. CY - Amsterdam AN - OPUS4-50952 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Adorjan, I. A1 - Rosenau, Th. A1 - Potthast, A. A1 - Kosma, P. A1 - Mereiter, K. A1 - Pauli, Jutta A1 - Jäger, Christian T1 - Crystal and molecular structure of methyl 4-O-methyl-beta-D-ribo-hex-3-ulopyranoside N2 - Methyl 4-O-methyl-?-Image-ribo-hex-3-ulopyranoside (2), a model compound for partially oxidized anhydroglucose units in cellulose, was crystallized from CHCl3/n-hexane by vapor diffusion to give colorless plates. Crystal structure determination revealed the monoclinic space group P21 with Z=2C8H14O6 and unit cell parameters of a=8.404(2), b=4.5716(10), c=13.916(3) Å, and ?=107.467(4)°. The structure was solved by direct methods and refined to R=0.0476 for 1655 reflections and 135 parameters. The hexulopyranoside occurs in a distorted chair conformation. Both hydroxyls are involved in hydrogen bonding and form zigzag bond chains along the b-axis. One of the two hydrogen bonds is bifurcated. The solid-state 13C NMR spectrum of 2 exhibits eight carbon resonances, with well-separated signals for the two methoxyls (1-OMe: 55.72 ppm, 4-OMe: 61.25 ppm) and a keto resonance with relatively large downfield shift (206.90 ppm). Differences in the C-4 and the methoxyls’ chemical shifts in the solid and liquid states were found KW - Crystal structure KW - Solid-state NMR KW - Cellulose KW - Carbonyl groups PY - 2004 DO - https://doi.org/10.1016/j.carres.2004.01.006 SN - 0008-6215 SN - 1873-426X VL - 339 IS - 4 SP - 795 EP - 799 PB - Elsevier CY - Amsterdam AN - OPUS4-5341 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -