TY - GEN A1 - Hasenstab, Andreas A1 - Krause, Martin A1 - Lutz, J. A1 - Hillemeier, B. A1 - Rieck, C. T1 - Niederfrequente Ultraschall-Echo-Verfahren und Bohrwiderstandsmessung zur Untersuchung von Holzbauteilen T2 - DGZfP Jahrestagung CY - Rostock, Deutschland DA - 2005-05-02 KW - ZfP an Holzbauteilen KW - Fehlstellen KW - Minderdicken KW - Ultraschallecho-Experimente an Probekörpern KW - Ultraschall-Echo KW - Fäulnis KW - Bauwesen PY - 2005 SN - 3-931381-64-1 N1 - Serientitel: Berichtsband / Deutsche Gesellschaft für zerstörungsfreie Prüfung e. V. – Series title: Berichtsband / Deutsche Gesellschaft für zerstörungsfreie Prüfung e. V. IS - 94-CD SP - 1(?) EP - 11(?) PB - DGZfP CY - Berlin AN - OPUS4-11960 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Segebade, Christian A1 - Lutz, G. J. A1 - Schmitt, B. F. T1 - Bestimmung von Pd, Ag, Pt und Au in Elektrolytkupfer durch Aktivierung mit hochenergetischen Photonen PY - 1979 SN - 0016-1152 VL - 296 SP - 263 EP - 265 PB - Springer CY - Berlin AN - OPUS4-9201 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Segebade, Christian A1 - Lutz, G. J. T1 - Aktivierungsanalytische Untersuchungen an Keramik (Terra Sigillata) PY - 1976 SN - 0342-4510 VL - 7 SP - 4,1 EP - 4,20 PB - Habelt CY - Bonn AN - OPUS4-8561 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Panik, F. A1 - Drosdol, J. A1 - Auersch, Lutz T1 - Anwendungsorientierte Untersuchungsmethoden des Lenkverhaltens von Kraftfahrzeugen T2 - VDI-Schwingungstagung CY - Düsseldorf, Deutschland DA - 1980-10-02 PY - 1980 SN - 3-18-090381-3 SN - 0083-5560 N1 - Serientitel: VDI-Berichte – Series title: VDI-Berichte IS - 381 SP - 89 EP - 98 PB - VDI-Verl. CY - Düsseldorf AN - OPUS4-9293 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reimers, Peter A1 - Lutz, G. J. A1 - Segebade, Christian T1 - The Non-Destructive Determination of Gold, Silver and Copper by Photon Activation Analysis of Coins and Art Objects PY - 1977 SN - 0003-813X SN - 1475-4754 SN - 0365-6004 VL - 19 IS - 1 SP - 167 EP - 172 PB - Blackwell CY - Oxford AN - OPUS4-8783 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schmidt, B.V.K.J. A1 - Fechler, N. A1 - Falkenhagen, Jana A1 - Lutz, J.-F. T1 - Controlled folding of synthetic polymer chains through the formation of positionable covalent bridges N2 - Covalent bridges play a crucial role in the folding process of sequence-defined biopolymers. This feature, however, has not been recreated in synthetic polymers because, apart from some simple regular arrangements (such as block co-polymers), these macromolecules generally do not exhibit a controlled primary structure—that is, it is difficult to predetermine precisely the sequence of their monomers. Herein, we introduce a versatile strategy for preparing foldable linear polymer chains. Well-defined polymers were synthesized by the atom transfer radical polymerization of styrene. The controlled addition of discrete amounts of protected maleimide at precise times during the synthesis enabled the formation of polystyrene chains that contained positionable reactive alkyne functions. Intramolecular reactions between these functions subsequently led to the formation of different types of covalently folded polymer chains. For example, tadpole (P-shaped), pseudocyclic (Q-shaped), bicyclic (8-shaped) and knotted (α-shaped) macromolecular origamis were prepared in a relatively straightforward manner. KW - Copolymerization KW - Chain folding KW - SEC KW - NMR KW - FT-IR KW - LAC KW - MALDI PY - 2011 DO - https://doi.org/10.1038/NCHEM.964 SN - 1755-4330 SN - 1755-4349 VL - 3 SP - 234 EP - 238 PB - Nature Publishing Group CY - London, UK AN - OPUS4-23888 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nöll, G. A1 - Daub, J. A1 - Lutz, M. A1 - Rurack, Knut T1 - Synthesis, spectroscopic properties, and electropolymerization of azulene dyads N2 - Four azulene dyads have been synthesized and studied by spectroscopic and electrochemical methods. A triarylamine, a boron-dipyrromethene (BDP or BODIPY), a porphyrin, and an isoalloxazine moiety have been linked to an extended π electron system at the 2-position of azulene, leading to the dyads 1–4, respectively. For the synthesis of 1–4, first 2-(4-ethynyl-phenyl)azulene (EPA) was prepared, which was further reacted with the halogenated chromophores by Pd-catalyzed cross-coupling reactions. The dyads 1–4 exhibit strong absorption bands in the visible range, which are dominated by the absorption spectra of the individual subchromophores. Fluorometric studies of 2–4 revealed that after excitation of the subchromophoric unit attached to the parent azulene moiety, quenching mainly through energy transfer to azulene is effective, whereas possible charge-transfer interactions play only a minor role. Potentiodynamic oxidation of the dyads 1–4 leads to the formation of polymer films, which are deposited at the electrode. The polymer film derived from 1 was further characterized by spectroelectrochemistry. During positive doping of poly-1, a strong absorption band appears at 13,200 cm–1, which is typical for triarylamine radical cations. This band is overlapping with a broad absorption band in the low-energy region that might be caused by charge-transfer interactions within the polymer. KW - Azulen KW - Elektropolymerisation KW - Energietransfer KW - Farbstoffe KW - Fluoreszenz PY - 2011 DO - https://doi.org/10.1021/jo200080v SN - 0022-3263 SN - 1520-6904 VL - 76 IS - 12 SP - 4859 EP - 4873 PB - American Chemical Society CY - Washington, DC AN - OPUS4-23987 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Segebade, Christian A1 - Lutz, George J. T1 - Die Untersuchung einiger Bodenlagerungseinflüsse auf die Zusammensetzung von römischer Keramik (Terra sigillata) PY - 1981 SN - 0344-5089 VL - 5 SP - 69 EP - 83 PB - Staatliche Museen CY - Berlin AN - OPUS4-33359 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Segebade, C. A1 - Lutz, G. J. A1 - Weise, Hans-Peter A1 - Fusban, H.-U. T1 - Quantitative Evaluation of Interference Reactions in Photon Activation Analysis PY - 1981 SN - 0134-0719 SN - 0022-4081 VL - 67 IS - 1 SP - 205 EP - 214 PB - Elsevier Sequoia CY - Lausanne AN - OPUS4-33361 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lutz, J.-F. A1 - Kubowicz, St. A1 - Baussard, J.-F. A1 - Thünemann, Andreas A1 - v. Berlepsch, H. A1 - Laschewsky, A. T1 - Multicompartment Micelles Obtained via the Self-Assembly of a Well-Defined Triblock Macrosurfactant Prepared by RAFT Polymerization KW - Micelles KW - Living polymerization KW - RAFT KW - Block copolymers PY - 2005 SN - 0032-3934 VL - 46 IS - 2 SP - 297 EP - 298 PB - American Chemical Society CY - Newark, NJ AN - OPUS4-10534 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kubowicz, St. A1 - Baussard, J.-F. A1 - Lutz, J.-F. A1 - Thünemann, Andreas A1 - v. Berlepsch, H. A1 - Laschewsky, A. T1 - Multicompartment Micelles Formed by Self-Assembly of Linear ABC Triblock Copolymers in Aqueous Medium KW - Small-angle x-ray scattering KW - Micelles PY - 2005 DO - https://doi.org/10.1002/anie.200500584 SN - 1433-7851 SN - 1521-3773 SN - 0570-0833 VL - 44 SP - 5262 EP - 5265 PB - Wiley-VCH CY - Weinheim AN - OPUS4-10537 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lutz, W. A1 - Kurzhals, R. A1 - Sauerbeck, S. A1 - Toufar, H. A1 - Buhl, J.-C. A1 - Gesing, T. A1 - Altenburg, Wolfgang A1 - Jäger, Christian T1 - Hydrothermal stability of zeolite SAPO-11 N2 - The hydrothermal stability of SAPO-11 was studied in water of autogenous pressure as function of the temperature. SAPO-11 remained crystalline up to 190 °C. Thereby, it was observed, parent as well as hydrothermally treated samples showed similarities to the isotypic structure of zeolite AlPO-11 called here AELdry. After fully hydration of the samples, AELdry changed completely into a hydrated AELwet structure of another framework symmetry. The transition from calcined to hydrated state was reversible for both the parent and the hydrothermally treated samples. 27Al and 31P NMR MAS spectra showed a single resonance typical for AlPO4 type tetrahedra for the calcined parent and hydrothermally treated samples. Upon hydration, the single AlPO4 resonance signal split into three different signals as is the case for the corresponding 31P signals. By means of NH3-TPD measurement a loss of acidity was detected after the hydrothermal treatment as follows from a framework desilication. Nitrogen and water adsorption decreased systematically. At 210 °C a non-zeolitic, non-porous phase was irreversibly formed. The XRD pattern of this phase shows resemblance to a synthetic aluminium phosphate of the tridymite structure type. KW - Zeolite KW - Silicoaluminophosphate KW - SAPO-11 KW - Hydrothermal stability KW - Phase transformation PY - 2010 DO - https://doi.org/10.1016/j.micromeso.2009.08.003 SN - 1387-1811 SN - 1873-3093 VL - 132 IS - 1-2 SP - 31 EP - 36 PB - Elsevier CY - Amsterdam AN - OPUS4-21131 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Giese, Lutz A1 - Weritz, Friederike A1 - Weimann, Karin A1 - Niederleithinger, Ernst A1 - Ulbricht, J.P. ED - Dincer, I. T1 - Bricks made of sludge from the Izmir bay - an integrative approach for the recycling of sludge - preliminary results T2 - 1st International Exergy, Energy and Environment Symposium ; IEEES-1 CY - Izmir, Turkey DA - 2003-07-13 PY - 2003 SN - 975-288440-7 SP - 995 EP - 1003 CY - Izmir AN - OPUS4-2829 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lutz, J.-F. A1 - Thünemann, Andreas A1 - Nehring, R. T1 - Preparation by Controlled Radical Polymerization and Self-Assembly via Base-Recognition of Synthetic Polymers Bearing Complementary Nucleobases N2 - The radical polymerization of three monomers bearing nucleobases 1-(4-vinylbenzyl)thymine (VBT), 1-(4-vinylbenzyl)uracil (VBU) and 9-(4-vinylbenzyl)adenine (VBA) was investigated. The corresponding homopolymers could be prepared in high yields via conventional radical polymerization. However, the resulting polymers were found to be only soluble in a few polar solvents. On the other hand, copolymers of dodecyl methacrylate (DMA) with either VBT or VBA could be prepared via both free radical polymerization and atom transfer radical polymerization and could be dissolved in a large variety of organic solvents. Moreover, the formed complementary copolymers P(VBT-co-DMA) and P(VBA-co-DMA) were found to self-assemble in dilute solutions in dioxane or chloroform via base recognition, as evidenced by a significant hypochromicity effect in UV spectroscopy. Nevertheless, at higher concentrations in chloroform, both dynamic light scattering and optical microscopy indicate that P(VBT-co-DMA), P(VBA-co-DMA), or P(VBT-co-DMA)/P(VBA-co-DMA) mixtures spontaneously self-assemble into micron size spherical aggregates. 1H NMR and FTIR studies confirmed that the self-assembly process is driven in all cases via H-bond formation. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 4805-4818, 2005 KW - ATRP KW - Living polymerization KW - Nucleic acids KW - Polymersomes KW - Self-assembly PY - 2005 DO - https://doi.org/10.1002/pola.20976 SN - 0360-6376 SN - 0887-624X VL - 43 IS - 20 SP - 4805 EP - 4818 PB - Wiley CY - Hoboken, NJ AN - OPUS4-10842 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lutz, J.-F. A1 - Thünemann, Andreas A1 - Rurack, Knut T1 - DNA-like "Melting" of Adenine- and Thymine-Functionalized Synthetic Copolymers KW - Polymers KW - Micelles KW - Amyloid beta-peptide KW - Proteins KW - Secondary structure PY - 2005 SN - 0024-9297 SN - 1520-5835 VL - 38 IS - 20 SP - 8124 EP - 8126 PB - American Chemical Society CY - Washington, DC AN - OPUS4-11068 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lutz, J.-F. A1 - Nehring, R. A1 - Thünemann, Andreas T1 - Solution Self-Assembly of Synthetic Copolymers bearing Complementary Nucleic Acid Funtionalities KW - DNA KW - Living polymerization KW - ATRP KW - Copolymers PY - 2005 SN - 0032-3934 VL - 46 IS - 2 SP - 397 EP - 398 PB - American Chemical Society CY - Newark, NJ AN - OPUS4-10535 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Lutz, J.-F. A1 - Kubowicz, S. A1 - Laschewsky, A. A1 - Nehring, R. A1 - Pfeifer, Sebastian A1 - Schütt, Dagmar A1 - Thünemann, Andreas T1 - Solution self-assembly of tailor-made macromolecular building-blocks designed by controlled radical polymerization techniques T2 - Makromolekulares Kolloquium Freiburg CY - Freiburg, Germany DA - 2006-02-23 PY - 2006 AN - OPUS4-12389 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Lutz, J.-F. A1 - Pfeifer, S. A1 - Chanana, M. A1 - Thünemann, Andreas A1 - Bienert, Ralf T1 - H-Bonding-Directed Self-Assembly of Synthetic Copolymers Containing Nucleobases: Organization and Colloidal Fusion in a Noncompetitive Solvent N2 - The self-organization of random copolymers composed of a nucleobase monomer (either 1-(4-vinylbenzyl)thymine or 9-(4-vinylbenzyl)adenine) and dodecyl methacrylate (DMA) was studied in dilute chloroform solutions. The balance between the molar fractions of the nucleobase monomer (leading to intermolecular H-bonding) and DMA (soluble moiety in chloroform) in the polymer chains was found to be the parameter that principally influences the self-organization. DMA-rich copolymers are molecularly soluble in chloroform, whereas nucleobase-rich copolymers are insoluble in this solvent. Copolymers possessing an equimolar comonomer composition self-assemble into micrometer-sized particles physically cross-linked by intermolecular H-bonds (either thymine-thymine or adenine-adenine interactions, depending on the studied copolymer). Nevertheless, when mixed together, thymine- and adenine-based colloids fuse into thermodynamically stable microspheres cross linked by adenine-thymine interactions. KW - Synthetic polymers KW - Self-organization KW - H-bonding KW - Nucleobases KW - Confocal fluorescence microscopy PY - 2006 DO - https://doi.org/10.1021/la061382a SN - 0743-7463 SN - 1520-5827 VL - 22 IS - 17 SP - 7411 EP - 7415 PB - American Chemical Society CY - Washington, DC AN - OPUS4-12637 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Roszak, I. A1 - Oswald, L. A1 - Ouahabi, A. A. A1 - Bertin, Annabelle A1 - Laurent, E. A1 - Felix, O. A1 - Carvin-Sergent, I. A1 - Charles, L. A1 - Lutz, J.-F. T1 - Synthesis and sequencing of informational poly(amino phosphodiester)s N2 - Sequence-defined poly(amino phosphodiester)s containing main-chain tertiary amines were synthesized by automated solid-phase phosphoramidite chemistry. These polymers were prepared using four monomers with different substituents. The formed polymers were characterized by HPLC and mass spectrometry. These methods evidenced preparation of molecularly-defined polymers. Furthermore, the presence of tertiary amines in the polymer backbones facilitates sequencing by tandem mass spectrometry. KW - Poly(amino phosphodiester) KW - Synthesis KW - HPLC KW - Mass spectrometry PY - 2021 DO - https://doi.org/10.1039/d1py01052b SN - 1759-9954 VL - 12 IS - 37 SP - 5279 EP - 5282 PB - Royal Society of Chemistry AN - OPUS4-53732 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -