TY - JOUR A1 - Franco, O. A1 - Reck, Günter A1 - Orgzall, I. A1 - Schulz, Burkhard A1 - Schulz, B. T1 - Characterization of a new non-centrosymmetric polymorph of diphenyl-1,3,4-oxadiazole N2 - Diphenyl-1,3,4-oxadiazole (DPO) crystallization experiments from solutions clearly reveal the polymorphism of the substance. Besides the formerly known centrosymmetric monoclinic structure with space group P21/c (DPO I) a new monoclinic structure with the non-centrosymmetric space group Cc is found (DPO II): a=2.4134(4) nm, b=2.4099(3) nm, c=1.2879(2) nm,?=110.048(3)°, and V=7.0363(17) nm3. The asymmetric unit contains six independent molecules in a complex packing motif. A re-determination of the crystal structure of DPO I at room temperature gives lattice parameters a=0.51885(6) nm, b=1.8078(2) nm, c=1.21435(14) nm, ?=93.193(3)°, and V=1.1373(2) nm3. X-ray measurements at 363 K show a significant increase of the unit cell volume by 1.6%. Differences between both structures concerning morphology and characteristic Raman bands are outlined in detail. DSC investigations show an irreversible transition from DPO I to DPO II at 97 °C. DPO II does not show any transition in the temperature range up to the melting point at 141 °C. The non-centrosymmetric DPO II structure shows triboluminescence. KW - Diphenyl-1,3,4-oxadiazole KW - X-ray structure KW - Polymorphism KW - Non-centrosymmetric structure PY - 2003 DO - https://doi.org/10.1016/S0022-2860(02)00569-0 SN - 0022-2860 SN - 1872-8014 SN - 0377-046X VL - 649 SP - 219 EP - 230 PB - Elsevier CY - Amsterdam AN - OPUS4-2465 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Emmerling, Franziska A1 - Orgzall, I. A1 - Dietzel, B. A1 - Schulz, Burkhard A1 - Reck, Günter A1 - Schulz, B. T1 - Structural studies on trifluoromethyl substituted 2,5-diphenyl-1,3,4-oxadiazoles N2 - Three new compounds have been synthesized based on the molecular motif 2-[2,6-bis(trifluoromethyl)phenyl]-5-phenyl-1,3,4-oxadiazole, with subsequent CF3-substitution in the ortho-positions of the phenylene ring. The crystal structures of the compounds have been determined by single crystal X-ray diffraction. All compounds have a monoclinic structure. The solid state structure of the compounds is influenced by the electronic properties of the fluorine atoms, leading to the occurrence of C–H...F, and C–F...ϖ interactions, partly replacing ϖ–ϖ interactions usually observed in the crystal structures of 2,5-diphenyl-1,3,4-oxadiazole derivatives. Other significant interactions than those involving fluorine appear only in rare cases. The strong impact of the fluorine atoms on the intra- and intermolecular interactions, and the molecular conformation lead to novel inputs for the understanding of molecular recognition, supramolecular assembly, and crystal packing of fluorine containing compounds. KW - Crystal structure KW - 1,3,4-oxadiazole KW - Molecular conformation KW - Weak interactions PY - 2007 SN - 0022-2860 SN - 1872-8014 SN - 0377-046X VL - 832 IS - 1-3 SP - 124 EP - 131 PB - Elsevier CY - Amsterdam AN - OPUS4-14644 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Emmerling, Franziska A1 - Orgzall, I. A1 - Reck, Günter A1 - Schulz, Burkhard A1 - Stockhause, S. A1 - Schulz, B. T1 - Structures of substituted di-aryl-1,3,4-oxadiazole derivatives: 2,5-bis(pyridyl)- and 2,5-bis(aminophenyl)-substitution N2 - Crystal structures of four different di-aryl-1,3,4-oxadiazole compounds (aryl = 2-pyridyl-, 3-pyridyl-, 2-aminophenyl-, 3-aminophenyl-) are determined. Crystallization of di(2-pyridyl)-1,3,4-oxadiazole yielded monoclinic and triclinic polymorphs. The structures are characterized by the occurrence of π–π interactions. Additionally, in case of the aminophenyl compounds intra- as well as intermolecular hydrogen bonds are found that influence the packing motif as well. Since these molecules are often used as ligands in metal–organic complexes similarities and differences of the molecular conformation between the molecules in the pure crystals and that of the ligands in the complexes are discussed. KW - Crystal structure KW - 1,3,4-Oxadiazole KW - Molecular conformation KW - Hydrogen bonds PY - 2006 DO - https://doi.org/10.1016/j.molstruc.2006.03.076 SN - 0022-2860 SN - 1872-8014 SN - 0377-046X VL - 800 IS - 1-3 SP - 74 EP - 84 PB - Elsevier CY - Amsterdam AN - OPUS4-13799 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rudert, R. A1 - Schulz, Burkhard A1 - Reck, Günter A1 - Vollhardt, D. A1 - Kriwanek, J. T1 - (Carboxymethyl)dimethylundecylammonium bromide N2 - The title compound, C₁₅H₃₂NO₂⁺.Br⁻, crystallizes to form layers with interdigitating hydrocarbon chains stabilized by Br⁻۰۰۰H—O hydrogen bonds and Br⁻۰۰۰N⁺ contacts. KW - (Carboxymethyl)dimethylundecylammonium bromide KW - Crystal structure PY - 1995 DO - https://doi.org/10.1107/s0108270194011443 SN - 0108-2701 VL - 51 SP - 768 EP - 770 PB - Wiley-Blackwell CY - Oxford AN - OPUS4-56998 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Vossmeyer, T. A1 - Reck, Günter A1 - Katsikas, L. A1 - Haupt, E. T. K. A1 - Schulz, Burkhard A1 - Weller, H. T1 - A "double-diamond superlattice" built up of Cd17S4(SCH2CH20H)26 clusters N2 - A simple preparation of Cd17S4(SCH2CH2OH)26 clusters in aqueous solution leads to the formation of colorless blocky crystals. X-ray structure determinations revealed a superlattice framework built up of covalently linked clusters. This superlattice is best described as two enlarged and interlaced diamond or zinc blende lattices. Because both the superlattice and the clusters display the same structural features, the crystal structure resembles the self-similarities known from fractal geometry. The optical spectrum of the cluster solution displays a sharp transition around 290 nanometers with a large Absorption coefficient (~84,000 per molar per centimeter). KW - superlattice KW - cluster KW - X-ray structure determination PY - 1995 DO - https://doi.org/10.1126/science.267.5203.1476 SN - 0036-8075 SN - 1095-9203 VL - 267 IS - 5203 SP - 1476 EP - 1479 PB - AAAS, American Association for the Advancement of Science CY - Washington, DC AN - OPUS4-44409 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Rikowski, E. T1 - Zur Charakterisierung von Si-Polymeren durch flüssigchromatographische Verfahren in Kopplung mit der MALDI-TOF-MS N2 - Summary. The coupling of the three liquid chromatographic modes with MALDI-TOF mass spectrometry is suitable for the determination of the molecular, functional, and chemical heterogeneities of Si polymers. Silsesquioxanes and siloxanes serve as examples for this method of structure identification. The substance specific construction of the SEC calibration curve by means of MALDI-MS is shown. Zusammenfassung. Die Kopplung der drei flüssigchromatographischen Modi mit MALDI-TOF-Massenspektrometrie ist zur Bestimmung der molekularen, funktionalen und chemischen Verteilungen von Si-Polymeren geeignet. Silsesquioxane und Siloxane dienen als Beispiele für diese Art der Strukturerkennung. Die substanzspezifische Konstruktion einer SEC-Eichkurve mit Hilfe der MALDI-MS wird gezeigt. KW - Si polymer characterization KW - LC/MALDI-TOF-MS PY - 1999 DO - https://doi.org/10.1007/PL00010162 SN - 0026-9247 SN - 1434-4475 VL - 130 IS - 1 SP - 163 EP - 174 PB - Springer CY - Wien AN - OPUS4-2163 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. A1 - Hauser, K. A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Macrocycles 12. Ring-Opening Polycondensations of Tin-Containing Macrocycles with Bis(Thioarylester)s N2 - 2,2-Dibutyl-2-stanna-1,3-dioxepane (DSDOP) was polycondensed with bis(4-chlorothiophenyl) suberat under various reaction conditions, but only moderate molecular weights (Mn 10000) were obtained. The MALDI-TOF mass spectrosmetry revealed the formation of cyclic oligo- and polyesters in addition to linear species having OH, CO2H, and unreacted 4-chlorothiophenyl ester endgroups. Furthermore, -Caprolactone (-CL) was polymerized with DSDOP as the initiator at monomer/initiator (M/I) ratios of 20 and 50. The resulting tin-containing macrocyclic polylactones were reacted with sebacic acid bis(4-thiocresyl)ester at three different temperatures and with different reaction times. Analogous polycondensations were conducted with suberic acid bis(4-chlorothiophenyl) ester. The presence of thioarylester endgroups in the isolated polyesters was checked by 1H NMR spectroscopy. The highest conversions were found at long reaction times (24 or 72 hours), or after the addition of pyridine and N,N-dimethylaminopyridine as catalysts. Despite high conversions, the number average molecular weights (Mn's) did not exceed values around 20000. Even in the samples having the highest molecular weights, unreacted 4-chlorothiophenylester endgroups were detected by GPC measurements evaluated with a UV-detector. It is concluded that both factors, cyclization and incomplete conversion, contribute to the limitation of the chain growth. KW - Ring-Opening Polycondensations KW - Macrocycles KW - Polyesters PY - 2000 DO - https://doi.org/10.1081/MA-100101099 SN - 1060-1325 SN - 1520-5738 VL - 37 IS - 4 SP - 379 EP - 394 PB - Taylor & Francis CY - Philadelphia, PA AN - OPUS4-2167 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H. A1 - Probst, N. A1 - Schwarz, G. A1 - Schulz, Günter A1 - Krüger, Ralph-Peter T1 - New Polymer Syntheses - 107. Aliphatic Poly(thio ester)s by Ring-Opening Polycondensation of 2-Stanna-1,3-Dithiacycloalkanes N2 - We prepared 2,2-dibutyl-2-stanna-1,3-dithiacycloalkanes from dibutyltin oxide and ,-dimercaptoalkanes. Heterocycles with five-, six-, seven-, or nine-ring members were used as bifunctional monomers for polycondensations with aliphatic dicarboxylic acid chlorides. These polycondensations conducted in bulk were highly exothermic and yielded poly(thio ester)s with number average molecular weights (Mn's) in the range of 5000-30,000 Da. These poly(thio ester)s proved to be rapidly crystallizing materials with melting temperatures in the range of 90-150 °C. In addition to the success of the new synthetic approach, two interesting and unpredictable results were obtained. All volatile species detectable by matrix assisted laser desorption induced-time of flight (MALDI-TOF) mass spectrometry were cyclic oligo- and poly(thio ester)s. Second, several polyesters showed a reversible first-order change of the crystal modification as identified by differential scanning calorimetry measurements and X-ray scattering with variation of the temperature. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 3656-3664, 2000 KW - Poly(thio-ester)s KW - Ring-opening polycondensation KW - Macrocycles KW - Change of crystal structure PY - 2000 DO - https://doi.org/10.1002/1099-0518(20001001)38:19<3656::AID-POLA190>3.0.CO;2-M SN - 0360-6376 SN - 0887-624X VL - 38 IS - 19 SP - 3656 EP - 3664 PB - Wiley CY - Hoboken, NJ AN - OPUS4-2170 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Reuther, F. A1 - Krüger, Ralph-Peter A1 - Schulz, Günter A1 - Baehr, G. A1 - Westerwelle, U. A1 - Gruetzner, G. ED - Houlihan, F. M. T1 - Tailored novolak resins for advanced photoresists by a two-step procedure - new insight into the molecular structure by coupling GPC and MALDI-TOF-MS T2 - 17th Annual SPIE Conference on Advances in Resist Technology and Processing CY - Santa Clara, CA, USA DA - 2000-02-28 KW - Novolak KW - Structure KW - Synthesis KW - Gel permeation KW - Chromatography KW - MALDI-TOF-MS PY - 2000 SN - 0-8194-3617-8 SN - 1605-7422 N1 - Serientitel: SPIE proceedings series – Series title: SPIE proceedings series IS - 3999 SP - 464 EP - 471 PB - SPIE CY - Bellingham AN - OPUS4-2171 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reck, Günter A1 - Orgzall, I. A1 - Schulz, B. A1 - Dietzel, B. T1 - Two polymorphic forms of 2,5-bis(4-methoxycarbonylphenyl)-1,3,4-oxadiazole N2 - In the title compound, C13H14BN3O, the aziridine ring is an almost equilateral triangle, the C—C distance being slightly shorter than the C—N distances, probably because of the dative B—N bond. The five-membered ring, composed of two C atoms and N, B and O atoms, is fused with the aziridine ring to form a six-membered ring with a chair conformation. PY - 2003 DO - https://doi.org/10.1107/S0108270103022698 SN - 0108-2701 SN - 1600-5759 VL - 59 SP - o634 EP - o635 PB - Blackwell Publ. CY - Oxford AN - OPUS4-2694 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schulz, Günter A1 - Starfinger, Käthe T1 - Pilzwidrige Wirksamkeit verschiedener Steinkohlenteeröle PY - 1961 SN - 0417-2000 VL - 48 SP - 53 EP - 56 PB - Deutsche Gesellschaft für Holzforschung CY - München AN - OPUS4-10112 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Determination of functionality and molar mass distribution of aliphatic polyesters by orthogonal liquid chromatography, Part I: Off-line investigation of poly-(1,6-hexanediol adipates) PY - 1994 SN - 0148-3919 VL - 17 SP - 3069 EP - 3090 PB - Dekker CY - New York, NY AN - OPUS4-2139 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - New Results of Determination of Polymer Heterogeneity by Two-Dimensional Orthogonal Liquid Chromatography T2 - International GPC Symposium CY - Lake Buena Vista, FL, USA DA - 1994-06-05 PY - 1994 SP - 273 EP - 275 PB - Gordon and Breach CY - St. Helier, Jersey AN - OPUS4-2140 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wachsen, O. A1 - Reichert, K.H. A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Thermal decomposition of biodegradable polyesters - III. Studies on the mechanisms of thermal degradation of oligo-L-lactide using SEC, LACCC and MALDI-TOF-MS PY - 1997 SN - 0141-3910 SN - 1873-2321 VL - 55 SP - 225 EP - 231 PB - Applied Science Publ. CY - London AN - OPUS4-2154 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Leitner, M.B. A1 - Schinkel, G. A1 - Springer, J. A1 - Ruhmann, R. A1 - Schulz, Günter A1 - Niesel, F.T. T1 - Methacrylate copolymers containing azoanthraquinone units: synthesis by direct copolymerization and by polymer-analogous esterfication reaction PY - 1997 SN - 1381-5148 SN - 1873-166X VL - 33 SP - 137 PB - Elsevier CY - Amsterdam AN - OPUS4-2155 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Determination of polymer heterogeneity by two-dimensional orthogonal liquid chromatography KW - Orthogonal chromatography KW - Size exclusion chromatography KW - Liquid adsorption chromatography at critical conditions KW - Matrix-assisted laser desorption ionization time-of-flight mass spectrometry KW - Polyester KW - Polyether PY - 1996 SN - 1023-666X SN - 1563-5341 VL - 2 SP - 221 EP - 235 PB - Gordon and Breach Publ. CY - Amsterdam AN - OPUS4-2146 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Leukel, J. A1 - Burchard, W. A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Mechanism of the anionic copolymerization of anhydride- cured epoxies-analysisted by matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF-MS) PY - 1996 SN - 1022-1336 SN - 1521-3927 VL - 17 SP - 359 EP - 366 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-2148 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Bestimmung der Polymerheterogenität durch Kopplung von HPLC und MALDI-TOF-MS KW - Zweidimensionale Flüssigchromatographie KW - Flugzeit-Massenspektrometrie KW - Synthetische Polymere PY - 1996 SN - 0016-3538 VL - 40 IS - 4 SP - 398 EP - 402 PB - GIT-Verlag CY - Darmstadt AN - OPUS4-2149 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Wachsen, O. T1 - New aspects of determination of polymer heterogeneity by 2-dimensional orthogonal liquid chromatography and MALDI-TOF-MS PY - 1996 SN - 1022-1360 SN - 0258-0322 SN - 1521-3900 VL - 110 SP - 155 EP - 176 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-2150 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mix, Renate A1 - Gähde, J. A1 - Goering, Harald A1 - Schulz, Günter T1 - Segmented polyurethanes with 4,4-bis-(6-hydroxyhexoxy)biphenyl as chain extender - Part 2. Synthesis and properties of MDI-polyurethanes in comparison with 2,4-TDI-polyurethanes N2 - Linear segmented polyurethanes based on poly(butylene adipate)s (PBA) of different molecular weight (Mn 2000, 1000, and 600), 4,4-diphenylmethane diisocyanate (MDI) and the mesogenic diol 4,4-bis-(6-hydroxyhexoxy)biphenyl (BHHBP) as well as the unsegmented polyurethane consisting of MDI/BHHBP units have been synthesized and characterized by elemental analysis, 13C-NMR and SEC. The thermal behavior and the morphology were studied by DSC, polarizing microscopy, and DMA. The properties of the MDI-polyurethanes were discussed in relation to the BHHBP chain extended 2,4-TDI-polyurethanes and common 1,4-butanediol chain-extended MDI products. MDI polyurethanes based on PBA (Mn 2000) exhibit a glass transition temperature Tg of about -40°C independent of the hard segment content up to 50% hard segments. At higher hard segment contents increasing Tgs were observed. Polyurethanes, based on the shorter polyester soft segments PBA (Mn 1000 or 600), reveal an increase in the glass transition temperatures with growing hard segment content. The thermal transitions caused by melting of the MDI/BHHBP hard segment domains are found at 50 K higher temperatures in comparison with the analogous TDI products with mesogenic BHHBP/TDI hard segments. Shortening of the PBA chain length causes a shift of the thermal transitions to lower temperatures. Polarizing microscopy experiments indicate that liquid crystalline behavior is influenced by both the content of mesogenic hard segments and the chain length of the polyester. © 1996 John Wiley & Sons, Inc. PY - 1996 DO - https://doi.org/10.1002/(SICI)1099-0518(19960115)34:1<33::AID-POLA3>3.0.CO;2-4 SN - 0360-6376 SN - 0887-624X VL - 34 IS - 1 SP - 33 EP - 44 PB - Wiley CY - Hoboken, NJ AN - OPUS4-2151 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter ED - Günther, W. T1 - Strukturaufklärung von heterogenen Polymeren durch zweidimensionale Flüssigchromatographie und MALDI-TOF-Massenspektrometrie T2 - InCom '94 - International Symposium on Instrumentalized Analytical Chemistry and Computer Technology CY - Düsseldorf, Deutschland DA - 1994-03-14 PY - 1994 VL - 94 PB - InCom-Bureau CY - Düsseldorf AN - OPUS4-2195 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Polymer Characterization by Two-Dimensional HPLC and MALDI-TOF-MS T2 - 7th International Symposium on Polymer Analysis and Characterization (ISPAC) CY - Les Diablerets, Switzerland DA - 1994-05-24 PY - 1994 PB - Gordon and Breach CY - St. Helier, Jersey AN - OPUS4-2196 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Paulus, G. A1 - Resch, M. A1 - Schulz, Günter ED - Darms, R. ED - Suter, U. T1 - Polymer Characterization by MALDI-TOF-MS and Combination with HPLC T2 - 5th European Polymer Federation Symposium on Polymeric Materials (EPF) CY - Basel, Switzerland DA - 1994-10-09 PY - 1994 SN - 3-85739-297-5 SN - 0258-0322 VL - 5 PB - Hüthig & Wepf CY - Zug AN - OPUS4-2200 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schulz, Günter A1 - Krüger, Ralph-Peter A1 - Much, Helmut ED - Günther, W. T1 - Polymercharakterisierung durch MALDI-TOF-MS und Kopplung mit der HPLC T2 - InCom '95 - International Symposium on Instrumentalized Analytical Chemistry and Computer Technology CY - Düsseldorf, Germany DA - 1995-03-20 PY - 1995 CY - Moers AN - OPUS4-2201 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wachsen, O. A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Reichert, K.H. T1 - Untersuchungen zur Charakterisierung des Abbaus von Polylactiden mittels 2D-HPLC und MALDI-TOF-MS T2 - Sitznung des Berliner Verband für Polymerforschung e.V. CY - Berlin DA - 1995-05-18 PY - 1995 CY - Berlin AN - OPUS4-2202 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Kilz, P. A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter ED - Provder, T. T1 - Two-dimensional chromatography for the deformulation of complex copolymers PY - 1995 SN - 0-8412-3132-X N1 - Serientitel: Advances in chemistry series – Series title: Advances in chemistry series IS - 247 SP - 223 EP - 241 PB - American Chemical Society CY - Washington AN - OPUS4-2185 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Rikowski, E. ED - Auner, N. T1 - Synthesis of Polyhedral Hexa-, Octa-, Deca- and Dodeca-Silsesquioxanes, Separation by NP-HPLC, SEC and LAC, Characterization by MALDI-TOF-MS KW - Silsesquioxanes KW - NP-HPLC KW - LAC KW - SEC KW - MALDI-TOF-MS PY - 2000 SN - 3-527-29854-1 SP - 545 ff. PB - Wiley-VCH CY - Weinheim AN - OPUS4-2187 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Much, Helmut A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Investigation of Macromer Heterogeneity by Two-Dimensional HPLC and MALDI-TOF-MS T2 - 19th International Symposium on Column Liquid Chromatography CY - Innsbruck, Austria DA - 1995-05-28 PY - 1995 CY - Innsbruck AN - OPUS4-2204 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Reichert, K.H. A1 - Schulz, Günter A1 - Wachsen, O. T1 - Untersuchungen zur Charakterisierung des Polylactidabbaus mittels HPLC und MALDI-TOF-MS T2 - Präsentationsveranstaltung des Instituts für Angewandte Chemie Berlin-Adlershof e.V. CY - Berlin, Germany DA - 1995-09-26 PY - 1995 CY - Berlin AN - OPUS4-2206 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Investigation of Macromer Heterogeneity by 2D-HPLC and MALDI-TOF-MS T2 - Präsentationsveranstaltung des Instituts für Angewandte Chemie Berlin-Adlershof e.V. CY - Berlin, Germany DA - 1995-09-26 PY - 1995 CY - Berlin AN - OPUS4-2207 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Flatau, S. A1 - Much, Helmut A1 - Schulz, Günter T1 - Hochleistungsflüssigchromatographie T2 - Statusseminar des ACA CY - Berlin, Deutschland DA - 1996-11-05 PY - 1996 AN - OPUS4-2210 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brehme, R. A1 - Gründemann, E. A1 - Schneider, M. A1 - Radeglia, Reiner A1 - Reck, Günter A1 - Schulz, Burkhard T1 - Aza-enamines X - Formylation of Pyrazole-4-carbaldehyde Hydrazones at the Hydrazonoazomethine C-Atom N2 - 1,3-Disubstituted 1H-pyrazole-4-carbaldehyde-N,N-di­methylhydrazones 1 reacted with the Vilsmeier-Haackreagent, corresponding to the aza-enamine concept, in an electrophilicsubstitution reaction at the azomethine C-atom yielding the 1,4,5-triaza-pentadieniumsalts 2. These were hydrolysed to give2-hydrazono-2-(1H-pyrazole-4-yl)ethanals 3. The electrophilic attack did not takeplace at the vinylogous position 5' of the pyrazoles. KW - Aza-enamines KW - Hydrazones KW - Heterocycles KW - Formylation KW - Alpha-oxoethanals PY - 2003 DO - https://doi.org/10.1055/s-2003-40527 SN - 0039-7881 SN - 1437-210X IS - 10 SP - 1615 EP - 1619 PB - Thieme [u.a.] CY - Stuttgart AN - OPUS4-2617 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Brehme, R. A1 - Reck, Günter A1 - Schulz, Burkhard A1 - Radeglia, Reiner T1 - Synthesis and Reactions of (1E,2Z)-2-N,N-Dialkylhydrazono-2-phenylethanal N,N-Dimethylhydrazones N2 - (1E,2Z)-2-N,N-Dialkylhydrazono-2-phenylethanal N,N-dimethylhydrazones 3a-e weresynthesised by the reaction of 1,4,5-triazapentadienium salts 2 with N,N-dimethylhydrazine. The compounds 3a and 3d didnot react with tosyl isocyanate in an electrophilic substitutionreaction at the azomethine C-1 as aza-enamines, but they reactedat room temperature in benzene in a 1,4-dipolar cycloaddition toyield 1,3,5-triazinan-2,4-diones 5a and 5d, whereas at 70 °Coctahydroimidazoimidazol-2,5-dione 6a wasformed via criss-cross addition reaction. With dimethyl sulfatein DMF, 3a was transformed into the trimethylhydrazoniumsalts 7a and 8a,isolated as co-crystallised perchlorates (molar ratio 1:1). KW - Aza-enamines KW - Heterocycles KW - Hydrazonium salts KW - 1,4-dipolar cycloaddition KW - Criss-cross addition reaction PY - 2003 DO - https://doi.org/10.1055/s-2003-40528 SN - 0039-7881 SN - 1437-210X IS - 10 SP - 1620 EP - 1625 PB - Thieme [u.a.] CY - Stuttgart AN - OPUS4-2618 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H.R. A1 - Vakhtangishvili, L. A1 - Schwarz, G. A1 - Schulz, Günter A1 - Krüger, Ralph-Peter T1 - Macrocycles 25. Cyclic poly(ether sulfone)s derived from 4-tert-butylcatechol N2 - Poly(ether sulfone)s were prepared by polycondensation of silylated 4-tert-butylcatechol and 4,4?-difluorodiphenylsulfone in N-methylpyrrolidone. The feed ratio and the reaction time were varied to study the influence of stoichiometry and conversion on molecular weight and extent of cyclization. Molecular weights and molecular weight distributions (MWD)s were characterized by SEC measurements calibrated with polystyrene. Light scattering confirmed that calibration with polystyrene gives reasonable results and revealed a tendency towards a bimodal MWD for the samples rich in cycles. The MALDI-TOF mass spectrometry indicated that the extent of cyclization increased with higher conversion and with optimization of the stoichiometry. This interpretation was confirmed by 1H NMR endgroup analyses. For the samples with the highest molar masses only mass peaks of cycles were found, which were detectable up to 20 000 Da before and up to 27 000 Da after fractionation. Via the pseudo-high dilution method low molar mass poly(ether sulfone) containing more than 95 mol% of cycles were prepared, and even these low molar mass samples had broad MWDs. DSC measurements indicated that the glass transition temperatures depend on the structure of the endgroups and increase with higher fractions of cycles. KW - Poly(ether sulfone)s KW - Polycondensation KW - MALDI-TOF mass spectrometry PY - 2003 DO - https://doi.org/10.1016/S0032-3861(03)00410-5 SN - 0032-3861 SN - 1873-2291 VL - 44 SP - 4471 EP - 4480 PB - Springer CY - Berlin AN - OPUS4-2623 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reck, Günter A1 - Orgzall, I. A1 - Schulz, B. T1 - 2,5-Di-p-tolyl-1,3,4-oxa­diazo­le N2 - The mol­ecule of the title compound, C16H14N2O, consists of two equivalent parts related by a twofold axis of the space group. The O atom occupies a special position on this twofold axis. PY - 2003 DO - https://doi.org/10.1107/S1600536803014867 SN - 1600-5368 VL - 59 IS - 8 SP - o1135 EP - o1136 PB - Munksgaard CY - Copenhagen AN - OPUS4-2609 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Aree, T. A1 - Reck, Günter A1 - Schulz, Burkhard T1 - Crystal Structures of ß-Cyclodextrin Complexes with Formic Acid and Acetic Acid N2 - ß-Cyclodextrin (ߖCD)-formic acid (1) and ß-CD–acetic acid (2) inclusion complexes crystallizeas ß-CD...0.3HCOOH...7.7H2O and ß-CD...0.4CH3COOH...7.7H2O in themonoclinic space group P21 with comparable unit cell constants. Anisotropic refinement of atomic parameters against X-ray diffractiondata with Fo 2 > 2 (Fo 2) (986/8563 and 991/8358) converged at R-factors of 0.051 and 0.054 for 1 and 2,respectively. In both complexes, the ß-CD molecularconformation, hydration pattern and crystal packing are similar,but the inclusion geometries of the guest molecules are different.The ß-CD macrocycles adopt a ``round'' conformationstabilized by intramolecular, interglucose O3(n)...O2(n + 1)hydrogen bonds and their O6–H groups are systematically hydratedby water molecules. In the asymmetric unit, each complex contains one ß-CD, 0.3 formic acid (or 0.4 acetic acid), and 7.7 water moleculesthat are distributed over 9 positions. Water sites located in the ß-CD cavity hydrogen bond to the guest molecule. In thecrystal lattice, ß-CD molecules are packed in a typical ``herringbone'' fashion. In 1, the formic acid (occupancy 0.3) is entirely included in the ß-CD cavity such that its C atom is shifted from the O4-plane center to the ß-CD O6-side by 2.90 Å and C=O, C–-O bonds point to this side. In 2, the acetic acid (occupancy 0.4) is completely embedded in the ß-CD cavity, in which the carboxylic C atom is displaced from the O4-plane centerto the ß-CD O6-side by 0.87 Å; the C=O bond directsto the ß-CD O6-side and makes an angle of 15°to the ß-CD molecular axis. Furthermore, bothdimethyl-ß-CD-acetic acid and ß-CD-acetic acidcomplexes form a cage structure, showing that the small guestsenclosed entirely in the cavity either in ß-CD or indimethyl--CD do not affect the packing of the host macrocycles. KW - Acetic acid KW - Crystal structures KW - Beta-cyclodextrin KW - Formic acid KW - Hydrogen bond KW - Inclusion complex KW - X-ray analysis PY - 2003 DO - https://doi.org/10.1023/B:JIPH.0000003923.92981.0f SN - 1388-3127 SN - 0923-0750 SN - 1573-1111 VL - 47 IS - 1-2 SP - 39 EP - 45 PB - Kluwer Academics Publishers CY - Dordrecht AN - OPUS4-3707 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kricheldorf, H.R. A1 - Böhme, S. A1 - Schwarz, G. A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Macrocycles 18. The Role of Cyclization in Syntheses of Poly(ether-sulfone)s N2 - Poly(ether-sulfone)s having an identical backbone were prepared by four different methods. First, silylated bisphenol A (BSBA) was polycondensed with 4,4'-difluorodiphenyl sulfone (DFDPS) and K2CO3 in N-methylpyrrolidone with variation of the temperature. Second, analogous polycondensation were conducted using CsF as catalyst (and no K2CO3). Third, CsF-catalyzed polycondensations BSBA and DFDPS were conducted in bulk up to 290 C. Fourth, free bisphenol was polycondensed with DFDPS or 4,4'-dichlorodiphenyl sulfone and K2CO3 in DMSO with azeotropic removal of water. MALDI-TOF mass spectroscopy revealed that the first method mainly yielded cyclic poly(ether-sulfone)s which were detected up to masses around 13 000 Da. These and other results suggest that these polycondensations take a kinetically kontrolled course at tempeatures 145 C. This interpretation is also valid for the fourth method where high yields of cycles were obtained with DFDPS. With the less reactive 4,4'-dichlorodiphenyl sulfone lower conversions, lower molecular weights and lower fractions of cycles were found. In contrast to KF (resulting from K2CO3) CsF cleaves the poly(ether sulfone) backbone at temperatures > 145 C. Smaller amounts of smaller cycles were found in these CsF-catalyzed polycondensations which were in this case the result of thermodynamically controlled "back-biting degradation". PY - 2001 DO - https://doi.org/10.1021/ma010218l SN - 0024-9297 SN - 1520-5835 VL - 34 SP - 8886 EP - 8893 PB - American Chemical Society CY - Washington, DC AN - OPUS4-2176 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Heß, H. A1 - Hübner, H. A1 - Sobisch, T. T1 - Umfassende analytische Charakterisierung handelsüblicher nichtionischer Tenside durch Kopplung von HPLC und MALDI-TOF-MS T2 - Dechema-Jahrestagung 1996 CY - Wiesbaden, Deutschland DA - 1996-05-21 PY - 1996 PB - DECHEMA CY - Frankfurt am Main AN - OPUS4-2220 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Frey, H. T1 - Characterization of unusual Silsesquioxane-Based Polymer Architectures Based on the Coupling of Liquid Chromatography and MALDI-TOF-MS T2 - 11th International Symposium on Organosilicon Chemistry CY - Montpellier, France DA - 1996-09-01 PY - 1996 CY - Montpellier AN - OPUS4-2222 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Pickard, M. A1 - Schulz, Günter A1 - Wachsen, O. T1 - Characterization of thermal and hydrolytic degradation of polylactides by Liquid Chromatography and MALDI-TOF mass spectrometry T2 - International Symposium on "Biodegradable Materials" and Hamburger Makromolekulares Symposium CY - Hamburg, Germany DA - 1996-10-07 PY - 1996 CY - Hamburg AN - OPUS4-2225 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rikowski, E. A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Synthesis of Polyhedral Hexa-, Octa-, Deca- and Dodeca Silsesquioxanes, Separation by NP-HPLC, SEC and LACCC, Characterization by MALDI-TOF-MS T2 - 4. Münchener Silikontage CY - München, Germany DA - 1998-04-07 PY - 1998 VL - 4 AN - OPUS4-2234 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Rikowski, E. A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Characterization of silicon-polymers by liquid chromatography and MALDI-TOF-MS T2 - 37th IUPAC Congress ; 27th GDCh General Meeting CY - Berlin, Germany DA - 1999-08-14 PY - 1999 SN - 3-924763-80-1 PB - Gesellschaft Deutscher Chemiker CY - Frankfurt am Main AN - OPUS4-2241 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Becker, Roland A1 - Reck, Günter A1 - Radeglia, Reiner A1 - Springer, A. A1 - Schulz, Burkhard T1 - Designed self-assembly of a bimolecular calix[4]resorcinarene capsule held together by hydrogen bonds N2 - The X-ray crystallographic study of the macrocyclic tetrakis-N[N-2-hydroxyethyl-piperazino]calix[4]resorcinarene·3CH3CH2OH·H2O (3) reveals a self-assembled dimeric capsule-like complex held together by an array of intermolecular hydrogen bonds. Pairs of concave molecules associate directly in bowl-to-bowl fashion and enclose an accessible supramolecular cavity of Å3 hosting one water and three ethanol molecules. The supramolecular arrangement displays alternating layers of facing bowls and interlocking lower rim aliphatic moieties. The helical conformation of the 2-hydroxyethyl piperazinomethyl moieties displays chirality of a bimolecular capsule frozen in the solid state. 3 crystallises in the triclinic space group P-1 with two symmetry independent molecules in the asymmetric unit. Two enantiomeric capsules form a racemic pair in the unit cell. KW - Hydrogen bonded molecular capsule KW - Conformational chirality KW - Calix[4]resorcinarenes KW - Crystal structure PY - 2006 DO - https://doi.org/10.1016/j.molstruc.2005.08.027 SN - 0022-2860 SN - 1872-8014 SN - 0377-046X VL - 784 IS - 1-3 SP - 157 EP - 161 PB - Elsevier CY - Amsterdam AN - OPUS4-12241 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Emmerling, Franziska A1 - Reck, Günter A1 - Kraus, Werner A1 - Orgzall, I. A1 - Schulz, B. T1 - Structure determination of two asymmetrically substituted oxadiazoles from powder diffraction data N2 - The crystal structures of the 1,3,4 oxadiazole compounds N,N-dimethyl-N-[4-(1,3,4-oxadiazol-2-yl)phenyl]amine (1) and 2-methyl-5-phenyl-1,3,4-oxadiazole (2) have been determined. In case of 1 no adequate crystals were available; therefore the structure was solved at room temperature from X-ray powder diffraction data using the method of simulated annealing. This solution is compared to a second one obtained by applying the molecular replacement method. Subsequent Rietveld refinements combined with the so called two stage method based on the data collected to 1.6 Å resolution yielded an Rwp value of 7.27% for 1. Compound 1 crystallizes in the orthorhombic space group P212121 with lattice parameters of a = 7.599(4) Å, b = 6.004(2) Å, c = 21.736(3) Å. The crystal structure of 2 was solved by means of single crystal structure analysis (monoclinic space group P21/c, a = 8.010(3) Å, b = 10.783(4) Å, c = 19.234(7) Å, β = 90.794(9)°). KW - Crystal structure KW - Oxadiazoles KW - Powder diffraction X-ray investigations KW - Structure determination PY - 2008 DO - https://doi.org/10.1002/crat.200711053 SN - 0023-4753 SN - 1521-4079 SN - 0232-1300 VL - 43 IS - 1 SP - 99 EP - 107 PB - Wiley-VCH Verlag GmbH & Co. KGaA CY - Weinheim AN - OPUS4-16582 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Franco, O. A1 - Reck, Günter A1 - Orgzall, I. A1 - Schulz, B. T1 - Structure and high pressure behaviour of organic crystals based on aromatically substituted 1,3,4-oxadiazoles KW - C. High pressure KW - D. Equations-of-state KW - D. Crystal structure PY - 2002 SN - 0022-3697 VL - 63 SP - 1805 EP - 1813 PB - Pergamon Press CY - New York, NY AN - OPUS4-1555 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dushenko, G. A1 - Mikhailov, I. A1 - Reck, Günter A1 - Schulz, Burkhard A1 - Zschunke, Adolf A1 - Kharabaev, N. A1 - Minkin, V. T1 - Structure and Tautomerism of Cyclopentadiene Derivatives - IX. Synthesis and Structure of Substituted N-Cyclopentadienyl Amidinium Ylides N2 - A procedure has been developed for the synthesis of N-cyclopentadienyl amidinium ylides of the general formula C5(CO2Me)4[ArNC(Ar')NHAr]. According to the X-ray diffraction data, 1H and 13C NMR spectroscopy, and MNDO quantum-chemical calculations, the title compounds have a zwitterionic structure with the positive charge localized over the amidine NÄCÄN triad, and the negative charge, over the cyclopentadiene fragment. The configuration of the amidine moiety is stabilized by additional interaction of the NH hydrogen atom with the negatively charged cyclopentadiene ring (-bonding). The ylides are chiral due to atropoisomerism arising from a high energy barrier (G 298 >25 kcal/mol) to rotation of the Ar' substituent about the ordinary CÄC bond in the amidinium fragment. PY - 2002 DO - https://doi.org/10.1023/A:1020897411534 SN - 1070-4280 SN - 1608-3393 VL - 38 IS - 7 SP - 982 EP - 994 PB - MAIK Nauka/Interperiodica Publ. CY - Moscow AN - OPUS4-1556 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Shen, Z. A1 - Röhr, Holger A1 - Rurack, Knut A1 - Uno, H. A1 - Spieles, Monika A1 - Schulz, Burkhard A1 - Reck, Günter A1 - Ono, N. T1 - Boron-Diindomethene (BDI) Dyes and Their Tetrahydrobicyclo Precursors - en Route to a New Class of Highly Emissive Fluorophores for the Red Spectral Range N2 - The X-ray crystallographic, optical spectroscopic, and electrochemical properties of a newly synthesized class of boron-diindomethene (BDI) dyes and their tetrahydrobicyclo precursors (bc-BDP) are presented. The BDI chromophore was designed to show intensive absorption and strong fluorescence in an applicationary advantageous spectral range. Its modular architecture permits fusion of a second subunit, for example, a receptor moiety to the dye's core to yield directly linked yet perpendicularly prearranged composite systems. The synthesis was developed to allow facile tuning of the chromophore platform and to thus adjust its redox properties. X-ray analysis revealed a pronounced planarity of the chromophore in the case of the BDIs, which led to a remarkable close packing in the crystal of the simplest derivative. On the other hand, deviation from planarity was found for the diester-substituted bc-BDP benzocrown that exhibits a butterfly-like conformation in the crystal. Both families of dyes show charge- or electron-transfer-type fluorescence-quenching characteristics in polar solvents when equipped with a strong donor in the meso-position of the core. These processes can be utilized for signaling purposes if an appropriate receptor is introduced. Further modification of the chromophore can invoke such a guest-responsive intramolecular quenching process, also for receptor groups of low electron density, for example, benzocrowns. In addition to the design of various prototype molecules, a promising fluoroionophore for Na+ was obtained that absorbs and emits in the 650 nm region and shows a strong fluorescence enhancement upon analyte binding. Furthermore, investigation of the remarkable solvatokinetic fluorescence properties of the butterfly-like bc-BDP derivatives suggested that a second intrinsic nonradiative deactivation channel can play a role in the photophysics of boron-dipyrromethene dyes. KW - Charge KW - Transfer KW - Dyes/pigments KW - Electron transfer KW - Fluorescence KW - Farbstoffe KW - Chemosensoren KW - NIR-Bereich KW - Photophysik KW - Röntgenstrukturanalyse PY - 2004 DO - https://doi.org/10.1002/chem.200400173 SN - 0947-6539 SN - 1521-3765 VL - 10 SP - 4853 EP - 4871 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-4125 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Kovalchuck, Anton V. A1 - Bricks, Julia A1 - Reck, Günter A1 - Rurack, Knut A1 - Schulz, Burkhard A1 - Szumna, A. A1 - Weißhoff, Hardy T1 - A charge transfer-type fluorescent molecular sensor that "lights up" in the visible upon hydrogen bond-assisted complexation of anions PY - 2004 DO - https://doi.org/10.1039/b405207b SN - 0022-4936 SN - 0009-241x SN - 1359-7345 SN - 1364-548x SP - 1946 EP - 1947 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-4123 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rurack, Knut A1 - Bricks, J. L. A1 - Reck, Günter A1 - Schulz, Burkhard A1 - Spieles, Monika T1 - Cation coordination of bisamidopyridine-derived receptors as investigated in the solid-state and in solution N2 - A bisamidopyridine-type receptor, N,N'-bis(6-methyl-2-pyridyl)pyridine-2,6-dicarboxamide (1), and its CoIII complex were prepared and their X-ray structures were compared to those of N,N'-diphenylpyridine-2,6-dicarboxamide (2) and CoIII(2)2. Introduction of the two additional coordinative groups resulted in second-order interactions between the central ion and the nitrogen atoms of the terminal pyridine moieties in the crystalline state. Solution studies in acetonitrile revealed the importance of these interactions for the ligand's metal ion recognition ability. Whereas 2 only binds to PbII and CuII, 1 yields complexes with a majority of the heavy and transition metal ions studied, CoII, NiII, CuII, ZnII, FeIII, FeII, HgII, and PbII, respectively. The cation binding properties in solution were investigated by absorption spectroscopy and in the case of 1-MII/III, the formation of two spectroscopically distinguishable types of complexes was found. Protonation experiments and theoretical considerations helped to gain further insight into possible modes of coordination in solution. KW - Pyridine carboxamides KW - Ion recognition KW - Crystal structure KW - N-coordination PY - 2003 DO - https://doi.org/10.1080/1061027031000078239 SN - 1061-0278 SN - 1029-0478 VL - 15 IS - 3 SP - 189 EP - 197 PB - Gordon and Breach Science Publ. CY - New York, NY AN - OPUS4-2106 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rurack, Knut A1 - Radeglia, Reiner A1 - Reck, Günter A1 - Schulz, Burkhard A1 - Resch-Genger, Ute A1 - Bricks, J. A1 - Sonnenschein, H. T1 - Reaction of a N-anthrylcarbonylthiourea derivative with Cu2+ or H+ - unusual rearrangement to a highly fluorescent S-(9-anthryl)-isothiouronium salt N2 - For the fluorescent ligand 1-(9-anthrylcarbonyl)-3,3-tetramethylenethiourea with Cu(ClO4)2 or strong acids an unusual rearrangement reaction occurred yielding a highly emissive S-(9-anthryl)isothiouronium salt. This rearrangement product was characterised by NMR spectroscopy and X-ray analysis as well as absorption and fluorescence spectroscopy. Additionally, the chemical and complexation behaviour of the N-anthrylcarbonylthiourea derivative is compared to that of its naphthyl and phenyl analogues. PY - 2000 DO - https://doi.org/10.1039/b000138o SN - 1472-779X IS - 6 SP - 1209 EP - 1214 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-857 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Reck, Günter A1 - Schulz, Burkhard A1 - Bricks, J. A1 - Li, Yanqin A1 - Resch-Genger, Ute T1 - Monoalkylated 4'-aryl-substituted terpyridines N2 - 1-Methyl-2-[4-phenyl-6-(pyridinium-2-yl)­pyridin-2-yl]­pyridinium diperchlorate, C22H19N32+·2ClO4-, (I), and 2-[4-(methoxy­phenyl)-2,2'-bipyridin-6-yl]-1-methyl­pyridinium iodide, C23H20N3O+·I-, (II), both crystallize in the monoclinic space group P21/c. In contrast with the monocharged mol­ecule of (II), the doubly charged mol­ecule of (I) contains an additional protonated pyridine ring. One of the two perchlorate counter-anions of (I) interacts with the cation of (I) via an N—HO hydrogen bond. In (II), two mol­ecules related by a centre of symmetry are connected by weak ?–? interactions, forming dimers in the crystal structure. KW - X-ray structure analysis KW - Fluorescent sensors KW - Molecular conformation KW - Intermolecular interactions PY - 2004 DO - https://doi.org/10.1107/S010827010400825X SN - 0108-2701 SN - 1600-5759 VL - 60 SP - o402 EP - o404 PB - Blackwell Publ. CY - Oxford AN - OPUS4-3563 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Rurack, Knut A1 - Schulz, Burkhard A1 - Reck, Günter A1 - Resch-Genger, Ute A1 - Bricks, J. A1 - Maus, M. T1 - Substituted 1,5-Diphenyl-3-benzothiazol-2-yl-Delta2-pyrazolines - Synthesis, X-ray Structure, Photophysics, and Cation Complexation Properties N2 - The spectroscopic properties of 1-phenyl-3-benzothiazol-2-yl-5-(4-R-phenyl)-2-pyrazolines are strongly dependent on both the electronic nature of the substituent R and solvent polarity. As revealed by spectroscopic studies as a function of solvent polarity as well as temperature, for electron-rich amino donor substituents in polar solvents, deactivation of the strongly emissive charge transfer (CT) state of the basic 1-phenyl-3-benzothiazol-2-yl-2-pyrazoline chromophore has to compete with a fast intramolecular electron transfer (ET) quenching reaction. In the case of the dimethylamino derivative (R = DMA), the rate constant of ET in acetonitrile was determined to ket = 3 × 1010 s-1. This ET process can be utilized for metal ion sensing by introducing nitrogen containing aza crown ether receptor units to the 4-position of the 5-phenyl group. The spectroscopically determined ET rates of the 5-(N-alkyl)anilino substituents, a DMA, a tetrathia- (AT415C5), and a tetraoxa-monoaza-15-crown-5 (A15C5) group, correlate with electrochemical data and increase in the order AT415C5 < A15C5 < DMA. The metal ion sensing abilities of the two crowned derivatives are presented, and the different signaling mechanisms include binding to the crown ether in the 4-R-position, chelate formation in the 3-benzothiazol-2-yl-2-pyrazoline moiety, and electrophotochemical detection. Furthermore, the rigid "pseudo spiro" geometry of the molecules, which holds the three substituents of the central 2-pyrazoline ring in a fixed prearrangement, was confirmed by X-ray structure analysis. KW - Farbstoff KW - Fluoreszenz KW - Kationen KW - Photophysik PY - 2000 DO - https://doi.org/10.1021/jp993404q SN - 1089-5639 SN - 1520-5215 VL - 104 IS - 26 SP - 6171 EP - 6188 PB - Soc. CY - Washington, DC AN - OPUS4-841 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Friedrich, Jörg Florian T1 - Beiträge zur Charakterisierung von synthetischen Si-Polymeren durch Kopplung von HPLC-Trennmethoden mit der MALDI-TOF-MS T2 - DFG-Symposium zum Schwerpunktprogramm "Silicium-Chemie" CY - Werfenweng, Österreich DA - 2000-09-27 PY - 2000 AN - OPUS4-2251 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Maier, Bärbel A1 - Much, Helmut A1 - Schulz, Günter T1 - Orthogonal two-dimensional chromatography of poly(ethylene oxid) adducts T2 - HPLC '96 CY - San Francisco, CA, USA DA - 1996-06-16 PY - 1996 CY - San Francisco AN - OPUS4-2221 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Falkenhagen, Jana A1 - Friedrich, Jörg Florian A1 - Schulz, Günter A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Weidner, Steffen T1 - Liquid Adsorption Chromatography near Critical Conditions of Adsorption coupled with Matrix-assisted Laser Desorption/Ionization Mass Spectrometry N2 - Chemical heterogeneities and molecular weight distributions of poly(ethylene oxide) (PEO)-co-polymethylene (PM) model oligomers, which are relevant to the synthesis of commonly used tensides, were investigated. For analytical characterization, the well-known principle of liquid adsorption chromatography at 'critical conditions' (LACCC) was modified. Near the critical conditions of adsorption of the PEO unit, e.g., at slight adsorption conditions of PM, the copolymers could be separated according to their PM chain length. The eluates were separated and single fractions of each peak were continuously transferred onto the MALDI target by means of a commercially available device. Simultaneously, the MALDI matrix solution was continuously added with a second pump. This procedure offers the possibility of the formation of homogeneous matrix-polymer textures. By MALDI-MS a complete characterization of the chemical composition (PEO and PM chain length) of each peak could be achieved. The obtained MALDI mass spectra of the eluates at different retention times could be used for the molecular weight calibration of the LAC system. In this way, an additional application of SEC, as in conventional 2D-chromatography, was avoided by using the MALDI method as quasi chromatographic separation KW - Liquid adsorption chromatography KW - Matrix-assisted laser desorption KW - Ionization mass spectrometry KW - Coupling methods KW - MALDI PY - 2000 DO - https://doi.org/10.1080/10236660008034644 SN - 1023-666X SN - 1563-5341 VL - 5 SP - 549 EP - 562 PB - Gordon and Breach Publ. CY - Amsterdam AN - OPUS4-2168 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Weidner, Steffen A1 - Falkenhagen, Jana A1 - Friedrich, Jörg Florian A1 - Krüger, Ralph-Peter A1 - Schulz, Günter A1 - Much, Helmut T1 - Liquid Adsorption Chromatography near Critical Conditions of Adsorption coupled with Matrix-assisted Laser/Ionization Mass Spectrometry T2 - 47th ASMS Conference on Mass Spectrometry and Allied Topics CY - Dallas, TX, USA DA - 1999-06-13 PY - 1999 CY - Dallas, Tex AN - OPUS4-2165 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Friedrich, Jörg Florian A1 - Much, Helmut A1 - Schulz, Günter A1 - Falkenhagen, Jana T1 - Zur Charakterisierung von Si-Polymeren durch Kopplung flüssigchromatographischer Arbeitsweisen mit der MALDI-TOF-MS T2 - DFG-Symposium zum Schwerpunktprogramm "Silicium-Chemie" CY - Bielefeld, Deutschland DA - 1999-05-09 PY - 1999 AN - OPUS4-2239 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Friedrich, Jörg Florian T1 - Beiträge zur Charakterisierung von synthetischen Si-Polymeren durch Kopplung von HPLC-Trennmethoden mit der MALDI-TOF-MS T2 - Incom 2001 - International Symposium on Instrumentalized Analytical Chemistry and Computer Technology CY - Düsseldorf, Deutschland DA - 2001-03-27 PY - 2001 AN - OPUS4-2254 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Weidner, Steffen T1 - Charakterisierung von synthetischen Polymeren durch Kopplung flüssigchromato-graphischer Trennmethoden mit der MALDI-TOF-Massenspektrometrie T2 - 1. Berliner Werkstofftag CY - Berlin, Deutschland DA - 1999-09-16 PY - 1999 AN - OPUS4-2242 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Weidner, Steffen ED - Grellmann, W. T1 - Characterization and identification of new polymer structures by optimization and coupling of HPLC and MALDI-TOF-MS T2 - Polymerwerkstoffe 2000 CY - Halle (Saale), Germany DA - 2000-09-25 PY - 2000 SN - 3-86010-605-8 PB - Martin-Luther-Univ. CY - Halle AN - OPUS4-2250 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Emmerling, Franziska A1 - Bricks, J. L. A1 - Resch-Genger, Ute A1 - Kraus, Werner A1 - Schulz, Burkhard A1 - Li, Yanqin A1 - Reck, Günter T1 - Influence of the donor substituent and acceptor alkylation on the structure-analytical properties of mono- and bifunctional biphenyl-type fluorescent reporters N2 - A systematic structural investigation of R-phenyl-substituted 2,2':6',2"-terpyridines, a family of mono- and bifunctional charge transfer (CT)-operated fluorescent reporters for protons and metal ions, is presented. These molecules are equipped with non-binding and analyte coordinating donor substituents R (R = CF3, H, OMe, OH, DMA, A15C5 equaling monoaza-15-crown-5) of various donor strength and display CT-controlled spectroscopic properties and communication of analyte–receptor interactions. The crystal structures of the neutral fluorescent probes are compared to the structures of their terpyridine-alkylated or -protonated counterparts that represent model systems for acceptor protonation or cation coordination. The aim is here a better understanding of the complexation-induced structural and spectroscopic changes and the identification of common packing motifs of bpb-R thereby taking into account the importance of terpyridine building blocks for the construction of supramolecular systems and coordination arrays revealing π–π interactions. KW - Biphenyl KW - Terpyridine KW - Crystal structure KW - Fluorescent probe KW - Charge transfer KW - Bifunctional PY - 2008 DO - https://doi.org/10.1016/j.molstruc.2007.03.025 SN - 0022-2860 SN - 1872-8014 SN - 0377-046X VL - 874 IS - 1-3 SP - 14 EP - 27 PB - Elsevier CY - Amsterdam AN - OPUS4-17087 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hoffmann, Katrin A1 - Dietzel, B. A1 - Schulz, B. A1 - Reck, Günter A1 - Hoffmann, Angelika A1 - Orgzall, I. A1 - Resch-Genger, Ute A1 - Emmerling, Franziska T1 - Combined structural and fluorescence studies of methyl-substituted 2,5-diphenyl-1,3,4-oxadiazoles - relation between electronic properties and packing motifs N2 - Prerequisite for the rational design of functional organic materials with tailor-made electronic properties is the knowledge of the structure–property relationship for the specific class of molecules under consideration. This encouraged us to systematically study the influence of the molecular structure and substitution pattern of aromatically substituted 1,3,4-oxadiazoles on the electronic properties and packing motifs of these molecules and on the interplay of these factors. For this purpose, seven diphenyl-oxadiazoles equipped with methyl substituents in the ortho- and meta-position(s) were synthesized and characterized. Absorption and fluorescence spectra in solution served here as tools to monitor substitution-induced changes in the electronic properties of the individual molecules whereas X-ray and optical measurements in the solid state provided information on the interplay of electronic and packing effects. In solution, the spectral position of the absorption maximum, the size of Stokes shift, and the fluorescence quantum yield are considerably affected by ortho-substitution in three or four ortho-positions. This results in blue shifted absorption bands, increased Stokes shifts, and reduced fluorescence quantum yields whereas the spectral position and vibrational structure of the emission bands remain more or less unaffected. In the crystalline state, however, the spectral position and shape of the emission bands display a strong dependence on the molecular structure and/or packing motifs that seem to control the amount of dye–dye-interactions. These observations reveal the limited value of commonly reported absorption and fluorescence measurements in solution for a straightforward comparison of spectroscopic results with single X-ray crystallography. This underlines the importance of solid state spectroscopic studies for a better understanding of the interplay of electronic effects and molecular order. KW - Diphenyl-oxadiazoles KW - X-ray structure KW - Packing motif KW - Optical properties KW - Fluorescence quantum yield PY - 2011 DO - https://doi.org/10.1016/j.molstruc.2010.11.071 SN - 0022-2860 SN - 1872-8014 SN - 0377-046X VL - 988 IS - 1-3 SP - 35 EP - 46 PB - Elsevier CY - Amsterdam AN - OPUS4-23253 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schulz, Günter A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter T1 - Kopplung von HPLC-Trennmethoden mit der MALDI-TOF-Massenspektrometrie zur Charakterisierung von Si-haltigen Verbindungen T2 - DFG-Symposium zum Schwerpunktprogramm "Silicium-Chemie" CY - Werfenweng, Österreich DA - 2002-05-02 PY - 2002 AN - OPUS4-1797 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Gerstung, Vanessa A1 - Much, Helmut A1 - Schulz, Günter A1 - Friedrich, Jörg Florian T1 - Beiträge zur Charakterisierung von synthetischen Si-Polymeren durch Kopplung von HPLC-Trennmethoden mit der MALDI-TOF-Massenspektrometrie T2 - Berliner Polymeren-Tage 2000 CY - Berlin, Deutschland DA - 2000-10-09 PY - 2000 CY - Berlin AN - OPUS4-2252 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Rikowski, E. T1 - Characterization of silicon polymers (silsesquioxanes, dendrimers and copolymers) by means of different modes of Liquid Chromatography and MALDI-TOF-MS PY - 1998 PB - Messe München GmbH CY - München AN - OPUS4-2236 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Schulz, Günter A1 - Gloede, J. T1 - Charakterisierung von Calixarenen durch Kopplung von Flüssigchromatographie und MALDI-TOF-MS KW - Flüssigchromatographie KW - Kopplung LACCC KW - MALDI-TOF-MS KW - Calixarene KW - Novolake PY - 2001 SN - 0016-3538 VL - 45 IS - 4 SP - 380 EP - 384 PB - GIT-Verlag CY - Darmstadt AN - OPUS4-2177 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Schulz, Günter A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Rikowski, E. ED - Cherdron, H. T1 - Nachweis neuer Si-Polymerstrukturen durch die Kopplung der SEC mit der MALDI-TOF-MS T2 - Symposium on Tailormade Polymers CY - Merseburg, Deutschland DA - 2000-03-20 PY - 2000 SN - 3-527-30325-1 SN - 1022-1360 N1 - Serientitel: Macromolecular symposia – Series title: Macromolecular symposia IS - 163 PB - Wiley-VCH CY - Weinheim AN - OPUS4-2244 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Rikowski, E. T1 - Zur Charakterisierung von Si-Polymeren durch MALDI-TOF-MS in Kopplung mit flüssigchromatographischen Arbeitsweisen T2 - InCom '99 CY - Düsseldorf, Deutschland DA - 1999-03-22 PY - 1999 AN - OPUS4-2238 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Much, Helmut A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter ED - Berger, T. T1 - New methods for characterization of polymer heterogeneity by combination of HPLC with MALDI-TOF-MS T2 - 21st International Symposium on Chromatography CY - Stuttgart, Germany DA - 1996-09-15 PY - 1996 SN - 0009-5893 IS - 45 PB - Vieweg CY - Wiesbaden AN - OPUS4-2223 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Characterization of polylactides by coupling of chromatographic methods with MALDI-TOF-MS T2 - Polydays 2002 ; ISPAC 2002 CY - Berlin, Germany DA - 2002-09-30 PY - 2002 AN - OPUS4-1807 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter A1 - Weidner, Steffen T1 - Polymer Characterization by LC / MALDI-MS Coupling T2 - Vortragstagung "Funktionspolymere für Systemlösungen" CY - Darmstadt, Germany DA - 2002-03-18 PY - 2002 AN - OPUS4-1805 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Polymercharakterisierung durch Kombination chromatographischer Verfahren sowie HPLC - MALDI-TOF-MS - Kopplung T2 - Tagung der BASF AG 2002 CY - Ludwigshafen, Deutschland DA - 2002-12-03 PY - 2002 AN - OPUS4-1804 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Schulz, Günter A1 - Weinmann, S. ED - Radusch, H.-J. ED - Fiedler, L. T1 - Beiträge zur Charakterisierung von Polyactiden durch Kopplung von HPLC-Trennmethoden mit der MALDI-Flugzeitmassenspektrometrie T2 - Internationale Fachtagung Polymerwerkstoffe ; P-2002 CY - Halle (Saale), Deutschland DA - 2002-09-25 PY - 2002 SN - 3-86010-656-2 PB - Martin-Luther-Univ. Halle-Wittenberg CY - Halle (Saale) AN - OPUS4-2189 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Investigations of Polymer Heterogeneity by Two-Dimensional HPLC, MALDI-TOF-MS and FTIR Coupling T2 - ISPAC 8, HPLC ´95 CY - Sanibel Island, FL, USA DA - 1995-05-20 PY - 1995 PB - Gordon and Breach CY - Sant Helier AN - OPUS4-2203 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter ED - Jutzi, P. ED - Schubert, U. T1 - Characterization of Si-polymers by coupling of HPLC-separation methods with MALDI-TOF-MS T2 - Symposium on Silicon Chemistry CY - Werfenweng, Österreich DA - 2002-01-01 PY - 2003 SN - 3-527-30647-1 SP - 406 EP - 418 PB - Wiley-VCH CY - Weinheim AN - OPUS4-2194 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Schulz, Günter T1 - Calixarene in Photoresisten (Kopplung von flüssigchromatographischen Methoden mit der MALDI-TOF-MS) T2 - Fachgruppenvollversammlung BAM CY - Berlin, Deutschland DA - 2002-01-29 PY - 2002 AN - OPUS4-2191 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Schulz, Günter A1 - Heinemann, M. T1 - Methodenkopplung zur Polylactidcharakterisierung PY - 2003 SN - 0344-1733 SN - 1610-8256 VL - 27 SP - 56 EP - 57 PB - Vogel CY - Würzburg AN - OPUS4-2597 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Coupling of different modes of liquid chromatography of polymers with spectroscopic methods and MALDI-TOF-MS-key for determination of polymer heterogeneity T2 - 6th SPSJ International Polymer Conference (IPC 97) CY - Kusatsu, Japan DA - 1997-10-20 PY - 1997 VL - 6 AN - OPUS4-2233 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter T1 - Charakterisierung von Si-Polymerarchitekturen durch Kopplung von flüssigchromatographischen Methoden mit der MALDI-TOF-Massenspektrometrie im DFG-Schwerpunktprogramm T2 - DFG-Kolloquium zum Schwerpunktprogramm "Silicium-Chemie" CY - Bielefeld, Deutschland DA - 1997-05-12 PY - 1997 AN - OPUS4-2231 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter A1 - Weidner, Steffen T1 - Polymer characterization by LC / MALDI-MS coupling T2 - Bayreuther Polymer Symposium 2001 CY - Bayreuth, Germany DA - 2001-09-16 PY - 2001 CY - Bayreuth AN - OPUS4-2256 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter T1 - Neue Ergebnisse der HPLC/MALDI-TOF-MS - Kopplung zur Charakterisierung von synthetischen Polymeren T2 - Analytica Conference 98 CY - München, Deutschland DA - 1998-04-21 PY - 1998 CY - München AN - OPUS4-2235 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Schulz, Günter A1 - Weinmann, S. T1 - Beiträge zur Charakterisierung von Polyactiden durch Kopplung von HPLC-Trennmethoden mit der MALDI-TOF-MS T2 - Analytica Conference 2002 CY - München, Deutschland DA - 2002-04-23 PY - 2002 AN - OPUS4-2188 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Falkenhagen, Jana A1 - Jancke, Harald A1 - Krüger, Ralph-Peter A1 - Rikowski, Eckhard A1 - Schulz, Günter T1 - Characterization of Silsesquioxanes by Size-exclusion chromatography and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry N2 - Liquid chromatography in combination with spectroscopic methods like matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) or nuclear magnetic resonance (NMR) spectroscopy is a powerful method to characterize silsesquioxanes and silsesquioxane mixtures. As new examples, the formation of silsesquioxyl-substituted silsesquioxanes [(n-octyl)7(SiO1.5)8]2O and [(n-octyl)7(SiO1.5)8O]2[(n-octyl)6(SiO1.5)8] as well as the cage rearrangement of octa-[(n-heptyl)silsesquioxane] to larger structur es [(n-heptyl)SiO1.5)]n up to n=28 are shown. PY - 2003 DO - https://doi.org/10.1002/rcm.911 SN - 0951-4198 SN - 1097-0231 VL - 17 IS - 4 SP - 285 EP - 290 PB - Wiley CY - Chichester AN - OPUS4-2182 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Spranger, K. T1 - Neue Möglichkeiten der Polymercharakterisierung durch 2D-HPLC, Kopplung mit spektroskopischen Methoden und MALDI-TOF-MS T2 - Gesellschaft Deutscher Chemiker, "Klassische Polymere im Aufwind, Polymerchemie aktuell" CY - Dresden, Deutschland DA - 1996-03-25 PY - 1996 CY - Dresden AN - OPUS4-2212 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Spranger, K. ED - Günther, W. T1 - MALDI-TOF-MS zur Charakterisierung von synthetischen Polymeren in Kopplung mit der HPLC T2 - InCom '96 - International Symposium on Instrumentalized Analytical Chemistry and Computer Technology CY - Düsseldorf, Deutschland DA - 1996-03-25 PY - 1996 PB - IAS CY - Moers AN - OPUS4-2213 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Schulz, Günter T1 - Einführung in die MALDI-TOF-Massenspektrometrie an synthetischen Polymeren T2 - Innovent Technologieentwicklung CY - Jena, Deutschland DA - 2002-08-14 PY - 2002 AN - OPUS4-1800 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Mehrdimensionale Analysenverfahren für komplexe Polymere - Arbeitskreis Polymeranalytik T2 - Tagung des Arbeitskreises Polymeranalytik CY - Darmstadt, Deutschland DA - 2002-09-25 PY - 2002 AN - OPUS4-1802 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Polymercharakterisierung mittels flüssigchromatographischer und spektroskopischer Methoden T2 - Innovent Technologieentwicklung CY - Jena, Deutschland DA - 2002-08-14 PY - 2002 AN - OPUS4-1801 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter ED - Fell, A. T1 - Two-dimensional chromatography, their optimization and coupling with different detection techniques for investigation of polymer heterogeneity T2 - 21st International Symposium on High Performance Liquid Phase Separations and Related Techniques (HPLC) CY - Birmingham, England, UK DA - 1997-06-22 PY - 1997 SN - 0021-9673 PB - Elsevier CY - Amsterdam AN - OPUS4-2232 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter A1 - Just, Ulrich ED - Yeung, E. T1 - Characterization of silicon polymers by coupling of liquid chromatographic methods with MALDI-TOF-MS T2 - 24th International Symposium on High Performance Liquid Phase Separations and Related Techniques ; 24th HPLC 2000 CY - Seattle, WA, USA DA - 2000-06-24 PY - 2000 SN - 0021-9673 PB - Elsevier CY - Amsterdam AN - OPUS4-2247 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Much, Helmut A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Schulz, Günter T1 - Charakterisierung von synthetischen Polymeren durch Kopplung flüssigchromato-graphischer Trennmethoden mit der MALDI-TOF-Massenspektrometrie T2 - Workshop "Hierarchic Structure Formation and Function of Organic-Inorganic Hybrid Systems" CY - Ulm, Deutschland DA - 1999-11-26 PY - 1999 AN - OPUS4-2243 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter ED - Günther, W. T1 - Neue Ergebnisse der MALDI-TOF-Massenspektrometrie von synthetischen Polymeren T2 - InCom '97 - International Symposium on Instrumentalized Analytical Chemistry and Computer Technology CY - Düsseldorf, Deutschland DA - 1997-03-17 PY - 1997 VL - 97 PB - IAS CY - Moers AN - OPUS4-2230 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Much, Helmut A1 - Schulz, Günter T1 - Characterization and identification of new polymer structures by optimization and coupling of HPLC and MALDI-TOF-MS T2 - Dechema-Diskussionstagung "Neue Methoden der Polymeranalytik" CY - Mainz, Germany DA - 2001-04-02 PY - 2001 CY - Mainz AN - OPUS4-2255 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter T1 - Beiträge zur Charakterisierung von synthetischen Si-Polymeren durch Kopplung von HPLC-Trennmethoden mit der MALDI-TOF-MS T2 - Analytica Conference 2000 CY - München, Deutschland DA - 2000-04-11 PY - 2000 CY - München AN - OPUS4-2245 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter A1 - Spranger, K. T1 - Zur Charakterisierung von synthetischen Polymeren durch MALDI-TOF in Kopplung mit der LACCC T2 - Analytica Conference 96 CY - München, Deutschland DA - 1996-04-23 PY - 1996 PB - Messe München GmbH CY - München AN - OPUS4-2219 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schulz, Günter T1 - Characterization of silicon polymers by coupling of chromatographic methods with MALDI-TOF-MS T2 - XXIII. Hamburger Makromolekulares Symposium CY - Hamburg, Germany DA - 2000-09-25 PY - 2000 AN - OPUS4-3457 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Falkenhagen, Jana A1 - Krüger, Ralph-Peter A1 - Rikowski, Eckhard A1 - Schulz, Günter A1 - Friedrich, Jörg Florian ED - Grellmann, W. T1 - Synthesis and Characterisation of Polyhedral Silsesquioxanes with Nanotubular Structures T2 - 23. DVM-Vortrags- und Diskussionstagung "Werkstoffprüfung 2005", DA - 2005-12-01 PY - 2005 SP - 25 EP - 30 PB - DVM AN - OPUS4-11947 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Much, Helmut A1 - Schulz, Günter T1 - Characterization of silicon polymers (silsesquioxanes, dendrimers and copolymers) by means of different modes of Liquid Chromatography and MALDI-TOF-MS T2 - 11th International Symposium on Polymer Analysis and Characterization CY - Santa Margherita Ligure, Italien DA - 1998-05-25 PY - 1999 N1 - Serientitel: International journal of polymer analysis and characterization – Series title: International journal of polymer analysis and characterization IS - 5.1999,3 PB - Gordon and Breach CY - St. Helier AN - OPUS4-19053 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Krüger, Ralph-Peter A1 - Falkenhagen, Jana A1 - Schulz, Günter A1 - Heinemann, M. A1 - Weinmann, S. A1 - Friedrich, Jörg Florian A1 - Fritz, H.-G. ED - Fritz, H.-G. ED - Eisenbach, C. D. T1 - Synthese von Polylactiden mittels reaktiver Extrusion und Produktcharakterisierung durch Kopplung von HPLC-Methoden mit der MALDI-TOF-MS T2 - 18. Stuttgarter Kunststoff-Kolloquium CY - Stuttgart, Deutschland DA - 2003-03-19 PY - 2003 SN - 3-00-010663-4 IS - CD-ROM PB - Univ., IKT, IAMC CY - Stuttgart AN - OPUS4-2190 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -