TY - JOUR A1 - Simões, R. G. A1 - Melo, P. L. T. A1 - Bernardes, C. E. S. A1 - Heilmann, Maria A1 - Emmerling, Franziska A1 - Minas da Piedade, M. E. T1 - Linking Aggregation in Solution, Solvation, and Solubility of Simvastatin: An Experimental and MD Simulation Study N2 - The solubility is generally thought to be higher if the solvent effectively solvates solute molecules that are well-separated from each other. The present work suggests, however, that the formation of large solute aggregates does not necessarily imply less effective solvation and lower solubility. Measurements of the solubility of simvastatin (one of the most commonly prescribed antihyperlipidemic drugs) in three solvents with different polarities and protic characters, led to the solubility order acetone > ethyl acetate > ethanol, in the full temperature range covered by the experiments (283–308 K). An analysis of the structures of the different solutions on the basis of molecular dynamics simulation results indicated that this trend seems to be determined by a balance between the solute tendency toward aggregation and the ability of the solvent to efficiently solvate it, by integrating the cluster structures, regardless of their size, and effectively establishing solvent–solute interactions. KW - Simvastatin KW - Solubility KW - API KW - Aggregation PY - 2021 DO - https://doi.org/10.1021/acs.cgd.0c01325 VL - 21 IS - 1 SP - 544 EP - 551 AN - OPUS4-52185 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Emmerling, Franziska A1 - Chewle, S. A1 - Weber, M. T1 - Revealing Kinetics of Paracetamol Crystallization Using Time Resolved Raman Spectroscopy, Orthogonal Time-Lapse Photography, and Non-Negative Matrix Factorization (OSANO) N2 - Crystallization is a complex phenomenon with farreaching implications for the production and formulation of active pharmaceutical ingredients. Understanding this process is critical for achieving control over key physicochemical properties that can affect, for example, the bioavailability and stability of a drug. In this study, we were able to reveal intricate and diverse dynamics of the formation of metastable intermediates of paracetamol crystallization varying with the choice of solvent. We demonstrate the efficacy of our novel approach utilizing an objective function-based non-negative matrix factorization technique for the analysis of time-resolved Raman spectroscopy data, in conjunction with time-lapse photography. Furthermore, we emphasize the crucial importance of integrating Raman spectroscopy with supplementary experimental instrumentation for the mathematical analysis of the obtained spectra. KW - Polymorphism KW - Crystallization KW - Measurement KW - Algorithm PY - 2023 DO - https://doi.org/10.1021/acs.cgd.3c00617 SN - 1528-7483 VL - 23 SP - 6737 EP - 6746 PB - ACS Publications AN - OPUS4-58193 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Alić, Jasna A1 - Schlegel, Moritz-Caspar A1 - Emmerling, Franziska A1 - Stolar, Tomislav T1 - Meeting the UN Sustainable Development Goals with Mechanochemistry N2 - Chemistry traditionally relies on reactions in solution, but this method is increasingly problematic due to the scale of chemical processes and their economic and environmental impact. Handling residual chemical waste, including solvents, incurs significant costs and environmental pressure. Conversely, novel chemical approaches are needed to address pressing societal issues such as climate change, energy scarcity, food insecurity, and waste pollution. Mechanochemistry, a sustainable chemistry discipline that uses mechanical action to induce chemical reactivity without bulk solvents, is a hot topic in academic research on sustainable and green chemistry. Given its fundamentally different working principles from solution chemistry, mechanochemistry offers more efficient chemical processes and the opportunity to design new chemical reactions. Mechanochemistry has a profound impact on many urgent issues facing our society and it is now necessary to use mechanochemistry to address them. This Minireview aims to provide a guide for using mechanochemistry to meet the United Nations (UN) Sustainable Development Goals (SDGs), thereby contributing to a prosperous society. Detailed analysis shows that mechanochemistry connects with most UN SDGs and offers more cost‐efficiency than other approaches together with a superior environmental performance. KW - Mechanochemistry KW - SDGs PY - 2024 DO - https://doi.org/10.1002/anie.202414745 SP - 1 EP - 3 PB - Wiley AN - OPUS4-61108 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nag, Sayak A1 - Emmerling, Franziska A1 - Tothadi, Srinu A1 - Bhattacharya, Biswajit A1 - Ghosh, Soumyajit T1 - Distinct photomechanical responses of two new 1,3-dimethylbarbituric acid derivative crystals N2 - We demonstrate two distinct photomechanical responses (i.e. photomechanical bending and photosalient bursting) of two new 1,3-dimethylbarbituric acid derivative crystals based on tailoring their substituents and the modulation of their spacers. KW - Crystal engineering KW - Fexible crystals PY - 2024 DO - https://doi.org/10.1039/D4CE00233D SP - 1 EP - 12 PB - Royal Society of Chemistry (RSC) AN - OPUS4-60141 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - Licht ins Dunkle - In situ Untersuchungen mechanochemischer Reaktionen N2 - Mechanochemistry is increasingly used for synthesizing soft matter materials including metal organic compounds and cocrystals. The ever-increasing interest in this method is contrasted by a limited mechanistic understanding of the mechanochemical reactivity and selectivity. Time-resolved in situ investigations of milling reactions provide direct insights in the underlying mechanisms. We recently introduced a setup enabling in situ investigation of mechanochemical reactions using synchrotron XRD combined with Raman spectroscopy. The specific combination allows to study milling processes comprehensively on the level of the molecular and crystalline structure and thus obtaining reliable data for mechanistic studies. In this contribution, I will discuss our recent results investigating the formation of (polymorphic) cocrystals and metal phosphonates. First investigations of a mechanochemical synthesis under controlled temperature which allow determining the activation barrier are presented. Furthermore, in situ Raman spectroscopy coupled with thermography revealed a low temperature increase during milling reactions due to the mechanical impact and clear temperature increases as a result of the reaction heat.5 Our results indicate that in situ investigation of milling reactions offer a new approach to tune and optimize mechanochemically synthesized compounds. T2 - PRORA Fachtagung Prozessnahe Röntgenanalytik CY - Berlin, Germany DA - 30.11.2017 KW - Mechanochemie KW - XRD KW - In situ PY - 2017 AN - OPUS4-43562 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - In situ investigations of mechanochemical reactions - new insights in formation pathways N2 - Mechanochemistry is increasingly used for synthesizing soft matter materials including metal organic compounds and cocrystals. The ever-increasing interest in this method is contrasted by a limited mechanistic understanding of the mechanochemical reactivity and selectivity. Time-resolved in situ investigations of milling reactions provide direct insights in the underlying mechanisms. We recently introduced a setup enabling in situ investigation of mechanochemical reactions using synchrotron XRD combined with Raman spectroscopy. The specific combination allows to study milling processes comprehensively on the level of the molecular and crystalline structure and thus obtaining reliable data for mechanistic studies. In situ Raman spectroscopy coupled with thermography revealed a low temperature increase during milling reactions due to the mechanical impact and clear temperature increases because of the reaction heat. Based on the data, temperature rises as postulated in the magma plasma and hot spot theory can be excluded for soft matter milling syntheses. Our results indicate that in situ investigation of milling reactions offer a new approach to tune and optimize mechanochemically synthesized compounds. T2 - Wissenschaftsforum Chemie CY - Berlin, Germany DA - 10.09.17 KW - Mechanochemistry KW - In situ PY - 2017 AN - OPUS4-43563 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Al-Terkawi, Abdal-Azim A1 - Scholz, Gudrun A1 - Emmerling, Franziska A1 - Kemnitz, Erhard T1 - Ca-Tetrafluorophthalate and Sr-isophthalate: mechanochemical synthesis and characterization in comparison with other Ca-and Sr-coordination polymers N2 - New Ca- and Sr-based coordination polymers (CPs) were mechanochemically synthesized by milling metal hydroxide samples (M = Ca, Sr) with tetrafluorophthalic acid (H2oBDC-F4) and isophthalic acid (H2mBDC). [Ca(oBDC-F4)(H2O)2] (1) exhibits a small surface area which is slightly increased after removing the crystal water. On the other hand, the hydrated sample of the nonfluorinated [Sr(mBDC)(H2O)3.4] (2) reveals a small BET surface area which remains unchanged even after the release of crystal water via thermal treatment. The new compounds 1 and 2 are similar to their Sr- and Ca-analogs, respectively. These findings are confirmed by thermal analysis, MAS NMR, and ATR-IR measurements, in addition to the Le Bail refinements for the measured powder X-ray data of 1 and 2. Ca- and Sr-CPs based on perfluorinated dicarboxylic systems and their nonfluorinated analogs diverse in structural and chemical properties depending on the geometries of the organic linkers and the presence of fluorine atoms. The fluorinations of organic ligands lead to the formation of fluorinated CPs with higher dimensionalities compared to their nonfluorinated counterparts. Conversely, the thermal stabilities of the latter are higher than those of the fluorinated CPs. KW - Mechanochemistry PY - 2018 DO - https://doi.org/10.1039/c8dt00695d SN - 1477-9226 SN - 1477-9234 VL - 47 IS - 16 SP - 5743 EP - 5754 PB - Royal Society of Chemistry CY - Cambridge AN - OPUS4-44696 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - In situ investigations of mechanochemical reactions N2 - Mechanochemistry is increasingly used for synthesizing soft matter materials including metal organic compounds and cocrystals.1,2 The ever-increasing interest in this method is contrasted by a limited mechanistic understanding of the mechanochemical reactivity and selectivity. Time-resolved in situ investigations of milling reactions provide direct insights in the underlying mechanisms.3,4 We recently introduced a setup enabling in situ investigation of mechanochemical reactions using synchrotron XRD combined with Raman spectroscopy (Fig.1a) The specific combination allows to study milling processes comprehensively on the level of the molecular and crystalline structure and thus obtaining reliable data for mechanistic studies. In this talk I will discuss our recent results investigating the formation of (polymorphic) cocrystals.6-7 First investigations of a mechanochemical synthesis under controlled temperature (Fig 2a) which allow determining the activation barrier are presented.8 Furthermore, in situ Raman spectroscopy coupled with thermography revealed a low temperature increase during milling reactions due to the mechanical impact and clear temperature increases as a result of the reaction heat. T2 - Kolloquium Anorganische und Analytische Chemie Universität Freiburg CY - Freiburg, Germany DA - 20.12.2017 KW - In situ KW - Mechanochemistry KW - Rietveld PY - 2017 AN - OPUS4-43566 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - In situ investigations of mechanochemical syntheses: New insights in formation pathways N2 - Mechanochemistry is increasingly used for synthesizing soft matter materials including metal organic compounds and cocrystals.1,2 The ever-increasing interest in this method is contrasted by a limited mechanistic understanding of the mechanochemical reactivity and selectivity. Time-resolved in situ investigations of milling reactions provide direct insights in the underlying mechanisms.3,4 We recently introduced a setup enabling in situ investigation of mechanochemical reactions using synchrotron XRD combined with Raman spectroscopy (Fig.1a) The specific combination allows to study milling processes comprehensively on the level of the molecular and crystalline structure and thus obtaining reliable data for mechanistic studies. In this talk I will discuss our recent results investigating the formation of (polymorphic) cocrystals. T2 - CF@Bo2017 Crystal Forms Bologna 2017 CY - Bologna, Italy DA - 04.06.2017 KW - Mechanochemistry PY - 2017 AN - OPUS4-43567 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Breitfeld, Steffen A1 - Scholz, G. A1 - Emmerling, Franziska A1 - Kemnitz, E. T1 - BaF-benzenedicarboxylate: the first mechanochemical N2 - Anewbariumcoordination polymer, BaF-benzenedicarboxylate (BaF(p-BDC)0.5), with fluorine directly coordinated to the metal cation, was prepared by mechanochemical synthesis routes. Phase-pure BaF-benzenedicarboxylate was synthesized by milling starting either from barium hydroxide or from Barium acetate as sources for barium cations. In both cases, the second reactant was 1,4-benzenedicarboxylic acid (H2(p-BDC)). Ammonium fluoride was used as fluorinating agent directly at milling. This is the first mechanochemical synthesis of coordination polymers where fluorine is directly coordinated to the metal cation. Following the second possibility, barium acetate fluoride (Ba(OAc)F) is formed as ntermediate product after milling, and the new coordination polymer is accessible only after washing with water and dimethyl sulfoxide. The new compound BaF(p-BDC)0.5 was characterized by X-ray powder diffraction, FTIR-, and 19F, 1H-13C CP MAS NMR spectroscopies, DTA-TG, and elemental Analysis. KW - Milling KW - MOF PY - 2018 DO - https://doi.org/10.1007/s10853-018-2331-3 SN - 0022-2461 VL - 53 IS - 19 SP - 13682 EP - 13689 PB - Springer AN - OPUS4-45677 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dolai, Malay A1 - Saha, Urmila A1 - Goswami, Juli Nanda A1 - Bhattacharya, Biswajit A1 - Emmerling, Franziska A1 - Ifseisi, Ahmad A. A1 - Biswas, Surajit ED - Bhattacharya, Biswajit T1 - Nickel(II)-mediated in situ complex formation with unexpected ligand transformations: crystal structures, DFT calculations, and catalytic activity in CO2 fixation reactions N2 - Two transformed ligands, namely 1,3,5-triazapentadienato(imidoylamidinato) and N-(methoxy(pyrimidin-2-yl)(pyrimidine-2-carboxamido)methyl)pyrimidine-2-carboxamide, are reported here as the first products derived from 2-cyano pyridine/pyrimidine, respectively, under nickel metal mediation in the presence of hydroxylamine hydrochloride in situ. Two different nickel-coordinated complexes (1 and 2) were formed. Single crystal X-ray diffraction revealed that complex 1 is a mononuclear complex with tetra-coordinated square planar geometry, whereas complex 2 is a dinuclear complex with hexa-coordinated distorted octahedral geometry. The synthetic pathways of both transformed ligands are explained with the support of energy calculations of different states via density functional theory (DFT) calculations. The catalytic addition reactions of epoxides and carbon dioxide efficiently produce organic cyclic carbonates in the presence of complexes 1–2, attributed to the presence of Lewis acidic nickel and Lewis basic centers, such as free amine, imine, methoxy, or nitrogen in complexes 1 and 2. Under mild reaction conditions (1 atm CO2 pressure and 60 °C temperature), different types of epoxides (exocyclic, endocyclic, and aromatic epoxides) yield high levels of respective cyclic carbonates in the presence of both complexes 1–2 as catalysts, with tert-butylammonium bromide (TBAB) acting as a co-catalyst. The high turnover number (TON) and turnover frequency (TOF) of these catalytic reactions clearly indicate the efficacy of the two catalysts. KW - Catalytic activity in CO2 fixation reactions DFT calculations KW - Nickel(II)-complex KW - In situ complex formation KW - Crystal Structure PY - 2025 DO - https://doi.org/10.1039/d4nj01801j SN - 1369-9261 VL - 49 IS - 11 SP - 4451 EP - 4463 PB - Royal Society of Chemistry (RSC) AN - OPUS4-62782 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Takao, S. A1 - Takao, K. A1 - Kraus, Werner A1 - Emmerling, Franziska A1 - Scheinost, A.C. A1 - Bernhard, G. A1 - Hennig, C. T1 - First hexanuclear U IV and Th IV formate complexes - Structure and stability range in aqueous solution N2 - The actinide(IV) hexanuclear [M6(μ3-O)4(μ3-OH)4(HCOO)12(LT)6] complexes were prepared (LT = H2O or CH3OH). Their structures were investigated by single-crystal X-ray analysis and XAFS spectroscopy. HCOO– acts as a bridging ligand, which prevents the formation of polynuclear hydrolysis species like UIV hydrous oxide colloids at least up to pH = 3.25, and stabilizes the nanosized clusters in solution. The charge of the hexamer is balanced by the O/OH ratio of the μ3-bridges.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) KW - Actinides KW - Polynuclear species KW - Formic acid KW - Bridging ligands PY - 2009 DO - https://doi.org/10.1002/ejic.200900899 SN - 1434-1948 SN - 1099-0682 VL - 2009 IS - 32 SP - 4771 EP - 4775 PB - Wiley-VCH Verl. CY - Weinheim AN - OPUS4-20329 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stroh, Julia A1 - Meng, Birgit A1 - Emmerling, Franziska T1 - Deterioration of hardened cement paste under combined sulphatechloride attack investigated by synchrotron XRD N2 - The exact mechanisms of the phase transitions caused by a combined sulphate-chloride attack are discussed controversially. The main points concern the mutual influences of sulphate and chloride ions during the secondary binding processes of these anions within cement hydrate phases. We simulated combined sulphate-chloride attack under laboratory conditions using solutions containing NaCl and Na2SO4 in different concentrations. Three sample compositions were used for the preparation of the specimens. In two of them, 30% of Portland cement was replaced by supplementary cementitious materials (fly ash, slag). The phase distribution in the samples was determined using synchrotron X-ray diffraction. The analysis with high spatial resolution allows the localisation of the secondary phase formation in the microstructural profile of the sample. A mechanism of the phase developments under combined sulphate-chloride attack is derived. KW - Cement paste KW - Sulphate-chloride attack KW - Portland cement KW - Mineral additions PY - 2016 DO - https://doi.org/10.1016/j.solidstatesciences.2016.04.002 IS - 56 SP - 29 EP - 44 PB - Elsevier Masson SAS CY - Issy les Moulineaux cedex; France AN - OPUS4-35936 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - Coordination of U(IV) sulfate in aqueous solution of high ionic strength and in solid state T2 - Jahrestagung der Deutschen Gesellschaft für Kristallographie CY - Erlangen, Germany DA - 2008-03-03 PY - 2008 AN - OPUS4-18726 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Klobes, Peter A1 - Klimakow, Maria A1 - Emmerling, Franziska T1 - Gas adsorption and SAXS studies of mechanochemically prepared Cu3 (BTC)2 T2 - CPM-5 - 5th - International Workshop "Characterization of Porous Materials: from Angstroms to Millimeters", New Brunswick, NJ, USA CY - New Brunswick, NJ, USA DA - 2009-06-24 PY - 2009 AN - OPUS4-18713 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bentrup, U. A1 - Radnik, J. A1 - Armbruster, U. A1 - Martin, A. A1 - Leiterer, Jork A1 - Emmerling, Franziska A1 - Brückner, A. T1 - Linking simultaneous in situ WAXS/SAXS/Raman with Raman/ATR/UV-vis spectroscopy: comprehensive insight into the synthesis of molybdate catalyst precursors N2 - A new setup is presented which enables simultaneous wide- and small-angle X-ray scattering (WAXS/SAXS) and Raman spectroscopic experiments during the synthesis of Mo-based mixed oxide catalyst precursors at the µ-spot beamline at the Berliner Elektronenspeicherring-Gesellschaft für Synchrotronstrahlung (BESSY). Furthermore, we report about the separate monitoring of the same reactions under comparable conditions by simultaneous combined ATR/UV–vis/Raman spectroscopic measurements. For testing the performance of both experimental setups two syntheses were described comprising the precipitation of metal molybdates by mixing solutions of metal nitrates and ammonium heptamolybdate. Additionally, the effect of H3PO4 admixture on precipitation was investigated. The combined evaluation of spectroscopic and WAXS/SAXS data allows the discrimination between different molybdate species appearing in solution and precipitate. Furthermore, these molybdate species could be assigned to separate phases of different crystallinity. KW - In situ KW - WAXS/SAXS KW - Raman KW - ATR KW - UV-vis KW - Mixed oxide catalyst KW - Synthesis PY - 2009 DO - https://doi.org/10.1007/s11244-009-9309-y SN - 1022-5528 VL - 52 IS - 10 SP - 1350 EP - 1359 PB - Springer Science + Business Media CY - Dordrecht AN - OPUS4-19794 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Winterlik, J. A1 - Fecher, G.H. A1 - Jenkins, C.A. A1 - Medvedev, S. A1 - Felser, C. A1 - Kübler, J. A1 - Mühle, C. A1 - Doll, K. A1 - Jansen, M. A1 - Palasyuk, T. A1 - Trojan, I. A1 - Eremets, M.I. A1 - Emmerling, Franziska T1 - Exotic magnetism in the alkali sesquioxides Rb4O6 and Cs4O6 KW - Caesium compounds KW - Crystal structure KW - Density functional theory KW - Electronic structure KW - Ferromagnetic materials KW - Frustration KW - Magnetic transitions KW - Magnetisation KW - Raman spectra KW - Rubidium compounds KW - Spin glasses KW - X-ray diffraction PY - 2009 DO - https://doi.org/10.1103/PhysRevB.79.214410 SN - 1098-0121 SN - 0163-1829 SN - 0556-2805 SN - 1095-3795 SN - 1550-235X VL - 79 IS - 21 SP - 214410-1 - 214410-6 PB - American Institute of Physics CY - Melville, NY AN - OPUS4-19796 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - New insight into the crystallization process of calcium carbonate by a contact-free in situ scattering technique using a levitating drop method T2 - 14. Vortragstagung Gesellschaft Deutscher Chemiker CY - Bayreuth, Germany DA - 2008-09-24 PY - 2008 AN - OPUS4-17954 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Juran, S. A1 - Walther, M. A1 - Stephan, H. A1 - Bergmann, R. A1 - Steinbach, J. A1 - Kraus, Werner A1 - Emmerling, Franziska A1 - Comba, P. T1 - Hexadentate Bispidine derivatives as versatile bifunctional chelate agents for Copper(II) radioisotopes PY - 2009 DO - https://doi.org/10.1021/bc800461e SN - 1043-1802 SN - 1520-4812 VL - 20 IS - 2 SP - 347 EP - 359 CY - Washington, DC AN - OPUS4-19068 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - Gas Adsorption and SAXS Studies of Mechanochemically Prepared MOFs T2 - XV. POROTEC-Workshop über die Charakterisierung von feinteiligen und porösen Festkörpern CY - Bad Soden, Germany DA - 2010-11-16 PY - 2010 AN - OPUS4-22834 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -