@inproceedings{47347,
  author       = {{Berndt, Axel}},
  booktitle    = {{{Kolloquium zur Musik des 20. Jahrhunderts}}},
  title        = {{{Musik im Spiel}}},
  year         = {{2018}},
}

@article{63739,
  author       = {{Kaczmarek, K. T. and Ledingham, P. M. and Brecht, Benjamin and Thomas, S. E. and Thekkadath, G. S. and Lazo-Arjona, O. and Munns, J. H. D. and Poem, E. and Feizpour, A. and Saunders, D. J. and Nunn, J. and Walmsley, I. A.}},
  issn         = {{2469-9926}},
  journal      = {{Physical Review A}},
  number       = {{4}},
  publisher    = {{American Physical Society (APS)}},
  title        = {{{High-speed noise-free optical quantum memory}}},
  doi          = {{10.1103/physreva.97.042316}},
  volume       = {{97}},
  year         = {{2018}},
}

@article{64031,
  abstract     = {{The activation of C-H bonds of alkanes remains a major challenge for chemistry. In a series of deuteration experiments with D-2 in contact with bis-(diphenylphosphino) butane (dppb) stabilized ruthenium nanoparticles (liquid substrates, 60 degrees C, 6 bar D-2) we have observed a surprisingly large reactivity of cyclopentane as compared to cyclohexane and other alkanes. DFT calculations using a ligand-free Ru13H17 model cluster as catalyst indicate oxidative C-H cleavage of the bound substrates as rate limiting reaction step. They also indicate similar binding and activation enthalpies of reactions of cyclopentane and cyclohexane.}},
  author       = {{Rothermel, N. and Bouzouita, D. and Rother, T. and Rosal, I. and Tricard, S. and Poteau, R. and Gutmann, Torsten and Chaudret, B. and Limbach, H. H. and Buntkowsky, G.}},
  journal      = {{ChemCatChem}},
  number       = {{19}},
  pages        = {{4243–4247}},
  title        = {{{Surprising Differences of Alkane C-H Activation Catalyzed by Ruthenium Nanoparticles: Complex Surface-Substrate Recognition?}}},
  doi          = {{10.1002/cctc.201801022}},
  volume       = {{10}},
  year         = {{2018}},
}

@article{64007,
  abstract     = {{The equilibration of H2, HD and D2 between the gas phase and surface hydrides of solid organic-ligand-stabilized Ru metal nanoparticles has been studied by gas phase 1H NMR spectroscopy using closed NMR tubes as batch reactors at room temperature and 800 mbar. When two different nanoparticle systems, Ru/PVP (PVP [identical with] polyvinylpyrrolidone) and Ru/HDA (HDA [identical with] hexadecylamine) were exposed to D2 gas, only the release of HD from the hydride containing surface could be detected in the initial stages of the reaction, but no H2. In the case of Ru/HDA also the reverse experiment was performed where surface deuterated nanoparticles were exposed to H2. In that case, the conversion of H2 into gaseous HD was detected. In order to analyze the experimental kinetic and spectroscopic data, we explored two different mechanisms taking into account potential kinetic and equilibrium H/D isotope effects. Firstly, we explored the dissociative exchange mechanism consisting of dissociative adsorption of dihydrogen, fast hydride surface diffusion and associative desorption of dihydrogen. It is shown that if D2 is the reaction partner, only H2 will be released in the beginning of the reaction, and HD only in later reaction stages. The second mechanism, dubbed here associative exchange consists of the binding of dihydrogen to Ru surface atoms, followed by a H-transfer to or by H-exchange with an adjacent hydride site, and finally of the associative desorption of dihydrogen. In that case, in the exchange with D2, only HD will be released in the beginning of the reaction. Our experimental results are not compatible with the dissociative exchange but can be explained in terms of the associative exchange. Whereas the former will dominate at low temperatures and pressures, the latter will prevail around room temperature and normal pressures where transition metal nanoparticles are generally used as reaction catalysts.}},
  author       = {{Limbach, Hans-Heinrich and Pery, Tal and Rothermel, Niels and Chaudret, Bruno and Gutmann, Torsten and Buntkowsky, Gerd}},
  journal      = {{Physical Chemistry Chemical Physics}},
  number       = {{16}},
  pages        = {{10697–10712}},
  publisher    = {{The Royal Society of Chemistry}},
  title        = {{{Gas phase 1H NMR studies and kinetic modeling of dihydrogen isotope equilibration catalyzed by Ru-nanoparticles under normal conditions: dissociative vs. associative exchange}}},
  doi          = {{10.1039/C7CP07770J}},
  volume       = {{20}},
  year         = {{2018}},
}

@article{64000,
  abstract     = {{Surface enhanced solid-state NMR by dynamic nuclear polarization (DNP SENS) enables the characterization of the inner-pore surface functionalization of porous etched ion-track membranes exhibiting low specific surface areas compared to typical SBA- or MCM-type mesoporous silica materials. The membranes were conformally coated with a 5 nm thin SiO2 layer by atomic layer deposition. This layer was subsequently modified by aminopropyl silane linkers that allow further functionalization via the terminal amine group. The results evidence that in principle DNP SENS is a capable tool to analyze more complex porous systems, e.g. bioinspired functional etched ion-track membranes down to the molecular level. These results are relevant also for single nanopore systems, for which a direct analysis of the channel surface functionalization is not feasible by classical characterization methods. The applicability of DNP SENS to complex porous systems requires the optimization of the sample preparation and measurement parameters.}},
  author       = {{Kumari, B. and John, D. and Hoffmann, P. and Spende, A. and Toimil-Molares, M. E. and Trautmann, C. and Hess, C. and Ruff, P. and Schulze, M. and Stark, R. and Buntkowsky, G. and Andrieu-Brunsen, A. and Gutmann, Torsten}},
  issn         = {{0942-9352}},
  journal      = {{Zeitschrift Fur Physikalische Chemie-International Journal of Research in Physical Chemistry & Chemical Physics}},
  number       = {{7-8}},
  pages        = {{1173–1186}},
  title        = {{{Surface Enhanced DNP Assisted Solid-State NMR of Functionatized SiO2 Coated Potycarbonate Membranes}}},
  doi          = {{10.1515/zpch-2017-1032}},
  volume       = {{232}},
  year         = {{2018}},
}

@article{63999,
  abstract     = {{The behavior of mixtures of 1-octanol with water with different molar ratios confined inside the mesoporous silica SBA-15 was investigated by a combination of solid-state NMR spectroscopy and molecular dynamics (MD) simulations. Two-dimensional H-1-Si-29 FSLG-HET-COR NMR spectra revealed the orientation of 1-octanol relative to the pore walls. These arrangements are in good agreement with the preferred structures found by MD. In addition, MD simulations also shed light on molecular orientations and interactions in the pore center region, which are not resolvable by solid-state NMR.}},
  author       = {{Kumari, B. and Brodrecht, M. and Breitzke, H. and Werner, M. and Grunberg, B. and Limbach, H. H. and Forg, S. and Sanjon, E. P. and Drossel, B. and Gutmann, Torsten and Buntkowsky, G.}},
  issn         = {{1932-7447}},
  journal      = {{Journal of Physical Chemistry C}},
  number       = {{34}},
  pages        = {{19540–19550}},
  title        = {{{Mixtures of Alcohols and Water confined in Mesoporous Silica: A Combined Solid-State NMR and Molecular Dynamics Simulation Study}}},
  doi          = {{10.1021/acs.jpcc.8b04745}},
  volume       = {{122}},
  year         = {{2018}},
}

@article{63926,
  abstract     = {{Synthesis of novel trityl-nitroxyl biradicals and their performance as polarization agents in DNP-enhanced solid-state MAS NMR spectroscopy is presented. Signal enhancements in H-1, H-1 -{\textgreater} C-13 CP MAS, and C-13 MAS experiments obtained with these radicals dissolved in 1,1,2,2-tetrachloroethane (TCE) solution are compared with the enhancements obtained from TCE solutions of binitroxyl radicals. The signal enhancements are correlated with the distance between the radical centers of the biradicals, as determined by theoretical structure calculations. Some of the biradical TCE solutions display direct-channel resonances in C-13 MAS experiments as well as indirect channel resonances induced via the proton spin reservoir. Differential scanning calorimetry reveals that only these solutions do not form any solid crystalline phases upon rapid cooling, suggesting that molecular motions needed for polarization transfer from radicals to C-13 via the proton spin reservoir remain active at the experimental low temperatures of nominal 120 K. DNP magnetic field sweep enhancement profiles for selected new biradicals are presented as well. These indicate that the DNP transfer is dominated by the cross-effect mechanism.}},
  author       = {{Bothe, S. and Nowag, J. and Klimavicius, V. and Hoffmann, M. and Troitskaya, T. I. and Amosov, E. V. and Tormyshev, V. M. and Kirilyuk, I. and Taratayko, A. and Kuzhelev, A. and Parkhomenko, D. and Bagryanskaya, E. and Gutmann, Torsten and Buntkowsky, G.}},
  issn         = {{1932-7447}},
  journal      = {{Journal of Physical Chemistry C}},
  number       = {{21}},
  pages        = {{11422–11432}},
  title        = {{{Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization}}},
  doi          = {{10.1021/acs.jpcc.8b02570}},
  volume       = {{122}},
  year         = {{2018}},
}

@article{63928,
  abstract     = {{A series of novel functionalized mesoporous silica-based materials with well-defined pore diameters, surface functionalization and surface morphology is synthesized by co-condensation or grafting techniques and characterized by solid-state NMR spectroscopy, DNP enhanced solid state-NMR and thermodynamic techniques. These materials are employed as host-systems for small-guest molecules like water, small alcohols, carbonic acids, small aromatic molecules, binary mixtures and others. The phase-behavior of these confined guests is studied by combinations of one dimensional solid-state NMR techniques (H-1 MAS, H-2-line shape analysis, C-13 CPMAS) and two-dimensional correlation experiments like H-1-Si-29- solid-state HETCOR.}},
  author       = {{Brodrecht, M. and Kumari, B. and Breitzke, H. and Gutmann, Torsten and Buntkowsky, G.}},
  issn         = {{0942-9352}},
  journal      = {{Zeitschrift Fur Physikalische Chemie-International Journal of Research in Physical Chemistry & Chemical Physics}},
  number       = {{7-8}},
  pages        = {{1127–1146}},
  title        = {{{Chemically Modified Silica Materials as Model Systems for the Characterization of Water-Surface Interactions}}},
  doi          = {{10.1515/zpch-2017-1059}},
  volume       = {{232}},
  year         = {{2018}},
}

@inproceedings{64374,
  author       = {{Gerhardt, Nils Christopher and Neutsch, Krisztian and Göring, Lena}},
  booktitle    = {{Nanoimaging and Nanospectroscopy VI}},
  title        = {{{Common-path digital holographic microscopy for 3D nanoparticle localization}}},
  doi          = {{10.1117/12.2321175}},
  year         = {{2018}},
}

@techreport{62740,
  author       = {{Bornemann, Tobias}},
  title        = {{{Do Transfer Pricing Rules distort R&D Investment Decisions?}}},
  doi          = {{10.2139/ssrn.3114071}},
  volume       = {{2018-02}},
  year         = {{2018}},
}

@article{13902,
  author       = {{Belobo, D. Belobo and Meier, T.}},
  issn         = {{2045-2322}},
  journal      = {{Scientific Reports}},
  pages        = {{3706}},
  title        = {{{Exotic complexes in one-dimensional Bose-Einstein condensates with spin-orbit coupling}}},
  doi          = {{10.1038/s41598-018-22008-2}},
  volume       = {{8}},
  year         = {{2018}},
}

@article{4365,
  author       = {{Belobo, D. Belobo and Meier, Torsten}},
  issn         = {{2045-2322}},
  journal      = {{Scientific Reports}},
  number       = {{1}},
  publisher    = {{Springer Nature}},
  title        = {{{Exotic complexes in one-dimensional Bose-Einstein condensates with spin-orbit coupling}}},
  doi          = {{10.1038/s41598-018-22008-2}},
  volume       = {{8}},
  year         = {{2018}},
}

@inproceedings{47006,
  author       = {{Güldenpenning, Iris and Weigelt, Matthias}},
  booktitle    = {{Abstracts of the 60th Conference of Experimental Psychologists (TeaP)}},
  editor       = {{Schütz, A. C. and Schubö, A. and Endres, D. and Lachnit, H.}},
  location     = {{Marburg}},
  pages        = {{97}},
  publisher    = {{Pabst Science Publishers}},
  title        = {{{Is the head-fake effect in basketball robust against practice?}}},
  year         = {{2018}},
}

@techreport{45131,
  author       = {{Kißgen, R. and Austermühle, J. and Franke, Sebastian and Limburg, D. and Wöhrle, J.}},
  publisher    = {{Universität Siegen}},
  title        = {{{Rheinland-Kita-Studie: Inklusion von Kindern mit Behinderung in Tageseinrichtungen für Kinder. Zwischenbericht zur quantitativ-empirischen Online-Erhebung der Leiterinnen und Leiter}}},
  year         = {{2018}},
}

@inbook{45136,
  author       = {{Mays, D. and Franke, Sebastian and Metzner, F. and Boyle, C. and Jindal-Snape, D. and Schneider, L. and Zielemanns, H. and Pawils, Z. and Wichmann, M.}},
  booktitle    = {{Pathways to Belonging - Contemporary Research in School Belonging}},
  editor       = {{Allen, K. and Boyle, C.}},
  pages        = {{168--187}},
  publisher    = {{Sense Publishers}},
  title        = {{{School belonging and successful transition practice - academic self-concept and achievement motivation in primary school students}}},
  year         = {{2018}},
}

@article{45132,
  author       = {{Mays, D. and Schneider, L. and Wichmann, M. and Metzner, F. and Zielemanns, H. and Pawils, S. and Franke, Sebastian}},
  journal      = {{Zeitschrift für Heilpädagogik}},
  pages        = {{133--146}},
  title        = {{{Schulisches Selbstkonzept sowie Lern- und Leistungsmotivation bei Schülerinnen und Schülern mit einem prognostizierten ungünstigen Entwicklungsverlauf im Bereich der emotionalen und sozialen Entwicklung während der Transition in die Sekundarstufe I}}},
  volume       = {{69}},
  year         = {{2018}},
}

@inbook{45133,
  author       = {{Mays, D. and Zielemanns, H. and Franke, Sebastian and Wichmann, M. and Metzner, F.}},
  booktitle    = {{Grundlagen für die Lehrerausbildung und Praxis}},
  pages        = {{139--164}},
  publisher    = {{UTB}},
  title        = {{{Der Übergang von der Grundschule auf die weiterführende Schule im Kontext inklusiver Bildung - Ein Blick in die Forschung und Praxis. In Porsch, R. (Hrsg.). Der Übergang von der Grundschule auf weiterführende Schulen}}},
  year         = {{2018}},
}

@inbook{57493,
  author       = {{Karaca, Resul and Schmitz, Sabine}},
  booktitle    = {{Le fait religieux dans les manuels d’histoire : Contenus-Institutions-Pratiques. Approches comparées à l’échelle internationale}},
  editor       = {{Avon, Dominique and Tolan,  John and Saint-Martin, Isabelle}},
  isbn         = {{979-10-90129-29-0}},
  pages        = {{77--101}},
  publisher    = {{Arbre Bleu Éditions}},
  title        = {{{La représentation de l’Islam dans les manuels d’histoire en Espagne et Allemagne : une narration de plus en plus vouée aux images}}},
  year         = {{2018}},
}

@inproceedings{58666,
  abstract     = {{<jats:p>In this paper, a questionnaire-based survey on the use of online videos by undergraduate engineering students for study-related purposes is presented. Over the last few years, a large number of instructional videos has been uploaded to websites such as YouTube. Due to the widespread distribution of high-speed internet connections and (mobile) devices, such as smartphones or laptops, which are nowadays routinely used by students, online videos are also frequently used in higher education. While much research on this subject focuses on Massive Open Online Courses (MOOCs) or flipped classroom approaches, this survey examines use of videos for self-study, complementary to traditional face-to-face courses. Furthermore, we analyze the acceptance of a characteristic video production style, which uses specific 3D animations to clarify complex connections between technical and mathematical aspects. The results indicate extensive use of short videos which address subjects that are particularly difficult for the students. This survey can help educators to develop an impression of current video use by undergraduate engineering students. In this paper, a questionnaire-based survey on the use of online videos by undergraduate engineering students for study-related purposes is presented. Especially over the last few years, a large number of instructional videos has been uploaded to websites such as YouTube. Due to the widespread distribution of high-speed internet connections and (mobile) devices, such as smartphones or laptops, which are nowadays routinely used by students, online videos are also frequently used in higher education. While much research on this subject focuses on Massive Open Online Courses (MOOCs) or flipped classroom approaches, this survey examines usage behavior concerning the apparently much more common use of videos for self-study, complementary to traditional face-to-face courses. Furthermore, we analyze the acceptance of a characteristic video production style using specific 3D animations to clarify complex connections between technical and mathematical aspects. The results indicate that short videos addressing subjects that are particularly difficult for the students are extensively used. Additionally, this survey can help educators to develop a realistic understanding of current video use by undergraduate engineering students.</jats:p>}},
  author       = {{Hennig, Markus and Mertsching, Bärbel}},
  booktitle    = {{Proceedings of the 4th International Conference on Higher Education Advances (HEAd'18)}},
  publisher    = {{Universitat Politècnica València}},
  title        = {{{Study-related Use of Instructional Videos by Undergraduate Engineering Students}}},
  doi          = {{10.4995/head18.2018.8207}},
  year         = {{2018}},
}

@inproceedings{60448,
  author       = {{Lim, Isaak and Dielen, Alexander and Campen, Marcel and Kobbelt, Leif}},
  booktitle    = {{Computer Vision - ECCV 2018 Workshops - Munich, Germany, September 8-14, 2018, Proceedings, Part III}},
  editor       = {{Leal-Taixé, Laura and Roth, Stefan}},
  pages        = {{349–362}},
  publisher    = {{Springer}},
  title        = {{{A Simple Approach to Intrinsic Correspondence Learning on Unstructured 3D Meshes}}},
  doi          = {{10.1007/978-3-030-11015-4_26}},
  volume       = {{11131}},
  year         = {{2018}},
}