@article{46548, abstract = {{The use of iron as a replacement for noble metals in photochemical and photophysical applications is challenging due to the typically fast deactivation of short-lived catalytically active states. Recent success of a cyclometalated iron(III) complex utilizing a bis-tridentate ligand motif inspired the use of phenyl-1H-pyrazole as a bidentate ligand. Five complexes using the tris(1-phenylpyrazolato-N,C2)iron(III) complex scaffold are presented. In addition to the parent complex, four derivatives with functionalization in the meta-position of the phenyl ring are thoroughly investigated by single crystal diffractometry, UV-Vis-spectroscopy, and cyclic voltammetry. Advanced X-ray spectroscopy in the form of X-ray absorption and emission spectroscopy allows unique insights into the electronic structure as well as DFT calculations. The ligand design leads to overlapping MLCT and LMCT absorption bands, and emissive behavior is suppressed by low-lying MC states.}}, author = {{Hirschhausen, Tanja and Fritsch, Lorena and Lux, Franziska and Steube, Jakob and Schoch, Roland and Neuba, Adam and Egold, Hans and Bauer, Matthias}}, issn = {{2304-6740}}, journal = {{Inorganics}}, keywords = {{Inorganic Chemistry, Computing Resources Provided by the Paderborn Center for Parallel Computing, pc2-ressources}}, number = {{7}}, publisher = {{MDPI AG}}, title = {{{Iron(III)-Complexes with N-Phenylpyrazole-Based Ligands}}}, doi = {{10.3390/inorganics11070282}}, volume = {{11}}, year = {{2023}}, } @article{46547, author = {{Rogolino, Andrea and Filho, José B. G. and Fritsch, Lorena and Ardisson, José D. and da Silva, Marcos A. R. and Atta Diab, Gabriel Ali and Silva, Ingrid Fernandes and Moraes, Carlos André Ferreira and Forim, Moacir Rossi and Bauer, Matthias and Kühne, Thomas D. and Antonietti, Markus and Teixeira, Ivo F.}}, issn = {{2155-5435}}, journal = {{ACS Catalysis}}, keywords = {{Catalysis, General Chemistry, pc2-ressources, Computing Resources Provided by the Paderborn Center for Parallel Computing}}, number = {{13}}, pages = {{8662--8669}}, publisher = {{American Chemical Society (ACS)}}, title = {{{Direct Synthesis of Acetone by Aerobic Propane Oxidation Promoted by Photoactive Iron(III) Chloride under Mild Conditions}}}, doi = {{10.1021/acscatal.3c02092}}, volume = {{13}}, year = {{2023}}, } @article{52345, abstract = {{Photoactive chromium(III) complexes saw a conceptual breakthrough with the discovery of the prototypical molecular ruby mer-[Cr(ddpd)2]3+ (ddpd = N,N′-dimethyl-N,N′-dipyridin-2-ylpyridine-2,6-diamine), which shows intense long-lived near-infrared (NIR) phosphorescence from metal-centered spin-flip states. In contrast to the numerous studies on chromium(III) photophysics, only 10 luminescent molybdenum(III) complexes have been reported so far. Here, we present the synthesis and characterization of mer-MoX3(ddpd) (1, X = Cl; 2, X = Br) and cisfac-[Mo(ddpd)2]3+ (cisfac-[3]3+), an isomeric heavy homologue of the prototypical molecular ruby. For cisfac-[3]3+, we found strong zero-field splitting using magnetic susceptibility measurements and electron paramagnetic resonance spectroscopy. Electronic spectra covering the spin-forbidden transitions show that the spin-flip states in mer-1, mer-2, and cisfac-[3]3+ are much lower in energy than those in comparable chromium(III) compounds. While all three complexes show weak spin-flip phosphorescence in NIR-II, the emission of cisfac-[3]3+ peaking at 1550 nm is particularly low in energy. Femtosecond transient absorption spectroscopy reveals a short excited-state lifetime of 1.4 ns, 6 orders of magnitude shorter than that of mer-[Cr(ddpd)2]3+. Using density functional theory and ab initio multireference calculations, we break down the reasons for this disparity and derive principles for the design of future stable photoactive molybdenum(III) complexes.}}, author = {{Kitzmann, Winald R. and Hunger, David and Reponen, Antti-Pekka M. and Förster, Christoph and Schoch, Roland and Bauer, Matthias and Feldmann, Sascha and van Slageren, Joris and Heinze, Katja}}, issn = {{0020-1669}}, journal = {{Inorganic Chemistry}}, keywords = {{Inorganic Chemistry, Physical and Theoretical Chemistry}}, number = {{39}}, pages = {{15797--15808}}, publisher = {{American Chemical Society (ACS)}}, title = {{{Electronic Structure and Excited-State Dynamics of the NIR-II Emissive Molybdenum(III) Analogue to the Molecular Ruby}}}, doi = {{10.1021/acs.inorgchem.3c02186}}, volume = {{62}}, year = {{2023}}, } @article{52344, abstract = {{Macrocyclization reactions are still challenging due to competing oligomerization, which requires the use of small substrate concentrations. Here, the cationic tungsten imido and tungsten oxo alkylidene N-heterocyclic carbene complexes [[W(N-2,6-Cl2-C6H3)(CHCMe2Ph(OC6F5)(pivalonitrile)(IMes)+ B(ArF)4−] (W1) and [W(O)(CHCMe2Ph(OCMe(CF3)2)(IMes)(CH3CN)+ B(ArF)4−] (W2) (IMes=1,3-dimesitylimidazol-2-ylidene; B(ArF)4−=tetrakis(3,5-bis(trifluoromethyl)phenyl borate) have been immobilized inside the pores of ordered mesoporous silica (OMS) with pore diameters of 3.3 and 6.8 nm, respectively, using a pore-selective immobilization protocol. X-ray absorption spectroscopy of W1@OMS showed that even though the catalyst structure is contracted due to confinement by the mesopores, both the oxidation state and structure of the catalyst stayed intact upon immobilization. Catalytic testing with four differently sized α,ω-dienes revealed a dramatically increased macrocyclization (MC) and Z-selectivity of the supported catalysts compared to the homogenous progenitors, allowing high substrate concentrations of 25 mM. With the supported complexes, a maximum increase in MC-selectivity from 27 to 81 % and in Z-selectivity from 17 to 34 % was achieved. In general, smaller mesopores exhibited a stronger confinement effect. A comparison of the two supported tungsten-based catalysts showed that W1@OMS possesses a higher MC-selectivity, while W2@OMS exhibits a higher Z-selectivity which can be rationalized by the structures of the catalysts.}}, author = {{Ziegler, Felix and Bruckner, Johanna R. and Nowakowski, Michal and Bauer, Matthias and Probst, Patrick and Atwi, Boshra and Buchmeiser, Michael R.}}, issn = {{1867-3880}}, journal = {{ChemCatChem}}, keywords = {{Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Catalysis}}, number = {{21}}, publisher = {{Wiley}}, title = {{{Macrocyclization of Dienes under Confinement with Cationic Tungsten Imido/Oxo Alkylidene N‐Heterocyclic Carbene Complexes}}}, doi = {{10.1002/cctc.202300871}}, volume = {{15}}, year = {{2023}}, } @article{49608, abstract = {{The effects of backbone amine functionalization in three new homoleptic C^N^C type ruthenium(II) complexes bearing a tridentate bis‐imidazole‐2‐ylidene pyridine ligand framework are characterized and studied by single crystal diffraction, electrochemistry, optical spectroscopy and transient absorption spectroscopy in combination with ab initio DFT calculations. Functionalization by dimethylamine groups in 4‐position of the pyridine backbone significantly influences the properties of the complexes as revealed by comparison with the unfunctionalized references. As a result of the amine functionalization, a higher molar absorption coefficient of the MLCT bands, a decreased photoluminescence quantum yield at room temperature together with a shortened excited state lifetime but an improved photostability is observed. Introduction of electron donating and withdrawing groups at the NHC unit modifies the electronic and optical properties, such as the oxidation potential, absorption and emission properties, and the lifetimes of the excited states.}}, author = {{Fritsch, Lorena and Vukadinovic, Yannik and Lang, Moritz and Naumann, Robert and Bertrams, Maria-Sophie and Kruse, Ayla and Schoch, Roland and Müller, Patrick and Neuba, Adam and Dierks, Philipp and Lochbrunner, Stefan and Kerzig, Christoph and Heinze, Katja and Bauer, Matthias}}, issn = {{2367-0932}}, journal = {{ChemPhotoChem}}, keywords = {{Organic Chemistry, Physical and Theoretical Chemistry, Analytical Chemistry, Computing Resources Provided by the Paderborn Center for Parallel Computing, pc2-ressources}}, publisher = {{Wiley}}, title = {{{Chemical and photophysical properties of amine functionalized bis‐NHC‐pyridine‐RuII complexes}}}, doi = {{10.1002/cptc.202300281}}, year = {{2023}}, } @misc{47901, author = {{Beutner, Marc and Schneider, Jennifer Nicole}}, booktitle = {{International Conference on Industry Sciences and Computer Science Innovation}}, title = {{{The use of IT and OER to support remote sustainable work in Europeans Green Economy}}}, year = {{2023}}, } @inbook{52330, author = {{Schwede, Jana and Harteis, Christian}}, booktitle = {{Nachhaltigkeitsorientierte Weiterbildungsdidaktik: Die doppelte Multiplikatorenqualifizierung}}, editor = {{Müller, Claudia and Pranger, Jan and Reißland, Jens}}, pages = {{147--164}}, publisher = {{wbv Publikation}}, title = {{{Weiterbildung des Weiterbildungspersonals – Vorwiegend eine Aufgabe des Lernens am Arbeitsplatz}}}, doi = {{10.3278/9783763974382}}, volume = {{73}}, year = {{2023}}, } @article{52358, author = {{Diederich, Malte and Spatz, Verena and Bauer, Anna Brigitte}}, journal = {{Phydid B, Didaktik der Physik, Beiträge zur DPG-Frühjahrstagung (2022)}}, title = {{{Auswirkungen einer Online-Intervention (Mindset, Lerntechniken) auf den Studieneinstieg}}}, year = {{2023}}, } @inproceedings{52369, abstract = {{Megatrends, such as digitization or sustainability, are confronting the product management of manufacturing companies with a variety of challenges regarding the design of future products, but also the management of the actual products. To successfully position their products in the market, product managers need to gather and analyze comprehensive information about customers, developments in the products’ environment, product usage, and more. The digitization of all aspects of life is making data on these topics increasingly available – via social media, documents, or the internet of things from the products themselves. The systematic collection and analysis of these data enable the exploitation of new potentials for the adaption of existing products and the creation of the products of tomorrow. However, there are still no insights into the main concepts and cause-effect relationships in exploiting data-driven approaches for product management. Therefore, this paper aims to identify the main concepts and advantages of data-driven product management. To answer the corresponding research questions a comprehensive systematic literature review is conducted. From its results, a detailed description of the main concepts of data-driven product management is derived. Furthermore, a taxonomy for the advantages of data-driven product management is presented. The main concepts and the taxonomy allow for a deeper understanding of the topic while highlighting necessary future actions and research needs.}}, author = {{Fichtler, Timm and Grigoryan, Khoren and Koldewey, Christian and Dumitrescu, Roman}}, booktitle = {{2023 IEEE International Conference on Technology Management, Operations and Decisions (ICTMOD)}}, keywords = {{Product Lifecyle Management (PLM), Data Analytics, Data-driven Design, Engineering Management, Lifecycle Data}}, location = {{Rabat, Morocco}}, publisher = {{IEEE}}, title = {{{Towards a Data-Driven Product Management – Concepts, Advantages, and Future Research}}}, doi = {{10.1109/ictmod59086.2023.10438135}}, year = {{2023}}, } @inproceedings{52370, author = {{Vernholz, Mats}}, booktitle = {{Living and Leading in the Next Era: Connecting Teaching, Research, Citizenship and Equity}}, editor = {{Perla, Loredana and Agrati, Laura Sara and Vinci, Viviana and Scarinci, Alessia}}, isbn = {{9791255681038}}, location = {{Bari}}, publisher = {{Pensa Multimedia}}, title = {{{Academic self-concepts of pre-service technology teachers for vocational education in Germany according to the TPACK- Model}}}, year = {{2023}}, }