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Nevertheless, we hardly pay attention to ideologies, their narratives, functions and organizations in economic theory today. Ideologies as “non-rational beliefs” seem incompatible with rationality in economic models. \r\n\r\nTherefore, the book examines the role of ideologies and belief systems in individual decision-making behavior from an economic and rational perspective. Due to the fact that people have incomplete information, belief systems and ideologies fulfill a number of important functions. While ideologies themselves serve psychological needs, they are used as a cognitive framework for rational decision-making once they have been adopted through a Bayesian learning process. They influence decisions in a wide range of areas, from consumption and work to politics. This is where the role of ideological organizations becomes important, because they determine the ideological direction of the narratives and their dissemination. \r\n\r\nThus, ideologies give a normative direction, for better or for worse. The “quality” of ideological leadership can be evaluated normatively on the basis of principles such as individual sovereignty and human dignity. A democratic discourse requires an information and communication system that enables an evaluation of precisely these ideologies, free from resource and information power.\r\n"}],"status":"public","publisher":"Springer Nature Switzerland","date_updated":"2025-11-09T09:52:35Z","author":[{"first_name":"Thomas","full_name":"Gries, Thomas","id":"186","last_name":"Gries"},{"last_name":"Burs","full_name":"Burs, Carina","first_name":"Carina"},{"first_name":"Veronika","last_name":"Müller","full_name":"Müller, Veronika"}],"date_created":"2025-07-13T18:02:56Z","title":"The Economics of Ideologies","doi":"10.1007/978-3-031-93514-5","publication_identifier":{"issn":["2731-5908","2731-5916"],"isbn":["9783031935138","9783031935145"]},"publication_status":"published","place":"Cham","year":"2025","citation":{"apa":"Gries, T., Burs, C., &#38; Müller, V. (2025). <i>The Economics of Ideologies</i>. 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Decision-Driven Analytics in Smart Factories: Enterprise Architecture Framework for Use Case Specification and Engineering (FUSE). <i>Electronics</i>, <i>14</i>(21), Article 4271. <a href=\"https://doi.org/10.3390/electronics14214271\">https://doi.org/10.3390/electronics14214271</a>","mla":"Weller, Julian, and Roman Dumitrescu. “Decision-Driven Analytics in Smart Factories: Enterprise Architecture Framework for Use Case Specification and Engineering (FUSE).” <i>Electronics</i>, vol. 14, no. 21, 4271, MDPI AG, 2025, doi:<a href=\"https://doi.org/10.3390/electronics14214271\">10.3390/electronics14214271</a>.","short":"J. Weller, R. Dumitrescu, Electronics 14 (2025).","bibtex":"@article{Weller_Dumitrescu_2025, title={Decision-Driven Analytics in Smart Factories: Enterprise Architecture Framework for Use Case Specification and Engineering (FUSE)}, volume={14}, DOI={<a href=\"https://doi.org/10.3390/electronics14214271\">10.3390/electronics14214271</a>}, number={214271}, journal={Electronics}, publisher={MDPI AG}, author={Weller, Julian and Dumitrescu, Roman}, year={2025} }","chicago":"Weller, Julian, and Roman Dumitrescu. “Decision-Driven Analytics in Smart Factories: Enterprise Architecture Framework for Use Case Specification and Engineering (FUSE).” <i>Electronics</i> 14, no. 21 (2025). <a href=\"https://doi.org/10.3390/electronics14214271\">https://doi.org/10.3390/electronics14214271</a>.","ieee":"J. Weller and R. 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The motivation behind this research lies in challenges faced by manufacturing companies, such as skilled labor shortages and increasing global competition, alongside the imperative for sustainable production. This journal provides a novel approach for designing and documenting prescriptive analytics use cases in manufacturing environments. The framework addresses the need for effective integration of advanced data analytics and prescriptive analytics solutions within existing production environments, thereby enhancing operational efficiency and decision-making processes. A Design Science Research approach is used to iteratively derive a framework based on stakeholder needs and activities along the prescriptive analytics use case development cycle. The resulting framework is demonstrated and evaluated in an IoT Factory setup in a research facility. From a practical perspective, the framework supports manufacturing companies in systematically designing prescriptive analytics use cases. From a research perspective, it contributes to the body of knowledge on Enterprise Architecture Management (EAM) by operationalizing the design of prescriptive analytics use cases in manufacturing contexts. The main contributions of this study include the development of a framework that supports the planning, design, and integration of prescriptive analytics use cases. This framework fosters interdisciplinary collaboration and aids in managing the complexity of data-driven projects.</jats:p>","lang":"eng"}],"status":"public"},{"page":"131-142","citation":{"ama":"Schroeter-Wittke H. Mache dich auf, werde licht! Ein Abriss des weihnachtlichen Ab und Auf anhand des Weihnachtsfilms von Penny 2022 Der Riss / Let’s Talk. In: Janus R, ed. <i>Weihnachts-Werbespots Als Moderne Krippenspiele</i>. Springer VS; 2025:131-142.","ieee":"H. Schroeter-Wittke, “Mache dich auf, werde licht! 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Published online 2025. doi:<a href=\"https://doi.org/10.1109/TVLSI.2025.3625787\">10.1109/TVLSI.2025.3625787</a>"},"year":"2025","date_created":"2025-11-10T08:31:47Z","author":[{"id":"93634","full_name":"Sadiye, Babak","last_name":"Sadiye","first_name":"Babak"},{"last_name":"Iftekhar","id":"47944","full_name":"Iftekhar, Mohammed","first_name":"Mohammed"},{"last_name":"Müller","full_name":"Müller, Wolfgang","id":"16243","first_name":"Wolfgang"},{"full_name":"Scheytt, J. Christoph","id":"37144","orcid":"0000-0002-5950-6618 ","last_name":"Scheytt","first_name":"J. Christoph"}],"publisher":"IEEE","date_updated":"2025-11-10T08:38:07Z","doi":"10.1109/TVLSI.2025.3625787","title":"60-Gb/s 1:4 Demultiplexer in 22-nm FD-SOI Technology Using TSPC Logic: A Circuit-to-System-Level Analysis and Design"},{"_id":"61335","user_id":"89271","department":[{"_id":"2"},{"_id":"389"}],"article_number":"202500394","keyword":["T2","T","CSSD"],"language":[{"iso":"eng"}],"type":"journal_article","publication":"Advanced Synthesis and Catalysis","abstract":[{"lang":"eng","text":"<jats:p>Amidines are a ubiquitous class of bioactive compounds found in a wide variety of natural products; thus, efficient strategies for their preparation are in great demand. Herein, a novel protocol is reported for the synthesis of amidines based on P<jats:sup>III</jats:sup>/P<jats:sup>V</jats:sup>O redox catalysis. This two‐step, one‐pot approach involves the activation of amides via P<jats:sup>III</jats:sup>/P<jats:sup>V</jats:sup>O catalyzed in situ formation of imidoyl chloride intermediates which are directly converted upon reaction with amines into the corresponding amidines. Instead of traditionally used toxic and corrosive chloride sources, hexachloroacetone (HCA) is successfully employed as a halide source. The reaction proceeds with low catalyst loading (2 mol%) in BuOAc as the solvent. Under the optimized conditions, 20 amidines are prepared in yields up to 99%. A feasible mechanism is proposed based on experimental results. The synthetic potential of this method is evaluated in the preparation of the tyrosine kinase inhibitor (TKI) Erlotinib.</jats:p>"}],"status":"public","date_updated":"2025-11-10T08:44:04Z","publisher":"Wiley","author":[{"first_name":"Viktorija","id":"92677","full_name":"Medvaric, Viktorija","last_name":"Medvaric"},{"first_name":"Jan","full_name":"Paradies, Jan","id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"date_created":"2025-09-17T15:16:49Z","title":"Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides","doi":"10.1002/adsc.70059","publication_status":"published","publication_identifier":{"issn":["1615-4150","1615-4169"]},"year":"2025","citation":{"apa":"Medvaric, V., Paradies, J., &#38; Werner, T. (2025). Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides. <i>Advanced Synthesis and Catalysis</i>, Article 202500394. <a href=\"https://doi.org/10.1002/adsc.70059\">https://doi.org/10.1002/adsc.70059</a>","mla":"Medvaric, Viktorija, et al. “Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides.” <i>Advanced Synthesis and Catalysis</i>, 202500394, Wiley, 2025, doi:<a href=\"https://doi.org/10.1002/adsc.70059\">10.1002/adsc.70059</a>.","short":"V. Medvaric, J. Paradies, T. Werner, Advanced Synthesis and Catalysis (2025).","bibtex":"@article{Medvaric_Paradies_Werner_2025, title={Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides}, DOI={<a href=\"https://doi.org/10.1002/adsc.70059\">10.1002/adsc.70059</a>}, number={202500394}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Medvaric, Viktorija and Paradies, Jan and Werner, Thomas}, year={2025} }","ieee":"V. Medvaric, J. Paradies, and T. Werner, “Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides,” <i>Advanced Synthesis and Catalysis</i>, Art. no. 202500394, 2025, doi: <a href=\"https://doi.org/10.1002/adsc.70059\">10.1002/adsc.70059</a>.","chicago":"Medvaric, Viktorija, Jan Paradies, and Thomas Werner. “Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides.” <i>Advanced Synthesis and Catalysis</i>, 2025. <a href=\"https://doi.org/10.1002/adsc.70059\">https://doi.org/10.1002/adsc.70059</a>.","ama":"Medvaric V, Paradies J, Werner T. Synthesis of Amidines Via P(III)/P(V)=O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides. <i>Advanced Synthesis and Catalysis</i>. Published online 2025. doi:<a href=\"https://doi.org/10.1002/adsc.70059\">10.1002/adsc.70059</a>"}},{"_id":"62086","department":[{"_id":"35"},{"_id":"2"}],"user_id":"89271","status":"public","type":"journal_article","doi":"10.1021/acs.joc.5c00889","date_updated":"2025-11-10T08:43:33Z","volume":90,"author":[{"first_name":"Vivian","full_name":"Stefanow, Vivian","last_name":"Stefanow"},{"first_name":"Lukas","last_name":"Kell","full_name":"Kell, Lukas"},{"last_name":"Leduskrasta","full_name":"Leduskrasta, Aiga","first_name":"Aiga"},{"first_name":"Marcus","last_name":"Eh","full_name":"Eh, Marcus"},{"first_name":"Johannes","last_name":"Panten","full_name":"Panten, Johannes"},{"full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"page":"12877-12887","intvolume":"        90","citation":{"ama":"Stefanow V, Kell L, Leduskrasta A, Eh M, Panten J, Werner T. Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients. <i>The Journal of Organic Chemistry</i>. 2025;90(37):12877-12887. doi:<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>","ieee":"V. Stefanow, L. Kell, A. Leduskrasta, M. Eh, J. Panten, and T. Werner, “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients,” <i>The Journal of Organic Chemistry</i>, vol. 90, no. 37, pp. 12877–12887, 2025, doi: <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>.","chicago":"Stefanow, Vivian, Lukas Kell, Aiga Leduskrasta, Marcus Eh, Johannes Panten, and Thomas Werner. “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients.” <i>The Journal of Organic Chemistry</i> 90, no. 37 (2025): 12877–87. <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">https://doi.org/10.1021/acs.joc.5c00889</a>.","mla":"Stefanow, Vivian, et al. “Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients.” <i>The Journal of Organic Chemistry</i>, vol. 90, no. 37, American Chemical Society (ACS), 2025, pp. 12877–87, doi:<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>.","short":"V. Stefanow, L. Kell, A. Leduskrasta, M. Eh, J. Panten, T. Werner, The Journal of Organic Chemistry 90 (2025) 12877–12887.","bibtex":"@article{Stefanow_Kell_Leduskrasta_Eh_Panten_Werner_2025, title={Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients}, volume={90}, DOI={<a href=\"https://doi.org/10.1021/acs.joc.5c00889\">10.1021/acs.joc.5c00889</a>}, number={37}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Stefanow, Vivian and Kell, Lukas and Leduskrasta, Aiga and Eh, Marcus and Panten, Johannes and Werner, Thomas}, year={2025}, pages={12877–12887} }","apa":"Stefanow, V., Kell, L., Leduskrasta, A., Eh, M., Panten, J., &#38; Werner, T. (2025). Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients. <i>The Journal of Organic Chemistry</i>, <i>90</i>(37), 12877–12887. <a href=\"https://doi.org/10.1021/acs.joc.5c00889\">https://doi.org/10.1021/acs.joc.5c00889</a>"},"publication_identifier":{"issn":["0022-3263","1520-6904"]},"publication_status":"published","keyword":["T4","CSSD"],"language":[{"iso":"eng"}],"publication":"The Journal of Organic Chemistry","title":"Straightforward Access to Terpene-Based 1,2-Diols and Their Acetals as Fragrance Ingredients","publisher":"American Chemical Society (ACS)","date_created":"2025-11-05T15:10:13Z","year":"2025","issue":"37"},{"publication":"Journal of the American Chemical Society","type":"journal_article","status":"public","department":[{"_id":"2"},{"_id":"389"}],"user_id":"89271","_id":"61336","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"article_number":"jacs.5c06190","publication_identifier":{"issn":["0002-7863","1520-5126"]},"publication_status":"published","citation":{"apa":"Zhou, R., Medvaric, V., Werner, T., &#38; Paradies, J. (2025). Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance. <i>Journal of the American Chemical Society</i>, Article jacs. 5c06190. <a href=\"https://doi.org/10.1021/jacs.5c06190\">https://doi.org/10.1021/jacs.5c06190</a>","short":"R. Zhou, V. Medvaric, T. Werner, J. Paradies, Journal of the American Chemical Society (2025).","mla":"Zhou, Rundong, et al. “Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance.” <i>Journal of the American Chemical Society</i>, jacs. 5c06190, American Chemical Society (ACS), 2025, doi:<a href=\"https://doi.org/10.1021/jacs.5c06190\">10.1021/jacs.5c06190</a>.","bibtex":"@article{Zhou_Medvaric_Werner_Paradies_2025, title={Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance}, DOI={<a href=\"https://doi.org/10.1021/jacs.5c06190\">10.1021/jacs.5c06190</a>}, number={jacs. 5c06190}, journal={Journal of the American Chemical Society}, publisher={American Chemical Society (ACS)}, author={Zhou, Rundong and Medvaric, Viktorija and Werner, Thomas and Paradies, Jan}, year={2025} }","ieee":"R. Zhou, V. Medvaric, T. Werner, and J. Paradies, “Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance,” <i>Journal of the American Chemical Society</i>, Art. no. jacs. 5c06190, 2025, doi: <a href=\"https://doi.org/10.1021/jacs.5c06190\">10.1021/jacs.5c06190</a>.","chicago":"Zhou, Rundong, Viktorija Medvaric, Thomas Werner, and Jan Paradies. “Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance.” <i>Journal of the American Chemical Society</i>, 2025. <a href=\"https://doi.org/10.1021/jacs.5c06190\">https://doi.org/10.1021/jacs.5c06190</a>.","ama":"Zhou R, Medvaric V, Werner T, Paradies J. Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance. <i>Journal of the American Chemical Society</i>. Published online 2025. doi:<a href=\"https://doi.org/10.1021/jacs.5c06190\">10.1021/jacs.5c06190</a>"},"year":"2025","date_created":"2025-09-17T15:18:11Z","author":[{"full_name":"Zhou, Rundong","last_name":"Zhou","first_name":"Rundong"},{"first_name":"Viktorija","id":"92677","full_name":"Medvaric, Viktorija","last_name":"Medvaric"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"https://orcid.org/0000-0001-9025-3244"},{"id":"53339","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","first_name":"Jan"}],"date_updated":"2025-11-10T08:43:50Z","publisher":"American Chemical Society (ACS)","doi":"10.1021/jacs.5c06190","title":"Metal-Free Reduction of Nitrous Oxide via P<sup>III</sup>/P<sup>V</sup>═O Cycling: Mechanistic Insights and Catalytic Performance"}]