[{"doi":"10.1002/ejoc.202301207","date_updated":"2024-03-13T17:17:37Z","language":[{"iso":"eng"}],"title":"A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes","publication_status":"published","publication_identifier":{"issn":["1434-193X","1099-0690"]},"department":[{"_id":"2"},{"_id":"389"}],"issue":"8","intvolume":" 27","_id":"52541","year":"2024","type":"journal_article","citation":{"bibtex":"@article{Peschtrich_Schoch_Kuckling_Paradies_2024, title={A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes}, volume={27}, DOI={10.1002/ejoc.202301207}, number={8}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Peschtrich, Sebastian and Schoch, Roland and Kuckling, Dirk and Paradies, Jan}, year={2024} }","mla":"Peschtrich, Sebastian, et al. “A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes.” European Journal of Organic Chemistry, vol. 27, no. 8, Wiley, 2024, doi:10.1002/ejoc.202301207.","chicago":"Peschtrich, Sebastian, Roland Schoch, Dirk Kuckling, and Jan Paradies. “A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes.” European Journal of Organic Chemistry 27, no. 8 (2024). https://doi.org/10.1002/ejoc.202301207.","ama":"Peschtrich S, Schoch R, Kuckling D, Paradies J. A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes. European Journal of Organic Chemistry. 2024;27(8). doi:10.1002/ejoc.202301207","apa":"Peschtrich, S., Schoch, R., Kuckling, D., & Paradies, J. (2024). A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes. European Journal of Organic Chemistry, 27(8). https://doi.org/10.1002/ejoc.202301207","ieee":"S. Peschtrich, R. Schoch, D. Kuckling, and J. Paradies, “A Comparative Kinetic and Computational Investigation of the Carbon‐Sulfur Cross Coupling of Potassium Thioacetate and 2‐Bromo Thiophene Using Palladium/Bisphosphine Complexes,” European Journal of Organic Chemistry, vol. 27, no. 8, 2024, doi: 10.1002/ejoc.202301207.","short":"S. Peschtrich, R. Schoch, D. Kuckling, J. Paradies, European Journal of Organic Chemistry 27 (2024)."},"user_id":"53339","abstract":[{"lang":"eng","text":"AbstractWe conducted an investigation into the palladium‐catalyzed carbon‐sulfur cross‐coupling reaction involving a 2‐bromothiophene derivative and potassium thioacetate as a substitute for hydrogen sulfide. This investigation utilized kinetic and computational methods. We synthesized two palladium complexes supported by the bisphosphane ligands bis(diphenylphosphino)ferrocene (DPPF) and bis(diisopropylphosphino)ferrocene (DiPPF), as well as their tentative intermediates in the catalytic cycle. Reaction rates were measured and then compared to computational predictions."}],"status":"public","date_created":"2024-03-13T17:15:14Z","volume":27,"author":[{"last_name":"Peschtrich","first_name":"Sebastian","full_name":"Peschtrich, Sebastian"},{"full_name":"Schoch, Roland","orcid":"0000-0003-2061-7289","first_name":"Roland","id":"48467","last_name":"Schoch"},{"full_name":"Kuckling, Dirk","first_name":"Dirk","id":"287","last_name":"Kuckling"},{"id":"53339","last_name":"Paradies","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"publisher":"Wiley","keyword":["Organic Chemistry","Physical and Theoretical Chemistry"],"publication":"European Journal of Organic Chemistry"},{"doi":"10.1002/ejic.202400057","_id":"52572","date_updated":"2024-03-14T07:10:37Z","language":[{"iso":"eng"}],"citation":{"bibtex":"@article{Köring_Birenheide_Krämer_Wenzel_Schoch_Brehm_Breher_Paradies_2024, title={Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements}, DOI={10.1002/ejic.202400057}, journal={European Journal of Inorganic Chemistry}, publisher={Wiley}, author={Köring, Laura and Birenheide, Bernhard and Krämer, Felix and Wenzel, Jonas O. and Schoch, Roland and Brehm, Martin and Breher, Frank and Paradies, Jan}, year={2024} }","mla":"Köring, Laura, et al. “Synthesis of Ferrocenyl Boranes and Their Application as Lewis Acids in Epoxide Rearrangements.” European Journal of Inorganic Chemistry, Wiley, 2024, doi:10.1002/ejic.202400057.","ama":"Köring L, Birenheide B, Krämer F, et al. Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements. European Journal of Inorganic Chemistry. Published online 2024. doi:10.1002/ejic.202400057","apa":"Köring, L., Birenheide, B., Krämer, F., Wenzel, J. O., Schoch, R., Brehm, M., Breher, F., & Paradies, J. (2024). Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements. European Journal of Inorganic Chemistry. https://doi.org/10.1002/ejic.202400057","chicago":"Köring, Laura, Bernhard Birenheide, Felix Krämer, Jonas O. Wenzel, Roland Schoch, Martin Brehm, Frank Breher, and Jan Paradies. “Synthesis of Ferrocenyl Boranes and Their Application as Lewis Acids in Epoxide Rearrangements.” European Journal of Inorganic Chemistry, 2024. https://doi.org/10.1002/ejic.202400057.","ieee":"L. Köring et al., “Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements,” European Journal of Inorganic Chemistry, 2024, doi: 10.1002/ejic.202400057.","short":"L. Köring, B. Birenheide, F. Krämer, J.O. Wenzel, R. Schoch, M. Brehm, F. Breher, J. Paradies, European Journal of Inorganic Chemistry (2024)."},"year":"2024","type":"journal_article","user_id":"53339","title":"Synthesis of Ferrocenyl Boranes and their Application as Lewis Acids in Epoxide Rearrangements","abstract":[{"text":"A series of substituted ferrocenyl boron derivatives was synthesized. The oxidation of the ferrocenyl unit resulted in a significant increase of the boron‐centered Lewis acidity. The neutral and cationic Lewis acids were characterized by NMR‐spectroscopy, crystal structure analysis and by computational methods. The new Lewis acids were then applied in the Meinwald rearrangement of epoxides, predominantly furnishing aldehydes as the kinetic products.","lang":"eng"}],"status":"public","date_created":"2024-03-14T07:09:09Z","publication_status":"published","publication_identifier":{"issn":["1434-1948","1099-0682"]},"author":[{"last_name":"Köring","first_name":"Laura","full_name":"Köring, Laura"},{"last_name":"Birenheide","full_name":"Birenheide, Bernhard","first_name":"Bernhard"},{"first_name":"Felix","full_name":"Krämer, Felix","last_name":"Krämer"},{"full_name":"Wenzel, Jonas O.","first_name":"Jonas O.","last_name":"Wenzel"},{"last_name":"Schoch","id":"48467","first_name":"Roland","full_name":"Schoch, Roland","orcid":"0000-0003-2061-7289"},{"last_name":"Brehm","id":"100167","first_name":"Martin","full_name":"Brehm, Martin"},{"last_name":"Breher","full_name":"Breher, Frank","first_name":"Frank"},{"orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","first_name":"Jan","id":"53339","last_name":"Paradies"}],"publisher":"Wiley","publication":"European Journal of Inorganic Chemistry","department":[{"_id":"2"},{"_id":"389"}],"keyword":["Inorganic Chemistry"]},{"title":"Stimuli‐accelerated polymeric drug delivery systems","department":[{"_id":"163"}],"publication_status":"published","publication_identifier":{"issn":["0959-8103","1097-0126"]},"date_updated":"2023-01-10T08:31:31Z","doi":"10.1002/pi.6474","language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"The controlled delivery of active pharmaceutical ingredients to the site of disease represents a major challenge in drug therapy. Particularly when drugs have to be transported across biological barriers, suitable drug delivery systems are of importance. In recent years responsive delivery systems have been developed which enable a controlled drug release depending on internal or external stimuli such as changes in pH, redox environment or light and temperature. In some studies delivery systems with reactivity against two different stimuli were established either to enhance the response by synergies of the stimuli or to broaden the window of possible trigger events. In the present review numerous exciting developments of pH-, light- and redox-cleavable polymers suitable for the preparation of smart delivery systems are described. The review discusses the different stimuli that can be used for a controlled drug release of polymer-based delivery systems. It puts a focus on the different polymers described for the preparation of stimuli-sensitive systems, their preparation techniques as well as their stimuli-responsive degradation. © 2022 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry."}],"article_type":"original","user_id":"94","publication":"Polymer International","keyword":["drug delivery system","stimuli","polymer","cleavable"],"author":[{"last_name":"Rust","full_name":"Rust, Tarik","first_name":"Tarik"},{"first_name":"Dimitri","full_name":"Jung, Dimitri","last_name":"Jung"},{"first_name":"Klaus","full_name":"Langer, Klaus","last_name":"Langer"},{"last_name":"Kuckling","id":"287","first_name":"Dirk","full_name":"Kuckling, Dirk"}],"publisher":"Wiley","date_created":"2023-01-10T08:25:22Z","status":"public","volume":72,"_id":"35657","intvolume":" 72","issue":"1","main_file_link":[{"url":"https://onlinelibrary.wiley.com/doi/10.1002/pi.6474"}],"page":"5-19","citation":{"ama":"Rust T, Jung D, Langer K, Kuckling D. Stimuli‐accelerated polymeric drug delivery systems. Polymer International. 2023;72(1):5-19. doi:10.1002/pi.6474","apa":"Rust, T., Jung, D., Langer, K., & Kuckling, D. (2023). Stimuli‐accelerated polymeric drug delivery systems. Polymer International, 72(1), 5–19. https://doi.org/10.1002/pi.6474","chicago":"Rust, Tarik, Dimitri Jung, Klaus Langer, and Dirk Kuckling. “Stimuli‐accelerated Polymeric Drug Delivery Systems.” Polymer International 72, no. 1 (2023): 5–19. https://doi.org/10.1002/pi.6474.","mla":"Rust, Tarik, et al. “Stimuli‐accelerated Polymeric Drug Delivery Systems.” Polymer International, vol. 72, no. 1, Wiley, 2023, pp. 5–19, doi:10.1002/pi.6474.","bibtex":"@article{Rust_Jung_Langer_Kuckling_2023, title={Stimuli‐accelerated polymeric drug delivery systems}, volume={72}, DOI={10.1002/pi.6474}, number={1}, journal={Polymer International}, publisher={Wiley}, author={Rust, Tarik and Jung, Dimitri and Langer, Klaus and Kuckling, Dirk}, year={2023}, pages={5–19} }","short":"T. Rust, D. Jung, K. Langer, D. Kuckling, Polymer International 72 (2023) 5–19.","ieee":"T. Rust, D. Jung, K. Langer, and D. Kuckling, “Stimuli‐accelerated polymeric drug delivery systems,” Polymer International, vol. 72, no. 1, pp. 5–19, 2023, doi: 10.1002/pi.6474."},"type":"journal_article","year":"2023"},{"status":"public","date_created":"2023-03-08T19:27:25Z","publication_identifier":{"issn":["1433-7851","1521-3773"]},"publication_status":"published","publisher":"Wiley","author":[{"last_name":"Köring","first_name":"Laura","full_name":"Köring, Laura"},{"last_name":"Stepen","full_name":"Stepen, Arne","first_name":"Arne"},{"full_name":"Birenheide, Bernhard","first_name":"Bernhard","last_name":"Birenheide"},{"last_name":"Barth","full_name":"Barth, Simon","first_name":"Simon"},{"full_name":"Leskov, Maxim","first_name":"Maxim","last_name":"Leskov"},{"full_name":"Schoch, Roland","first_name":"Roland","last_name":"Schoch"},{"last_name":"Krämer","full_name":"Krämer, Felix","first_name":"Felix"},{"full_name":"Breher, Frank","first_name":"Frank","last_name":"Breher"},{"last_name":"Paradies","id":"53339","first_name":"Jan","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X"}],"keyword":["General Chemistry","Catalysis"],"department":[{"_id":"2"},{"_id":"389"}],"publication":"Angewandte Chemie International Edition","user_id":"53339","title":"Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation","language":[{"iso":"eng"}],"citation":{"bibtex":"@article{Köring_Stepen_Birenheide_Barth_Leskov_Schoch_Krämer_Breher_Paradies_2023, title={Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation}, DOI={10.1002/anie.202301632}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Köring, Laura and Stepen, Arne and Birenheide, Bernhard and Barth, Simon and Leskov, Maxim and Schoch, Roland and Krämer, Felix and Breher, Frank and Paradies, Jan}, year={2023} }","mla":"Köring, Laura, et al. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” Angewandte Chemie International Edition, Wiley, 2023, doi:10.1002/anie.202301632.","chicago":"Köring, Laura, Arne Stepen, Bernhard Birenheide, Simon Barth, Maxim Leskov, Roland Schoch, Felix Krämer, Frank Breher, and Jan Paradies. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” Angewandte Chemie International Edition, 2023. https://doi.org/10.1002/anie.202301632.","ama":"Köring L, Stepen A, Birenheide B, et al. Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation. Angewandte Chemie International Edition. Published online 2023. doi:10.1002/anie.202301632","apa":"Köring, L., Stepen, A., Birenheide, B., Barth, S., Leskov, M., Schoch, R., Krämer, F., Breher, F., & Paradies, J. (2023). Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.202301632","ieee":"L. Köring et al., “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation,” Angewandte Chemie International Edition, 2023, doi: 10.1002/anie.202301632.","short":"L. Köring, A. Stepen, B. Birenheide, S. Barth, M. Leskov, R. Schoch, F. Krämer, F. Breher, J. Paradies, Angewandte Chemie International Edition (2023)."},"year":"2023","type":"journal_article","doi":"10.1002/anie.202301632","_id":"42878","date_updated":"2023-03-08T19:31:59Z"},{"language":[{"iso":"eng"}],"citation":{"short":"L. Köring, A. Stepen, B. Birenheide, S. Barth, M. Leskov, R. Schoch, F. Krämer, F. Breher, J. Paradies, Angewandte Chemie (2023).","ieee":"L. Köring et al., “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation,” Angewandte Chemie, 2023, doi: 10.1002/ange.202301632.","apa":"Köring, L., Stepen, A., Birenheide, B., Barth, S., Leskov, M., Schoch, R., Krämer, F., Breher, F., & Paradies, J. (2023). Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation. Angewandte Chemie. https://doi.org/10.1002/ange.202301632","ama":"Köring L, Stepen A, Birenheide B, et al. Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation. Angewandte Chemie. Published online 2023. doi:10.1002/ange.202301632","chicago":"Köring, Laura, Arne Stepen, Bernhard Birenheide, Simon Barth, Maxim Leskov, Roland Schoch, Felix Krämer, Frank Breher, and Jan Paradies. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” Angewandte Chemie, 2023. https://doi.org/10.1002/ange.202301632.","bibtex":"@article{Köring_Stepen_Birenheide_Barth_Leskov_Schoch_Krämer_Breher_Paradies_2023, title={Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation}, DOI={10.1002/ange.202301632}, journal={Angewandte Chemie}, publisher={Wiley}, author={Köring, Laura and Stepen, Arne and Birenheide, Bernhard and Barth, Simon and Leskov, Maxim and Schoch, Roland and Krämer, Felix and Breher, Frank and Paradies, Jan}, year={2023} }","mla":"Köring, Laura, et al. “Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation.” Angewandte Chemie, Wiley, 2023, doi:10.1002/ange.202301632."},"year":"2023","type":"journal_article","doi":"10.1002/ange.202301632","date_updated":"2023-03-08T19:32:09Z","_id":"42879","date_created":"2023-03-08T19:31:03Z","status":"public","publication_identifier":{"issn":["0044-8249","1521-3757"]},"publication_status":"published","publication":"Angewandte Chemie","department":[{"_id":"2"},{"_id":"389"}],"keyword":["General Medicine"],"publisher":"Wiley","author":[{"first_name":"Laura","full_name":"Köring, Laura","last_name":"Köring"},{"full_name":"Stepen, Arne","first_name":"Arne","last_name":"Stepen"},{"first_name":"Bernhard","full_name":"Birenheide, Bernhard","last_name":"Birenheide"},{"first_name":"Simon","full_name":"Barth, Simon","last_name":"Barth"},{"full_name":"Leskov, Maxim","first_name":"Maxim","last_name":"Leskov"},{"last_name":"Schoch","full_name":"Schoch, Roland","first_name":"Roland"},{"last_name":"Krämer","full_name":"Krämer, Felix","first_name":"Felix"},{"last_name":"Breher","full_name":"Breher, Frank","first_name":"Frank"},{"id":"53339","last_name":"Paradies","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","first_name":"Jan"}],"user_id":"53339","title":"Boron‐Centered Lewis Superacid through Redox‐Active Ligands: Application in C−F and S−F Bond Activation"},{"issue":"7","intvolume":" 56","_id":"44523","page":"821-834","year":"2023","type":"journal_article","citation":{"ieee":"J. Paradies, “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations,” Accounts of Chemical Research, vol. 56, no. 7, pp. 821–834, 2023, doi: 10.1021/acs.accounts.2c00832.","short":"J. Paradies, Accounts of Chemical Research 56 (2023) 821–834.","mla":"Paradies, Jan. “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations.” Accounts of Chemical Research, vol. 56, no. 7, American Chemical Society (ACS), 2023, pp. 821–34, doi:10.1021/acs.accounts.2c00832.","bibtex":"@article{Paradies_2023, title={Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations}, volume={56}, DOI={10.1021/acs.accounts.2c00832}, number={7}, journal={Accounts of Chemical Research}, publisher={American Chemical Society (ACS)}, author={Paradies, Jan}, year={2023}, pages={821–834} }","chicago":"Paradies, Jan. “Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations.” Accounts of Chemical Research 56, no. 7 (2023): 821–34. https://doi.org/10.1021/acs.accounts.2c00832.","apa":"Paradies, J. (2023). Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations. Accounts of Chemical Research, 56(7), 821–834. https://doi.org/10.1021/acs.accounts.2c00832","ama":"Paradies J. Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations. Accounts of Chemical Research. 2023;56(7):821-834. doi:10.1021/acs.accounts.2c00832"},"user_id":"53339","volume":56,"date_created":"2023-05-05T13:25:50Z","status":"public","publication":"Accounts of Chemical Research","keyword":["General Medicine","General Chemistry"],"author":[{"id":"53339","last_name":"Paradies","full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","first_name":"Jan"}],"publisher":"American Chemical Society (ACS)","doi":"10.1021/acs.accounts.2c00832","date_updated":"2023-05-05T13:27:06Z","language":[{"iso":"eng"}],"title":"Structure–Reactivity Relationships in Borane-Based FLP-Catalyzed Hydrogenations, Dehydrogenations, and Cycloisomerizations","publication_identifier":{"issn":["0001-4842","1520-4898"]},"publication_status":"published","department":[{"_id":"2"},{"_id":"389"}]},{"doi":"10.1002/anie.202308752","date_updated":"2023-08-03T09:01:41Z","_id":"46277","year":"2023","citation":{"chicago":"Sieland, Benedikt, Marcel Stahn, Roland Schoch, Constantin Daniliuc, Sebastian Spicher, Stefan Grimme, Andreas Hansen, and Jan Paradies. “Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs.” Angewandte Chemie International Edition, 2023. https://doi.org/10.1002/anie.202308752.","ama":"Sieland B, Stahn M, Schoch R, et al. Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs. Angewandte Chemie International Edition. Published online 2023. doi:10.1002/anie.202308752","apa":"Sieland, B., Stahn, M., Schoch, R., Daniliuc, C., Spicher, S., Grimme, S., Hansen, A., & Paradies, J. (2023). Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.202308752","mla":"Sieland, Benedikt, et al. “Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs.” Angewandte Chemie International Edition, Wiley, 2023, doi:10.1002/anie.202308752.","bibtex":"@article{Sieland_Stahn_Schoch_Daniliuc_Spicher_Grimme_Hansen_Paradies_2023, title={Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs}, DOI={10.1002/anie.202308752}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Sieland, Benedikt and Stahn, Marcel and Schoch, Roland and Daniliuc, Constantin and Spicher, Sebastian and Grimme, Stefan and Hansen, Andreas and Paradies, Jan}, year={2023} }","short":"B. Sieland, M. Stahn, R. Schoch, C. Daniliuc, S. Spicher, S. Grimme, A. Hansen, J. Paradies, Angewandte Chemie International Edition (2023).","ieee":"B. Sieland et al., “Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs,” Angewandte Chemie International Edition, 2023, doi: 10.1002/anie.202308752."},"type":"journal_article","language":[{"iso":"eng"}],"title":"Dispersion Energy‐Stabilized Boron and Phosphorus Lewis Pairs","user_id":"53339","publication_status":"published","publication_identifier":{"issn":["1433-7851","1521-3773"]},"status":"public","date_created":"2023-08-03T09:00:33Z","author":[{"first_name":"Benedikt","full_name":"Sieland, Benedikt","last_name":"Sieland"},{"full_name":"Stahn, Marcel","first_name":"Marcel","last_name":"Stahn"},{"last_name":"Schoch","first_name":"Roland","full_name":"Schoch, Roland"},{"first_name":"Constantin","full_name":"Daniliuc, Constantin","last_name":"Daniliuc"},{"full_name":"Spicher, Sebastian","first_name":"Sebastian","last_name":"Spicher"},{"full_name":"Grimme, Stefan","first_name":"Stefan","last_name":"Grimme"},{"full_name":"Hansen, Andreas","first_name":"Andreas","last_name":"Hansen"},{"first_name":"Jan","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","last_name":"Paradies","id":"53339"}],"publisher":"Wiley","keyword":["General Chemistry","Catalysis"],"publication":"Angewandte Chemie International Edition","department":[{"_id":"2"},{"_id":"389"}]},{"user_id":"53339","title":"A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media","department":[{"_id":"2"},{"_id":"389"}],"keyword":["General Chemical Engineering","General Chemistry"],"publication":"Nature Chemistry","author":[{"last_name":"Krämer","first_name":"Felix","full_name":"Krämer, Felix"},{"full_name":"Paradies, Jan","orcid":"0000-0002-3698-668X","first_name":"Jan","id":"53339","last_name":"Paradies"},{"last_name":"Fernández","full_name":"Fernández, Israel","first_name":"Israel"},{"last_name":"Breher","first_name":"Frank","full_name":"Breher, Frank"}],"publisher":"Springer Science and Business Media LLC","date_created":"2023-10-04T14:40:07Z","status":"public","publication_identifier":{"issn":["1755-4330","1755-4349"]},"publication_status":"published","_id":"47589","date_updated":"2023-10-04T14:41:12Z","doi":"10.1038/s41557-023-01340-9","language":[{"iso":"eng"}],"citation":{"apa":"Krämer, F., Paradies, J., Fernández, I., & Breher, F. (2023). A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media. Nature Chemistry. https://doi.org/10.1038/s41557-023-01340-9","ama":"Krämer F, Paradies J, Fernández I, Breher F. A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media. Nature Chemistry. Published online 2023. doi:10.1038/s41557-023-01340-9","chicago":"Krämer, Felix, Jan Paradies, Israel Fernández, and Frank Breher. “A Crystalline Aluminium–Carbon-Based Ambiphile Capable of Activation and Catalytic Transfer of Ammonia in Non-Aqueous Media.” Nature Chemistry, 2023. https://doi.org/10.1038/s41557-023-01340-9.","mla":"Krämer, Felix, et al. “A Crystalline Aluminium–Carbon-Based Ambiphile Capable of Activation and Catalytic Transfer of Ammonia in Non-Aqueous Media.” Nature Chemistry, Springer Science and Business Media LLC, 2023, doi:10.1038/s41557-023-01340-9.","bibtex":"@article{Krämer_Paradies_Fernández_Breher_2023, title={A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media}, DOI={10.1038/s41557-023-01340-9}, journal={Nature Chemistry}, publisher={Springer Science and Business Media LLC}, author={Krämer, Felix and Paradies, Jan and Fernández, Israel and Breher, Frank}, year={2023} }","short":"F. Krämer, J. Paradies, I. Fernández, F. Breher, Nature Chemistry (2023).","ieee":"F. Krämer, J. Paradies, I. Fernández, and F. Breher, “A crystalline aluminium–carbon-based ambiphile capable of activation and catalytic transfer of ammonia in non-aqueous media,” Nature Chemistry, 2023, doi: 10.1038/s41557-023-01340-9."},"year":"2023","type":"journal_article"},{"date_created":"2024-03-13T17:17:52Z","status":"public","volume":30,"publication":"Chemistry – A European Journal","keyword":["General Chemistry","Catalysis","Organic Chemistry"],"author":[{"last_name":"Krämer","first_name":"Felix","full_name":"Krämer, Felix"},{"last_name":"Paradies","id":"53339","first_name":"Jan","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan"},{"full_name":"Fernández, Israel","first_name":"Israel","last_name":"Fernández"},{"last_name":"Breher","full_name":"Breher, Frank","first_name":"Frank"}],"publisher":"Wiley","user_id":"53339","abstract":[{"lang":"eng","text":"AbstractWe report on so‐called “hidden FLPs” (FLP: frustrated Lewis pair) consisting of a phosphorus ylide featuring a group 13 fragment in the ortho position of a phenyl ring scaffold to form five‐membered ring structures. Although the formation of the Lewis acid/base adducts was observed in the solid state, most of the title compounds readily react with carbon dioxide to provide stable insertion products. Strikingly, 0.3–3.0 mol% of the reported aluminum and gallium/carbon‐based ambiphiles catalyze the reduction of CO2 to methanol with satisfactory high selectivity and yields using pinacol borane as stoichiometric reduction equivalent. Comprehensive computational studies provided valuable mechanistic insights and shed more light on activity differences."}],"year":"2023","type":"journal_article","citation":{"mla":"Krämer, Felix, et al. “Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles.” Chemistry – A European Journal, vol. 30, no. 5, Wiley, 2023, doi:10.1002/chem.202303380.","bibtex":"@article{Krämer_Paradies_Fernández_Breher_2023, title={Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles}, volume={30}, DOI={10.1002/chem.202303380}, number={5}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Krämer, Felix and Paradies, Jan and Fernández, Israel and Breher, Frank}, year={2023} }","ama":"Krämer F, Paradies J, Fernández I, Breher F. Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles. Chemistry – A European Journal. 2023;30(5). doi:10.1002/chem.202303380","apa":"Krämer, F., Paradies, J., Fernández, I., & Breher, F. (2023). Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles. Chemistry – A European Journal, 30(5). https://doi.org/10.1002/chem.202303380","chicago":"Krämer, Felix, Jan Paradies, Israel Fernández, and Frank Breher. “Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles.” Chemistry – A European Journal 30, no. 5 (2023). https://doi.org/10.1002/chem.202303380.","ieee":"F. Krämer, J. Paradies, I. Fernández, and F. Breher, “Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles,” Chemistry – A European Journal, vol. 30, no. 5, 2023, doi: 10.1002/chem.202303380.","short":"F. Krämer, J. Paradies, I. Fernández, F. Breher, Chemistry – A European Journal 30 (2023)."},"issue":"5","intvolume":" 30","_id":"52542","publication_identifier":{"issn":["0947-6539","1521-3765"]},"publication_status":"published","department":[{"_id":"2"},{"_id":"389"}],"title":"Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles","language":[{"iso":"eng"}],"doi":"10.1002/chem.202303380","date_updated":"2024-03-13T17:18:17Z"},{"issue":"12","article_number":"768","intvolume":" 8","_id":"35642","citation":{"bibtex":"@article{Völlmecke_Afroz_Bierbach_Brenker_Frücht_Glass_Giebelhaus_Hoppe_Kanemaru_Lazarek_et al._2022, title={Hydrogel-Based Biosensors}, volume={8}, DOI={10.3390/gels8120768}, number={12768}, journal={Gels}, publisher={MDPI AG}, author={Völlmecke, Katharina and Afroz, Rowshon and Bierbach, Sascha and Brenker, Lee Josephine and Frücht, Sebastian and Glass, Alexandra and Giebelhaus, Ryland and Hoppe, Axel and Kanemaru, Karen and Lazarek, Michal and et al.}, year={2022} }","mla":"Völlmecke, Katharina, et al. “Hydrogel-Based Biosensors.” Gels, vol. 8, no. 12, 768, MDPI AG, 2022, doi:10.3390/gels8120768.","chicago":"Völlmecke, Katharina, Rowshon Afroz, Sascha Bierbach, Lee Josephine Brenker, Sebastian Frücht, Alexandra Glass, Ryland Giebelhaus, et al. “Hydrogel-Based Biosensors.” Gels 8, no. 12 (2022). https://doi.org/10.3390/gels8120768.","apa":"Völlmecke, K., Afroz, R., Bierbach, S., Brenker, L. J., Frücht, S., Glass, A., Giebelhaus, R., Hoppe, A., Kanemaru, K., Lazarek, M., Rabbe, L., Song, L., Velasco Suarez, A., Wu, S., Serpe, M., & Kuckling, D. (2022). Hydrogel-Based Biosensors. Gels, 8(12), Article 768. https://doi.org/10.3390/gels8120768","ama":"Völlmecke K, Afroz R, Bierbach S, et al. Hydrogel-Based Biosensors. Gels. 2022;8(12). doi:10.3390/gels8120768","ieee":"K. Völlmecke et al., “Hydrogel-Based Biosensors,” Gels, vol. 8, no. 12, Art. no. 768, 2022, doi: 10.3390/gels8120768.","short":"K. Völlmecke, R. Afroz, S. Bierbach, L.J. Brenker, S. Frücht, A. Glass, R. Giebelhaus, A. Hoppe, K. Kanemaru, M. Lazarek, L. Rabbe, L. Song, A. Velasco Suarez, S. Wu, M. Serpe, D. Kuckling, Gels 8 (2022)."},"type":"journal_article","year":"2022","main_file_link":[{"url":"https://www.mdpi.com/2310-2861/8/12/768"}],"user_id":"94","article_type":"review","abstract":[{"text":"There is an increasing interest in sensing applications for a variety of analytes in aqueous environments, as conventional methods do not work reliably under humid conditions or they require complex equipment with experienced operators. Hydrogel sensors are easy to fabricate, are incredibly sensitive, and have broad dynamic ranges. Experiments on their robustness, reliability, and reusability have indicated the possible long-term applications of these systems in a variety of fields, including disease diagnosis, detection of pharmaceuticals, and in environmental testing. It is possible to produce hydrogels, which, upon sensing a specific analyte, can adsorb it onto their 3D-structure and can therefore be used to remove them from a given environment. High specificity can be obtained by using molecularly imprinted polymers. Typical detection principles involve optical methods including fluorescence and chemiluminescence, and volume changes in colloidal photonic crystals, as well as electrochemical methods. Here, we explore the current research utilizing hydrogel-based sensors in three main areas: (1) biomedical applications, (2) for detecting and quantifying pharmaceuticals of interest, and (3) detecting and quantifying environmental contaminants in aqueous environments.","lang":"eng"}],"status":"public","date_created":"2023-01-10T08:02:50Z","volume":8,"publisher":"MDPI AG","author":[{"last_name":"Völlmecke","full_name":"Völlmecke, Katharina","first_name":"Katharina"},{"full_name":"Afroz, Rowshon","first_name":"Rowshon","last_name":"Afroz"},{"last_name":"Bierbach","first_name":"Sascha","full_name":"Bierbach, Sascha"},{"full_name":"Brenker, Lee Josephine","first_name":"Lee Josephine","last_name":"Brenker"},{"last_name":"Frücht","first_name":"Sebastian","full_name":"Frücht, Sebastian"},{"last_name":"Glass","full_name":"Glass, Alexandra","first_name":"Alexandra"},{"last_name":"Giebelhaus","first_name":"Ryland","full_name":"Giebelhaus, Ryland"},{"full_name":"Hoppe, Axel","first_name":"Axel","last_name":"Hoppe"},{"full_name":"Kanemaru, Karen","first_name":"Karen","last_name":"Kanemaru"},{"last_name":"Lazarek","first_name":"Michal","full_name":"Lazarek, Michal"},{"last_name":"Rabbe","full_name":"Rabbe, Lukas","first_name":"Lukas"},{"first_name":"Longfei","full_name":"Song, Longfei","last_name":"Song"},{"first_name":"Andrea","full_name":"Velasco Suarez, Andrea","last_name":"Velasco Suarez"},{"full_name":"Wu, Shuang","first_name":"Shuang","last_name":"Wu"},{"first_name":"Michael","full_name":"Serpe, Michael","last_name":"Serpe"},{"id":"287","last_name":"Kuckling","full_name":"Kuckling, Dirk","first_name":"Dirk"}],"keyword":["Polymers and Plastics","Organic Chemistry","Biomaterials","Bioengineering"],"publication":"Gels","doi":"10.3390/gels8120768","date_updated":"2023-01-10T08:05:30Z","language":[{"iso":"eng"}],"title":"Hydrogel-Based Biosensors","publication_identifier":{"issn":["2310-2861"]},"publication_status":"published","department":[{"_id":"163"}]},{"publisher":"Informa UK Limited","author":[{"first_name":"Marie-Theres","full_name":"Berg, Marie-Theres","last_name":"Berg"},{"last_name":"Herberg","id":"94","first_name":"Artjom","full_name":"Herberg, Artjom"},{"last_name":"Kuckling","id":"287","first_name":"Dirk","full_name":"Kuckling, Dirk"}],"publication":"International Journal of Polymer Analysis and Characterization","keyword":["Ultra-high-performance liquid chromatography","ion mobility separation","mass spectrometry","LC-MS hyphenation","sequence-defined oligomers"],"status":"public","date_created":"2022-07-26T06:38:52Z","article_type":"original","abstract":[{"lang":"eng","text":"In recent years, sequence-defined oligomers (SDOs) gained increasing interest due to their perfectly controlled molecular structure, thus providing defined properties. In order to tune the properties, different functionalities need to be incorporated into the oligomers and the chain tacticity needs to be controlled. Beside the synthesis of SDOs, suitable methods need to be found to analyze the molecular structure. In this work, oligomers exhibiting an alternating or block-wise sequence of side chain functionalities were analyzed using a hyphenation of ultra-high-performance liquid chromatography and electrospray ionization mass spectrometry enhanced by ion mobility separation (IMS). Moieties in the side chains were varied according to polarity and bulkiness. Moreover, chain tacticity was varied. Drift times in the IMS cell and the corresponding collision cross section (CCS) values were shown to be individual parameters allowing the identification of SDOs, even in the case that SDO structures only differ in sequence or tacticity of side chain functionalities. Thus, a library of CCS values was obtained as reference used for the analysis of complex mixtures of SDOs."}],"user_id":"94","citation":{"ieee":"M.-T. Berg, A. Herberg, and D. Kuckling, “Hyphenation of ultra-high-performance liquid chromatography and ion mobility mass spectrometry for the analysis of sequence-defined oligomers with different functionalities and tacticity,” International Journal of Polymer Analysis and Characterization, pp. 1–12, 2022, doi: 10.1080/1023666x.2022.2100968.","short":"M.-T. Berg, A. Herberg, D. Kuckling, International Journal of Polymer Analysis and Characterization (2022) 1–12.","bibtex":"@article{Berg_Herberg_Kuckling_2022, title={Hyphenation of ultra-high-performance liquid chromatography and ion mobility mass spectrometry for the analysis of sequence-defined oligomers with different functionalities and tacticity}, DOI={10.1080/1023666x.2022.2100968}, journal={International Journal of Polymer Analysis and Characterization}, publisher={Informa UK Limited}, author={Berg, Marie-Theres and Herberg, Artjom and Kuckling, Dirk}, year={2022}, pages={1–12} }","mla":"Berg, Marie-Theres, et al. “Hyphenation of Ultra-High-Performance Liquid Chromatography and Ion Mobility Mass Spectrometry for the Analysis of Sequence-Defined Oligomers with Different Functionalities and Tacticity.” International Journal of Polymer Analysis and Characterization, Informa UK Limited, 2022, pp. 1–12, doi:10.1080/1023666x.2022.2100968.","apa":"Berg, M.-T., Herberg, A., & Kuckling, D. (2022). Hyphenation of ultra-high-performance liquid chromatography and ion mobility mass spectrometry for the analysis of sequence-defined oligomers with different functionalities and tacticity. International Journal of Polymer Analysis and Characterization, 1–12. https://doi.org/10.1080/1023666x.2022.2100968","ama":"Berg M-T, Herberg A, Kuckling D. Hyphenation of ultra-high-performance liquid chromatography and ion mobility mass spectrometry for the analysis of sequence-defined oligomers with different functionalities and tacticity. International Journal of Polymer Analysis and Characterization. Published online 2022:1-12. doi:10.1080/1023666x.2022.2100968","chicago":"Berg, Marie-Theres, Artjom Herberg, and Dirk Kuckling. “Hyphenation of Ultra-High-Performance Liquid Chromatography and Ion Mobility Mass Spectrometry for the Analysis of Sequence-Defined Oligomers with Different Functionalities and Tacticity.” International Journal of Polymer Analysis and Characterization, 2022, 1–12. https://doi.org/10.1080/1023666x.2022.2100968."},"year":"2022","type":"journal_article","page":"1-12","_id":"32416","department":[{"_id":"163"}],"publication_identifier":{"issn":["1023-666X","1563-5341"]},"publication_status":"published","title":"Hyphenation of ultra-high-performance liquid chromatography and ion mobility mass spectrometry for the analysis of sequence-defined oligomers with different functionalities and tacticity","language":[{"iso":"eng"}],"date_updated":"2023-01-10T08:14:52Z","doi":"10.1080/1023666x.2022.2100968"},{"citation":{"mla":"Kumar, Amit, et al. “Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction.” ACS Applied Polymer Materials, vol. 4, no. 12, American Chemical Society (ACS), 2022, pp. 8996–9005, doi:10.1021/acsapm.2c01330.","bibtex":"@article{Kumar_Kuckling_Nebhani_2022, title={Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction}, volume={4}, DOI={10.1021/acsapm.2c01330}, number={12}, journal={ACS Applied Polymer Materials}, publisher={American Chemical Society (ACS)}, author={Kumar, Amit and Kuckling, Dirk and Nebhani, Leena}, year={2022}, pages={8996–9005} }","chicago":"Kumar, Amit, Dirk Kuckling, and Leena Nebhani. “Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction.” ACS Applied Polymer Materials 4, no. 12 (2022): 8996–9005. https://doi.org/10.1021/acsapm.2c01330.","ama":"Kumar A, Kuckling D, Nebhani L. Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction. ACS Applied Polymer Materials. 2022;4(12):8996-9005. doi:10.1021/acsapm.2c01330","apa":"Kumar, A., Kuckling, D., & Nebhani, L. (2022). Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction. ACS Applied Polymer Materials, 4(12), 8996–9005. https://doi.org/10.1021/acsapm.2c01330","ieee":"A. Kumar, D. Kuckling, and L. Nebhani, “Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction,” ACS Applied Polymer Materials, vol. 4, no. 12, pp. 8996–9005, 2022, doi: 10.1021/acsapm.2c01330.","short":"A. Kumar, D. Kuckling, L. Nebhani, ACS Applied Polymer Materials 4 (2022) 8996–9005."},"type":"journal_article","year":"2022","page":"8996-9005","main_file_link":[{"url":"https://pubs.acs.org/doi/10.1021/acsapm.2c01330"}],"issue":"12","_id":"35645","intvolume":" 4","volume":4,"status":"public","date_created":"2023-01-10T08:07:12Z","publisher":"American Chemical Society (ACS)","author":[{"last_name":"Kumar","full_name":"Kumar, Amit","first_name":"Amit"},{"id":"287","last_name":"Kuckling","full_name":"Kuckling, Dirk","first_name":"Dirk"},{"full_name":"Nebhani, Leena","first_name":"Leena","last_name":"Nebhani"}],"keyword":["distillation−precipitation polymerization","porous microparticles","heterogeneous catalysis Baylis−Hillman reaction","reusable catalyst"],"publication":"ACS Applied Polymer Materials","user_id":"94","article_type":"original","abstract":[{"lang":"eng","text":"Poly(quinuclidin-3-yl methacrylate-co-divinylbenzene) microparticles having porous as well as nonporous morphology and varying contents of quinuclidine functionality were synthesized by distillation–precipitation polymerization. Further, the synthesized microparticles were explored to catalyze the Baylis–Hillman reaction between 4-nitrobenzaldehyde and acrylonitrile. Porous and nonporous microparticles functionalized with a catalytic moiety with a loading of 70% (labeled as P70 and NP70) were employed to optimize reaction parameters such as water content, solvent, and temperature for the Baylis–Hillman reaction between 4-nitrobenzaldehyde and acrylonitrile. Using optimal conditions, the catalytic efficiency of porous and nonporous microparticles at different feed compositions was determined. Porous microparticles containing 70% of quinuclidine (P70) displayed 100% conversion within 16 h at 50 °C, while nonporous microparticles containing 70% of quinuclidine (NP70) displayed a relatively less catalytic conversion, which is attributed to their lower surface area. Furthermore, the catalytic activity of porous microparticles containing 70% of quinuclidine (P70) for the Baylis–Hillman reaction involving a variety of aryl aldehyde derivatives was determined, where the microparticles displayed impressive catalytic efficiency. In addition, the reusability of the microparticles functionalized with a catalytic moiety was evaluated for five cycles of catalytic reaction."}],"language":[{"iso":"eng"}],"doi":"10.1021/acsapm.2c01330","date_updated":"2023-01-10T08:12:15Z","publication_status":"published","publication_identifier":{"issn":["2637-6105","2637-6105"]},"department":[{"_id":"163"}],"title":"Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction"},{"date_created":"2022-08-17T06:28:55Z","status":"public","publication_status":"published","publication_identifier":{"issn":["1023-666X","1563-5341"]},"publication":"International Journal of Polymer Analysis and Characterization","department":[{"_id":"163"}],"keyword":["Size-exclusion chromatography","triple detection","branching analysis","star polymers","poly(N-isopropylacrylamide)","β-cyclodextrin"],"publisher":"Informa UK Limited","author":[{"full_name":"Herberg, Artjom","first_name":"Artjom","id":"94","last_name":"Herberg"},{"last_name":"Kuckling","id":"287","first_name":"Dirk","full_name":"Kuckling, Dirk"}],"user_id":"94","title":"Branching analysis of β-cyclodextrin-based poly(N-isopropylacrylamide) star polymers using triple detection SEC","abstract":[{"text":"For the first time, poly(N-isopropylacrylamide) (PNIPAAm) star polymers with a β-cyclodextrin core are characterized in detail by size-exclusion chromatography (SEC) with triple detection to experimentally verify the number of arms. A combination of a refractive index detector, multi-angle laser light scattering detector, and an online-viscosimeter was used for branching analysis. At first, the SEC system was calibrated and the detector setup was validated using linear polystyrene reference polymers. The applicability of the established triple detection SEC for branching analysis was shown by the analysis of two commercially available polystyrene star polymers. Due to the high molar masses of the star polymers, both the contraction ratio g and g′ could be determined independently, thus allowing the calculation of the viscosity shielding ratio ε. Finally, the branching analysis of the PNIPAAm star polymers could experimentally confirm the assumed arm number of up to 21 arms. Moreover, an increasingly compact molecular structure and the influence of the arm number on the viscosity shielding ratio could be shown.","lang":"eng"}],"language":[{"iso":"eng"}],"page":"1-19","type":"journal_article","year":"2022","citation":{"ama":"Herberg A, Kuckling D. Branching analysis of β-cyclodextrin-based poly(N-isopropylacrylamide) star polymers using triple detection SEC. International Journal of Polymer Analysis and Characterization. Published online 2022:1-19. doi:10.1080/1023666x.2022.2110133","apa":"Herberg, A., & Kuckling, D. (2022). Branching analysis of β-cyclodextrin-based poly(N-isopropylacrylamide) star polymers using triple detection SEC. International Journal of Polymer Analysis and Characterization, 1–19. https://doi.org/10.1080/1023666x.2022.2110133","chicago":"Herberg, Artjom, and Dirk Kuckling. “Branching Analysis of β-Cyclodextrin-Based Poly(N-Isopropylacrylamide) Star Polymers Using Triple Detection SEC.” International Journal of Polymer Analysis and Characterization, 2022, 1–19. https://doi.org/10.1080/1023666x.2022.2110133.","bibtex":"@article{Herberg_Kuckling_2022, title={Branching analysis of β-cyclodextrin-based poly(N-isopropylacrylamide) star polymers using triple detection SEC}, DOI={10.1080/1023666x.2022.2110133}, journal={International Journal of Polymer Analysis and Characterization}, publisher={Informa UK Limited}, author={Herberg, Artjom and Kuckling, Dirk}, year={2022}, pages={1–19} }","mla":"Herberg, Artjom, and Dirk Kuckling. “Branching Analysis of β-Cyclodextrin-Based Poly(N-Isopropylacrylamide) Star Polymers Using Triple Detection SEC.” International Journal of Polymer Analysis and Characterization, Informa UK Limited, 2022, pp. 1–19, doi:10.1080/1023666x.2022.2110133.","short":"A. Herberg, D. Kuckling, International Journal of Polymer Analysis and Characterization (2022) 1–19.","ieee":"A. Herberg and D. Kuckling, “Branching analysis of β-cyclodextrin-based poly(N-isopropylacrylamide) star polymers using triple detection SEC,” International Journal of Polymer Analysis and Characterization, pp. 1–19, 2022, doi: 10.1080/1023666x.2022.2110133."},"doi":"10.1080/1023666x.2022.2110133","date_updated":"2023-01-10T08:13:52Z","_id":"32865"},{"_id":"37942","intvolume":" 70","issue":"3","year":"2022","type":"journal_article","citation":{"ieee":"J. N. Andexer et al., “Trendbericht Organische Chemie 2022,” Nachrichten aus der Chemie, vol. 70, no. 3, pp. 42–69, 2022, doi: 10.1002/nadc.20224122453.","short":"J.N. Andexer, U. Beifuss, M. Brasholz, R. Breinbauer, M. Breugst, O. Dumele, M. Ernst, R. Ganardi, M. Giese, T.A.M. Gulder, W. Hüttel, S. Kath‐Schorr, K. Körber, M. Kordes, T. Lindel, C. Mück‐Lichtenfeld, J. Niemeyer, R. Pfau, F. Pfrengle, J. Pietruszka, J.L. Röckl, N. Schaschke, H. Sebode, M.O. Senge, B.F. Straub, J. Teichert, S.R. Waldvogel, T. Werner, C. Winter, Nachrichten Aus Der Chemie 70 (2022) 42–69.","bibtex":"@article{Andexer_Beifuss_Brasholz_Breinbauer_Breugst_Dumele_Ernst_Ganardi_Giese_Gulder_et al._2022, title={Trendbericht Organische Chemie 2022}, volume={70}, DOI={10.1002/nadc.20224122453}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Andexer, Jennifer N. and Beifuss, Uwe and Brasholz, Malte and Breinbauer, Rolf and Breugst, Martin and Dumele, Oliver and Ernst, Martin and Ganardi, Ruth and Giese, Michael and Gulder, Tobias A. M. and et al.}, year={2022}, pages={42–69} }","mla":"Andexer, Jennifer N., et al. “Trendbericht Organische Chemie 2022.” Nachrichten Aus Der Chemie, vol. 70, no. 3, Wiley, 2022, pp. 42–69, doi:10.1002/nadc.20224122453.","chicago":"Andexer, Jennifer N., Uwe Beifuss, Malte Brasholz, Rolf Breinbauer, Martin Breugst, Oliver Dumele, Martin Ernst, et al. “Trendbericht Organische Chemie 2022.” Nachrichten Aus Der Chemie 70, no. 3 (2022): 42–69. https://doi.org/10.1002/nadc.20224122453.","apa":"Andexer, J. N., Beifuss, U., Brasholz, M., Breinbauer, R., Breugst, M., Dumele, O., Ernst, M., Ganardi, R., Giese, M., Gulder, T. A. M., Hüttel, W., Kath‐Schorr, S., Körber, K., Kordes, M., Lindel, T., Mück‐Lichtenfeld, C., Niemeyer, J., Pfau, R., Pfrengle, F., … Winter, C. (2022). Trendbericht Organische Chemie 2022. Nachrichten Aus Der Chemie, 70(3), 42–69. https://doi.org/10.1002/nadc.20224122453","ama":"Andexer JN, Beifuss U, Brasholz M, et al. Trendbericht Organische Chemie 2022. Nachrichten aus der Chemie. 2022;70(3):42-69. doi:10.1002/nadc.20224122453"},"page":"42-69","user_id":"14931","publisher":"Wiley","author":[{"last_name":"Andexer","first_name":"Jennifer N.","full_name":"Andexer, Jennifer N."},{"last_name":"Beifuss","full_name":"Beifuss, Uwe","first_name":"Uwe"},{"full_name":"Brasholz, Malte","first_name":"Malte","last_name":"Brasholz"},{"full_name":"Breinbauer, Rolf","first_name":"Rolf","last_name":"Breinbauer"},{"last_name":"Breugst","first_name":"Martin","full_name":"Breugst, Martin"},{"first_name":"Oliver","full_name":"Dumele, Oliver","last_name":"Dumele"},{"first_name":"Martin","full_name":"Ernst, Martin","last_name":"Ernst"},{"first_name":"Ruth","full_name":"Ganardi, Ruth","last_name":"Ganardi"},{"last_name":"Giese","first_name":"Michael","full_name":"Giese, Michael"},{"full_name":"Gulder, Tobias A. M.","first_name":"Tobias A. M.","last_name":"Gulder"},{"full_name":"Hüttel, Wolfgang","first_name":"Wolfgang","last_name":"Hüttel"},{"full_name":"Kath‐Schorr, Stephanie","first_name":"Stephanie","last_name":"Kath‐Schorr"},{"first_name":"Karsten","full_name":"Körber, Karsten","last_name":"Körber"},{"last_name":"Kordes","full_name":"Kordes, Markus","first_name":"Markus"},{"last_name":"Lindel","full_name":"Lindel, Thomas","first_name":"Thomas"},{"last_name":"Mück‐Lichtenfeld","full_name":"Mück‐Lichtenfeld, Christian","first_name":"Christian"},{"last_name":"Niemeyer","first_name":"Jochen","full_name":"Niemeyer, Jochen"},{"first_name":"Roland","full_name":"Pfau, Roland","last_name":"Pfau"},{"last_name":"Pfrengle","full_name":"Pfrengle, Fabian","first_name":"Fabian"},{"last_name":"Pietruszka","full_name":"Pietruszka, Jörg","first_name":"Jörg"},{"last_name":"Röckl","first_name":"Johannes L.","full_name":"Röckl, Johannes L."},{"last_name":"Schaschke","first_name":"Norbert","full_name":"Schaschke, Norbert"},{"full_name":"Sebode, Hanna","first_name":"Hanna","last_name":"Sebode"},{"full_name":"Senge, Mathias O.","first_name":"Mathias O.","last_name":"Senge"},{"last_name":"Straub","full_name":"Straub, Bernd F.","first_name":"Bernd F."},{"first_name":"Johannes","full_name":"Teichert, Johannes","last_name":"Teichert"},{"last_name":"Waldvogel","full_name":"Waldvogel, Siegfried R.","first_name":"Siegfried R."},{"id":"89271","last_name":"Werner","full_name":"Werner, Thomas","first_name":"Thomas"},{"full_name":"Winter, Christian","first_name":"Christian","last_name":"Winter"}],"keyword":["General Chemical Engineering","General Chemistry"],"publication":"Nachrichten aus der Chemie","volume":70,"status":"public","date_created":"2023-01-22T20:22:02Z","date_updated":"2023-01-23T10:45:25Z","doi":"10.1002/nadc.20224122453","language":[{"iso":"eng"}],"title":"Trendbericht Organische Chemie 2022","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"publication_status":"published","publication_identifier":{"issn":["1439-9598","1868-0054"]}},{"language":[{"iso":"eng"}],"doi":"10.1021/acssuschemeng.2c03210","date_updated":"2023-01-23T10:46:08Z","publication_status":"published","publication_identifier":{"issn":["2168-0485","2168-0485"]},"department":[{"_id":"2"},{"_id":"657"}],"title":"Synthesis of Cyclic Carbonates Catalyzed by CaI2–Et3N and Studies on Their Biocatalytic Kinetic Resolution","year":"2022","citation":{"short":"C. Terazzi, K. Laatz, J. von Langermann, T. Werner, ACS Sustainable Chemistry and Engineering 10 (2022) 13335–13342.","ieee":"C. Terazzi, K. Laatz, J. von Langermann, and T. Werner, “Synthesis of Cyclic Carbonates Catalyzed by CaI2–Et3N and Studies on Their Biocatalytic Kinetic Resolution,” ACS Sustainable Chemistry and Engineering, vol. 10, no. 40, pp. 13335–13342, 2022, doi: 10.1021/acssuschemeng.2c03210.","ama":"Terazzi C, Laatz K, von Langermann J, Werner T. Synthesis of Cyclic Carbonates Catalyzed by CaI2–Et3N and Studies on Their Biocatalytic Kinetic Resolution. ACS Sustainable Chemistry and Engineering. 2022;10(40):13335-13342. doi:10.1021/acssuschemeng.2c03210","apa":"Terazzi, C., Laatz, K., von Langermann, J., & Werner, T. (2022). Synthesis of Cyclic Carbonates Catalyzed by CaI2–Et3N and Studies on Their Biocatalytic Kinetic Resolution. ACS Sustainable Chemistry and Engineering, 10(40), 13335–13342. https://doi.org/10.1021/acssuschemeng.2c03210","chicago":"Terazzi, Constanza, Karoline Laatz, Jan von Langermann, and Thomas Werner. “Synthesis of Cyclic Carbonates Catalyzed by CaI2–Et3N and Studies on Their Biocatalytic Kinetic Resolution.” ACS Sustainable Chemistry and Engineering 10, no. 40 (2022): 13335–42. https://doi.org/10.1021/acssuschemeng.2c03210.","mla":"Terazzi, Constanza, et al. “Synthesis of Cyclic Carbonates Catalyzed by CaI2–Et3N and Studies on Their Biocatalytic Kinetic Resolution.” ACS Sustainable Chemistry and Engineering, vol. 10, no. 40, American Chemical Society (ACS), 2022, pp. 13335–42, doi:10.1021/acssuschemeng.2c03210.","bibtex":"@article{Terazzi_Laatz_von Langermann_Werner_2022, title={Synthesis of Cyclic Carbonates Catalyzed by CaI2–Et3N and Studies on Their Biocatalytic Kinetic Resolution}, volume={10}, DOI={10.1021/acssuschemeng.2c03210}, number={40}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Terazzi, Constanza and Laatz, Karoline and von Langermann, Jan and Werner, Thomas}, year={2022}, pages={13335–13342} }"},"type":"journal_article","page":"13335-13342","issue":"40","_id":"37938","intvolume":" 10","status":"public","date_created":"2023-01-22T20:10:44Z","volume":10,"author":[{"full_name":"Terazzi, Constanza","first_name":"Constanza","last_name":"Terazzi"},{"last_name":"Laatz","full_name":"Laatz, Karoline","first_name":"Karoline"},{"last_name":"von Langermann","full_name":"von Langermann, Jan","first_name":"Jan"},{"last_name":"Werner","id":"89271","first_name":"Thomas","full_name":"Werner, Thomas"}],"publisher":"American Chemical Society (ACS)","keyword":["Renewable Energy","Sustainability and the Environment","General Chemical Engineering","Environmental Chemistry","General Chemistry"],"publication":"ACS Sustainable Chemistry and Engineering","user_id":"14931"},{"volume":11,"status":"public","date_created":"2023-01-22T20:19:21Z","author":[{"full_name":"Ren, Changyue","first_name":"Changyue","last_name":"Ren"},{"last_name":"Spannenberg","first_name":"Anke","full_name":"Spannenberg, Anke"},{"id":"89271","last_name":"Werner","full_name":"Werner, Thomas","first_name":"Thomas"}],"publisher":"Wiley","publication":"Asian Journal of Organic Chemistry","keyword":["Organic Chemistry"],"user_id":"14931","citation":{"ieee":"C. Ren, A. Spannenberg, and T. Werner, “Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO 2,” Asian Journal of Organic Chemistry, vol. 11, no. 9, 2022, doi: 10.1002/ajoc.202200156.","short":"C. Ren, A. Spannenberg, T. Werner, Asian Journal of Organic Chemistry 11 (2022).","mla":"Ren, Changyue, et al. “Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO 2.” Asian Journal of Organic Chemistry, vol. 11, no. 9, Wiley, 2022, doi:10.1002/ajoc.202200156.","bibtex":"@article{Ren_Spannenberg_Werner_2022, title={Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO 2}, volume={11}, DOI={10.1002/ajoc.202200156}, number={9}, journal={Asian Journal of Organic Chemistry}, publisher={Wiley}, author={Ren, Changyue and Spannenberg, Anke and Werner, Thomas}, year={2022} }","chicago":"Ren, Changyue, Anke Spannenberg, and Thomas Werner. “Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO 2.” Asian Journal of Organic Chemistry 11, no. 9 (2022). https://doi.org/10.1002/ajoc.202200156.","apa":"Ren, C., Spannenberg, A., & Werner, T. (2022). Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO 2. Asian Journal of Organic Chemistry, 11(9). https://doi.org/10.1002/ajoc.202200156","ama":"Ren C, Spannenberg A, Werner T. Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO 2. Asian Journal of Organic Chemistry. 2022;11(9). doi:10.1002/ajoc.202200156"},"year":"2022","type":"journal_article","issue":"9","intvolume":" 11","_id":"37940","publication_status":"published","publication_identifier":{"issn":["2193-5807","2193-5815"]},"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"title":"Synthesis of Bifunctional Phosphonium Salts Bearing Perfluorinated Side Chains and Their Application in the Synthesis of Cyclic Carbonates from Epoxides and CO 2","language":[{"iso":"eng"}],"doi":"10.1002/ajoc.202200156","date_updated":"2023-01-23T10:45:43Z"},{"user_id":"53339","publication":"Chemistry – A European Journal","keyword":["General Chemistry","Catalysis","Organic Chemistry"],"publisher":"Wiley","author":[{"last_name":"Hou","first_name":"Peng","full_name":"Hou, Peng"},{"full_name":"Peschtrich, Sebastian","first_name":"Sebastian","last_name":"Peschtrich"},{"full_name":"Huber, Nils","first_name":"Nils","last_name":"Huber"},{"last_name":"Feuerstein","first_name":"Wolfram","full_name":"Feuerstein, Wolfram"},{"first_name":"Angela","full_name":"Bihlmeier, Angela","last_name":"Bihlmeier"},{"last_name":"Krummenacher","full_name":"Krummenacher, Ivo","first_name":"Ivo"},{"full_name":"Schoch, Roland","first_name":"Roland","last_name":"Schoch"},{"last_name":"Klopper","full_name":"Klopper, Wim","first_name":"Wim"},{"last_name":"Breher","first_name":"Frank","full_name":"Breher, Frank"},{"first_name":"Jan","orcid":"0000-0002-3698-668X","full_name":"Paradies, Jan","last_name":"Paradies","id":"53339"}],"date_created":"2023-01-10T09:10:15Z","status":"public","volume":28,"_id":"35703","intvolume":" 28","issue":"23","citation":{"short":"P. Hou, S. Peschtrich, N. Huber, W. Feuerstein, A. Bihlmeier, I. Krummenacher, R. Schoch, W. Klopper, F. Breher, J. Paradies, Chemistry – A European Journal 28 (2022).","ieee":"P. Hou et al., “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022),” Chemistry – A European Journal, vol. 28, no. 23, 2022, doi: 10.1002/chem.202200982.","chicago":"Hou, Peng, Sebastian Peschtrich, Nils Huber, Wolfram Feuerstein, Angela Bihlmeier, Ivo Krummenacher, Roland Schoch, Wim Klopper, Frank Breher, and Jan Paradies. “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022).” Chemistry – A European Journal 28, no. 23 (2022). https://doi.org/10.1002/chem.202200982.","apa":"Hou, P., Peschtrich, S., Huber, N., Feuerstein, W., Bihlmeier, A., Krummenacher, I., Schoch, R., Klopper, W., Breher, F., & Paradies, J. (2022). Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022). Chemistry – A European Journal, 28(23). https://doi.org/10.1002/chem.202200982","ama":"Hou P, Peschtrich S, Huber N, et al. Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022). Chemistry – A European Journal. 2022;28(23). doi:10.1002/chem.202200982","mla":"Hou, Peng, et al. “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022).” Chemistry – A European Journal, vol. 28, no. 23, Wiley, 2022, doi:10.1002/chem.202200982.","bibtex":"@article{Hou_Peschtrich_Huber_Feuerstein_Bihlmeier_Krummenacher_Schoch_Klopper_Breher_Paradies_2022, title={Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022)}, volume={28}, DOI={10.1002/chem.202200982}, number={23}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Hou, Peng and Peschtrich, Sebastian and Huber, Nils and Feuerstein, Wolfram and Bihlmeier, Angela and Krummenacher, Ivo and Schoch, Roland and Klopper, Wim and Breher, Frank and Paradies, Jan}, year={2022} }"},"year":"2022","type":"journal_article","title":"Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022)","department":[{"_id":"2"},{"_id":"389"}],"publication_identifier":{"issn":["0947-6539","1521-3765"]},"publication_status":"published","date_updated":"2023-01-23T12:47:43Z","doi":"10.1002/chem.202200982","language":[{"iso":"eng"}]},{"article_number":"120326","doi":"10.1016/j.ijpharm.2021.120326","intvolume":" 597","_id":"23701","date_updated":"2022-07-28T09:57:44Z","language":[{"iso":"eng"}],"year":"2021","type":"journal_article","citation":{"chicago":"Schoppa, Timo, Dimitri Jung, Tarik Rust, Dennis Mulac, Dirk Kuckling, and Klaus Langer. “Light-Responsive Polymeric Nanoparticles Based on a Novel Nitropiperonal Based Polyester as Drug Delivery Systems for Photosensitizers in PDT.” International Journal of Pharmaceutics 597 (2021). https://doi.org/10.1016/j.ijpharm.2021.120326.","apa":"Schoppa, T., Jung, D., Rust, T., Mulac, D., Kuckling, D., & Langer, K. (2021). Light-responsive polymeric nanoparticles based on a novel nitropiperonal based polyester as drug delivery systems for photosensitizers in PDT. International Journal of Pharmaceutics, 597, Article 120326. https://doi.org/10.1016/j.ijpharm.2021.120326","ama":"Schoppa T, Jung D, Rust T, Mulac D, Kuckling D, Langer K. Light-responsive polymeric nanoparticles based on a novel nitropiperonal based polyester as drug delivery systems for photosensitizers in PDT. International Journal of Pharmaceutics. 2021;597. doi:10.1016/j.ijpharm.2021.120326","mla":"Schoppa, Timo, et al. “Light-Responsive Polymeric Nanoparticles Based on a Novel Nitropiperonal Based Polyester as Drug Delivery Systems for Photosensitizers in PDT.” International Journal of Pharmaceutics, vol. 597, 120326, Elsevier, 2021, doi:10.1016/j.ijpharm.2021.120326.","bibtex":"@article{Schoppa_Jung_Rust_Mulac_Kuckling_Langer_2021, title={Light-responsive polymeric nanoparticles based on a novel nitropiperonal based polyester as drug delivery systems for photosensitizers in PDT}, volume={597}, DOI={10.1016/j.ijpharm.2021.120326}, number={120326}, journal={International Journal of Pharmaceutics}, publisher={Elsevier}, author={Schoppa, Timo and Jung, Dimitri and Rust, Tarik and Mulac, Dennis and Kuckling, Dirk and Langer, Klaus}, year={2021} }","short":"T. Schoppa, D. Jung, T. Rust, D. Mulac, D. Kuckling, K. Langer, International Journal of Pharmaceutics 597 (2021).","ieee":"T. Schoppa, D. Jung, T. Rust, D. Mulac, D. Kuckling, and K. Langer, “Light-responsive polymeric nanoparticles based on a novel nitropiperonal based polyester as drug delivery systems for photosensitizers in PDT,” International Journal of Pharmaceutics, vol. 597, Art. no. 120326, 2021, doi: 10.1016/j.ijpharm.2021.120326."},"user_id":"94","title":"Light-responsive polymeric nanoparticles based on a novel nitropiperonal based polyester as drug delivery systems for photosensitizers in PDT","status":"public","date_created":"2021-09-02T12:48:00Z","publication_status":"published","volume":597,"publication_identifier":{"issn":["0378-5173"]},"author":[{"last_name":"Schoppa","full_name":"Schoppa, Timo","first_name":"Timo"},{"full_name":"Jung, Dimitri","first_name":"Dimitri","last_name":"Jung"},{"full_name":"Rust, Tarik","first_name":"Tarik","last_name":"Rust"},{"full_name":"Mulac, Dennis","first_name":"Dennis","last_name":"Mulac"},{"id":"287","last_name":"Kuckling","full_name":"Kuckling, Dirk","first_name":"Dirk"},{"last_name":"Langer","full_name":"Langer, Klaus","first_name":"Klaus"}],"publisher":"Elsevier","department":[{"_id":"311"}],"publication":"International Journal of Pharmaceutics"},{"doi":"10.1021/acsapm.1c00411","date_updated":"2022-07-28T10:00:40Z","language":[{"iso":"eng"}],"title":"Backbone-Degradable (Co-)Polymers for Light-Triggered Drug Delivery","publication_identifier":{"issn":["2637-6105","2637-6105"]},"publication_status":"published","department":[{"_id":"311"}],"issue":"8","intvolume":" 3","_id":"23662","type":"journal_article","citation":{"bibtex":"@article{Rust_Jung_Hoppe_Schoppa_Langer_Kuckling_2021, title={Backbone-Degradable (Co-)Polymers for Light-Triggered Drug Delivery}, volume={3}, DOI={10.1021/acsapm.1c00411}, number={8}, journal={ACS Applied Polymer Materials}, publisher={ACS}, author={Rust, Tarik and Jung, Dimitri and Hoppe, Axel and Schoppa, Timo and Langer, Klaus and Kuckling, Dirk}, year={2021}, pages={3831–3842} }","mla":"Rust, Tarik, et al. “Backbone-Degradable (Co-)Polymers for Light-Triggered Drug Delivery.” ACS Applied Polymer Materials, vol. 3, no. 8, ACS, 2021, pp. 3831–42, doi:10.1021/acsapm.1c00411.","chicago":"Rust, Tarik, Dimitri Jung, Axel Hoppe, Timo Schoppa, Klaus Langer, and Dirk Kuckling. “Backbone-Degradable (Co-)Polymers for Light-Triggered Drug Delivery.” ACS Applied Polymer Materials 3, no. 8 (2021): 3831–42. https://doi.org/10.1021/acsapm.1c00411.","ama":"Rust T, Jung D, Hoppe A, Schoppa T, Langer K, Kuckling D. Backbone-Degradable (Co-)Polymers for Light-Triggered Drug Delivery. ACS Applied Polymer Materials. 2021;3(8):3831-3842. doi:10.1021/acsapm.1c00411","apa":"Rust, T., Jung, D., Hoppe, A., Schoppa, T., Langer, K., & Kuckling, D. (2021). Backbone-Degradable (Co-)Polymers for Light-Triggered Drug Delivery. ACS Applied Polymer Materials, 3(8), 3831–3842. https://doi.org/10.1021/acsapm.1c00411","ieee":"T. Rust, D. Jung, A. Hoppe, T. Schoppa, K. Langer, and D. Kuckling, “Backbone-Degradable (Co-)Polymers for Light-Triggered Drug Delivery,” ACS Applied Polymer Materials, vol. 3, no. 8, pp. 3831–3842, 2021, doi: 10.1021/acsapm.1c00411.","short":"T. Rust, D. Jung, A. Hoppe, T. Schoppa, K. Langer, D. Kuckling, ACS Applied Polymer Materials 3 (2021) 3831–3842."},"year":"2021","page":"3831-3842","user_id":"94","status":"public","date_created":"2021-09-02T06:41:16Z","volume":3,"publisher":"ACS","author":[{"last_name":"Rust","full_name":"Rust, Tarik","first_name":"Tarik"},{"full_name":"Jung, Dimitri","first_name":"Dimitri","last_name":"Jung"},{"last_name":"Hoppe","first_name":"Axel","full_name":"Hoppe, Axel"},{"first_name":"Timo","full_name":"Schoppa, Timo","last_name":"Schoppa"},{"last_name":"Langer","full_name":"Langer, Klaus","first_name":"Klaus"},{"full_name":"Kuckling, Dirk","first_name":"Dirk","id":"287","last_name":"Kuckling"}],"publication":"ACS Applied Polymer Materials"},{"_id":"23699","date_updated":"2022-07-28T09:57:57Z","doi":"10.1002/ejoc.202100268","type":"journal_article","citation":{"mla":"Schmiegel, Carsten J., et al. “Direct Asymmetric Aldol Reaction in Continuous Flow Using Gel‐Bound Organocatalysts.” European Journal of Organic Chemistry, Wiley-VCH, 2021, pp. 2578–86, doi:10.1002/ejoc.202100268.","bibtex":"@article{Schmiegel_Baier_Kuckling_2021, title={Direct Asymmetric Aldol Reaction in Continuous Flow Using Gel‐Bound Organocatalysts}, DOI={10.1002/ejoc.202100268}, journal={European Journal of Organic Chemistry}, publisher={Wiley-VCH}, author={Schmiegel, Carsten J. and Baier, Rene and Kuckling, Dirk}, year={2021}, pages={2578–2586} }","ama":"Schmiegel CJ, Baier R, Kuckling D. Direct Asymmetric Aldol Reaction in Continuous Flow Using Gel‐Bound Organocatalysts. European Journal of Organic Chemistry. Published online 2021:2578-2586. doi:10.1002/ejoc.202100268","apa":"Schmiegel, C. J., Baier, R., & Kuckling, D. (2021). Direct Asymmetric Aldol Reaction in Continuous Flow Using Gel‐Bound Organocatalysts. European Journal of Organic Chemistry, 2578–2586. https://doi.org/10.1002/ejoc.202100268","chicago":"Schmiegel, Carsten J., Rene Baier, and Dirk Kuckling. “Direct Asymmetric Aldol Reaction in Continuous Flow Using Gel‐Bound Organocatalysts.” European Journal of Organic Chemistry, 2021, 2578–86. https://doi.org/10.1002/ejoc.202100268.","ieee":"C. J. Schmiegel, R. Baier, and D. Kuckling, “Direct Asymmetric Aldol Reaction in Continuous Flow Using Gel‐Bound Organocatalysts,” European Journal of Organic Chemistry, pp. 2578–2586, 2021, doi: 10.1002/ejoc.202100268.","short":"C.J. Schmiegel, R. Baier, D. Kuckling, European Journal of Organic Chemistry (2021) 2578–2586."},"year":"2021","page":"2578-2586","language":[{"iso":"eng"}],"title":"Direct Asymmetric Aldol Reaction in Continuous Flow Using Gel‐Bound Organocatalysts","user_id":"94","publisher":"Wiley-VCH","author":[{"first_name":"Carsten J.","full_name":"Schmiegel, Carsten J.","last_name":"Schmiegel"},{"last_name":"Baier","first_name":"Rene","full_name":"Baier, Rene"},{"last_name":"Kuckling","id":"287","first_name":"Dirk","full_name":"Kuckling, Dirk"}],"department":[{"_id":"311"}],"publication":"European Journal of Organic Chemistry","publication_identifier":{"issn":["1434-193X","1099-0690"]},"publication_status":"published","status":"public","date_created":"2021-09-02T12:44:25Z"}]