[{"date_created":"2023-01-22T20:44:02Z","author":[{"first_name":"Lars","full_name":"Longwitz, Lars","last_name":"Longwitz"},{"full_name":"Jopp, Stefan","last_name":"Jopp","first_name":"Stefan"},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"volume":84,"date_updated":"2025-11-10T08:54:28Z","publisher":"American Chemical Society (ACS)","doi":"10.1021/acs.joc.9b00741","title":"Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling","issue":"12","publication_status":"published","publication_identifier":{"issn":["0022-3263","1520-6904"]},"citation":{"mla":"Longwitz, Lars, et al. “Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling.” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 12, American Chemical Society (ACS), 2019, pp. 7863–70, doi:<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>.","short":"L. Longwitz, S. Jopp, T. Werner, The Journal of Organic Chemistry 84 (2019) 7863–7870.","bibtex":"@article{Longwitz_Jopp_Werner_2019, title={Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling}, volume={84}, DOI={<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>}, number={12}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Longwitz, Lars and Jopp, Stefan and Werner, Thomas}, year={2019}, pages={7863–7870} }","apa":"Longwitz, L., Jopp, S., &#38; Werner, T. (2019). Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling. <i>The Journal of Organic Chemistry</i>, <i>84</i>(12), 7863–7870. <a href=\"https://doi.org/10.1021/acs.joc.9b00741\">https://doi.org/10.1021/acs.joc.9b00741</a>","ieee":"L. Longwitz, S. Jopp, and T. Werner, “Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling,” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 12, pp. 7863–7870, 2019, doi: <a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>.","chicago":"Longwitz, Lars, Stefan Jopp, and Thomas Werner. “Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling.” <i>The Journal of Organic Chemistry</i> 84, no. 12 (2019): 7863–70. <a href=\"https://doi.org/10.1021/acs.joc.9b00741\">https://doi.org/10.1021/acs.joc.9b00741</a>.","ama":"Longwitz L, Jopp S, Werner T. Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling. <i>The Journal of Organic Chemistry</i>. 2019;84(12):7863-7870. doi:<a href=\"https://doi.org/10.1021/acs.joc.9b00741\">10.1021/acs.joc.9b00741</a>"},"page":"7863-7870","intvolume":"        84","year":"2019","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37962","extern":"1","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"type":"journal_article","publication":"The Journal of Organic Chemistry","status":"public"},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37959","status":"public","type":"journal_article","doi":"10.1126/science.aay6635","volume":365,"author":[{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"date_updated":"2025-11-10T09:01:38Z","intvolume":"       365","page":"866-867","citation":{"bibtex":"@article{Longwitz_Werner_2019, title={The Mitsunobu reaction, reimagined}, volume={365}, DOI={<a href=\"https://doi.org/10.1126/science.aay6635\">10.1126/science.aay6635</a>}, number={6456}, journal={Science}, publisher={American Association for the Advancement of Science (AAAS)}, author={Longwitz, Lars and Werner, Thomas}, year={2019}, pages={866–867} }","short":"L. Longwitz, T. Werner, Science 365 (2019) 866–867.","mla":"Longwitz, Lars, and Thomas Werner. “The Mitsunobu Reaction, Reimagined.” <i>Science</i>, vol. 365, no. 6456, American Association for the Advancement of Science (AAAS), 2019, pp. 866–67, doi:<a href=\"https://doi.org/10.1126/science.aay6635\">10.1126/science.aay6635</a>.","apa":"Longwitz, L., &#38; Werner, T. (2019). The Mitsunobu reaction, reimagined. <i>Science</i>, <i>365</i>(6456), 866–867. <a href=\"https://doi.org/10.1126/science.aay6635\">https://doi.org/10.1126/science.aay6635</a>","chicago":"Longwitz, Lars, and Thomas Werner. “The Mitsunobu Reaction, Reimagined.” <i>Science</i> 365, no. 6456 (2019): 866–67. <a href=\"https://doi.org/10.1126/science.aay6635\">https://doi.org/10.1126/science.aay6635</a>.","ieee":"L. Longwitz and T. Werner, “The Mitsunobu reaction, reimagined,” <i>Science</i>, vol. 365, no. 6456, pp. 866–867, 2019, doi: <a href=\"https://doi.org/10.1126/science.aay6635\">10.1126/science.aay6635</a>.","ama":"Longwitz L, Werner T. The Mitsunobu reaction, reimagined. <i>Science</i>. 2019;365(6456):866-867. doi:<a href=\"https://doi.org/10.1126/science.aay6635\">10.1126/science.aay6635</a>"},"publication_identifier":{"issn":["0036-8075","1095-9203"]},"publication_status":"published","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"abstract":[{"text":"<jats:p>Catalytic nucleophilic substitution of alcohols makes organic synthesis greener</jats:p>","lang":"eng"}],"publication":"Science","title":"The Mitsunobu reaction, reimagined","date_created":"2023-01-22T20:42:20Z","publisher":"American Association for the Advancement of Science (AAAS)","year":"2019","issue":"6456"},{"publication":"ACS Catalysis","language":[{"iso":"eng"}],"keyword":["T4","CSSD"],"year":"2019","issue":"9","title":"Catalytic Approaches to Monomers for Polymers Based on Renewables","date_created":"2023-01-22T20:42:48Z","publisher":"American Chemical Society (ACS)","status":"public","type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37960","intvolume":"         9","page":"8012-8067","citation":{"ama":"Stadler BM, Wulf C, Werner T, Tin S, de Vries JG. Catalytic Approaches to Monomers for Polymers Based on Renewables. <i>ACS Catalysis</i>. 2019;9(9):8012-8067. doi:<a href=\"https://doi.org/10.1021/acscatal.9b01665\">10.1021/acscatal.9b01665</a>","ieee":"B. M. Stadler, C. Wulf, T. Werner, S. Tin, and J. G. de Vries, “Catalytic Approaches to Monomers for Polymers Based on Renewables,” <i>ACS Catalysis</i>, vol. 9, no. 9, pp. 8012–8067, 2019, doi: <a href=\"https://doi.org/10.1021/acscatal.9b01665\">10.1021/acscatal.9b01665</a>.","chicago":"Stadler, Bernhard M., Christoph Wulf, Thomas Werner, Sergey Tin, and Johannes G. de Vries. “Catalytic Approaches to Monomers for Polymers Based on Renewables.” <i>ACS Catalysis</i> 9, no. 9 (2019): 8012–67. <a href=\"https://doi.org/10.1021/acscatal.9b01665\">https://doi.org/10.1021/acscatal.9b01665</a>.","mla":"Stadler, Bernhard M., et al. “Catalytic Approaches to Monomers for Polymers Based on Renewables.” <i>ACS Catalysis</i>, vol. 9, no. 9, American Chemical Society (ACS), 2019, pp. 8012–67, doi:<a href=\"https://doi.org/10.1021/acscatal.9b01665\">10.1021/acscatal.9b01665</a>.","short":"B.M. Stadler, C. Wulf, T. Werner, S. Tin, J.G. de Vries, ACS Catalysis 9 (2019) 8012–8067.","bibtex":"@article{Stadler_Wulf_Werner_Tin_de Vries_2019, title={Catalytic Approaches to Monomers for Polymers Based on Renewables}, volume={9}, DOI={<a href=\"https://doi.org/10.1021/acscatal.9b01665\">10.1021/acscatal.9b01665</a>}, number={9}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Stadler, Bernhard M. and Wulf, Christoph and Werner, Thomas and Tin, Sergey and de Vries, Johannes G.}, year={2019}, pages={8012–8067} }","apa":"Stadler, B. M., Wulf, C., Werner, T., Tin, S., &#38; de Vries, J. G. (2019). Catalytic Approaches to Monomers for Polymers Based on Renewables. <i>ACS Catalysis</i>, <i>9</i>(9), 8012–8067. <a href=\"https://doi.org/10.1021/acscatal.9b01665\">https://doi.org/10.1021/acscatal.9b01665</a>"},"publication_identifier":{"issn":["2155-5435","2155-5435"]},"publication_status":"published","doi":"10.1021/acscatal.9b01665","volume":9,"author":[{"first_name":"Bernhard M.","last_name":"Stadler","full_name":"Stadler, Bernhard M."},{"first_name":"Christoph","full_name":"Wulf, Christoph","last_name":"Wulf"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"},{"full_name":"Tin, Sergey","last_name":"Tin","first_name":"Sergey"},{"first_name":"Johannes G.","full_name":"de Vries, Johannes G.","last_name":"de Vries"}],"date_updated":"2025-11-10T09:01:51Z"},{"abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title>\r\n               <jats:p>Numerous organic transformations are based on the use of stoichiometric amounts of phosphorus reagents. The formation of phosphane oxides from phosphanes is usually the thermodynamic driving force for these reactions. The stoichiometric amounts of phosphane oxide which are formed as by-products often significantly hamper the product purification. Organophosphorus catalysis based on P(III)/P(V) redox cycling aims to address these problems. Herein we present our recent advances in developing catalytic Wittig-type reactions. More specifically, we reported our results on catalytic Wittig reactions based on readily available Bu<jats:sub>3</jats:sub>P=O as pre-catalyst as well as the first microwave-assisted version of this reaction and the first enantioselective catalytic Wittig reaction utilizing chiral phosphane catalysts. Further developments led to the implementation of catalytic base-free Wittig reactions yielding highly functionalized alkylidene and arylidene succinates.</jats:p>"}],"status":"public","type":"journal_article","publication":"Pure and Applied Chemistry","keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"extern":"1","_id":"37966","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"year":"2019","citation":{"ama":"Longwitz L, Werner T. Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling. <i>Pure and Applied Chemistry</i>. 2019;91(1):95-102. doi:<a href=\"https://doi.org/10.1515/pac-2018-0920\">10.1515/pac-2018-0920</a>","chicago":"Longwitz, Lars, and Thomas Werner. “Recent Advances in Catalytic Wittig-Type Reactions Based on P(III)/P(V) Redox Cycling.” <i>Pure and Applied Chemistry</i> 91, no. 1 (2019): 95–102. <a href=\"https://doi.org/10.1515/pac-2018-0920\">https://doi.org/10.1515/pac-2018-0920</a>.","ieee":"L. Longwitz and T. Werner, “Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling,” <i>Pure and Applied Chemistry</i>, vol. 91, no. 1, pp. 95–102, 2019, doi: <a href=\"https://doi.org/10.1515/pac-2018-0920\">10.1515/pac-2018-0920</a>.","apa":"Longwitz, L., &#38; Werner, T. (2019). Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling. <i>Pure and Applied Chemistry</i>, <i>91</i>(1), 95–102. <a href=\"https://doi.org/10.1515/pac-2018-0920\">https://doi.org/10.1515/pac-2018-0920</a>","mla":"Longwitz, Lars, and Thomas Werner. “Recent Advances in Catalytic Wittig-Type Reactions Based on P(III)/P(V) Redox Cycling.” <i>Pure and Applied Chemistry</i>, vol. 91, no. 1, Walter de Gruyter GmbH, 2019, pp. 95–102, doi:<a href=\"https://doi.org/10.1515/pac-2018-0920\">10.1515/pac-2018-0920</a>.","short":"L. Longwitz, T. Werner, Pure and Applied Chemistry 91 (2019) 95–102.","bibtex":"@article{Longwitz_Werner_2019, title={Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling}, volume={91}, DOI={<a href=\"https://doi.org/10.1515/pac-2018-0920\">10.1515/pac-2018-0920</a>}, number={1}, journal={Pure and Applied Chemistry}, publisher={Walter de Gruyter GmbH}, author={Longwitz, Lars and Werner, Thomas}, year={2019}, pages={95–102} }"},"page":"95-102","intvolume":"        91","publication_status":"published","publication_identifier":{"issn":["1365-3075","0033-4545"]},"issue":"1","title":"Recent advances in catalytic Wittig-type reactions based on P(III)/P(V) redox cycling","doi":"10.1515/pac-2018-0920","publisher":"Walter de Gruyter GmbH","date_updated":"2025-11-10T09:06:58Z","date_created":"2023-01-22T20:45:38Z","author":[{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"volume":91},{"type":"journal_article","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37965","extern":"1","publication_status":"published","publication_identifier":{"issn":["0022-3263","1520-6904"]},"citation":{"chicago":"Grandane, Aiga, Lars Longwitz, Catrin Roolf, Anke Spannenberg, Hugo Murua Escobar, Christian Junghanss, Edgars Suna, and Thomas Werner. “Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones.” <i>The Journal of Organic Chemistry</i> 84, no. 3 (2019): 1320–29. <a href=\"https://doi.org/10.1021/acs.joc.8b02789\">https://doi.org/10.1021/acs.joc.8b02789</a>.","ieee":"A. Grandane <i>et al.</i>, “Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones,” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 3, pp. 1320–1329, 2019, doi: <a href=\"https://doi.org/10.1021/acs.joc.8b02789\">10.1021/acs.joc.8b02789</a>.","ama":"Grandane A, Longwitz L, Roolf C, et al. Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones. <i>The Journal of Organic Chemistry</i>. 2019;84(3):1320-1329. doi:<a href=\"https://doi.org/10.1021/acs.joc.8b02789\">10.1021/acs.joc.8b02789</a>","apa":"Grandane, A., Longwitz, L., Roolf, C., Spannenberg, A., Murua Escobar, H., Junghanss, C., Suna, E., &#38; Werner, T. (2019). Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones. <i>The Journal of Organic Chemistry</i>, <i>84</i>(3), 1320–1329. <a href=\"https://doi.org/10.1021/acs.joc.8b02789\">https://doi.org/10.1021/acs.joc.8b02789</a>","bibtex":"@article{Grandane_Longwitz_Roolf_Spannenberg_Murua Escobar_Junghanss_Suna_Werner_2019, title={Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones}, volume={84}, DOI={<a href=\"https://doi.org/10.1021/acs.joc.8b02789\">10.1021/acs.joc.8b02789</a>}, number={3}, journal={The Journal of Organic Chemistry}, publisher={American Chemical Society (ACS)}, author={Grandane, Aiga and Longwitz, Lars and Roolf, Catrin and Spannenberg, Anke and Murua Escobar, Hugo and Junghanss, Christian and Suna, Edgars and Werner, Thomas}, year={2019}, pages={1320–1329} }","short":"A. Grandane, L. Longwitz, C. Roolf, A. Spannenberg, H. Murua Escobar, C. Junghanss, E. Suna, T. Werner, The Journal of Organic Chemistry 84 (2019) 1320–1329.","mla":"Grandane, Aiga, et al. “Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones.” <i>The Journal of Organic Chemistry</i>, vol. 84, no. 3, American Chemical Society (ACS), 2019, pp. 1320–29, doi:<a href=\"https://doi.org/10.1021/acs.joc.8b02789\">10.1021/acs.joc.8b02789</a>."},"intvolume":"        84","page":"1320-1329","author":[{"first_name":"Aiga","last_name":"Grandane","full_name":"Grandane, Aiga"},{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"first_name":"Catrin","last_name":"Roolf","full_name":"Roolf, Catrin"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"first_name":"Hugo","full_name":"Murua Escobar, Hugo","last_name":"Murua Escobar"},{"first_name":"Christian","last_name":"Junghanss","full_name":"Junghanss, Christian"},{"last_name":"Suna","full_name":"Suna, Edgars","first_name":"Edgars"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"volume":84,"date_updated":"2025-11-10T09:10:18Z","doi":"10.1021/acs.joc.8b02789","publication":"The Journal of Organic Chemistry","language":[{"iso":"eng"}],"keyword":["T2","T4","CSSD"],"issue":"3","year":"2019","date_created":"2023-01-22T20:45:12Z","publisher":"American Chemical Society (ACS)","title":"Intramolecular Base-Free Catalytic Wittig Reaction: Synthesis of Benzoxepinones"},{"status":"public","type":"book_chapter","publication":"Homogeneous Hydrogenation with Non‐Precious Catalysts","language":[{"iso":"eng"}],"_id":"64890","user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"year":"2019","citation":{"mla":"Paradies, Jan, and Sebastian Tussing. “Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen.” <i>Homogeneous Hydrogenation with Non‐Precious Catalysts</i>, Wiley, 2019, doi:<a href=\"https://doi.org/10.1002/9783527814237.ch7\">10.1002/9783527814237.ch7</a>.","short":"J. Paradies, S. Tussing, in: Homogeneous Hydrogenation with Non‐Precious Catalysts, Wiley, 2019.","bibtex":"@inbook{Paradies_Tussing_2019, title={Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen}, DOI={<a href=\"https://doi.org/10.1002/9783527814237.ch7\">10.1002/9783527814237.ch7</a>}, booktitle={Homogeneous Hydrogenation with Non‐Precious Catalysts}, publisher={Wiley}, author={Paradies, Jan and Tussing, Sebastian}, year={2019} }","apa":"Paradies, J., &#38; Tussing, S. (2019). Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen. In <i>Homogeneous Hydrogenation with Non‐Precious Catalysts</i>. Wiley. <a href=\"https://doi.org/10.1002/9783527814237.ch7\">https://doi.org/10.1002/9783527814237.ch7</a>","ama":"Paradies J, Tussing S. Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen. In: <i>Homogeneous Hydrogenation with Non‐Precious Catalysts</i>. Wiley; 2019. doi:<a href=\"https://doi.org/10.1002/9783527814237.ch7\">10.1002/9783527814237.ch7</a>","chicago":"Paradies, Jan, and Sebastian Tussing. “Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen.” In <i>Homogeneous Hydrogenation with Non‐Precious Catalysts</i>. Wiley, 2019. <a href=\"https://doi.org/10.1002/9783527814237.ch7\">https://doi.org/10.1002/9783527814237.ch7</a>.","ieee":"J. Paradies and S. Tussing, “Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen,” in <i>Homogeneous Hydrogenation with Non‐Precious Catalysts</i>, Wiley, 2019."},"publication_status":"published","publication_identifier":{"isbn":["9783527344390","9783527814237"]},"title":"Frustrated Lewis Pair‐Catalyzed Reductions Using Molecular Hydrogen","doi":"10.1002/9783527814237.ch7","date_updated":"2026-03-11T10:17:35Z","publisher":"Wiley","author":[{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X"},{"first_name":"Sebastian","last_name":"Tussing","full_name":"Tussing, Sebastian"}],"date_created":"2026-03-11T10:17:22Z"},{"doi":"10.1016/j.ijpharm.2018.12.040","title":"Light-responsive nanoparticles based on new polycarbonate polymers as innovative drug delivery systems for photosensitizers in PDT","volume":557,"date_created":"2022-04-21T09:13:47Z","author":[{"full_name":"Anderski, Juliane","last_name":"Anderski","first_name":"Juliane"},{"full_name":"Mahlert, Laura","last_name":"Mahlert","first_name":"Laura"},{"last_name":"Sun","full_name":"Sun, Jingjiang","first_name":"Jingjiang"},{"full_name":"Birnbaum, Wolfgang","last_name":"Birnbaum","first_name":"Wolfgang"},{"last_name":"Mulac","full_name":"Mulac, Dennis","first_name":"Dennis"},{"full_name":"Schreiber, Sebastian","last_name":"Schreiber","first_name":"Sebastian"},{"first_name":"Fabian","last_name":"Herrmann","full_name":"Herrmann, Fabian"},{"first_name":"Dirk","last_name":"Kuckling","id":"287","full_name":"Kuckling, Dirk"},{"full_name":"Langer, Klaus","last_name":"Langer","first_name":"Klaus"}],"date_updated":"2022-04-21T09:14:49Z","publisher":"Elsevier BV","page":"182-191","intvolume":"       557","citation":{"apa":"Anderski, J., Mahlert, L., Sun, J., Birnbaum, W., Mulac, D., Schreiber, S., Herrmann, F., Kuckling, D., &#38; Langer, K. (2018). Light-responsive nanoparticles based on new polycarbonate polymers as innovative drug delivery systems for photosensitizers in PDT. <i>International Journal of Pharmaceutics</i>, <i>557</i>, 182–191. <a href=\"https://doi.org/10.1016/j.ijpharm.2018.12.040\">https://doi.org/10.1016/j.ijpharm.2018.12.040</a>","short":"J. Anderski, L. Mahlert, J. Sun, W. Birnbaum, D. Mulac, S. Schreiber, F. Herrmann, D. Kuckling, K. Langer, International Journal of Pharmaceutics 557 (2018) 182–191.","bibtex":"@article{Anderski_Mahlert_Sun_Birnbaum_Mulac_Schreiber_Herrmann_Kuckling_Langer_2018, title={Light-responsive nanoparticles based on new polycarbonate polymers as innovative drug delivery systems for photosensitizers in PDT}, volume={557}, DOI={<a href=\"https://doi.org/10.1016/j.ijpharm.2018.12.040\">10.1016/j.ijpharm.2018.12.040</a>}, journal={International Journal of Pharmaceutics}, publisher={Elsevier BV}, author={Anderski, Juliane and Mahlert, Laura and Sun, Jingjiang and Birnbaum, Wolfgang and Mulac, Dennis and Schreiber, Sebastian and Herrmann, Fabian and Kuckling, Dirk and Langer, Klaus}, year={2018}, pages={182–191} }","mla":"Anderski, Juliane, et al. “Light-Responsive Nanoparticles Based on New Polycarbonate Polymers as Innovative Drug Delivery Systems for Photosensitizers in PDT.” <i>International Journal of Pharmaceutics</i>, vol. 557, Elsevier BV, 2018, pp. 182–91, doi:<a href=\"https://doi.org/10.1016/j.ijpharm.2018.12.040\">10.1016/j.ijpharm.2018.12.040</a>.","ama":"Anderski J, Mahlert L, Sun J, et al. Light-responsive nanoparticles based on new polycarbonate polymers as innovative drug delivery systems for photosensitizers in PDT. <i>International Journal of Pharmaceutics</i>. 2018;557:182-191. doi:<a href=\"https://doi.org/10.1016/j.ijpharm.2018.12.040\">10.1016/j.ijpharm.2018.12.040</a>","ieee":"J. Anderski <i>et al.</i>, “Light-responsive nanoparticles based on new polycarbonate polymers as innovative drug delivery systems for photosensitizers in PDT,” <i>International Journal of Pharmaceutics</i>, vol. 557, pp. 182–191, 2018, doi: <a href=\"https://doi.org/10.1016/j.ijpharm.2018.12.040\">10.1016/j.ijpharm.2018.12.040</a>.","chicago":"Anderski, Juliane, Laura Mahlert, Jingjiang Sun, Wolfgang Birnbaum, Dennis Mulac, Sebastian Schreiber, Fabian Herrmann, Dirk Kuckling, and Klaus Langer. “Light-Responsive Nanoparticles Based on New Polycarbonate Polymers as Innovative Drug Delivery Systems for Photosensitizers in PDT.” <i>International Journal of Pharmaceutics</i> 557 (2018): 182–91. <a href=\"https://doi.org/10.1016/j.ijpharm.2018.12.040\">https://doi.org/10.1016/j.ijpharm.2018.12.040</a>."},"year":"2018","publication_identifier":{"issn":["0378-5173"]},"publication_status":"published","language":[{"iso":"eng"}],"keyword":["NanoparticlesLight-responsive polymersPhotodynamic therapyPoly(lactic-co-glycolic acid)Intestinal cancer"],"department":[{"_id":"311"}],"user_id":"94","_id":"30935","status":"public","publication":"International Journal of Pharmaceutics","type":"journal_article"},{"year":"2018","intvolume":"        40","citation":{"chicago":"Li, Jie, Xiaoqian Yu, Artjom Herberg, and Dirk Kuckling. “Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films.” <i>Macromolecular Rapid Communications</i> 40, no. 7 (2018). <a href=\"https://doi.org/10.1002/marc.201800674\">https://doi.org/10.1002/marc.201800674</a>.","ieee":"J. Li, X. Yu, A. Herberg, and D. Kuckling, “Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films,” <i>Macromolecular Rapid Communications</i>, vol. 40, no. 7, Art. no. 1800674, 2018, doi: <a href=\"https://doi.org/10.1002/marc.201800674\">10.1002/marc.201800674</a>.","ama":"Li J, Yu X, Herberg A, Kuckling D. Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films. <i>Macromolecular Rapid Communications</i>. 2018;40(7). doi:<a href=\"https://doi.org/10.1002/marc.201800674\">10.1002/marc.201800674</a>","apa":"Li, J., Yu, X., Herberg, A., &#38; Kuckling, D. (2018). Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films. <i>Macromolecular Rapid Communications</i>, <i>40</i>(7), Article 1800674. <a href=\"https://doi.org/10.1002/marc.201800674\">https://doi.org/10.1002/marc.201800674</a>","mla":"Li, Jie, et al. “Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films.” <i>Macromolecular Rapid Communications</i>, vol. 40, no. 7, 1800674, Wiley, 2018, doi:<a href=\"https://doi.org/10.1002/marc.201800674\">10.1002/marc.201800674</a>.","short":"J. Li, X. Yu, A. Herberg, D. Kuckling, Macromolecular Rapid Communications 40 (2018).","bibtex":"@article{Li_Yu_Herberg_Kuckling_2018, title={Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films}, volume={40}, DOI={<a href=\"https://doi.org/10.1002/marc.201800674\">10.1002/marc.201800674</a>}, number={71800674}, journal={Macromolecular Rapid Communications}, publisher={Wiley}, author={Li, Jie and Yu, Xiaoqian and Herberg, Artjom and Kuckling, Dirk}, year={2018} }"},"publication_identifier":{"issn":["1022-1336","1521-3927"]},"publication_status":"published","issue":"7","title":"Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films","doi":"10.1002/marc.201800674","publisher":"Wiley","date_updated":"2022-07-28T09:44:55Z","volume":40,"date_created":"2022-07-28T09:41:44Z","author":[{"last_name":"Li","full_name":"Li, Jie","first_name":"Jie"},{"last_name":"Yu","full_name":"Yu, Xiaoqian","first_name":"Xiaoqian"},{"full_name":"Herberg, Artjom","id":"94","last_name":"Herberg","first_name":"Artjom"},{"last_name":"Kuckling","id":"287","full_name":"Kuckling, Dirk","first_name":"Dirk"}],"status":"public","publication":"Macromolecular Rapid Communications","type":"journal_article","keyword":["Materials Chemistry","Polymers and Plastics","Organic Chemistry"],"article_number":"1800674","article_type":"original","language":[{"iso":"eng"}],"_id":"32444","department":[{"_id":"163"}],"user_id":"94"},{"abstract":[{"lang":"eng","text":"We describe the synthesis of mesoporous Al2O3 and MgO layers on silicon wafer substrates by using poly(dimethylacrylamide) hydrogels as porogenic matrices. Hydrogel films are prepared by spreading the polymer through spin-coating, followed by photo-cross-linking and anchoring to the substrate surface. The metal oxides are obtained by swelling the hydrogels in the respective metal nitrate solutions and subsequent thermal conversion. Combustion of the hydrogel results in mesoporous metal oxide layers with thicknesses in the μm range and high specific surface areas up to 558 m2∙g−1. Materials are characterized by SEM, FIB ablation, EDX, and Kr physisorption porosimetry."}],"publication":"Nanomaterials","language":[{"iso":"eng"}],"year":"2018","quality_controlled":"1","title":"Porous Aluminum Oxide and Magnesium Oxide Films Using Organic Hydrogels as Structure Matrices","date_created":"2021-10-08T10:48:59Z","status":"public","type":"journal_article","article_type":"original","article_number":"186","_id":"25910","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"},{"_id":"311"}],"user_id":"23547","citation":{"apa":"Chen, Z., Kuckling, D., &#38; Tiemann, M. (2018). Porous Aluminum Oxide and Magnesium Oxide Films Using Organic Hydrogels as Structure Matrices. <i>Nanomaterials</i>, Article 186. <a href=\"https://doi.org/10.3390/nano8040186\">https://doi.org/10.3390/nano8040186</a>","bibtex":"@article{Chen_Kuckling_Tiemann_2018, title={Porous Aluminum Oxide and Magnesium Oxide Films Using Organic Hydrogels as Structure Matrices}, DOI={<a href=\"https://doi.org/10.3390/nano8040186\">10.3390/nano8040186</a>}, number={186}, journal={Nanomaterials}, author={Chen, Zimei and Kuckling, Dirk and Tiemann, Michael}, year={2018} }","mla":"Chen, Zimei, et al. “Porous Aluminum Oxide and Magnesium Oxide Films Using Organic Hydrogels as Structure Matrices.” <i>Nanomaterials</i>, 186, 2018, doi:<a href=\"https://doi.org/10.3390/nano8040186\">10.3390/nano8040186</a>.","short":"Z. Chen, D. Kuckling, M. Tiemann, Nanomaterials (2018).","ieee":"Z. Chen, D. Kuckling, and M. Tiemann, “Porous Aluminum Oxide and Magnesium Oxide Films Using Organic Hydrogels as Structure Matrices,” <i>Nanomaterials</i>, Art. no. 186, 2018, doi: <a href=\"https://doi.org/10.3390/nano8040186\">10.3390/nano8040186</a>.","chicago":"Chen, Zimei, Dirk Kuckling, and Michael Tiemann. “Porous Aluminum Oxide and Magnesium Oxide Films Using Organic Hydrogels as Structure Matrices.” <i>Nanomaterials</i>, 2018. <a href=\"https://doi.org/10.3390/nano8040186\">https://doi.org/10.3390/nano8040186</a>.","ama":"Chen Z, Kuckling D, Tiemann M. Porous Aluminum Oxide and Magnesium Oxide Films Using Organic Hydrogels as Structure Matrices. <i>Nanomaterials</i>. Published online 2018. doi:<a href=\"https://doi.org/10.3390/nano8040186\">10.3390/nano8040186</a>"},"publication_identifier":{"issn":["2079-4991"]},"publication_status":"published","doi":"10.3390/nano8040186","main_file_link":[{"open_access":"1","url":"https://www.mdpi.com/2079-4991/8/4/186/pdf?version=1525344745"}],"date_updated":"2023-03-08T10:22:33Z","oa":"1","author":[{"last_name":"Chen","full_name":"Chen, Zimei","first_name":"Zimei"},{"first_name":"Dirk","id":"287","full_name":"Kuckling, Dirk","last_name":"Kuckling"},{"first_name":"Michael","id":"23547","full_name":"Tiemann, Michael","orcid":"0000-0003-1711-2722","last_name":"Tiemann"}]},{"language":[{"iso":"eng"}],"publication":"Gels","abstract":[{"text":"Organic polymer-hydrogels are known to be capable of directing the nucleation and growth of inorganic materials, such as silica, metal oxides, apatite or metal chalcogenides. This approach can be exploited in the synthesis of materials that exhibit defined nanoporosity. When the organic polymer-based hydrogel is incorporated in the inorganic product, a composite is formed from which the organic component may be selectively removed, yielding nanopores in the inorganic product. Such porogenic impact resembles the concept of using soft or hard templates for porous materials. This micro-review provides a survey of select examples from the literature.","lang":"eng"}],"date_created":"2021-10-08T10:47:59Z","title":"Hydrogels as Porogens for Nanoporous Inorganic Materials","quality_controlled":"1","year":"2018","_id":"25909","user_id":"23547","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"},{"_id":"311"}],"article_number":"83","article_type":"review","type":"journal_article","status":"public","date_updated":"2023-03-08T10:20:36Z","oa":"1","author":[{"last_name":"Weinberger","full_name":"Weinberger, Christian","id":"11848","first_name":"Christian"},{"id":"287","full_name":"Kuckling, Dirk","last_name":"Kuckling","first_name":"Dirk"},{"full_name":"Tiemann, Michael","id":"23547","orcid":"0000-0003-1711-2722","last_name":"Tiemann","first_name":"Michael"}],"main_file_link":[{"url":"https://www.mdpi.com/2310-2861/4/4/83/pdf?version=1539178292","open_access":"1"}],"doi":"10.3390/gels4040083","publication_status":"published","publication_identifier":{"issn":["2310-2861"]},"citation":{"ama":"Weinberger C, Kuckling D, Tiemann M. Hydrogels as Porogens for Nanoporous Inorganic Materials. <i>Gels</i>. Published online 2018. doi:<a href=\"https://doi.org/10.3390/gels4040083\">10.3390/gels4040083</a>","ieee":"C. Weinberger, D. Kuckling, and M. Tiemann, “Hydrogels as Porogens for Nanoporous Inorganic Materials,” <i>Gels</i>, Art. no. 83, 2018, doi: <a href=\"https://doi.org/10.3390/gels4040083\">10.3390/gels4040083</a>.","chicago":"Weinberger, Christian, Dirk Kuckling, and Michael Tiemann. “Hydrogels as Porogens for Nanoporous Inorganic Materials.” <i>Gels</i>, 2018. <a href=\"https://doi.org/10.3390/gels4040083\">https://doi.org/10.3390/gels4040083</a>.","apa":"Weinberger, C., Kuckling, D., &#38; Tiemann, M. (2018). Hydrogels as Porogens for Nanoporous Inorganic Materials. <i>Gels</i>, Article 83. <a href=\"https://doi.org/10.3390/gels4040083\">https://doi.org/10.3390/gels4040083</a>","short":"C. Weinberger, D. Kuckling, M. Tiemann, Gels (2018).","mla":"Weinberger, Christian, et al. “Hydrogels as Porogens for Nanoporous Inorganic Materials.” <i>Gels</i>, 83, 2018, doi:<a href=\"https://doi.org/10.3390/gels4040083\">10.3390/gels4040083</a>.","bibtex":"@article{Weinberger_Kuckling_Tiemann_2018, title={Hydrogels as Porogens for Nanoporous Inorganic Materials}, DOI={<a href=\"https://doi.org/10.3390/gels4040083\">10.3390/gels4040083</a>}, number={83}, journal={Gels}, author={Weinberger, Christian and Kuckling, Dirk and Tiemann, Michael}, year={2018} }"}},{"citation":{"chicago":"Straub, Bernd, Jennifer N. Andexer, Christoph Arenz, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, et al. “Trendbericht Organische Chemie 2017.” <i>Nachrichten Aus Der Chemie</i> 66, no. 3 (2018): 249–80. <a href=\"https://doi.org/10.1002/nadc.20184072148\">https://doi.org/10.1002/nadc.20184072148</a>.","ieee":"B. Straub <i>et al.</i>, “Trendbericht Organische Chemie 2017,” <i>Nachrichten aus der Chemie</i>, vol. 66, no. 3, pp. 249–280, 2018, doi: <a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>.","ama":"Straub B, Andexer JN, Arenz C, et al. Trendbericht Organische Chemie 2017. <i>Nachrichten aus der Chemie</i>. 2018;66(3):249-280. doi:<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>","apa":"Straub, B., Andexer, J. N., Arenz, C., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ditrich, K., Ernst, M., Gulder, T. A. M., Kordes, M., Krueger, A., Lehmann, M., Lindel, T., Lüdeke, S., Luy, B., Meier, M. A. R., Mück-Lichtenfeld, C., Muhle-Goll, C., … Worgull, D. (2018). Trendbericht Organische Chemie 2017. <i>Nachrichten Aus Der Chemie</i>, <i>66</i>(3), 249–280. <a href=\"https://doi.org/10.1002/nadc.20184072148\">https://doi.org/10.1002/nadc.20184072148</a>","mla":"Straub, Bernd, et al. “Trendbericht Organische Chemie 2017.” <i>Nachrichten Aus Der Chemie</i>, vol. 66, no. 3, Wiley, 2018, pp. 249–80, doi:<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>.","short":"B. Straub, J.N. Andexer, C. Arenz, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, K. Ditrich, M. Ernst, T.A.M. Gulder, M. Kordes, A. Krueger, M. Lehmann, T. Lindel, S. Lüdeke, B. Luy, M.A.R. Meier, C. Mück-Lichtenfeld, C. Muhle-Goll, A. Narine, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M.O. Senge, T. Werner, D.B. Werz, C. Winter, D. Worgull, Nachrichten Aus Der Chemie 66 (2018) 249–280.","bibtex":"@article{Straub_Andexer_Arenz_Beifuss_Beuerle_Brasholz_Breinbauer_Ditrich_Ernst_Gulder_et al._2018, title={Trendbericht Organische Chemie 2017}, volume={66}, DOI={<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Straub, Bernd and Andexer, Jennifer N. and Arenz, Christoph and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ditrich, Klaus and Ernst, Martin and Gulder, Tobias A. M. and et al.}, year={2018}, pages={249–280} }"},"page":"249-280","intvolume":"        66","publication_status":"published","publication_identifier":{"issn":["1439-9598"]},"doi":"10.1002/nadc.20184072148","author":[{"full_name":"Straub, Bernd","last_name":"Straub","first_name":"Bernd"},{"first_name":"Jennifer N.","last_name":"Andexer","full_name":"Andexer, Jennifer N."},{"first_name":"Christoph","last_name":"Arenz","full_name":"Arenz, Christoph"},{"first_name":"Uwe","full_name":"Beifuss, Uwe","last_name":"Beifuss"},{"full_name":"Beuerle, Florian","last_name":"Beuerle","first_name":"Florian"},{"last_name":"Brasholz","full_name":"Brasholz, Malte","first_name":"Malte"},{"last_name":"Breinbauer","full_name":"Breinbauer, Rolf","first_name":"Rolf"},{"last_name":"Ditrich","full_name":"Ditrich, Klaus","first_name":"Klaus"},{"last_name":"Ernst","full_name":"Ernst, Martin","first_name":"Martin"},{"first_name":"Tobias A. M.","full_name":"Gulder, Tobias A. 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R.","last_name":"Meier"},{"first_name":"Christian","last_name":"Mück-Lichtenfeld","full_name":"Mück-Lichtenfeld, Christian"},{"full_name":"Muhle-Goll, Claudia","last_name":"Muhle-Goll","first_name":"Claudia"},{"last_name":"Narine","full_name":"Narine, Arun","first_name":"Arun"},{"id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X","first_name":"Jan"},{"last_name":"Pfau","full_name":"Pfau, Roland","first_name":"Roland"},{"last_name":"Pietruszka","full_name":"Pietruszka, Jörg","first_name":"Jörg"},{"last_name":"Schaschke","full_name":"Schaschke, Norbert","first_name":"Norbert"},{"full_name":"Senge, Mathias O.","last_name":"Senge","first_name":"Mathias O."},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner"},{"full_name":"Werz, Daniel B.","last_name":"Werz","first_name":"Daniel B."},{"first_name":"Christian","last_name":"Winter","full_name":"Winter, Christian"},{"first_name":"Dennis","full_name":"Worgull, Dennis","last_name":"Worgull"}],"volume":66,"date_updated":"2025-11-10T09:03:49Z","status":"public","type":"journal_article","extern":"1","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"},{"_id":"389"}],"_id":"37971","year":"2018","issue":"3","title":"Trendbericht Organische Chemie 2017","date_created":"2023-01-22T20:48:24Z","publisher":"Wiley","publication":"Nachrichten aus der Chemie","language":[{"iso":"eng"}],"keyword":["General Chemical Engineering","General Chemistry"]},{"date_updated":"2025-11-10T09:05:47Z","volume":2018,"author":[{"last_name":"Hu","full_name":"Hu, Yuya","first_name":"Yuya"},{"first_name":"Zhiping","last_name":"Yin","full_name":"Yin, Zhiping"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"first_name":"Xiao-Feng","full_name":"Wu, Xiao-Feng","last_name":"Wu"}],"doi":"10.1002/ejoc.201701813","publication_identifier":{"issn":["1434-193X"]},"publication_status":"published","page":"1274-1276","intvolume":"      2018","citation":{"ieee":"Y. Hu, Z. Yin, T. Werner, A. Spannenberg, and X.-F. Wu, “1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur,” <i>European Journal of Organic Chemistry</i>, vol. 2018, no. 10, pp. 1274–1276, 2018, doi: <a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>.","chicago":"Hu, Yuya, Zhiping Yin, Thomas Werner, Anke Spannenberg, and Xiao-Feng Wu. “1,8-Diazabicyclo[5.4.0]Undec-7-Ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur.” <i>European Journal of Organic Chemistry</i> 2018, no. 10 (2018): 1274–76. <a href=\"https://doi.org/10.1002/ejoc.201701813\">https://doi.org/10.1002/ejoc.201701813</a>.","ama":"Hu Y, Yin Z, Werner T, Spannenberg A, Wu X-F. 1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur. <i>European Journal of Organic Chemistry</i>. 2018;2018(10):1274-1276. doi:<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>","apa":"Hu, Y., Yin, Z., Werner, T., Spannenberg, A., &#38; Wu, X.-F. (2018). 1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur. <i>European Journal of Organic Chemistry</i>, <i>2018</i>(10), 1274–1276. <a href=\"https://doi.org/10.1002/ejoc.201701813\">https://doi.org/10.1002/ejoc.201701813</a>","short":"Y. Hu, Z. Yin, T. Werner, A. Spannenberg, X.-F. Wu, European Journal of Organic Chemistry 2018 (2018) 1274–1276.","bibtex":"@article{Hu_Yin_Werner_Spannenberg_Wu_2018, title={1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur}, volume={2018}, DOI={<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>}, number={10}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Hu, Yuya and Yin, Zhiping and Werner, Thomas and Spannenberg, Anke and Wu, Xiao-Feng}, year={2018}, pages={1274–1276} }","mla":"Hu, Yuya, et al. “1,8-Diazabicyclo[5.4.0]Undec-7-Ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur.” <i>European Journal of Organic Chemistry</i>, vol. 2018, no. 10, Wiley, 2018, pp. 1274–76, doi:<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>."},"_id":"37968","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","extern":"1","alternative_title":["1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur"],"type":"journal_article","status":"public","publisher":"Wiley","date_created":"2023-01-22T20:46:32Z","title":"1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur","issue":"10","year":"2018","keyword":["Organic Chemistry","Physical and Theoretical Chemistry"],"language":[{"iso":"eng"}],"publication":"European Journal of Organic Chemistry"},{"year":"2018","issue":"8","title":"Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T20:46:04Z","publication":"ACS Sustainable Chemistry and Engineering","keyword":["T1","T2","CSSD"],"language":[{"iso":"eng"}],"intvolume":"         6","page":"10778-10788","citation":{"apa":"Steinbauer, J., Kubis, C., Ludwig, R., &#38; Werner, T. (2018). Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach. <i>ACS Sustainable Chemistry and Engineering</i>, <i>6</i>(8), 10778–10788. <a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">https://doi.org/10.1021/acssuschemeng.8b02093</a>","short":"J. Steinbauer, C. Kubis, R. Ludwig, T. Werner, ACS Sustainable Chemistry and Engineering 6 (2018) 10778–10788.","bibtex":"@article{Steinbauer_Kubis_Ludwig_Werner_2018, title={Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach}, volume={6}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">10.1021/acssuschemeng.8b02093</a>}, number={8}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Steinbauer, Johannes and Kubis, Christoph and Ludwig, Ralf and Werner, Thomas}, year={2018}, pages={10778–10788} }","mla":"Steinbauer, Johannes, et al. “Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 6, no. 8, American Chemical Society (ACS), 2018, pp. 10778–88, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">10.1021/acssuschemeng.8b02093</a>.","ama":"Steinbauer J, Kubis C, Ludwig R, Werner T. Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach. <i>ACS Sustainable Chemistry and Engineering</i>. 2018;6(8):10778-10788. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">10.1021/acssuschemeng.8b02093</a>","chicago":"Steinbauer, Johannes, Christoph Kubis, Ralf Ludwig, and Thomas Werner. “Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach.” <i>ACS Sustainable Chemistry and Engineering</i> 6, no. 8 (2018): 10778–88. <a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">https://doi.org/10.1021/acssuschemeng.8b02093</a>.","ieee":"J. Steinbauer, C. Kubis, R. Ludwig, and T. Werner, “Mechanistic Study on the Addition of CO<sub>2</sub> to Epoxides Catalyzed by Ammonium and Phosphonium Salts: A Combined Spectroscopic and Kinetic Approach,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 6, no. 8, pp. 10778–10788, 2018, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.8b02093\">10.1021/acssuschemeng.8b02093</a>."},"publication_identifier":{"issn":["2168-0485","2168-0485"]},"publication_status":"published","doi":"10.1021/acssuschemeng.8b02093","date_updated":"2025-11-10T09:04:50Z","volume":6,"author":[{"full_name":"Steinbauer, Johannes","last_name":"Steinbauer","first_name":"Johannes"},{"full_name":"Kubis, Christoph","last_name":"Kubis","first_name":"Christoph"},{"first_name":"Ralf","last_name":"Ludwig","full_name":"Ludwig, Ralf"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"status":"public","type":"journal_article","extern":"1","_id":"37967","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271"},{"type":"journal_article","publication":"RSC Advances","abstract":[{"text":"<p>Simple zinc organyls (R<sub>2</sub>Zn) efficiently catalyze the copolymerization of CO<sub>2</sub> and cyclohexene oxide. The effect of various reaction parameters has been studied. The reaction proceeds under halogen-free conditions and no co-catalyst is required.</p>","lang":"eng"}],"status":"public","_id":"37969","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}],"extern":"1","publication_status":"published","publication_identifier":{"issn":["2046-2069"]},"issue":"7","year":"2018","citation":{"ieee":"C. Wulf, U. Doering, and T. Werner, “Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls,” <i>RSC Advances</i>, vol. 8, no. 7, pp. 3673–3679, 2018, doi: <a href=\"https://doi.org/10.1039/c7ra12535f\">10.1039/c7ra12535f</a>.","chicago":"Wulf, Christoph, Ulrike Doering, and Thomas Werner. “Copolymerization of CO<sub>2</sub> and Epoxides Mediated by Zinc Organyls.” <i>RSC Advances</i> 8, no. 7 (2018): 3673–79. <a href=\"https://doi.org/10.1039/c7ra12535f\">https://doi.org/10.1039/c7ra12535f</a>.","ama":"Wulf C, Doering U, Werner T. Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls. <i>RSC Advances</i>. 2018;8(7):3673-3679. doi:<a href=\"https://doi.org/10.1039/c7ra12535f\">10.1039/c7ra12535f</a>","short":"C. Wulf, U. Doering, T. Werner, RSC Advances 8 (2018) 3673–3679.","mla":"Wulf, Christoph, et al. “Copolymerization of CO<sub>2</sub> and Epoxides Mediated by Zinc Organyls.” <i>RSC Advances</i>, vol. 8, no. 7, Royal Society of Chemistry (RSC), 2018, pp. 3673–79, doi:<a href=\"https://doi.org/10.1039/c7ra12535f\">10.1039/c7ra12535f</a>.","bibtex":"@article{Wulf_Doering_Werner_2018, title={Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls}, volume={8}, DOI={<a href=\"https://doi.org/10.1039/c7ra12535f\">10.1039/c7ra12535f</a>}, number={7}, journal={RSC Advances}, publisher={Royal Society of Chemistry (RSC)}, author={Wulf, Christoph and Doering, Ulrike and Werner, Thomas}, year={2018}, pages={3673–3679} }","apa":"Wulf, C., Doering, U., &#38; Werner, T. (2018). Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls. <i>RSC Advances</i>, <i>8</i>(7), 3673–3679. <a href=\"https://doi.org/10.1039/c7ra12535f\">https://doi.org/10.1039/c7ra12535f</a>"},"intvolume":"         8","page":"3673-3679","date_updated":"2025-11-10T09:03:07Z","publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-22T20:46:56Z","author":[{"last_name":"Wulf","full_name":"Wulf, Christoph","first_name":"Christoph"},{"last_name":"Doering","full_name":"Doering, Ulrike","first_name":"Ulrike"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"volume":8,"title":"Copolymerization of CO<sub>2</sub> and epoxides mediated by zinc organyls","doi":"10.1039/c7ra12535f"},{"title":"Trendbericht Organische Chemie 2017","date_created":"2026-03-11T10:24:32Z","publisher":"Wiley","year":"2018","issue":"3","language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"<jats:title>Abstract</jats:title><jats:p>Molekularer Knoten mit topologischer Chiralität – Strukturaufklärung des Polyol‐Makrolids Deplelid A – Totalsynthese von Crocagin A – Organokatalyse in supramolekularen Aggregaten – nachhaltige Oxidation an Oxymorphon – eisenkatalysierte enantioselektive C‐H‐Aktivierung‐ und Alkylierung – fluoreszierendes künstliches DNA‐Basenpaar</jats:p>"}],"publication":"Nachrichten aus der Chemie","doi":"10.1002/nadc.20184072148","volume":66,"author":[{"first_name":"Bernd","full_name":"Straub, Bernd","last_name":"Straub"},{"last_name":"Andexer","full_name":"Andexer, Jennifer N.","first_name":"Jennifer N."},{"first_name":"Christoph","full_name":"Arenz, Christoph","last_name":"Arenz"},{"full_name":"Beifuss, Uwe","last_name":"Beifuss","first_name":"Uwe"},{"first_name":"Florian","full_name":"Beuerle, Florian","last_name":"Beuerle"},{"full_name":"Brasholz, Malte","last_name":"Brasholz","first_name":"Malte"},{"first_name":"Rolf","last_name":"Breinbauer","full_name":"Breinbauer, Rolf"},{"last_name":"Ditrich","full_name":"Ditrich, Klaus","first_name":"Klaus"},{"last_name":"Ernst","full_name":"Ernst, Martin","first_name":"Martin"},{"last_name":"Gulder","full_name":"Gulder, Tobias A. M.","first_name":"Tobias A. M."},{"first_name":"Markus","last_name":"Kordes","full_name":"Kordes, Markus"},{"first_name":"Anke","full_name":"Krueger, Anke","last_name":"Krueger"},{"full_name":"Lehmann, Matthias","last_name":"Lehmann","first_name":"Matthias"},{"first_name":"Thomas","last_name":"Lindel","full_name":"Lindel, Thomas"},{"first_name":"Steffen","full_name":"Lüdeke, Steffen","last_name":"Lüdeke"},{"last_name":"Luy","full_name":"Luy, Burkhard","first_name":"Burkhard"},{"full_name":"Meier, Michael A. R.","last_name":"Meier","first_name":"Michael A. R."},{"full_name":"Mück‐Lichtenfeld, Christian","last_name":"Mück‐Lichtenfeld","first_name":"Christian"},{"first_name":"Claudia","full_name":"Muhle‐Goll, Claudia","last_name":"Muhle‐Goll"},{"full_name":"Narine, Arun","last_name":"Narine","first_name":"Arun"},{"first_name":"Jan","id":"53339","full_name":"Paradies, Jan","last_name":"Paradies","orcid":"0000-0002-3698-668X"},{"last_name":"Pfau","full_name":"Pfau, Roland","first_name":"Roland"},{"first_name":"Jörg","full_name":"Pietruszka, Jörg","last_name":"Pietruszka"},{"first_name":"Norbert","full_name":"Schaschke, Norbert","last_name":"Schaschke"},{"first_name":"Mathias O.","last_name":"Senge","full_name":"Senge, Mathias O."},{"first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"},{"first_name":"Daniel B.","last_name":"Werz","full_name":"Werz, Daniel B."},{"last_name":"Winter","full_name":"Winter, Christian","first_name":"Christian"},{"last_name":"Worgull","full_name":"Worgull, Dennis","first_name":"Dennis"}],"date_updated":"2026-03-11T10:24:43Z","page":"249-280","intvolume":"        66","citation":{"bibtex":"@article{Straub_Andexer_Arenz_Beifuss_Beuerle_Brasholz_Breinbauer_Ditrich_Ernst_Gulder_et al._2018, title={Trendbericht Organische Chemie 2017}, volume={66}, DOI={<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Straub, Bernd and Andexer, Jennifer N. and Arenz, Christoph and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ditrich, Klaus and Ernst, Martin and Gulder, Tobias A. M. and et al.}, year={2018}, pages={249–280} }","short":"B. Straub, J.N. Andexer, C. Arenz, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, K. Ditrich, M. Ernst, T.A.M. Gulder, M. Kordes, A. Krueger, M. Lehmann, T. Lindel, S. Lüdeke, B. Luy, M.A.R. Meier, C. Mück‐Lichtenfeld, C. Muhle‐Goll, A. Narine, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M.O. Senge, T. Werner, D.B. Werz, C. Winter, D. Worgull, Nachrichten Aus Der Chemie 66 (2018) 249–280.","mla":"Straub, Bernd, et al. “Trendbericht Organische Chemie 2017.” <i>Nachrichten Aus Der Chemie</i>, vol. 66, no. 3, Wiley, 2018, pp. 249–80, doi:<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>.","ama":"Straub B, Andexer JN, Arenz C, et al. Trendbericht Organische Chemie 2017. <i>Nachrichten aus der Chemie</i>. 2018;66(3):249-280. doi:<a href=\"https://doi.org/10.1002/nadc.20184072148\">10.1002/nadc.20184072148</a>","apa":"Straub, B., Andexer, J. 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Andexer, Christoph Arenz, Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, et al. “Trendbericht Organische Chemie 2017.” <i>Nachrichten Aus Der Chemie</i> 66, no. 3 (2018): 249–80. <a href=\"https://doi.org/10.1002/nadc.20184072148\">https://doi.org/10.1002/nadc.20184072148</a>."},"publication_identifier":{"issn":["1439-9598","1868-0054"]},"publication_status":"published","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"64897","status":"public","type":"journal_article"},{"department":[{"_id":"163"}],"user_id":"94","_id":"32445","article_type":"original","article_number":"1700506","type":"journal_article","status":"public","volume":219,"author":[{"last_name":"Yu","full_name":"Yu, Xiaoqian","first_name":"Xiaoqian"},{"first_name":"Marie-Theres","full_name":"Picker, Marie-Theres","last_name":"Picker"},{"first_name":"Martin","last_name":"Schneider","full_name":"Schneider, Martin"},{"id":"94","full_name":"Herberg, Artjom","last_name":"Herberg","first_name":"Artjom"},{"first_name":"Sagrario","last_name":"Pascual","full_name":"Pascual, Sagrario"},{"full_name":"Fontaine, Laurent","last_name":"Fontaine","first_name":"Laurent"},{"full_name":"Kuckling, Dirk","id":"287","last_name":"Kuckling","first_name":"Dirk"}],"date_updated":"2022-07-28T09:58:34Z","doi":"10.1002/macp.201700506","publication_identifier":{"issn":["1022-1352"]},"publication_status":"published","intvolume":"       219","citation":{"ama":"Yu X, Picker M-T, Schneider M, et al. Synthesis of Amphiphilic Block Copolymers Based on SKA by RAFT Polymerization. <i>Macromolecular Chemistry and Physics</i>. 2017;219(5). doi:<a href=\"https://doi.org/10.1002/macp.201700506\">10.1002/macp.201700506</a>","chicago":"Yu, Xiaoqian, Marie-Theres Picker, Martin Schneider, Artjom Herberg, Sagrario Pascual, Laurent Fontaine, and Dirk Kuckling. “Synthesis of Amphiphilic Block Copolymers Based on SKA by RAFT Polymerization.” <i>Macromolecular Chemistry and Physics</i> 219, no. 5 (2017). <a href=\"https://doi.org/10.1002/macp.201700506\">https://doi.org/10.1002/macp.201700506</a>.","ieee":"X. Yu <i>et al.</i>, “Synthesis of Amphiphilic Block Copolymers Based on SKA by RAFT Polymerization,” <i>Macromolecular Chemistry and Physics</i>, vol. 219, no. 5, Art. no. 1700506, 2017, doi: <a href=\"https://doi.org/10.1002/macp.201700506\">10.1002/macp.201700506</a>.","short":"X. Yu, M.-T. Picker, M. Schneider, A. Herberg, S. Pascual, L. Fontaine, D. Kuckling, Macromolecular Chemistry and Physics 219 (2017).","bibtex":"@article{Yu_Picker_Schneider_Herberg_Pascual_Fontaine_Kuckling_2017, title={Synthesis of Amphiphilic Block Copolymers Based on SKA by RAFT Polymerization}, volume={219}, DOI={<a href=\"https://doi.org/10.1002/macp.201700506\">10.1002/macp.201700506</a>}, number={51700506}, journal={Macromolecular Chemistry and Physics}, publisher={Wiley}, author={Yu, Xiaoqian and Picker, Marie-Theres and Schneider, Martin and Herberg, Artjom and Pascual, Sagrario and Fontaine, Laurent and Kuckling, Dirk}, year={2017} }","mla":"Yu, Xiaoqian, et al. “Synthesis of Amphiphilic Block Copolymers Based on SKA by RAFT Polymerization.” <i>Macromolecular Chemistry and Physics</i>, vol. 219, no. 5, 1700506, Wiley, 2017, doi:<a href=\"https://doi.org/10.1002/macp.201700506\">10.1002/macp.201700506</a>.","apa":"Yu, X., Picker, M.-T., Schneider, M., Herberg, A., Pascual, S., Fontaine, L., &#38; Kuckling, D. (2017). Synthesis of Amphiphilic Block Copolymers Based on SKA by RAFT Polymerization. <i>Macromolecular Chemistry and Physics</i>, <i>219</i>(5), Article 1700506. <a href=\"https://doi.org/10.1002/macp.201700506\">https://doi.org/10.1002/macp.201700506</a>"},"language":[{"iso":"eng"}],"keyword":["Materials Chemistry","Organic Chemistry","Polymers and Plastics","Physical and Theoretical Chemistry","Condensed Matter Physics"],"publication":"Macromolecular Chemistry and Physics","date_created":"2022-07-28T09:52:27Z","publisher":"Wiley","title":"Synthesis of Amphiphilic Block Copolymers Based on SKA by RAFT Polymerization","issue":"5","year":"2017"},{"volume":23,"date_created":"2023-01-10T09:12:03Z","author":[{"last_name":"Bestgen","full_name":"Bestgen, Sebastian","first_name":"Sebastian"},{"first_name":"Carmen","last_name":"Seidl","full_name":"Seidl, Carmen"},{"full_name":"Wiesner, Thomas","last_name":"Wiesner","first_name":"Thomas"},{"full_name":"Zimmer, Andreas","last_name":"Zimmer","first_name":"Andreas"},{"full_name":"Falk, Martina","last_name":"Falk","first_name":"Martina"},{"full_name":"Köberle, Beate","last_name":"Köberle","first_name":"Beate"},{"first_name":"Martina","last_name":"Austeri","full_name":"Austeri, Martina"},{"first_name":"Jan","orcid":"0000-0002-3698-668X","last_name":"Paradies","full_name":"Paradies, Jan","id":"53339"},{"full_name":"Bräse, Stefan","last_name":"Bräse","first_name":"Stefan"},{"first_name":"Ute","full_name":"Schepers, Ute","last_name":"Schepers"},{"first_name":"Peter W.","last_name":"Roesky","full_name":"Roesky, Peter W."}],"publisher":"Wiley","date_updated":"2023-01-23T12:46:34Z","doi":"10.1002/chem.201700517","title":"Inside Back Cover: Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes (Chem. Eur. J. 26/2017)","issue":"26","publication_identifier":{"issn":["0947-6539"]},"publication_status":"published","intvolume":"        23","page":"6459-6459","citation":{"chicago":"Bestgen, Sebastian, Carmen Seidl, Thomas Wiesner, Andreas Zimmer, Martina Falk, Beate Köberle, Martina Austeri, et al. “Inside Back Cover: Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes (Chem. Eur. J. 26/2017).” <i>Chemistry - A European Journal</i> 23, no. 26 (2017): 6459–6459. <a href=\"https://doi.org/10.1002/chem.201700517\">https://doi.org/10.1002/chem.201700517</a>.","ieee":"S. Bestgen <i>et al.</i>, “Inside Back Cover: Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes (Chem. Eur. J. 26/2017),” <i>Chemistry - A European Journal</i>, vol. 23, no. 26, pp. 6459–6459, 2017, doi: <a href=\"https://doi.org/10.1002/chem.201700517\">10.1002/chem.201700517</a>.","ama":"Bestgen S, Seidl C, Wiesner T, et al. Inside Back Cover: Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes (Chem. Eur. J. 26/2017). <i>Chemistry - A European Journal</i>. 2017;23(26):6459-6459. doi:<a href=\"https://doi.org/10.1002/chem.201700517\">10.1002/chem.201700517</a>","bibtex":"@article{Bestgen_Seidl_Wiesner_Zimmer_Falk_Köberle_Austeri_Paradies_Bräse_Schepers_et al._2017, title={Inside Back Cover: Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes (Chem. Eur. J. 26/2017)}, volume={23}, DOI={<a href=\"https://doi.org/10.1002/chem.201700517\">10.1002/chem.201700517</a>}, number={26}, journal={Chemistry - A European Journal}, publisher={Wiley}, author={Bestgen, Sebastian and Seidl, Carmen and Wiesner, Thomas and Zimmer, Andreas and Falk, Martina and Köberle, Beate and Austeri, Martina and Paradies, Jan and Bräse, Stefan and Schepers, Ute and et al.}, year={2017}, pages={6459–6459} }","short":"S. Bestgen, C. Seidl, T. Wiesner, A. Zimmer, M. Falk, B. Köberle, M. Austeri, J. Paradies, S. Bräse, U. Schepers, P.W. Roesky, Chemistry - A European Journal 23 (2017) 6459–6459.","mla":"Bestgen, Sebastian, et al. “Inside Back Cover: Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes (Chem. Eur. J. 26/2017).” <i>Chemistry - A European Journal</i>, vol. 23, no. 26, Wiley, 2017, pp. 6459–6459, doi:<a href=\"https://doi.org/10.1002/chem.201700517\">10.1002/chem.201700517</a>.","apa":"Bestgen, S., Seidl, C., Wiesner, T., Zimmer, A., Falk, M., Köberle, B., Austeri, M., Paradies, J., Bräse, S., Schepers, U., &#38; Roesky, P. W. (2017). Inside Back Cover: Double-Strand DNA Breaks Induced by Paracyclophane Gold(I) Complexes (Chem. Eur. J. 26/2017). <i>Chemistry - A European Journal</i>, <i>23</i>(26), 6459–6459. <a href=\"https://doi.org/10.1002/chem.201700517\">https://doi.org/10.1002/chem.201700517</a>"},"year":"2017","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339","_id":"35705","language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis","Organic Chemistry"],"publication":"Chemistry - A European Journal","type":"journal_article","status":"public"},{"doi":"10.1002/ejic.201601364","title":"Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina","author":[{"id":"11848","full_name":"Weinberger, Christian","last_name":"Weinberger","first_name":"Christian"},{"first_name":"Zimei","last_name":"Chen","full_name":"Chen, Zimei"},{"full_name":"Birnbaum, Wolfgang","last_name":"Birnbaum","first_name":"Wolfgang"},{"full_name":"Kuckling, Dirk","id":"287","last_name":"Kuckling","first_name":"Dirk"},{"first_name":"Michael","orcid":"0000-0003-1711-2722","last_name":"Tiemann","id":"23547","full_name":"Tiemann, Michael"}],"date_created":"2021-10-08T11:05:54Z","date_updated":"2023-03-08T10:24:33Z","page":"1026-1031","citation":{"mla":"Weinberger, Christian, et al. “Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina.” <i>European Journal of Inorganic Chemistry</i>, 2017, pp. 1026–31, doi:<a href=\"https://doi.org/10.1002/ejic.201601364\">10.1002/ejic.201601364</a>.","short":"C. Weinberger, Z. Chen, W. Birnbaum, D. Kuckling, M. Tiemann, European Journal of Inorganic Chemistry (2017) 1026–1031.","bibtex":"@article{Weinberger_Chen_Birnbaum_Kuckling_Tiemann_2017, title={Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina}, DOI={<a href=\"https://doi.org/10.1002/ejic.201601364\">10.1002/ejic.201601364</a>}, journal={European Journal of Inorganic Chemistry}, author={Weinberger, Christian and Chen, Zimei and Birnbaum, Wolfgang and Kuckling, Dirk and Tiemann, Michael}, year={2017}, pages={1026–1031} }","apa":"Weinberger, C., Chen, Z., Birnbaum, W., Kuckling, D., &#38; Tiemann, M. (2017). Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina. <i>European Journal of Inorganic Chemistry</i>, 1026–1031. <a href=\"https://doi.org/10.1002/ejic.201601364\">https://doi.org/10.1002/ejic.201601364</a>","ama":"Weinberger C, Chen Z, Birnbaum W, Kuckling D, Tiemann M. Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina. <i>European Journal of Inorganic Chemistry</i>. Published online 2017:1026-1031. doi:<a href=\"https://doi.org/10.1002/ejic.201601364\">10.1002/ejic.201601364</a>","chicago":"Weinberger, Christian, Zimei Chen, Wolfgang Birnbaum, Dirk Kuckling, and Michael Tiemann. “Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina.” <i>European Journal of Inorganic Chemistry</i>, 2017, 1026–31. <a href=\"https://doi.org/10.1002/ejic.201601364\">https://doi.org/10.1002/ejic.201601364</a>.","ieee":"C. Weinberger, Z. Chen, W. Birnbaum, D. Kuckling, and M. Tiemann, “Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina,” <i>European Journal of Inorganic Chemistry</i>, pp. 1026–1031, 2017, doi: <a href=\"https://doi.org/10.1002/ejic.201601364\">10.1002/ejic.201601364</a>."},"year":"2017","quality_controlled":"1","publication_identifier":{"issn":["1434-1948"]},"publication_status":"published","language":[{"iso":"eng"}],"article_type":"original","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"},{"_id":"311"}],"user_id":"23547","_id":"25915","status":"public","abstract":[{"lang":"eng","text":"Dimethylacrylamide-based hydrogels were utilized as porogenic matrices in the synthesis of mesoporous aluminum oxide (γ-Al2O3) with specific BET surface areas up to 360 m2 g–1. Polymers with molecular mass in the range 12000–35000 g mol–1 were synthesized from dimethylacrylamide and various comonomers by free-radical polymerization. Photo-cross-linking of the polymers and impregnation with aluminum nitrate [Al(NO3)3] was carried out in a single step, followed by formation of Al(OH)3/AlO(OH) and subsequent calcination. Calcination led to the formation of mesoporous Al2O3 and simultaneous combustion of the hydrogel. The structural properties of the products were characterized by powder XRD, N2 physisorption analysis, Hg intrusion porosimetry, and thermogravimetric analysis."}],"publication":"European Journal of Inorganic Chemistry","type":"journal_article"},{"language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"Dimethylacrylamide-based hydrogels were utilized as porogenic matrices in the synthesis of mesoporous aluminum oxide (γ-Al2O3) with specific BET surface areas up to 360 m2 g–1. Polymers with molecular mass in the range 12000–35000 g mol–1 were synthesized from dimethylacrylamide and various comonomers by free-radical polymerization. Photo-cross-linking of the polymers and impregnation with aluminum nitrate [Al(NO3)3] was carried out in a single step, followed by formation of Al(OH)3/AlO(OH) and subsequent calcination. Calcination led to the formation of mesoporous Al2O3 and simultaneous combustion of the hydrogel. The structural properties of the products were characterized by powder XRD, N2 physisorption analysis, Hg intrusion porosimetry, and thermogravimetric analysis."}],"publication":"Processes","title":"Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia","date_created":"2021-10-08T10:53:18Z","year":"2017","quality_controlled":"1","article_number":"70","article_type":"original","_id":"25914","user_id":"23547","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"},{"_id":"311"}],"status":"public","type":"journal_article","main_file_link":[{"url":"https://www.mdpi.com/2227-9717/5/4/70/pdf?version=1510132833","open_access":"1"}],"doi":"10.3390/pr5040070","date_updated":"2023-03-08T10:25:25Z","oa":"1","author":[{"first_name":"Zimei","last_name":"Chen","full_name":"Chen, Zimei"},{"first_name":"Christian","last_name":"Weinberger","full_name":"Weinberger, Christian","id":"11848"},{"full_name":"Tiemann, Michael","id":"23547","orcid":"0000-0003-1711-2722","last_name":"Tiemann","first_name":"Michael"},{"id":"287","full_name":"Kuckling, Dirk","last_name":"Kuckling","first_name":"Dirk"}],"citation":{"short":"Z. Chen, C. Weinberger, M. Tiemann, D. Kuckling, Processes (2017).","bibtex":"@article{Chen_Weinberger_Tiemann_Kuckling_2017, title={Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia}, DOI={<a href=\"https://doi.org/10.3390/pr5040070\">10.3390/pr5040070</a>}, number={70}, journal={Processes}, author={Chen, Zimei and Weinberger, Christian and Tiemann, Michael and Kuckling, Dirk}, year={2017} }","mla":"Chen, Zimei, et al. “Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia.” <i>Processes</i>, 70, 2017, doi:<a href=\"https://doi.org/10.3390/pr5040070\">10.3390/pr5040070</a>.","apa":"Chen, Z., Weinberger, C., Tiemann, M., &#38; Kuckling, D. (2017). Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia. <i>Processes</i>, Article 70. <a href=\"https://doi.org/10.3390/pr5040070\">https://doi.org/10.3390/pr5040070</a>","ama":"Chen Z, Weinberger C, Tiemann M, Kuckling D. Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia. <i>Processes</i>. Published online 2017. doi:<a href=\"https://doi.org/10.3390/pr5040070\">10.3390/pr5040070</a>","chicago":"Chen, Zimei, Christian Weinberger, Michael Tiemann, and Dirk Kuckling. “Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia.” <i>Processes</i>, 2017. <a href=\"https://doi.org/10.3390/pr5040070\">https://doi.org/10.3390/pr5040070</a>.","ieee":"Z. Chen, C. Weinberger, M. Tiemann, and D. Kuckling, “Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia,” <i>Processes</i>, Art. no. 70, 2017, doi: <a href=\"https://doi.org/10.3390/pr5040070\">10.3390/pr5040070</a>."},"publication_status":"published","publication_identifier":{"issn":["2227-9717"]}},{"publication":"ACS Catalysis","language":[{"iso":"eng"}],"keyword":["T1","T3","T4"],"issue":"1","year":"2017","date_created":"2023-01-22T20:47:19Z","publisher":"American Chemical Society (ACS)","title":"Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions","type":"journal_article","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37970","extern":"1","publication_status":"published","publication_identifier":{"issn":["2155-5435","2155-5435"]},"citation":{"apa":"Longwitz, L., Steinbauer, J., Spannenberg, A., &#38; Werner, T. (2017). Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions. <i>ACS Catalysis</i>, <i>8</i>(1), 665–672. <a href=\"https://doi.org/10.1021/acscatal.7b03367\">https://doi.org/10.1021/acscatal.7b03367</a>","short":"L. Longwitz, J. Steinbauer, A. Spannenberg, T. Werner, ACS Catalysis 8 (2017) 665–672.","mla":"Longwitz, Lars, et al. “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions.” <i>ACS Catalysis</i>, vol. 8, no. 1, American Chemical Society (ACS), 2017, pp. 665–72, doi:<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>.","bibtex":"@article{Longwitz_Steinbauer_Spannenberg_Werner_2017, title={Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions}, volume={8}, DOI={<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>}, number={1}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Longwitz, Lars and Steinbauer, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2017}, pages={665–672} }","chicago":"Longwitz, Lars, Johannes Steinbauer, Anke Spannenberg, and Thomas Werner. “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions.” <i>ACS Catalysis</i> 8, no. 1 (2017): 665–72. <a href=\"https://doi.org/10.1021/acscatal.7b03367\">https://doi.org/10.1021/acscatal.7b03367</a>.","ieee":"L. Longwitz, J. Steinbauer, A. Spannenberg, and T. Werner, “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions,” <i>ACS Catalysis</i>, vol. 8, no. 1, pp. 665–672, 2017, doi: <a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>.","ama":"Longwitz L, Steinbauer J, Spannenberg A, Werner T. Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions. <i>ACS Catalysis</i>. 2017;8(1):665-672. doi:<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>"},"page":"665-672","intvolume":"         8","author":[{"last_name":"Longwitz","full_name":"Longwitz, Lars","first_name":"Lars"},{"first_name":"Johannes","full_name":"Steinbauer, Johannes","last_name":"Steinbauer"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"orcid":"https://orcid.org/0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"volume":8,"date_updated":"2025-11-06T08:38:07Z","doi":"10.1021/acscatal.7b03367"}]