[{"date_created":"2021-09-07T10:23:25Z","type":"journal_article","department":[{"_id":"311"},{"_id":"35"},{"_id":"307"},{"_id":"2"}],"publication":"Nanotechnology","abstract":[{"text":"Micropatterned nanoporous aluminum oxide arrays are prepared on silicon wafer substrates by using photopolymerized poly(dimethylacrylamide) hydrogels as porogenic matrices. Hydrogel micropatterns are fabricated by spreading the prepolymer mixture on the substrate, followed by UV photopolymerization through a micropatterned mask. The hydrogel is covalently bonded to the substrate surface. Al2O3 is produced by swelling the hydrogel in a saturated aluminum nitrate solution and subsequent thermal conversion/calcination. As a result, micropatterned porous Al2O3 microdots with heights in µm range and large specific surface areas up to 274 m2 g−1 are obtained. Hence, the hydrogel fulfills a dual templating function, namely micropatterning and nanoporosity generation. The impact of varying the photopolymerization time on the properties of the products is studied. Samples are characterized by light and confocal laser scanning microscopy, scanning electron microscopy, energy-dispersive x-ray spectrometry, and Kr physisorption analysis.","lang":"eng"}],"main_file_link":[{"url":"https://iopscience.iop.org/article/10.1088/1361-6528/aba710/pdf","open_access":"1"}],"article_number":"445601","language":[{"iso":"eng"}],"doi":"10.1088/1361-6528/aba710","title":"Nanoporous aluminum oxide micropatterns prepared by hydrogel templating","year":"2020","author":[{"last_name":"Chen","first_name":"Zimei","full_name":"Chen, Zimei"},{"id":"287","last_name":"Kuckling","first_name":"Dirk","full_name":"Kuckling, Dirk"},{"id":"23547","last_name":"Tiemann","first_name":"Michael","orcid":"0000-0003-1711-2722","full_name":"Tiemann, Michael"}],"publication_identifier":{"issn":["0957-4484","1361-6528"]},"date_updated":"2023-03-08T08:26:12Z","publication_status":"published","intvolume":"        31","article_type":"original","oa":"1","citation":{"bibtex":"@article{Chen_Kuckling_Tiemann_2020, title={Nanoporous aluminum oxide micropatterns prepared by hydrogel templating}, volume={31}, DOI={<a href=\"https://doi.org/10.1088/1361-6528/aba710\">10.1088/1361-6528/aba710</a>}, number={445601}, journal={Nanotechnology}, publisher={IOP Publishing}, author={Chen, Zimei and Kuckling, Dirk and Tiemann, Michael}, year={2020} }","ama":"Chen Z, Kuckling D, Tiemann M. Nanoporous aluminum oxide micropatterns prepared by hydrogel templating. <i>Nanotechnology</i>. 2020;31. doi:<a href=\"https://doi.org/10.1088/1361-6528/aba710\">10.1088/1361-6528/aba710</a>","mla":"Chen, Zimei, et al. “Nanoporous Aluminum Oxide Micropatterns Prepared by Hydrogel Templating.” <i>Nanotechnology</i>, vol. 31, 445601, IOP Publishing, 2020, doi:<a href=\"https://doi.org/10.1088/1361-6528/aba710\">10.1088/1361-6528/aba710</a>.","short":"Z. Chen, D. Kuckling, M. Tiemann, Nanotechnology 31 (2020).","chicago":"Chen, Zimei, Dirk Kuckling, and Michael Tiemann. “Nanoporous Aluminum Oxide Micropatterns Prepared by Hydrogel Templating.” <i>Nanotechnology</i> 31 (2020). <a href=\"https://doi.org/10.1088/1361-6528/aba710\">https://doi.org/10.1088/1361-6528/aba710</a>.","ieee":"Z. Chen, D. Kuckling, and M. Tiemann, “Nanoporous aluminum oxide micropatterns prepared by hydrogel templating,” <i>Nanotechnology</i>, vol. 31, Art. no. 445601, 2020, doi: <a href=\"https://doi.org/10.1088/1361-6528/aba710\">10.1088/1361-6528/aba710</a>.","apa":"Chen, Z., Kuckling, D., &#38; Tiemann, M. (2020). Nanoporous aluminum oxide micropatterns prepared by hydrogel templating. <i>Nanotechnology</i>, <i>31</i>, Article 445601. <a href=\"https://doi.org/10.1088/1361-6528/aba710\">https://doi.org/10.1088/1361-6528/aba710</a>"},"quality_controlled":"1","publisher":"IOP Publishing","_id":"23854","user_id":"23547","volume":31,"status":"public"},{"citation":{"chicago":"Andexer, Jennifer N., Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, Julian Greb, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 68, no. 3 (2020): 42–72. <a href=\"https://doi.org/10.1002/nadc.20204095515\">https://doi.org/10.1002/nadc.20204095515</a>.","short":"J.N. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, J. Greb, T. Gulder, W. Hüttel, S. Kath‐Schorr, M. Kordes, M. Lehmann, T. Lindel, B. Luy, C. Mück‐Lichtenfeld, C. Muhle, A. Narine, J. Niemeyer, J. Paradies, R. Pfau, J. Pietruszka, N. Schaschke, M. Senge, B.F. Straub, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 68 (2020) 42–72.","ieee":"J. N. Andexer <i>et al.</i>, “Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 68, no. 3, pp. 42–72, 2020, doi: <a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>.","apa":"Andexer, J. N., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Greb, J., Gulder, T., Hüttel, W., Kath‐Schorr, S., Kordes, M., Lehmann, M., Lindel, T., Luy, B., Mück‐Lichtenfeld, C., Muhle, C., Narine, A., Niemeyer, J., Paradies, J., … Winter, C. (2020). Organische Chemie. <i>Nachrichten Aus Der Chemie</i>, <i>68</i>(3), 42–72. <a href=\"https://doi.org/10.1002/nadc.20204095515\">https://doi.org/10.1002/nadc.20204095515</a>","bibtex":"@article{Andexer_Beifuss_Beuerle_Brasholz_Breinbauer_Ernst_Greb_Gulder_Hüttel_Kath‐Schorr_et al._2020, title={Organische Chemie}, volume={68}, DOI={<a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>}, number={3}, journal={Nachrichten aus der Chemie}, publisher={Wiley}, author={Andexer, Jennifer N. and Beifuss, Uwe and Beuerle, Florian and Brasholz, Malte and Breinbauer, Rolf and Ernst, Martin and Greb, Julian and Gulder, Tobias and Hüttel, Wolfgang and Kath‐Schorr, Stephanie and et al.}, year={2020}, pages={42–72} }","ama":"Andexer JN, Beifuss U, Beuerle F, et al. Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2020;68(3):42-72. doi:<a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>","mla":"Andexer, Jennifer N., et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 68, no. 3, Wiley, 2020, pp. 42–72, doi:<a href=\"https://doi.org/10.1002/nadc.20204095515\">10.1002/nadc.20204095515</a>."},"status":"public","publisher":"Wiley","_id":"37956","page":"42-72","volume":68,"user_id":"89271","publication":"Nachrichten aus der Chemie","issue":"3","extern":"1","date_created":"2023-01-22T20:40:48Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"},{"_id":"389"}],"type":"journal_article","keyword":["General Chemical Engineering","General Chemistry"],"publication_identifier":{"issn":["1439-9598","1868-0054"]},"author":[{"first_name":"Jennifer N.","last_name":"Andexer","full_name":"Andexer, Jennifer N."},{"full_name":"Beifuss, Uwe","last_name":"Beifuss","first_name":"Uwe"},{"first_name":"Florian","last_name":"Beuerle","full_name":"Beuerle, Florian"},{"last_name":"Brasholz","first_name":"Malte","full_name":"Brasholz, Malte"},{"full_name":"Breinbauer, Rolf","last_name":"Breinbauer","first_name":"Rolf"},{"last_name":"Ernst","first_name":"Martin","full_name":"Ernst, Martin"},{"full_name":"Greb, Julian","first_name":"Julian","last_name":"Greb"},{"full_name":"Gulder, Tobias","last_name":"Gulder","first_name":"Tobias"},{"last_name":"Hüttel","first_name":"Wolfgang","full_name":"Hüttel, Wolfgang"},{"full_name":"Kath‐Schorr, Stephanie","first_name":"Stephanie","last_name":"Kath‐Schorr"},{"first_name":"Markus","last_name":"Kordes","full_name":"Kordes, Markus"},{"full_name":"Lehmann, Matthias","first_name":"Matthias","last_name":"Lehmann"},{"full_name":"Lindel, Thomas","last_name":"Lindel","first_name":"Thomas"},{"full_name":"Luy, Burkhard","first_name":"Burkhard","last_name":"Luy"},{"full_name":"Mück‐Lichtenfeld, Christian","first_name":"Christian","last_name":"Mück‐Lichtenfeld"},{"first_name":"Claudia","last_name":"Muhle","full_name":"Muhle, Claudia"},{"full_name":"Narine, Arun","first_name":"Arun","last_name":"Narine"},{"first_name":"Jörg","last_name":"Niemeyer","full_name":"Niemeyer, Jörg"},{"full_name":"Paradies, Jan","last_name":"Paradies","first_name":"Jan","orcid":"0000-0002-3698-668X","id":"53339"},{"full_name":"Pfau, Roland","last_name":"Pfau","first_name":"Roland"},{"full_name":"Pietruszka, Jörg","last_name":"Pietruszka","first_name":"Jörg"},{"last_name":"Schaschke","first_name":"Norbert","full_name":"Schaschke, Norbert"},{"first_name":"Mathias","last_name":"Senge","full_name":"Senge, Mathias"},{"first_name":"Bernd F.","last_name":"Straub","full_name":"Straub, Bernd F."},{"id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"},{"full_name":"Werz, Daniel B.","first_name":"Daniel B.","last_name":"Werz"},{"first_name":"Christian","last_name":"Winter","full_name":"Winter, Christian"}],"title":"Organische Chemie","year":"2020","intvolume":"        68","publication_status":"published","date_updated":"2025-11-10T08:13:43Z","language":[{"iso":"eng"}],"doi":"10.1002/nadc.20204095515"},{"citation":{"chicago":"Liu, Xin, Lars Longwitz, Brian Spiegelberg, Jan Tönjes, Torsten Beweries, and Thomas Werner. “Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions.” <i>ACS Catalysis</i> 10, no. 22 (2020): 13659–67. <a href=\"https://doi.org/10.1021/acscatal.0c03294\">https://doi.org/10.1021/acscatal.0c03294</a>.","short":"X. Liu, L. Longwitz, B. Spiegelberg, J. Tönjes, T. Beweries, T. Werner, ACS Catalysis 10 (2020) 13659–13667.","ieee":"X. Liu, L. Longwitz, B. Spiegelberg, J. Tönjes, T. Beweries, and T. Werner, “Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions,” <i>ACS Catalysis</i>, vol. 10, no. 22, pp. 13659–13667, 2020, doi: <a href=\"https://doi.org/10.1021/acscatal.0c03294\">10.1021/acscatal.0c03294</a>.","apa":"Liu, X., Longwitz, L., Spiegelberg, B., Tönjes, J., Beweries, T., &#38; Werner, T. (2020). Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions. <i>ACS Catalysis</i>, <i>10</i>(22), 13659–13667. <a href=\"https://doi.org/10.1021/acscatal.0c03294\">https://doi.org/10.1021/acscatal.0c03294</a>","bibtex":"@article{Liu_Longwitz_Spiegelberg_Tönjes_Beweries_Werner_2020, title={Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions}, volume={10}, DOI={<a href=\"https://doi.org/10.1021/acscatal.0c03294\">10.1021/acscatal.0c03294</a>}, number={22}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Liu, Xin and Longwitz, Lars and Spiegelberg, Brian and Tönjes, Jan and Beweries, Torsten and Werner, Thomas}, year={2020}, pages={13659–13667} }","ama":"Liu X, Longwitz L, Spiegelberg B, Tönjes J, Beweries T, Werner T. Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions. <i>ACS Catalysis</i>. 2020;10(22):13659-13667. doi:<a href=\"https://doi.org/10.1021/acscatal.0c03294\">10.1021/acscatal.0c03294</a>","mla":"Liu, Xin, et al. “Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions.” <i>ACS Catalysis</i>, vol. 10, no. 22, American Chemical Society (ACS), 2020, pp. 13659–67, doi:<a href=\"https://doi.org/10.1021/acscatal.0c03294\">10.1021/acscatal.0c03294</a>."},"_id":"37951","publisher":"American Chemical Society (ACS)","page":"13659-13667","volume":10,"user_id":"89271","status":"public","date_created":"2023-01-22T20:35:25Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T3","CSSD"],"type":"journal_article","publication":"ACS Catalysis","issue":"22","extern":"1","language":[{"iso":"eng"}],"doi":"10.1021/acscatal.0c03294","publication_identifier":{"issn":["2155-5435","2155-5435"]},"author":[{"last_name":"Liu","first_name":"Xin","full_name":"Liu, Xin"},{"first_name":"Lars","last_name":"Longwitz","full_name":"Longwitz, Lars"},{"last_name":"Spiegelberg","first_name":"Brian","full_name":"Spiegelberg, Brian"},{"full_name":"Tönjes, Jan","first_name":"Jan","last_name":"Tönjes"},{"last_name":"Beweries","first_name":"Torsten","full_name":"Beweries, Torsten"},{"last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"title":"Erbium-Catalyzed Regioselective Isomerization–Cobalt-Catalyzed Transfer Hydrogenation Sequence for the Synthesis of Anti-Markovnikov Alcohols from Epoxides under Mild Conditions","year":"2020","intvolume":"        10","date_updated":"2025-11-10T08:50:10Z","publication_status":"published"},{"intvolume":"         8","date_updated":"2025-11-10T08:51:03Z","publication_status":"published","publication_identifier":{"issn":["2168-0485","2168-0485"]},"author":[{"first_name":"Christoph","last_name":"Wulf","full_name":"Wulf, Christoph"},{"full_name":"Reckers, Matthias","last_name":"Reckers","first_name":"Matthias"},{"last_name":"Perechodjuk","first_name":"Anna","full_name":"Perechodjuk, Anna"},{"full_name":"Werner, Thomas","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271"}],"year":"2020","title":"Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes","doi":"10.1021/acssuschemeng.9b06662","language":[{"iso":"eng"}],"extern":"1","publication":"ACS Sustainable Chemistry and Engineering","issue":"3","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T3","CSSD"],"date_created":"2023-01-22T20:39:32Z","status":"public","volume":8,"user_id":"89271","publisher":"American Chemical Society (ACS)","_id":"37955","page":"1651-1658","citation":{"short":"C. Wulf, M. Reckers, A. Perechodjuk, T. Werner, ACS Sustainable Chemistry and Engineering 8 (2020) 1651–1658.","chicago":"Wulf, Christoph, Matthias Reckers, Anna Perechodjuk, and Thomas Werner. “Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes.” <i>ACS Sustainable Chemistry and Engineering</i> 8, no. 3 (2020): 1651–58. <a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">https://doi.org/10.1021/acssuschemeng.9b06662</a>.","ieee":"C. Wulf, M. Reckers, A. Perechodjuk, and T. Werner, “Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes,” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 8, no. 3, pp. 1651–1658, 2020, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">10.1021/acssuschemeng.9b06662</a>.","apa":"Wulf, C., Reckers, M., Perechodjuk, A., &#38; Werner, T. (2020). Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes. <i>ACS Sustainable Chemistry and Engineering</i>, <i>8</i>(3), 1651–1658. <a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">https://doi.org/10.1021/acssuschemeng.9b06662</a>","bibtex":"@article{Wulf_Reckers_Perechodjuk_Werner_2020, title={Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes}, volume={8}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">10.1021/acssuschemeng.9b06662</a>}, number={3}, journal={ACS Sustainable Chemistry and Engineering}, publisher={American Chemical Society (ACS)}, author={Wulf, Christoph and Reckers, Matthias and Perechodjuk, Anna and Werner, Thomas}, year={2020}, pages={1651–1658} }","ama":"Wulf C, Reckers M, Perechodjuk A, Werner T. Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes. <i>ACS Sustainable Chemistry and Engineering</i>. 2020;8(3):1651-1658. doi:<a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">10.1021/acssuschemeng.9b06662</a>","mla":"Wulf, Christoph, et al. “Catalytic Systems for the Synthesis of Biscarbonates and Their Impact on the Sequential Preparation of Non-Isocyanate Polyurethanes.” <i>ACS Sustainable Chemistry and Engineering</i>, vol. 8, no. 3, American Chemical Society (ACS), 2020, pp. 1651–58, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.9b06662\">10.1021/acssuschemeng.9b06662</a>."}},{"status":"public","volume":13,"user_id":"89271","_id":"37953","publisher":"Wiley","page":"1825-1833","citation":{"short":"Y. Hu, S. Peglow, L. Longwitz, M. Frank, J.D. Epping, V. Brüser, T. Werner, ChemSusChem 13 (2020) 1825–1833.","chicago":"Hu, Yuya, Sandra Peglow, Lars Longwitz, Marcus Frank, Jan Dirk Epping, Volker Brüser, and Thomas Werner. “Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>.” <i>ChemSusChem</i> 13, no. 7 (2020): 1825–33. <a href=\"https://doi.org/10.1002/cssc.201903384\">https://doi.org/10.1002/cssc.201903384</a>.","apa":"Hu, Y., Peglow, S., Longwitz, L., Frank, M., Epping, J. D., Brüser, V., &#38; Werner, T. (2020). Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>. <i>ChemSusChem</i>, <i>13</i>(7), 1825–1833. <a href=\"https://doi.org/10.1002/cssc.201903384\">https://doi.org/10.1002/cssc.201903384</a>","ieee":"Y. Hu <i>et al.</i>, “Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>,” <i>ChemSusChem</i>, vol. 13, no. 7, pp. 1825–1833, 2020, doi: <a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>.","ama":"Hu Y, Peglow S, Longwitz L, et al. Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>. <i>ChemSusChem</i>. 2020;13(7):1825-1833. doi:<a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>","bibtex":"@article{Hu_Peglow_Longwitz_Frank_Epping_Brüser_Werner_2020, title={Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>}, volume={13}, DOI={<a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>}, number={7}, journal={ChemSusChem}, publisher={Wiley}, author={Hu, Yuya and Peglow, Sandra and Longwitz, Lars and Frank, Marcus and Epping, Jan Dirk and Brüser, Volker and Werner, Thomas}, year={2020}, pages={1825–1833} }","mla":"Hu, Yuya, et al. “Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>.” <i>ChemSusChem</i>, vol. 13, no. 7, Wiley, 2020, pp. 1825–33, doi:<a href=\"https://doi.org/10.1002/cssc.201903384\">10.1002/cssc.201903384</a>."},"intvolume":"        13","date_updated":"2025-11-10T08:50:25Z","publication_status":"published","publication_identifier":{"issn":["1864-5631","1864-564X"]},"author":[{"full_name":"Hu, Yuya","first_name":"Yuya","last_name":"Hu"},{"full_name":"Peglow, Sandra","first_name":"Sandra","last_name":"Peglow"},{"full_name":"Longwitz, Lars","last_name":"Longwitz","first_name":"Lars"},{"full_name":"Frank, Marcus","last_name":"Frank","first_name":"Marcus"},{"full_name":"Epping, Jan Dirk","first_name":"Jan Dirk","last_name":"Epping"},{"full_name":"Brüser, Volker","first_name":"Volker","last_name":"Brüser"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"year":"2020","title":"Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>","doi":"10.1002/cssc.201903384","language":[{"iso":"eng"}],"extern":"1","publication":"ChemSusChem","issue":"7","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","T1","CSSD"],"type":"journal_article","date_created":"2023-01-22T20:38:11Z"},{"status":"public","_id":"37952","publisher":"Elsevier BV","volume":28,"user_id":"89271","citation":{"short":"A. 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In vitro evaluation of innovative light-responsive nanoparticles for controlled drug release in intestinal PDT. <i>International Journal of Pharmaceutics</i>. 2019;565:199-208. doi:<a href=\"https://doi.org/10.1016/j.ijpharm.2019.04.077\">10.1016/j.ijpharm.2019.04.077</a>","bibtex":"@article{Mahlert_Anderski_Schoppa_Mulac_Sun_Kuckling_Langer_2019, title={In vitro evaluation of innovative light-responsive nanoparticles for controlled drug release in intestinal PDT}, volume={565}, DOI={<a href=\"https://doi.org/10.1016/j.ijpharm.2019.04.077\">10.1016/j.ijpharm.2019.04.077</a>}, journal={International Journal of Pharmaceutics}, publisher={Elsevier BV}, author={Mahlert, Laura and Anderski, Juliane and Schoppa, Timo and Mulac, Dennis and Sun, Jingjiang and Kuckling, Dirk and Langer, Klaus}, year={2019}, pages={199–208} }"},"status":"public","page":"199-208","_id":"30934","publisher":"Elsevier BV","user_id":"94","volume":565},{"doi":"10.1021/acsabm.9b00347","language":[{"iso":"eng"}],"date_updated":"2022-04-21T09:16:31Z","publication_status":"published","intvolume":"         2","year":"2019","title":"Light-Responsive Serinol-Based Polycarbonate and Polyester as Degradable Scaffolds","publication_identifier":{"issn":["2576-6422","2576-6422"]},"author":[{"full_name":"Sun, Jingjiang","last_name":"Sun","first_name":"Jingjiang"},{"last_name":"Jung","first_name":"Dimitri","full_name":"Jung, Dimitri"},{"last_name":"Schoppa","first_name":"Timo","full_name":"Schoppa, Timo"},{"full_name":"Anderski, Juliane","first_name":"Juliane","last_name":"Anderski"},{"first_name":"Marie-Theres","last_name":"Picker","full_name":"Picker, Marie-Theres"},{"last_name":"Ren","first_name":"Yi","full_name":"Ren, Yi"},{"first_name":"Dennis","last_name":"Mulac","full_name":"Mulac, Dennis"},{"last_name":"Stein","first_name":"Nora","full_name":"Stein, Nora"},{"first_name":"Klaus","last_name":"Langer","full_name":"Langer, Klaus"},{"full_name":"Kuckling, Dirk","last_name":"Kuckling","first_name":"Dirk","id":"287"}],"type":"journal_article","keyword":["light-responsive polymers","biodegradable polymers","polycondensation"],"department":[{"_id":"311"}],"date_created":"2022-04-21T09:15:22Z","publication":"ACS Applied Bio Materials","issue":"7","user_id":"94","volume":2,"page":"3038-3051","publisher":"American Chemical Society (ACS)","_id":"30936","status":"public","citation":{"bibtex":"@article{Sun_Jung_Schoppa_Anderski_Picker_Ren_Mulac_Stein_Langer_Kuckling_2019, title={Light-Responsive Serinol-Based Polycarbonate and Polyester as Degradable Scaffolds}, volume={2}, DOI={<a href=\"https://doi.org/10.1021/acsabm.9b00347\">10.1021/acsabm.9b00347</a>}, number={7}, journal={ACS Applied Bio Materials}, publisher={American Chemical Society (ACS)}, author={Sun, Jingjiang and Jung, Dimitri and Schoppa, Timo and Anderski, Juliane and Picker, Marie-Theres and Ren, Yi and Mulac, Dennis and Stein, Nora and Langer, Klaus and Kuckling, Dirk}, year={2019}, pages={3038–3051} }","chicago":"Sun, Jingjiang, Dimitri Jung, Timo Schoppa, Juliane Anderski, Marie-Theres Picker, Yi Ren, Dennis Mulac, Nora Stein, Klaus Langer, and Dirk Kuckling. “Light-Responsive Serinol-Based Polycarbonate and Polyester as Degradable Scaffolds.” <i>ACS Applied Bio Materials</i> 2, no. 7 (2019): 3038–51. <a href=\"https://doi.org/10.1021/acsabm.9b00347\">https://doi.org/10.1021/acsabm.9b00347</a>.","ama":"Sun J, Jung D, Schoppa T, et al. Light-Responsive Serinol-Based Polycarbonate and Polyester as Degradable Scaffolds. <i>ACS Applied Bio Materials</i>. 2019;2(7):3038-3051. doi:<a href=\"https://doi.org/10.1021/acsabm.9b00347\">10.1021/acsabm.9b00347</a>","short":"J. Sun, D. Jung, T. Schoppa, J. Anderski, M.-T. Picker, Y. Ren, D. Mulac, N. Stein, K. Langer, D. Kuckling, ACS Applied Bio Materials 2 (2019) 3038–3051.","ieee":"J. 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Light-Responsive Serinol-Based Polycarbonate and Polyester as Degradable Scaffolds. <i>ACS Applied Bio Materials</i>, <i>2</i>(7), 3038–3051. <a href=\"https://doi.org/10.1021/acsabm.9b00347\">https://doi.org/10.1021/acsabm.9b00347</a>"}},{"doi":"10.1002/macp.201800539","language":[{"iso":"eng"}],"article_number":"1800539","intvolume":"       220","publication_status":"published","date_updated":"2022-04-21T09:11:32Z","author":[{"first_name":"Jingjiang","last_name":"Sun","full_name":"Sun, Jingjiang"},{"first_name":"Juliane","last_name":"Anderski","full_name":"Anderski, Juliane"},{"full_name":"Picker, Marie-Theres","first_name":"Marie-Theres","last_name":"Picker"},{"full_name":"Langer, Klaus","first_name":"Klaus","last_name":"Langer"},{"first_name":"Dirk","last_name":"Kuckling","full_name":"Kuckling, Dirk","id":"287"}],"publication_identifier":{"issn":["1022-1352"]},"title":"Preparation of Light-Responsive Aliphatic Polycarbonate via Versatile Polycondensation for Controlled Degradation","year":"2019","department":[{"_id":"311"}],"keyword":["Materials Chemistry","Organic Chemistry","Polymers and Plastics","Physical and Theoretical Chemistry","Condensed Matter Physics"],"type":"journal_article","date_created":"2022-04-21T09:09:59Z","issue":"5","publication":"Macromolecular Chemistry and Physics","volume":220,"user_id":"94","_id":"30933","publisher":"Wiley","status":"public","citation":{"mla":"Sun, Jingjiang, et al. “Preparation of Light-Responsive Aliphatic Polycarbonate via Versatile Polycondensation for Controlled Degradation.” <i>Macromolecular Chemistry and Physics</i>, vol. 220, no. 5, 1800539, Wiley, 2019, doi:<a href=\"https://doi.org/10.1002/macp.201800539\">10.1002/macp.201800539</a>.","ama":"Sun J, Anderski J, Picker M-T, Langer K, Kuckling D. Preparation of Light-Responsive Aliphatic Polycarbonate via Versatile Polycondensation for Controlled Degradation. <i>Macromolecular Chemistry and Physics</i>. 2019;220(5). doi:<a href=\"https://doi.org/10.1002/macp.201800539\">10.1002/macp.201800539</a>","bibtex":"@article{Sun_Anderski_Picker_Langer_Kuckling_2019, title={Preparation of Light-Responsive Aliphatic Polycarbonate via Versatile Polycondensation for Controlled Degradation}, volume={220}, DOI={<a href=\"https://doi.org/10.1002/macp.201800539\">10.1002/macp.201800539</a>}, number={51800539}, journal={Macromolecular Chemistry and Physics}, publisher={Wiley}, author={Sun, Jingjiang and Anderski, Juliane and Picker, Marie-Theres and Langer, Klaus and Kuckling, Dirk}, year={2019} }","apa":"Sun, J., Anderski, J., Picker, M.-T., Langer, K., &#38; Kuckling, D. (2019). Preparation of Light-Responsive Aliphatic Polycarbonate via Versatile Polycondensation for Controlled Degradation. <i>Macromolecular Chemistry and Physics</i>, <i>220</i>(5), Article 1800539. <a href=\"https://doi.org/10.1002/macp.201800539\">https://doi.org/10.1002/macp.201800539</a>","ieee":"J. Sun, J. Anderski, M.-T. Picker, K. Langer, and D. Kuckling, “Preparation of Light-Responsive Aliphatic Polycarbonate via Versatile Polycondensation for Controlled Degradation,” <i>Macromolecular Chemistry and Physics</i>, vol. 220, no. 5, Art. no. 1800539, 2019, doi: <a href=\"https://doi.org/10.1002/macp.201800539\">10.1002/macp.201800539</a>.","short":"J. Sun, J. Anderski, M.-T. Picker, K. Langer, D. 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(2019). Light‐Responsive Serinol‐Based Polyurethane Nanocarrier for Controlled Drug Release. <i>Macromolecular Rapid Communications</i>, <i>40</i>(22), Article 1900348. <a href=\"https://doi.org/10.1002/marc.201900348\">https://doi.org/10.1002/marc.201900348</a>","ieee":"J. Sun, T. Rust, and D. Kuckling, “Light‐Responsive Serinol‐Based Polyurethane Nanocarrier for Controlled Drug Release,” <i>Macromolecular Rapid Communications</i>, vol. 40, no. 22, Art. no. 1900348, 2019, doi: <a href=\"https://doi.org/10.1002/marc.201900348\">10.1002/marc.201900348</a>.","chicago":"Sun, Jingjiang, Tarik Rust, and Dirk Kuckling. “Light‐Responsive Serinol‐Based Polyurethane Nanocarrier for Controlled Drug Release.” <i>Macromolecular Rapid Communications</i> 40, no. 22 (2019). <a href=\"https://doi.org/10.1002/marc.201900348\">https://doi.org/10.1002/marc.201900348</a>.","short":"J. Sun, T. Rust, D. 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Synthesis and characterization of light-degradable bromocoumarin functionalized polycarbonates. <i>Polymer Chemistry</i>. 2019;11:721-733. doi:<a href=\"https://doi.org/10.1039/c9py01405e\">10.1039/c9py01405e</a>","bibtex":"@article{Müller_Jung_Sun_Kuckling_2019, title={Synthesis and characterization of light-degradable bromocoumarin functionalized polycarbonates}, volume={11}, DOI={<a href=\"https://doi.org/10.1039/c9py01405e\">10.1039/c9py01405e</a>}, journal={Polymer Chemistry}, publisher={RSC}, author={Müller, Ann-Kathrin and Jung, Dimitri and Sun, Jingjiang and Kuckling, Dirk}, year={2019}, pages={721–733} }","apa":"Müller, A.-K., Jung, D., Sun, J., &#38; Kuckling, D. (2019). Synthesis and characterization of light-degradable bromocoumarin functionalized polycarbonates. <i>Polymer Chemistry</i>, <i>11</i>, 721–733. <a href=\"https://doi.org/10.1039/c9py01405e\">https://doi.org/10.1039/c9py01405e</a>","ieee":"A.-K. Müller, D. Jung, J. Sun, and D. Kuckling, “Synthesis and characterization of light-degradable bromocoumarin functionalized polycarbonates,” <i>Polymer Chemistry</i>, vol. 11, pp. 721–733, 2019, doi: <a href=\"https://doi.org/10.1039/c9py01405e\">10.1039/c9py01405e</a>.","chicago":"Müller, Ann-Kathrin, Dimitri Jung, Jingjiang Sun, and Dirk Kuckling. “Synthesis and Characterization of Light-Degradable Bromocoumarin Functionalized Polycarbonates.” <i>Polymer Chemistry</i> 11 (2019): 721–33. <a href=\"https://doi.org/10.1039/c9py01405e\">https://doi.org/10.1039/c9py01405e</a>.","short":"A.-K. Müller, D. Jung, J. Sun, D. 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M. and Kath‐Schorr, Stephanie and Kordes, Markus and Lehmann, Matthias and et al.}, year={2019}, pages={46–78} }","ama":"Andexer JN, Beifuss U, Beuerle F, et al. Trendbericht Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2019;67(3):46-78. doi:<a href=\"https://doi.org/10.1002/nadc.20194085243\">10.1002/nadc.20194085243</a>","mla":"Andexer, Jennifer N., et al. “Trendbericht Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 67, no. 3, Wiley, 2019, pp. 46–78, doi:<a href=\"https://doi.org/10.1002/nadc.20194085243\">10.1002/nadc.20194085243</a>.","short":"J.N. Andexer, U. Beifuss, F. Beuerle, M. Brasholz, R. Breinbauer, M. Ernst, T.A.M. Gulder, S. Kath‐Schorr, M. Kordes, M. Lehmann, T. Lindel, S. Lüdeke, B. Luy, M. Mantel, C. Mück‐Lichtenfeld, C. Muhle‐Goll, A. Narine, J. Niemeyer, R. Pfau, J. Pietruszka, N. Schaschke, M.O. Senge, B.F. Straub, T. Werner, D.B. Werz, C. Winter, Nachrichten Aus Der Chemie 67 (2019) 46–78.","chicago":"Andexer, Jennifer N., Uwe Beifuss, Florian Beuerle, Malte Brasholz, Rolf Breinbauer, Martin Ernst, Tobias A. M. Gulder, et al. “Trendbericht Organische Chemie.” <i>Nachrichten Aus Der Chemie</i> 67, no. 3 (2019): 46–78. <a href=\"https://doi.org/10.1002/nadc.20194085243\">https://doi.org/10.1002/nadc.20194085243</a>.","ieee":"J. N. Andexer <i>et al.</i>, “Trendbericht Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 67, no. 3, pp. 46–78, 2019, doi: <a href=\"https://doi.org/10.1002/nadc.20194085243\">10.1002/nadc.20194085243</a>.","apa":"Andexer, J. N., Beifuss, U., Beuerle, F., Brasholz, M., Breinbauer, R., Ernst, M., Gulder, T. A. M., Kath‐Schorr, S., Kordes, M., Lehmann, M., Lindel, T., Lüdeke, S., Luy, B., Mantel, M., Mück‐Lichtenfeld, C., Muhle‐Goll, C., Narine, A., Niemeyer, J., Pfau, R., … Winter, C. (2019). Trendbericht Organische Chemie. <i>Nachrichten Aus Der Chemie</i>, <i>67</i>(3), 46–78. <a href=\"https://doi.org/10.1002/nadc.20194085243\">https://doi.org/10.1002/nadc.20194085243</a>"},"status":"public","user_id":"89271","volume":67,"page":"46-78","publisher":"Wiley","_id":"37964"},{"abstract":[{"lang":"eng","text":"<p>The reduction of poly and cyclic carbonates in the presence of an earth abundant metal catalyst using isopropanol as the hydrogen donor is reported.</p>"}],"extern":"1","issue":"19","publication":"Green Chemistry","keyword":["T3","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T20:43:38Z","date_updated":"2025-11-10T08:55:06Z","publication_status":"published","intvolume":"        21","year":"2019","title":"Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts","author":[{"last_name":"Liu","first_name":"Xin","full_name":"Liu, Xin"},{"full_name":"de Vries, Johannes G.","first_name":"Johannes G.","last_name":"de Vries"},{"id":"89271","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["1463-9262","1463-9270"]},"doi":"10.1039/c9gc02052g","language":[{"iso":"eng"}],"citation":{"apa":"Liu, X., de Vries, J. G., &#38; Werner, T. (2019). Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts. <i>Green Chemistry</i>, <i>21</i>(19), 5248–5255. <a href=\"https://doi.org/10.1039/c9gc02052g\">https://doi.org/10.1039/c9gc02052g</a>","ieee":"X. Liu, J. G. de Vries, and T. Werner, “Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts,” <i>Green Chemistry</i>, vol. 21, no. 19, pp. 5248–5255, 2019, doi: <a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>.","chicago":"Liu, Xin, Johannes G. de Vries, and Thomas Werner. “Transfer Hydrogenation of Cyclic Carbonates and Polycarbonate to Methanol and Diols by Iron Pincer Catalysts.” <i>Green Chemistry</i> 21, no. 19 (2019): 5248–55. <a href=\"https://doi.org/10.1039/c9gc02052g\">https://doi.org/10.1039/c9gc02052g</a>.","short":"X. Liu, J.G. de Vries, T. Werner, Green Chemistry 21 (2019) 5248–5255.","mla":"Liu, Xin, et al. “Transfer Hydrogenation of Cyclic Carbonates and Polycarbonate to Methanol and Diols by Iron Pincer Catalysts.” <i>Green Chemistry</i>, vol. 21, no. 19, Royal Society of Chemistry (RSC), 2019, pp. 5248–55, doi:<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>.","ama":"Liu X, de Vries JG, Werner T. Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts. <i>Green Chemistry</i>. 2019;21(19):5248-5255. doi:<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>","bibtex":"@article{Liu_de Vries_Werner_2019, title={Transfer hydrogenation of cyclic carbonates and polycarbonate to methanol and diols by iron pincer catalysts}, volume={21}, DOI={<a href=\"https://doi.org/10.1039/c9gc02052g\">10.1039/c9gc02052g</a>}, number={19}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Liu, Xin and de Vries, Johannes G. and Werner, Thomas}, year={2019}, pages={5248–5255} }"},"status":"public","user_id":"89271","volume":21,"page":"5248-5255","publisher":"Royal Society of Chemistry (RSC)","_id":"37961"},{"page":"2701-2707","_id":"37963","publisher":"Wiley","user_id":"89271","volume":12,"status":"public","citation":{"mla":"Büttner, Hendrik, et al. “Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate.” <i>ChemSusChem</i>, vol. 12, no. 12, Wiley, 2019, pp. 2701–07, doi:<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>.","apa":"Büttner, H., Kohrt, C., Wulf, C., Schäffner, B., Groenke, K., Hu, Y., Kruse, D., &#38; Werner, T. (2019). Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate. <i>ChemSusChem</i>, <i>12</i>(12), 2701–2707. <a href=\"https://doi.org/10.1002/cssc.201900678\">https://doi.org/10.1002/cssc.201900678</a>","ieee":"H. Büttner <i>et al.</i>, “Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate,” <i>ChemSusChem</i>, vol. 12, no. 12, pp. 2701–2707, 2019, doi: <a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>.","chicago":"Büttner, Hendrik, Christina Kohrt, Christoph Wulf, Benjamin Schäffner, Karsten Groenke, Yuya Hu, Daniela Kruse, and Thomas Werner. “Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate.” <i>ChemSusChem</i> 12, no. 12 (2019): 2701–7. <a href=\"https://doi.org/10.1002/cssc.201900678\">https://doi.org/10.1002/cssc.201900678</a>.","ama":"Büttner H, Kohrt C, Wulf C, et al. Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate. <i>ChemSusChem</i>. 2019;12(12):2701-2707. doi:<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>","short":"H. Büttner, C. Kohrt, C. Wulf, B. Schäffner, K. Groenke, Y. Hu, D. Kruse, T. Werner, ChemSusChem 12 (2019) 2701–2707.","bibtex":"@article{Büttner_Kohrt_Wulf_Schäffner_Groenke_Hu_Kruse_Werner_2019, title={Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate}, volume={12}, DOI={<a href=\"https://doi.org/10.1002/cssc.201900678\">10.1002/cssc.201900678</a>}, number={12}, journal={ChemSusChem}, publisher={Wiley}, author={Büttner, Hendrik and Kohrt, Christina and Wulf, Christoph and Schäffner, Benjamin and Groenke, Karsten and Hu, Yuya and Kruse, Daniela and Werner, Thomas}, year={2019}, pages={2701–2707} }"},"language":[{"iso":"eng"}],"doi":"10.1002/cssc.201900678","title":"Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate","year":"2019","publication_identifier":{"issn":["1864-5631","1864-564X"]},"author":[{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"first_name":"Christina","last_name":"Kohrt","full_name":"Kohrt, Christina"},{"first_name":"Christoph","last_name":"Wulf","full_name":"Wulf, Christoph"},{"full_name":"Schäffner, Benjamin","first_name":"Benjamin","last_name":"Schäffner"},{"last_name":"Groenke","first_name":"Karsten","full_name":"Groenke, Karsten"},{"full_name":"Hu, Yuya","first_name":"Yuya","last_name":"Hu"},{"full_name":"Kruse, Daniela","last_name":"Kruse","first_name":"Daniela"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"date_updated":"2025-11-10T08:56:56Z","publication_status":"published","intvolume":"        12","date_created":"2023-01-22T20:44:24Z","keyword":["T1","T4","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"issue":"12","publication":"ChemSusChem","extern":"1"}]