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Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis. <i>ChemSusChem</i>, <i>10</i>(15), 3025–3029. <a href=\"https://doi.org/10.1002/cssc.201700788\">https://doi.org/10.1002/cssc.201700788</a>","mla":"Steinbauer, Johannes, and Thomas Werner. “Poly(Ethylene Glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis.” <i>ChemSusChem</i>, vol. 10, no. 15, Wiley, 2017, pp. 3025–29, doi:<a href=\"https://doi.org/10.1002/cssc.201700788\">10.1002/cssc.201700788</a>.","bibtex":"@article{Steinbauer_Werner_2017, title={Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis}, volume={10}, DOI={<a href=\"https://doi.org/10.1002/cssc.201700788\">10.1002/cssc.201700788</a>}, number={15}, journal={ChemSusChem}, publisher={Wiley}, author={Steinbauer, Johannes and Werner, Thomas}, year={2017}, pages={3025–3029} }","chicago":"Steinbauer, Johannes, and Thomas Werner. “Poly(Ethylene Glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis.” <i>ChemSusChem</i> 10, no. 15 (2017): 3025–29. <a href=\"https://doi.org/10.1002/cssc.201700788\">https://doi.org/10.1002/cssc.201700788</a>.","short":"J. Steinbauer, T. Werner, ChemSusChem 10 (2017) 3025–3029.","ama":"Steinbauer J, Werner T. Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis. <i>ChemSusChem</i>. 2017;10(15):3025-3029. doi:<a href=\"https://doi.org/10.1002/cssc.201700788\">10.1002/cssc.201700788</a>"},"volume":10,"user_id":"89271","publisher":"Wiley","_id":"37974","page":"3025-3029","status":"public","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T3","CSSD"],"date_created":"2023-01-22T20:58:02Z","extern":"1","issue":"15","publication":"ChemSusChem","doi":"10.1002/cssc.201700788","language":[{"iso":"eng"}],"intvolume":"        10","publication_status":"published","date_updated":"2025-11-10T09:17:48Z","author":[{"full_name":"Steinbauer, Johannes","first_name":"Johannes","last_name":"Steinbauer"},{"id":"89271","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["1864-5631"]},"title":"Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis","year":"2017"},{"keyword":["T1","T3","CSSD"],"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:03:02Z","abstract":[{"text":"<p><bold>Taking Control!</bold>The binary catalyst system composed of MoO<sub>3</sub>and an organic phoshponium salt [Bu<sub>4</sub>P]X proved very efficient to produce oleochemical cyclic carbonates from renewables.</p>","lang":"eng"}],"extern":"1","issue":"13","publication":"Green Chemistry","doi":"10.1039/c6gc00671j","language":[{"iso":"eng"}],"date_updated":"2025-11-10T09:20:35Z","publication_status":"published","intvolume":"        18","title":"Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables","year":"2016","publication_identifier":{"issn":["1463-9262","1463-9270"]},"author":[{"full_name":"Tenhumberg, Nils","first_name":"Nils","last_name":"Tenhumberg"},{"last_name":"Büttner","first_name":"Hendrik","full_name":"Büttner, Hendrik"},{"full_name":"Schäffner, Benjamin","last_name":"Schäffner","first_name":"Benjamin"},{"full_name":"Kruse, Daniela","first_name":"Daniela","last_name":"Kruse"},{"last_name":"Blumenstein","first_name":"Michael","full_name":"Blumenstein, Michael"},{"full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","id":"89271"}],"citation":{"ieee":"N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, and T. Werner, “Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables,” <i>Green Chemistry</i>, vol. 18, no. 13, pp. 3775–3788, 2016, doi: <a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>.","apa":"Tenhumberg, N., Büttner, H., Schäffner, B., Kruse, D., Blumenstein, M., &#38; Werner, T. (2016). Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables. <i>Green Chemistry</i>, <i>18</i>(13), 3775–3788. <a href=\"https://doi.org/10.1039/c6gc00671j\">https://doi.org/10.1039/c6gc00671j</a>","chicago":"Tenhumberg, Nils, Hendrik Büttner, Benjamin Schäffner, Daniela Kruse, Michael Blumenstein, and Thomas Werner. “Cooperative Catalyst System for the Synthesis of Oleochemical Cyclic Carbonates from CO<sub>2</sub>and Renewables.” <i>Green Chemistry</i> 18, no. 13 (2016): 3775–88. <a href=\"https://doi.org/10.1039/c6gc00671j\">https://doi.org/10.1039/c6gc00671j</a>.","short":"N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, T. Werner, Green Chemistry 18 (2016) 3775–3788.","mla":"Tenhumberg, Nils, et al. “Cooperative Catalyst System for the Synthesis of Oleochemical Cyclic Carbonates from CO<sub>2</sub>and Renewables.” <i>Green Chemistry</i>, vol. 18, no. 13, Royal Society of Chemistry (RSC), 2016, pp. 3775–88, doi:<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>.","bibtex":"@article{Tenhumberg_Büttner_Schäffner_Kruse_Blumenstein_Werner_2016, title={Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables}, volume={18}, DOI={<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>}, number={13}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Tenhumberg, Nils and Büttner, Hendrik and Schäffner, Benjamin and Kruse, Daniela and Blumenstein, Michael and Werner, Thomas}, year={2016}, pages={3775–3788} }","ama":"Tenhumberg N, Büttner H, Schäffner B, Kruse D, Blumenstein M, Werner T. Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables. <i>Green Chemistry</i>. 2016;18(13):3775-3788. doi:<a href=\"https://doi.org/10.1039/c6gc00671j\">10.1039/c6gc00671j</a>"},"user_id":"89271","volume":18,"page":"3775-3788","publisher":"Royal Society of Chemistry (RSC)","_id":"37983","status":"public"},{"language":[{"iso":"eng"}],"doi":"10.1002/adsc.201500762","author":[{"full_name":"Schirmer, Marie-Luis","last_name":"Schirmer","first_name":"Marie-Luis"},{"full_name":"Jopp, Stefan","last_name":"Jopp","first_name":"Stefan"},{"full_name":"Holz, Jens","first_name":"Jens","last_name":"Holz"},{"full_name":"Spannenberg, Anke","first_name":"Anke","last_name":"Spannenberg"},{"full_name":"Werner, Thomas","first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271"}],"publication_identifier":{"issn":["1615-4150"]},"title":"Organocatalyzed Reduction of Tertiary Phosphine Oxides","year":"2016","intvolume":"       358","date_updated":"2025-11-10T09:22:07Z","publication_status":"published","date_created":"2023-01-22T21:05:14Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T2","CSSD"],"type":"journal_article","issue":"1","publication":"Advanced Synthesis and Catalysis","extern":"1","_id":"37989","publisher":"Wiley","page":"26-29","volume":358,"user_id":"89271","status":"public","citation":{"mla":"Schirmer, Marie-Luis, et al. “Organocatalyzed Reduction of Tertiary Phosphine Oxides.” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 1, Wiley, 2016, pp. 26–29, doi:<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>.","ama":"Schirmer M-L, Jopp S, Holz J, Spannenberg A, Werner T. Organocatalyzed Reduction of Tertiary Phosphine Oxides. <i>Advanced Synthesis and Catalysis</i>. 2016;358(1):26-29. doi:<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>","bibtex":"@article{Schirmer_Jopp_Holz_Spannenberg_Werner_2016, title={Organocatalyzed Reduction of Tertiary Phosphine Oxides}, volume={358}, DOI={<a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>}, number={1}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Schirmer, Marie-Luis and Jopp, Stefan and Holz, Jens and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={26–29} }","apa":"Schirmer, M.-L., Jopp, S., Holz, J., Spannenberg, A., &#38; Werner, T. (2016). Organocatalyzed Reduction of Tertiary Phosphine Oxides. <i>Advanced Synthesis and Catalysis</i>, <i>358</i>(1), 26–29. <a href=\"https://doi.org/10.1002/adsc.201500762\">https://doi.org/10.1002/adsc.201500762</a>","ieee":"M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, and T. Werner, “Organocatalyzed Reduction of Tertiary Phosphine Oxides,” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 1, pp. 26–29, 2016, doi: <a href=\"https://doi.org/10.1002/adsc.201500762\">10.1002/adsc.201500762</a>.","chicago":"Schirmer, Marie-Luis, Stefan Jopp, Jens Holz, Anke Spannenberg, and Thomas Werner. “Organocatalyzed Reduction of Tertiary Phosphine Oxides.” <i>Advanced Synthesis and Catalysis</i> 358, no. 1 (2016): 26–29. <a href=\"https://doi.org/10.1002/adsc.201500762\">https://doi.org/10.1002/adsc.201500762</a>.","short":"M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, T. Werner, Advanced Synthesis and Catalysis 358 (2016) 26–29."}},{"volume":14,"user_id":"89271","_id":"37981","publisher":"Royal Society of Chemistry (RSC)","page":"7480-7489","status":"public","citation":{"bibtex":"@article{Diebler_Spannenberg_Werner_2016, title={Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes}, volume={14}, DOI={<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>}, number={31}, journal={Organic and Biomolecular Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Diebler, J. and Spannenberg, A. and Werner, Thomas}, year={2016}, pages={7480–7489} }","ama":"Diebler J, Spannenberg A, Werner T. Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. <i>Organic and Biomolecular Chemistry</i>. 2016;14(31):7480-7489. doi:<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>","mla":"Diebler, J., et al. “Atom Economical Synthesis of Di- and Trithiocarbonates by the Lithium Tert-Butoxide Catalyzed Addition of Carbon Disulfide to Epoxides and Thiiranes.” <i>Organic and Biomolecular Chemistry</i>, vol. 14, no. 31, Royal Society of Chemistry (RSC), 2016, pp. 7480–89, doi:<a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>.","short":"J. Diebler, A. Spannenberg, T. Werner, Organic and Biomolecular Chemistry 14 (2016) 7480–7489.","chicago":"Diebler, J., A. Spannenberg, and Thomas Werner. “Atom Economical Synthesis of Di- and Trithiocarbonates by the Lithium Tert-Butoxide Catalyzed Addition of Carbon Disulfide to Epoxides and Thiiranes.” <i>Organic and Biomolecular Chemistry</i> 14, no. 31 (2016): 7480–89. <a href=\"https://doi.org/10.1039/c6ob01081d\">https://doi.org/10.1039/c6ob01081d</a>.","ieee":"J. Diebler, A. Spannenberg, and T. Werner, “Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes,” <i>Organic and Biomolecular Chemistry</i>, vol. 14, no. 31, pp. 7480–7489, 2016, doi: <a href=\"https://doi.org/10.1039/c6ob01081d\">10.1039/c6ob01081d</a>.","apa":"Diebler, J., Spannenberg, A., &#38; Werner, T. (2016). Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. <i>Organic and Biomolecular Chemistry</i>, <i>14</i>(31), 7480–7489. <a href=\"https://doi.org/10.1039/c6ob01081d\">https://doi.org/10.1039/c6ob01081d</a>"},"doi":"10.1039/c6ob01081d","language":[{"iso":"eng"}],"intvolume":"        14","date_updated":"2025-11-10T09:24:16Z","publication_status":"published","author":[{"first_name":"J.","last_name":"Diebler","full_name":"Diebler, J."},{"first_name":"A.","last_name":"Spannenberg","full_name":"Spannenberg, A."},{"id":"89271","full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244"}],"publication_identifier":{"issn":["1477-0520","1477-0539"]},"year":"2016","title":"Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["CSSD"],"type":"journal_article","date_created":"2023-01-22T21:01:59Z","abstract":[{"text":"<p>The lithium <italic>tert</italic>-butoxide catalyzed addition of CS<sub>2</sub> to epoxides and thiiranes under mild conditions is reported. A mechanism has been proposed taking into account the regio- and stereochemical outcome of the reaction.</p>","lang":"eng"}],"extern":"1","issue":"31","publication":"Organic and Biomolecular Chemistry"},{"intvolume":"         3","date_updated":"2025-11-10T09:26:28Z","publication_status":"published","publication_identifier":{"issn":["2052-4129"]},"author":[{"first_name":"Willi","last_name":"Desens","full_name":"Desens, Willi"},{"last_name":"Kohrt","first_name":"Christina","full_name":"Kohrt, Christina"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"}],"year":"2016","title":"A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions","doi":"10.1039/c5qo00356c","language":[{"iso":"eng"}],"abstract":[{"text":"<p>A novel zinc based binary catalytic system for the synthesis of cyclic carbonates under mild and solvent-free conditions utilizing CO<sub>2</sub>as a C1 building block is reported.</p>","lang":"eng"}],"extern":"1","issue":"2","publication":"Organic Chemistry Frontiers","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"keyword":["T1","T3","CSSD"],"type":"journal_article","date_created":"2023-01-22T21:04:30Z","status":"public","volume":3,"user_id":"89271","_id":"37987","publisher":"Royal Society of Chemistry (RSC)","page":"156-164","citation":{"mla":"Desens, Willi, et al. “A Novel Zinc Based Binary Catalytic System for CO<sub>2</sub>Utilization under Mild Conditions.” <i>Organic Chemistry Frontiers</i>, vol. 3, no. 2, Royal Society of Chemistry (RSC), 2016, pp. 156–64, doi:<a href=\"https://doi.org/10.1039/c5qo00356c\">10.1039/c5qo00356c</a>.","ama":"Desens W, Kohrt C, Spannenberg A, Werner T. A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions. <i>Organic Chemistry Frontiers</i>. 2016;3(2):156-164. doi:<a href=\"https://doi.org/10.1039/c5qo00356c\">10.1039/c5qo00356c</a>","bibtex":"@article{Desens_Kohrt_Spannenberg_Werner_2016, title={A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions}, volume={3}, DOI={<a href=\"https://doi.org/10.1039/c5qo00356c\">10.1039/c5qo00356c</a>}, number={2}, journal={Organic Chemistry Frontiers}, publisher={Royal Society of Chemistry (RSC)}, author={Desens, Willi and Kohrt, Christina and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={156–164} }","apa":"Desens, W., Kohrt, C., Spannenberg, A., &#38; Werner, T. (2016). A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions. <i>Organic Chemistry Frontiers</i>, <i>3</i>(2), 156–164. <a href=\"https://doi.org/10.1039/c5qo00356c\">https://doi.org/10.1039/c5qo00356c</a>","ieee":"W. Desens, C. Kohrt, A. Spannenberg, and T. Werner, “A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions,” <i>Organic Chemistry Frontiers</i>, vol. 3, no. 2, pp. 156–164, 2016, doi: <a href=\"https://doi.org/10.1039/c5qo00356c\">10.1039/c5qo00356c</a>.","chicago":"Desens, Willi, Christina Kohrt, Anke Spannenberg, and Thomas Werner. “A Novel Zinc Based Binary Catalytic System for CO<sub>2</sub>Utilization under Mild Conditions.” <i>Organic Chemistry Frontiers</i> 3, no. 2 (2016): 156–64. <a href=\"https://doi.org/10.1039/c5qo00356c\">https://doi.org/10.1039/c5qo00356c</a>.","short":"W. Desens, C. Kohrt, A. Spannenberg, T. Werner, Organic Chemistry Frontiers 3 (2016) 156–164."}},{"citation":{"apa":"Diebler, J., Komber, H., Häußler, L., Lederer, A., &#38; Werner, T. (2016). Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers. <i>Macromolecules</i>, <i>49</i>(13), 4723–4731. <a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">https://doi.org/10.1021/acs.macromol.6b00728</a>","ieee":"J. Diebler, H. Komber, L. Häußler, A. Lederer, and T. Werner, “Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers,” <i>Macromolecules</i>, vol. 49, no. 13, pp. 4723–4731, 2016, doi: <a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">10.1021/acs.macromol.6b00728</a>.","chicago":"Diebler, Johannes, Hartmut Komber, Liane Häußler, Albena Lederer, and Thomas Werner. “Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers.” <i>Macromolecules</i> 49, no. 13 (2016): 4723–31. <a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">https://doi.org/10.1021/acs.macromol.6b00728</a>.","short":"J. Diebler, H. Komber, L. Häußler, A. Lederer, T. Werner, Macromolecules 49 (2016) 4723–4731.","mla":"Diebler, Johannes, et al. “Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers.” <i>Macromolecules</i>, vol. 49, no. 13, American Chemical Society (ACS), 2016, pp. 4723–31, doi:<a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">10.1021/acs.macromol.6b00728</a>.","ama":"Diebler J, Komber H, Häußler L, Lederer A, Werner T. Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers. <i>Macromolecules</i>. 2016;49(13):4723-4731. doi:<a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">10.1021/acs.macromol.6b00728</a>","bibtex":"@article{Diebler_Komber_Häußler_Lederer_Werner_2016, title={Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers}, volume={49}, DOI={<a href=\"https://doi.org/10.1021/acs.macromol.6b00728\">10.1021/acs.macromol.6b00728</a>}, number={13}, journal={Macromolecules}, publisher={American Chemical Society (ACS)}, author={Diebler, Johannes and Komber, Hartmut and Häußler, Liane and Lederer, Albena and Werner, Thomas}, year={2016}, pages={4723–4731} }"},"status":"public","user_id":"89271","volume":49,"page":"4723-4731","_id":"37982","publisher":"American Chemical Society (ACS)","extern":"1","publication":"Macromolecules","issue":"13","type":"journal_article","keyword":["CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"date_created":"2023-01-22T21:02:41Z","date_updated":"2025-11-10T09:25:16Z","publication_status":"published","intvolume":"        49","title":"Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers","year":"2016","author":[{"full_name":"Diebler, Johannes","last_name":"Diebler","first_name":"Johannes"},{"first_name":"Hartmut","last_name":"Komber","full_name":"Komber, Hartmut"},{"last_name":"Häußler","first_name":"Liane","full_name":"Häußler, Liane"},{"full_name":"Lederer, Albena","first_name":"Albena","last_name":"Lederer"},{"id":"89271","orcid":"0000-0001-9025-3244","first_name":"Thomas","last_name":"Werner","full_name":"Werner, Thomas"}],"publication_identifier":{"issn":["0024-9297","1520-5835"]},"doi":"10.1021/acs.macromol.6b00728","language":[{"iso":"eng"}]},{"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T3","CSSD"],"date_created":"2023-01-22T21:01:04Z","extern":"1","publication":"ACS Sustainable Chemistry &amp; Engineering","issue":"9","doi":"10.1021/acssuschemeng.6b01092","language":[{"iso":"eng"}],"intvolume":"         4","date_updated":"2025-11-10T09:26:56Z","publication_status":"published","publication_identifier":{"issn":["2168-0485","2168-0485"]},"author":[{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"full_name":"Grimmer, Christoph","last_name":"Grimmer","first_name":"Christoph"},{"full_name":"Steinbauer, Johannes","last_name":"Steinbauer","first_name":"Johannes"},{"id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244","first_name":"Thomas","full_name":"Werner, Thomas"}],"year":"2016","title":"Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates","citation":{"ieee":"H. Büttner, C. Grimmer, J. Steinbauer, and T. Werner, “Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates,” <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>, vol. 4, no. 9, pp. 4805–4814, 2016, doi: <a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">10.1021/acssuschemeng.6b01092</a>.","mla":"Büttner, Hendrik, et al. “Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates.” <i>ACS Sustainable Chemistry &#38;amp; Engineering</i>, vol. 4, no. 9, American Chemical Society (ACS), 2016, pp. 4805–14, doi:<a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">10.1021/acssuschemeng.6b01092</a>.","apa":"Büttner, H., Grimmer, C., Steinbauer, J., &#38; Werner, T. (2016). 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