[{"publication_status":"published","publication_identifier":{"issn":["1864-5631"]},"citation":{"ieee":"J. Steinbauer and T. Werner, “Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis,” <i>ChemSusChem</i>, vol. 10, no. 15, pp. 3025–3029, 2017, doi: <a href=\"https://doi.org/10.1002/cssc.201700788\">10.1002/cssc.201700788</a>.","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>.","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>","apa":"Steinbauer, J., &#38; Werner, T. (2017). 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>","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} }","short":"J. Steinbauer, T. Werner, ChemSusChem 10 (2017) 3025–3029.","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>."},"intvolume":"        10","page":"3025-3029","date_updated":"2025-11-10T09:17:48Z","author":[{"full_name":"Steinbauer, Johannes","last_name":"Steinbauer","first_name":"Johannes"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"volume":10,"doi":"10.1002/cssc.201700788","type":"journal_article","status":"public","_id":"37974","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"extern":"1","issue":"15","year":"2017","publisher":"Wiley","date_created":"2023-01-22T20:58:02Z","title":"Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis","publication":"ChemSusChem","keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}]},{"author":[{"first_name":"Nils","last_name":"Tenhumberg","full_name":"Tenhumberg, Nils"},{"last_name":"Büttner","full_name":"Büttner, Hendrik","first_name":"Hendrik"},{"last_name":"Schäffner","full_name":"Schäffner, Benjamin","first_name":"Benjamin"},{"full_name":"Kruse, Daniela","last_name":"Kruse","first_name":"Daniela"},{"first_name":"Michael","full_name":"Blumenstein, Michael","last_name":"Blumenstein"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"volume":18,"date_updated":"2025-11-10T09:20:35Z","doi":"10.1039/c6gc00671j","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"citation":{"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>.","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>.","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>","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} }","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>"},"intvolume":"        18","page":"3775-3788","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37983","extern":"1","type":"journal_article","status":"public","date_created":"2023-01-22T21:03:02Z","publisher":"Royal Society of Chemistry (RSC)","title":"Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables","issue":"13","year":"2016","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"publication":"Green Chemistry","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"}]},{"citation":{"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>","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} }","short":"M.-L. Schirmer, S. Jopp, J. Holz, A. Spannenberg, T. Werner, Advanced Synthesis and Catalysis 358 (2016) 26–29.","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>","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>."},"page":"26-29","intvolume":"       358","year":"2016","issue":"1","publication_status":"published","publication_identifier":{"issn":["1615-4150"]},"doi":"10.1002/adsc.201500762","title":"Organocatalyzed Reduction of Tertiary Phosphine Oxides","author":[{"first_name":"Marie-Luis","last_name":"Schirmer","full_name":"Schirmer, Marie-Luis"},{"full_name":"Jopp, Stefan","last_name":"Jopp","first_name":"Stefan"},{"first_name":"Jens","last_name":"Holz","full_name":"Holz, Jens"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271","first_name":"Thomas"}],"date_created":"2023-01-22T21:05:14Z","volume":358,"publisher":"Wiley","date_updated":"2025-11-10T09:22:07Z","status":"public","type":"journal_article","publication":"Advanced Synthesis and Catalysis","extern":"1","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37989"},{"keyword":["CSSD"],"language":[{"iso":"eng"}],"publication":"Organic and Biomolecular Chemistry","abstract":[{"lang":"eng","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>"}],"publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-22T21:01:59Z","title":"Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes","issue":"31","year":"2016","_id":"37981","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"extern":"1","type":"journal_article","status":"public","date_updated":"2025-11-10T09:24:16Z","author":[{"first_name":"J.","full_name":"Diebler, J.","last_name":"Diebler"},{"first_name":"A.","last_name":"Spannenberg","full_name":"Spannenberg, A."},{"orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas"}],"volume":14,"doi":"10.1039/c6ob01081d","publication_status":"published","publication_identifier":{"issn":["1477-0520","1477-0539"]},"citation":{"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>","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>.","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} }","short":"J. Diebler, A. Spannenberg, T. Werner, Organic and Biomolecular Chemistry 14 (2016) 7480–7489.","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>.","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>"},"page":"7480-7489","intvolume":"        14"},{"extern":"1","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37987","status":"public","type":"journal_article","doi":"10.1039/c5qo00356c","volume":3,"author":[{"last_name":"Desens","full_name":"Desens, Willi","first_name":"Willi"},{"full_name":"Kohrt, Christina","last_name":"Kohrt","first_name":"Christina"},{"last_name":"Spannenberg","full_name":"Spannenberg, Anke","first_name":"Anke"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"date_updated":"2025-11-10T09:26:28Z","page":"156-164","intvolume":"         3","citation":{"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>","short":"W. Desens, C. Kohrt, A. Spannenberg, T. Werner, Organic Chemistry Frontiers 3 (2016) 156–164.","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} }","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>.","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>.","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>.","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>"},"publication_identifier":{"issn":["2052-4129"]},"publication_status":"published","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"abstract":[{"lang":"eng","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>"}],"publication":"Organic Chemistry Frontiers","title":"A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions","date_created":"2023-01-22T21:04:30Z","publisher":"Royal Society of Chemistry (RSC)","year":"2016","issue":"2"},{"date_updated":"2025-11-10T09:25:16Z","author":[{"last_name":"Diebler","full_name":"Diebler, Johannes","first_name":"Johannes"},{"first_name":"Hartmut","last_name":"Komber","full_name":"Komber, Hartmut"},{"last_name":"Häußler","full_name":"Häußler, Liane","first_name":"Liane"},{"last_name":"Lederer","full_name":"Lederer, Albena","first_name":"Albena"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"volume":49,"doi":"10.1021/acs.macromol.6b00728","publication_status":"published","publication_identifier":{"issn":["0024-9297","1520-5835"]},"citation":{"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} }","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>.","short":"J. Diebler, H. Komber, L. Häußler, A. Lederer, T. Werner, Macromolecules 49 (2016) 4723–4731.","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>","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>.","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>.","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>"},"intvolume":"        49","page":"4723-4731","_id":"37982","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"extern":"1","type":"journal_article","status":"public","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T21:02:41Z","title":"Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers","issue":"13","year":"2016","keyword":["CSSD"],"language":[{"iso":"eng"}],"publication":"Macromolecules"},{"publication":"ACS Sustainable Chemistry &amp; Engineering","language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"year":"2016","issue":"9","title":"Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates","date_created":"2023-01-22T21:01:04Z","publisher":"American Chemical Society (ACS)","status":"public","type":"journal_article","extern":"1","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","_id":"37980","page":"4805-4814","intvolume":"         4","citation":{"chicago":"Büttner, Hendrik, Christoph Grimmer, Johannes Steinbauer, and Thomas 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> 4, no. 9 (2016): 4805–14. <a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">https://doi.org/10.1021/acssuschemeng.6b01092</a>.","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>.","ama":"Büttner H, Grimmer C, Steinbauer J, Werner T. 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>. 2016;4(9):4805-4814. 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). 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>, <i>4</i>(9), 4805–4814. <a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">https://doi.org/10.1021/acssuschemeng.6b01092</a>","bibtex":"@article{Büttner_Grimmer_Steinbauer_Werner_2016, title={Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates}, volume={4}, DOI={<a href=\"https://doi.org/10.1021/acssuschemeng.6b01092\">10.1021/acssuschemeng.6b01092</a>}, number={9}, journal={ACS Sustainable Chemistry &#38;amp; Engineering}, publisher={American Chemical Society (ACS)}, author={Büttner, Hendrik and Grimmer, Christoph and Steinbauer, Johannes and Werner, Thomas}, year={2016}, pages={4805–4814} }","short":"H. Büttner, C. Grimmer, J. Steinbauer, T. 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