[{"extern":"1","_id":"37983","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"status":"public","type":"journal_article","doi":"10.1039/c6gc00671j","date_updated":"2025-11-10T09:20:35Z","author":[{"last_name":"Tenhumberg","full_name":"Tenhumberg, Nils","first_name":"Nils"},{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"first_name":"Benjamin","full_name":"Schäffner, Benjamin","last_name":"Schäffner"},{"first_name":"Daniela","last_name":"Kruse","full_name":"Kruse, Daniela"},{"first_name":"Michael","full_name":"Blumenstein, Michael","last_name":"Blumenstein"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"volume":18,"citation":{"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>","short":"N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, T. Werner, Green Chemistry 18 (2016) 3775–3788.","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} }","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>.","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>"},"intvolume":"        18","page":"3775-3788","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}],"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"}],"publication":"Green Chemistry","title":"Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO<sub>2</sub>and renewables","publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-22T21:03:02Z","year":"2016","issue":"13"},{"keyword":["T2","CSSD"],"language":[{"iso":"eng"}],"extern":"1","_id":"37989","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"status":"public","type":"journal_article","publication":"Advanced Synthesis and Catalysis","title":"Organocatalyzed Reduction of Tertiary Phosphine Oxides","doi":"10.1002/adsc.201500762","date_updated":"2025-11-10T09:22:07Z","publisher":"Wiley","author":[{"first_name":"Marie-Luis","last_name":"Schirmer","full_name":"Schirmer, Marie-Luis"},{"last_name":"Jopp","full_name":"Jopp, Stefan","first_name":"Stefan"},{"first_name":"Jens","full_name":"Holz, Jens","last_name":"Holz"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","full_name":"Werner, Thomas","id":"89271"}],"date_created":"2023-01-22T21:05:14Z","volume":358,"year":"2016","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>."},"intvolume":"       358","page":"26-29","publication_status":"published","publication_identifier":{"issn":["1615-4150"]},"issue":"1"},{"status":"public","type":"journal_article","extern":"1","_id":"37984","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","intvolume":"        72","page":"504-508","citation":{"chicago":"Schirmer, Marie-Luis, Anke Spannenberg, and Thomas Werner. “Highly Functionalized Alkenes Produced from Base-Free Organocatalytic Wittig Reactions: (<i>E</i>)-3-Benzylidenepyrrolidine-2,5-Dione, (<i>E</i>)-3-Benzylidene-1-Methylpyrrolidine-2,5-Dione and (<i>E</i>)-3-Benzylidene-1-<i>Tert</i>-Butylpyrrolidine-2,5-Dione.” <i>Acta Crystallographica Section C Structural Chemistry</i> 72, no. 6 (2016): 504–8. <a href=\"https://doi.org/10.1107/s2053229616008159\">https://doi.org/10.1107/s2053229616008159</a>.","ieee":"M.-L. Schirmer, A. Spannenberg, and T. Werner, “Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione,” <i>Acta Crystallographica Section C Structural Chemistry</i>, vol. 72, no. 6, pp. 504–508, 2016, doi: <a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>.","ama":"Schirmer M-L, Spannenberg A, Werner T. Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione. <i>Acta Crystallographica Section C Structural Chemistry</i>. 2016;72(6):504-508. doi:<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>","bibtex":"@article{Schirmer_Spannenberg_Werner_2016, title={Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione}, volume={72}, DOI={<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>}, number={6}, journal={Acta Crystallographica Section C Structural Chemistry}, publisher={International Union of Crystallography (IUCr)}, author={Schirmer, Marie-Luis and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={504–508} }","short":"M.-L. Schirmer, A. Spannenberg, T. Werner, Acta Crystallographica Section C Structural Chemistry 72 (2016) 504–508.","mla":"Schirmer, Marie-Luis, et al. “Highly Functionalized Alkenes Produced from Base-Free Organocatalytic Wittig Reactions: (<i>E</i>)-3-Benzylidenepyrrolidine-2,5-Dione, (<i>E</i>)-3-Benzylidene-1-Methylpyrrolidine-2,5-Dione and (<i>E</i>)-3-Benzylidene-1-<i>Tert</i>-Butylpyrrolidine-2,5-Dione.” <i>Acta Crystallographica Section C Structural Chemistry</i>, vol. 72, no. 6, International Union of Crystallography (IUCr), 2016, pp. 504–08, doi:<a href=\"https://doi.org/10.1107/s2053229616008159\">10.1107/s2053229616008159</a>.","apa":"Schirmer, M.-L., Spannenberg, A., &#38; Werner, T. (2016). Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione. <i>Acta Crystallographica Section C Structural Chemistry</i>, <i>72</i>(6), 504–508. <a href=\"https://doi.org/10.1107/s2053229616008159\">https://doi.org/10.1107/s2053229616008159</a>"},"publication_identifier":{"issn":["2053-2296"]},"publication_status":"published","doi":"10.1107/s2053229616008159","date_updated":"2025-11-10T09:23:46Z","volume":72,"author":[{"first_name":"Marie-Luis","last_name":"Schirmer","full_name":"Schirmer, Marie-Luis"},{"first_name":"Anke","full_name":"Spannenberg, Anke","last_name":"Spannenberg"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner"}],"abstract":[{"text":"<jats:p>The Wittig reaction is a fundamental transformation for the preparation of alkenes from carbonyl compounds and phosphonium ylides. The ylides are prepared prior to the olefination step from the respective phosphonium salts by deprotonation utilizing strong bases. A first free-base catalytic Wittig reaction for the preparation of highly functionalized alkenes was based on tributylphosphane as the catalyst. Subsequently we developed a system employing a phospholene oxide as a pre-catalyst and trimethoxysilane as reducing agent which operates under milder conditions. The title compounds, (<jats:italic>E</jats:italic>)-3-benzylidenepyrrolidine-2,5-dione, C<jats:sub>11</jats:sub>H<jats:sub>9</jats:sub>NO<jats:sub>2</jats:sub>, (I), the methylpyrrolidine derivative, C<jats:sub>12</jats:sub>H<jats:sub>11</jats:sub>NO<jats:sub>2</jats:sub>, (II), and the<jats:italic>tert-</jats:italic>butylpyrrolidine derivative, C<jats:sub>15</jats:sub>H<jats:sub>17</jats:sub>NO<jats:sub>2</jats:sub>, (III), have been synthesized by base-free catalytic Wittig reactions. In the crystal of (I), molecules are linked into centrosymmetric dimers<jats:italic>via</jats:italic>pairs of N—H...O hydrogen bonds. Furthermore, in the crystal structure of (III), there are two molecules in the asymmetric unit, whereas in (I) and (II), only one molecule is present.</jats:p>","lang":"eng"}],"publication":"Acta Crystallographica Section C Structural Chemistry","keyword":["T2"],"language":[{"iso":"eng"}],"year":"2016","issue":"6","title":"Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (<i>E</i>)-3-benzylidenepyrrolidine-2,5-dione, (<i>E</i>)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (<i>E</i>)-3-benzylidene-1-<i>tert</i>-butylpyrrolidine-2,5-dione","publisher":"International Union of Crystallography (IUCr)","date_created":"2023-01-22T21:03:23Z"},{"type":"journal_article","status":"public","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37981","extern":"1","publication_status":"published","publication_identifier":{"issn":["1477-0520","1477-0539"]},"citation":{"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>.","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>","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","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,"date_updated":"2025-11-10T09:24:16Z","doi":"10.1039/c6ob01081d","publication":"Organic and Biomolecular Chemistry","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"}],"language":[{"iso":"eng"}],"keyword":["CSSD"],"issue":"31","year":"2016","date_created":"2023-01-22T21:01:59Z","publisher":"Royal Society of Chemistry (RSC)","title":"Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes"},{"language":[{"iso":"eng"}],"keyword":["T1","T3","CSSD"],"publication":"Organic Chemistry Frontiers","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>"}],"date_created":"2023-01-22T21:04:30Z","publisher":"Royal Society of Chemistry (RSC)","title":"A novel zinc based binary catalytic system for CO<sub>2</sub>utilization under mild conditions","issue":"2","year":"2016","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37987","extern":"1","type":"journal_article","status":"public","author":[{"full_name":"Desens, Willi","last_name":"Desens","first_name":"Willi"},{"first_name":"Christina","full_name":"Kohrt, Christina","last_name":"Kohrt"},{"full_name":"Spannenberg, Anke","last_name":"Spannenberg","first_name":"Anke"},{"first_name":"Thomas","orcid":"0000-0001-9025-3244","last_name":"Werner","id":"89271","full_name":"Werner, Thomas"}],"volume":3,"date_updated":"2025-11-10T09:26:28Z","doi":"10.1039/c5qo00356c","publication_status":"published","publication_identifier":{"issn":["2052-4129"]},"citation":{"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>","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>.","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} }","short":"W. Desens, C. Kohrt, A. Spannenberg, T. Werner, Organic Chemistry Frontiers 3 (2016) 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>.","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>"},"page":"156-164","intvolume":"         3"},{"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","date_updated":"2025-11-10T09:25:16Z","volume":49,"author":[{"last_name":"Diebler","full_name":"Diebler, Johannes","first_name":"Johannes"},{"last_name":"Komber","full_name":"Komber, Hartmut","first_name":"Hartmut"},{"full_name":"Häußler, Liane","last_name":"Häußler","first_name":"Liane"},{"full_name":"Lederer, Albena","last_name":"Lederer","first_name":"Albena"},{"full_name":"Werner, Thomas","id":"89271","orcid":"0000-0001-9025-3244","last_name":"Werner","first_name":"Thomas"}],"doi":"10.1021/acs.macromol.6b00728","publication_identifier":{"issn":["0024-9297","1520-5835"]},"publication_status":"published","intvolume":"        49","page":"4723-4731","citation":{"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>.","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>","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.","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} }","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>"},"_id":"37982","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","extern":"1","type":"journal_article","status":"public"},{"citation":{"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>","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>.","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. Werner, ACS Sustainable Chemistry &#38;amp; Engineering 4 (2016) 4805–4814.","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). 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>"},"intvolume":"         4","page":"4805-4814","publication_status":"published","publication_identifier":{"issn":["2168-0485","2168-0485"]},"doi":"10.1021/acssuschemeng.6b01092","date_updated":"2025-11-10T09:26:56Z","author":[{"first_name":"Hendrik","last_name":"Büttner","full_name":"Büttner, Hendrik"},{"first_name":"Christoph","full_name":"Grimmer, Christoph","last_name":"Grimmer"},{"first_name":"Johannes","last_name":"Steinbauer","full_name":"Steinbauer, Johannes"},{"first_name":"Thomas","full_name":"Werner, Thomas","id":"89271","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"volume":4,"status":"public","type":"journal_article","extern":"1","_id":"37980","user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"year":"2016","issue":"9","title":"Iron-Based Binary Catalytic System for the Valorization of CO<sub>2</sub> into Biobased Cyclic Carbonates","publisher":"American Chemical Society (ACS)","date_created":"2023-01-22T21:01:04Z","publication":"ACS Sustainable Chemistry &amp; Engineering","keyword":["T1","T3","CSSD"],"language":[{"iso":"eng"}]},{"extern":"1","language":[{"iso":"eng"}],"keyword":["T2","CSSD"],"user_id":"89271","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"_id":"37986","status":"public","type":"journal_article","publication":"Chemistry - A European Journal","doi":"10.1002/chem.201503744","title":"Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes","date_created":"2023-01-22T21:04:06Z","author":[{"last_name":"Schirmer","full_name":"Schirmer, Marie-Luis","first_name":"Marie-Luis"},{"first_name":"Sven","full_name":"Adomeit, Sven","last_name":"Adomeit"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"first_name":"Thomas","id":"89271","full_name":"Werner, Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244"}],"volume":22,"date_updated":"2025-11-10T09:23:00Z","publisher":"Wiley","citation":{"apa":"Schirmer, M.-L., Adomeit, S., Spannenberg, A., &#38; Werner, T. (2016). Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes. <i>Chemistry - A European Journal</i>, <i>22</i>(7), 2458–2465. <a href=\"https://doi.org/10.1002/chem.201503744\">https://doi.org/10.1002/chem.201503744</a>","bibtex":"@article{Schirmer_Adomeit_Spannenberg_Werner_2016, title={Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes}, volume={22}, DOI={<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>}, number={7}, journal={Chemistry - A European Journal}, publisher={Wiley}, author={Schirmer, Marie-Luis and Adomeit, Sven and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={2458–2465} }","short":"M.-L. Schirmer, S. Adomeit, A. Spannenberg, T. Werner, Chemistry - A European Journal 22 (2016) 2458–2465.","mla":"Schirmer, Marie-Luis, et al. “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes.” <i>Chemistry - A European Journal</i>, vol. 22, no. 7, Wiley, 2016, pp. 2458–65, doi:<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>.","ama":"Schirmer M-L, Adomeit S, Spannenberg A, Werner T. Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes. <i>Chemistry - A European Journal</i>. 2016;22(7):2458-2465. doi:<a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>","chicago":"Schirmer, Marie-Luis, Sven Adomeit, Anke Spannenberg, and Thomas Werner. “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes.” <i>Chemistry - A European Journal</i> 22, no. 7 (2016): 2458–65. <a href=\"https://doi.org/10.1002/chem.201503744\">https://doi.org/10.1002/chem.201503744</a>.","ieee":"M.-L. Schirmer, S. Adomeit, A. Spannenberg, and T. Werner, “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes,” <i>Chemistry - A European Journal</i>, vol. 22, no. 7, pp. 2458–2465, 2016, doi: <a href=\"https://doi.org/10.1002/chem.201503744\">10.1002/chem.201503744</a>."},"page":"2458-2465","intvolume":"        22","year":"2016","issue":"7","publication_status":"published","publication_identifier":{"issn":["0947-6539"]}},{"publication":"ChemCatChem","keyword":["CSSD"],"language":[{"iso":"eng"}],"issue":"12","year":"2016","publisher":"Wiley","date_created":"2023-01-22T21:03:46Z","title":"Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions","type":"journal_article","status":"public","_id":"37985","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","extern":"1","publication_identifier":{"issn":["1867-3880"]},"publication_status":"published","intvolume":"         8","page":"2027-2030","citation":{"ama":"Diebler J, Spannenberg A, Werner T. Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions. <i>ChemCatChem</i>. 2016;8(12):2027-2030. doi:<a href=\"https://doi.org/10.1002/cctc.201600242\">10.1002/cctc.201600242</a>","chicago":"Diebler, Johannes, Anke Spannenberg, and Thomas Werner. “Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions.” <i>ChemCatChem</i> 8, no. 12 (2016): 2027–30. <a href=\"https://doi.org/10.1002/cctc.201600242\">https://doi.org/10.1002/cctc.201600242</a>.","ieee":"J. Diebler, A. Spannenberg, and T. Werner, “Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions,” <i>ChemCatChem</i>, vol. 8, no. 12, pp. 2027–2030, 2016, doi: <a href=\"https://doi.org/10.1002/cctc.201600242\">10.1002/cctc.201600242</a>.","mla":"Diebler, Johannes, et al. “Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions.” <i>ChemCatChem</i>, vol. 8, no. 12, Wiley, 2016, pp. 2027–30, doi:<a href=\"https://doi.org/10.1002/cctc.201600242\">10.1002/cctc.201600242</a>.","bibtex":"@article{Diebler_Spannenberg_Werner_2016, title={Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions}, volume={8}, DOI={<a href=\"https://doi.org/10.1002/cctc.201600242\">10.1002/cctc.201600242</a>}, number={12}, journal={ChemCatChem}, publisher={Wiley}, author={Diebler, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2016}, pages={2027–2030} }","short":"J. Diebler, A. Spannenberg, T. Werner, ChemCatChem 8 (2016) 2027–2030.","apa":"Diebler, J., Spannenberg, A., &#38; Werner, T. (2016). Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions. <i>ChemCatChem</i>, <i>8</i>(12), 2027–2030. <a href=\"https://doi.org/10.1002/cctc.201600242\">https://doi.org/10.1002/cctc.201600242</a>"},"date_updated":"2025-11-10T09:24:45Z","volume":8,"author":[{"first_name":"Johannes","full_name":"Diebler, Johannes","last_name":"Diebler"},{"first_name":"Anke","last_name":"Spannenberg","full_name":"Spannenberg, Anke"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"doi":"10.1002/cctc.201600242"},{"publication_identifier":{"issn":["1615-4150"]},"publication_status":"published","issue":"4","year":"2016","page":"622-630","intvolume":"       358","citation":{"ama":"Desens W, Werner T. Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates. <i>Advanced Synthesis and Catalysis</i>. 2016;358(4):622-630. doi:<a href=\"https://doi.org/10.1002/adsc.201500941\">10.1002/adsc.201500941</a>","ieee":"W. Desens and T. Werner, “Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates,” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 4, pp. 622–630, 2016, doi: <a href=\"https://doi.org/10.1002/adsc.201500941\">10.1002/adsc.201500941</a>.","chicago":"Desens, Willi, and Thomas Werner. “Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates.” <i>Advanced Synthesis and Catalysis</i> 358, no. 4 (2016): 622–30. <a href=\"https://doi.org/10.1002/adsc.201500941\">https://doi.org/10.1002/adsc.201500941</a>.","apa":"Desens, W., &#38; Werner, T. (2016). Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates. <i>Advanced Synthesis and Catalysis</i>, <i>358</i>(4), 622–630. <a href=\"https://doi.org/10.1002/adsc.201500941\">https://doi.org/10.1002/adsc.201500941</a>","short":"W. Desens, T. Werner, Advanced Synthesis and Catalysis 358 (2016) 622–630.","mla":"Desens, Willi, and Thomas Werner. “Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates.” <i>Advanced Synthesis and Catalysis</i>, vol. 358, no. 4, Wiley, 2016, pp. 622–30, doi:<a href=\"https://doi.org/10.1002/adsc.201500941\">10.1002/adsc.201500941</a>.","bibtex":"@article{Desens_Werner_2016, title={Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates}, volume={358}, DOI={<a href=\"https://doi.org/10.1002/adsc.201500941\">10.1002/adsc.201500941</a>}, number={4}, journal={Advanced Synthesis and Catalysis}, publisher={Wiley}, author={Desens, Willi and Werner, Thomas}, year={2016}, pages={622–630} }"},"date_updated":"2025-11-10T09:25:53Z","publisher":"Wiley","volume":358,"author":[{"last_name":"Desens","full_name":"Desens, Willi","first_name":"Willi"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"date_created":"2023-01-22T21:04:52Z","title":"Convergent Activation Concept for CO<sub>2</sub>Fixation in Carbonates","doi":"10.1002/adsc.201500941","publication":"Advanced Synthesis and Catalysis","type":"journal_article","status":"public","_id":"37988","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"user_id":"89271","keyword":["T1","CSSD"],"extern":"1","language":[{"iso":"eng"}]},{"doi":"10.1007/978-3-319-48135-7_4","title":"Hydrometallurgical Recovery of Rare Earth Metals from Spent FCC Catalysts","author":[{"last_name":"Wenzel","full_name":"Wenzel, M.","first_name":"M."},{"last_name":"Schnaars","full_name":"Schnaars, Kathleen","id":"117735","first_name":"Kathleen"},{"full_name":"Kelly, N.","last_name":"Kelly","first_name":"N."},{"last_name":"Götzke","full_name":"Götzke, L.","first_name":"L."},{"first_name":"S. M.","full_name":"Robles, S. M.","last_name":"Robles"},{"last_name":"Kretschmer","full_name":"Kretschmer, K.","first_name":"K."},{"last_name":"Le","full_name":"Le, Phuc Nguyen","first_name":"Phuc Nguyen"},{"last_name":"Tung","full_name":"Tung, Dang Thanh","first_name":"Dang Thanh"},{"full_name":"Luong, Nguyen Huu","last_name":"Luong","first_name":"Nguyen Huu"},{"first_name":"Nguyen Anh","last_name":"Duc","full_name":"Duc, Nguyen Anh"},{"last_name":"Sy","full_name":"Sy, Dang Van","first_name":"Dang Van"},{"first_name":"K.","last_name":"Gloe","full_name":"Gloe, K."},{"last_name":"Weigand","full_name":"Weigand, J. J.","first_name":"J. J."}],"date_created":"2025-12-04T12:15:35Z","date_updated":"2025-12-04T12:19:23Z","publisher":"Springer International Publishing","citation":{"ama":"Wenzel M, Schnaars K, Kelly N, et al. Hydrometallurgical Recovery of Rare Earth Metals from Spent FCC Catalysts. In: <i>Rare Metal Technology 2016</i>. Springer International Publishing; 2016. doi:<a href=\"https://doi.org/10.1007/978-3-319-48135-7_4\">10.1007/978-3-319-48135-7_4</a>","chicago":"Wenzel, M., Kathleen Schnaars, N. Kelly, L. Götzke, S. M. Robles, K. Kretschmer, Phuc Nguyen Le, et al. “Hydrometallurgical Recovery of Rare Earth Metals from Spent FCC Catalysts.” In <i>Rare Metal Technology 2016</i>. Cham: Springer International Publishing, 2016. <a href=\"https://doi.org/10.1007/978-3-319-48135-7_4\">https://doi.org/10.1007/978-3-319-48135-7_4</a>.","ieee":"M. Wenzel <i>et al.</i>, “Hydrometallurgical Recovery of Rare Earth Metals from Spent FCC Catalysts,” in <i>Rare Metal Technology 2016</i>, Cham: Springer International Publishing, 2016.","apa":"Wenzel, M., Schnaars, K., Kelly, N., Götzke, L., Robles, S. M., Kretschmer, K., Le, P. N., Tung, D. T., Luong, N. H., Duc, N. A., Sy, D. V., Gloe, K., &#38; Weigand, J. J. (2016). Hydrometallurgical Recovery of Rare Earth Metals from Spent FCC Catalysts. In <i>Rare Metal Technology 2016</i>. Springer International Publishing. <a href=\"https://doi.org/10.1007/978-3-319-48135-7_4\">https://doi.org/10.1007/978-3-319-48135-7_4</a>","bibtex":"@inbook{Wenzel_Schnaars_Kelly_Götzke_Robles_Kretschmer_Le_Tung_Luong_Duc_et al._2016, place={Cham}, title={Hydrometallurgical Recovery of Rare Earth Metals from Spent FCC Catalysts}, DOI={<a href=\"https://doi.org/10.1007/978-3-319-48135-7_4\">10.1007/978-3-319-48135-7_4</a>}, booktitle={Rare Metal Technology 2016}, publisher={Springer International Publishing}, author={Wenzel, M. and Schnaars, Kathleen and Kelly, N. and Götzke, L. and Robles, S. M. and Kretschmer, K. and Le, Phuc Nguyen and Tung, Dang Thanh and Luong, Nguyen Huu and Duc, Nguyen Anh and et al.}, year={2016} }","mla":"Wenzel, M., et al. “Hydrometallurgical Recovery of Rare Earth Metals from Spent FCC Catalysts.” <i>Rare Metal Technology 2016</i>, Springer International Publishing, 2016, doi:<a href=\"https://doi.org/10.1007/978-3-319-48135-7_4\">10.1007/978-3-319-48135-7_4</a>.","short":"M. Wenzel, K. Schnaars, N. Kelly, L. Götzke, S.M. Robles, K. Kretschmer, P.N. Le, D.T. Tung, N.H. Luong, N.A. Duc, D.V. Sy, K. Gloe, J.J. Weigand, in: Rare Metal Technology 2016, Springer International Publishing, Cham, 2016."},"place":"Cham","year":"2016","publication_status":"published","publication_identifier":{"isbn":["9783319486161","9783319481357"]},"quality_controlled":"1","extern":"1","language":[{"iso":"eng"}],"user_id":"117735","department":[{"_id":"985"}],"_id":"62857","status":"public","abstract":[{"text":"The recovery of rare earth metals from secondary sources has attracted much attention due to their ever expanding demand in the high-tech industry. The studies reported here focus on the hydrometallurgical recovery of lanthanum and cerium from spent fluid catalytic cracking (FCC) catalysts in a two-step process: leaching with nitric acid and solvent extraction by tri-n-butyl phosphate (TBP) and di(2-ethylhexyl)phosphoric acid (D2EHPA). The experiments show a high dissolution yield of about 93% lanthanum and 42% cerium in a single leaching step with 2 M (126 g/L) HNO3 at 80 °C; only 11% aluminum has been dissolved simultaneously. In the subsequent solvent extraction step the best results for this leach liquor could be achieved using a 1:1 mixture of 25% (v/v) TBP (0.92 M) and 25% (v/v) D2EHPA (0.76 M) in n-decane without the need for any pH adjustment. In that case La(III) and Ce(III) can be extracted with 60% and 74% yield respectively in one stage from the majority of accompanying matrix elements. In particular no extraction of Al(III) could be observed under these conditions.","lang":"eng"}],"type":"book_chapter","publication":"Rare Metal Technology 2016"},{"page":"11694-11706","intvolume":"        55","citation":{"chicago":"Vollmers, Nora Jenny, Patrick Müller, Alexander Hoffmann, Sonja Herres-Pawlis, Martin Rohrmüller, Wolf Gero Schmidt, Uwe Gerstmann, and Matthias Bauer. “Experimental and Theoretical High-Energy-Resolution X-Ray Absorption Spectroscopy: Implications for the Investigation of the Entatic State.” <i>Inorganic Chemistry</i> 55 (2016): 11694–706. <a href=\"https://doi.org/10.1021/acs.inorgchem.6b01704\">https://doi.org/10.1021/acs.inorgchem.6b01704</a>.","ieee":"N. J. Vollmers <i>et al.</i>, “Experimental and Theoretical High-Energy-Resolution X-ray Absorption Spectroscopy: Implications for the Investigation of the Entatic State,” <i>Inorganic Chemistry</i>, vol. 55, pp. 11694–11706, 2016, doi: <a href=\"https://doi.org/10.1021/acs.inorgchem.6b01704\">10.1021/acs.inorgchem.6b01704</a>.","ama":"Vollmers NJ, Müller P, Hoffmann A, et al. Experimental and Theoretical High-Energy-Resolution X-ray Absorption Spectroscopy: Implications for the Investigation of the Entatic State. <i>Inorganic Chemistry</i>. 2016;55:11694-11706. doi:<a href=\"https://doi.org/10.1021/acs.inorgchem.6b01704\">10.1021/acs.inorgchem.6b01704</a>","mla":"Vollmers, Nora Jenny, et al. “Experimental and Theoretical High-Energy-Resolution X-Ray Absorption Spectroscopy: Implications for the Investigation of the Entatic State.” <i>Inorganic Chemistry</i>, vol. 55, 2016, pp. 11694–706, doi:<a href=\"https://doi.org/10.1021/acs.inorgchem.6b01704\">10.1021/acs.inorgchem.6b01704</a>.","short":"N.J. Vollmers, P. Müller, A. Hoffmann, S. Herres-Pawlis, M. Rohrmüller, W.G. Schmidt, U. Gerstmann, M. Bauer, Inorganic Chemistry 55 (2016) 11694–11706.","bibtex":"@article{Vollmers_Müller_Hoffmann_Herres-Pawlis_Rohrmüller_Schmidt_Gerstmann_Bauer_2016, title={Experimental and Theoretical High-Energy-Resolution X-ray Absorption Spectroscopy: Implications for the Investigation of the Entatic State}, volume={55}, DOI={<a href=\"https://doi.org/10.1021/acs.inorgchem.6b01704\">10.1021/acs.inorgchem.6b01704</a>}, journal={Inorganic Chemistry}, author={Vollmers, Nora Jenny and Müller, Patrick and Hoffmann, Alexander and Herres-Pawlis, Sonja and Rohrmüller, Martin and Schmidt, Wolf Gero and Gerstmann, Uwe and Bauer, Matthias}, year={2016}, pages={11694–11706} }","apa":"Vollmers, N. J., Müller, P., Hoffmann, A., Herres-Pawlis, S., Rohrmüller, M., Schmidt, W. G., Gerstmann, U., &#38; Bauer, M. (2016). 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Beifuss, M. Lehmann, A. Krueger, F. Beuerle, M.O. Senge, R. Breinbauer, C. Mück‐Lichtenfeld, T.J.J. Müller, M. Denißen, T. Lindel, J. Pietruszka, D. Worgull, T. Gulder, J. Paradies, K. Muñiz, T. Bach, K. Ditrich, C. Winter, M. Kordes, W. von Deyn, R. Pfau, C. Muhle‐Goll, B. Luy, D.B. Werz, C. Arenz, W. Hüttel, J.N. Andexer, B.F. Straub, Nachrichten Aus Der Chemie 64 (2016) 255–294.","mla":"Itzen, Aymelt, et al. “Organische Chemie.” <i>Nachrichten Aus Der Chemie</i>, vol. 64, no. 3, Wiley, 2016, pp. 255–94, doi:<a href=\"https://doi.org/10.1002/nadc.20164047492\">10.1002/nadc.20164047492</a>.","ieee":"A. Itzen <i>et al.</i>, “Organische Chemie,” <i>Nachrichten aus der Chemie</i>, vol. 64, no. 3, pp. 255–294, 2016, doi: <a href=\"https://doi.org/10.1002/nadc.20164047492\">10.1002/nadc.20164047492</a>.","chicago":"Itzen, Aymelt, Norbert Schaschke, Uwe Beifuss, Matthias Lehmann, Anke Krueger, Florian Beuerle, Mathias O. 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Organische Chemie. <i>Nachrichten aus der Chemie</i>. 2016;64(3):255-294. doi:<a href=\"https://doi.org/10.1002/nadc.20164047492\">10.1002/nadc.20164047492</a>"},"publication_identifier":{"issn":["1439-9598","1868-0054"]},"publication_status":"published","issue":"3","title":"Organische Chemie","doi":"10.1002/nadc.20164047492","publisher":"Wiley","date_updated":"2026-03-11T10:25:23Z","volume":64,"date_created":"2026-03-11T10:25:12Z","author":[{"first_name":"Aymelt","last_name":"Itzen","full_name":"Itzen, Aymelt"},{"full_name":"Schaschke, Norbert","last_name":"Schaschke","first_name":"Norbert"},{"first_name":"Uwe","last_name":"Beifuss","full_name":"Beifuss, Uwe"},{"full_name":"Lehmann, Matthias","last_name":"Lehmann","first_name":"Matthias"},{"last_name":"Krueger","full_name":"Krueger, Anke","first_name":"Anke"},{"first_name":"Florian","full_name":"Beuerle, Florian","last_name":"Beuerle"},{"first_name":"Mathias O.","full_name":"Senge, Mathias O.","last_name":"Senge"},{"first_name":"Rolf","last_name":"Breinbauer","full_name":"Breinbauer, Rolf"},{"full_name":"Mück‐Lichtenfeld, Christian","last_name":"Mück‐Lichtenfeld","first_name":"Christian"},{"first_name":"Thomas J. J.","last_name":"Müller","full_name":"Müller, Thomas J. J."},{"full_name":"Denißen, Melanie","last_name":"Denißen","first_name":"Melanie"},{"last_name":"Lindel","full_name":"Lindel, Thomas","first_name":"Thomas"},{"last_name":"Pietruszka","full_name":"Pietruszka, Jörg","first_name":"Jörg"},{"first_name":"Dennis","full_name":"Worgull, Dennis","last_name":"Worgull"},{"first_name":"Tobias","last_name":"Gulder","full_name":"Gulder, Tobias"},{"orcid":"0000-0002-3698-668X","last_name":"Paradies","full_name":"Paradies, Jan","id":"53339","first_name":"Jan"},{"full_name":"Muñiz, Kilian","last_name":"Muñiz","first_name":"Kilian"},{"last_name":"Bach","full_name":"Bach, Thorsten","first_name":"Thorsten"},{"first_name":"Klaus","full_name":"Ditrich, Klaus","last_name":"Ditrich"},{"full_name":"Winter, Christian","last_name":"Winter","first_name":"Christian"},{"last_name":"Kordes","full_name":"Kordes, Markus","first_name":"Markus"},{"full_name":"von Deyn, Wolfgang","last_name":"von Deyn","first_name":"Wolfgang"},{"first_name":"Roland","last_name":"Pfau","full_name":"Pfau, Roland"},{"first_name":"Claudia","full_name":"Muhle‐Goll, Claudia","last_name":"Muhle‐Goll"},{"full_name":"Luy, Burkhard","last_name":"Luy","first_name":"Burkhard"},{"first_name":"Daniel B.","last_name":"Werz","full_name":"Werz, Daniel B."},{"last_name":"Arenz","full_name":"Arenz, Christoph","first_name":"Christoph"},{"last_name":"Hüttel","full_name":"Hüttel, Wolfgang","first_name":"Wolfgang"},{"last_name":"Andexer","full_name":"Andexer, Jennifer N.","first_name":"Jennifer N."},{"full_name":"Straub, Bernd F.","last_name":"Straub","first_name":"Bernd F."}],"abstract":[{"text":"<jats:title>Abstract</jats:title><jats:p>Siliciumrhodaminderivate weisen Formaldehyd nach – neues Nanomaterial: Graphitphasen polymeren Kohlenstoffnitrids – molekulare Drähte – homogene Cof‐Dünnschichten bei Raumtemperatur – Biosyntheserekord: 1,8 MDa großes kolGen – [3,3]‐sigmatrope Umlagerung führt zu quartären Stereozentren.</jats:p>","lang":"eng"}],"status":"public","publication":"Nachrichten aus der Chemie","type":"journal_article","language":[{"iso":"eng"}],"_id":"64898","department":[{"_id":"2"},{"_id":"389"}],"user_id":"53339"},{"publication_status":"published","publication_identifier":{"issn":["0143-7496"]},"year":"2015","citation":{"ieee":"O. 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