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Structural Transitions and Thermochromism of Linear Polynuclear Cobalt(II)-4-Octadecyl-1,2,4-triazole Complexes. <i>Journal of Inorganic and Organometallic Polymers and Materials</i>, <i>27</i>(3), 605–611. <a href=\"https://doi.org/10.1007/s10904-016-0486-4\">https://doi.org/10.1007/s10904-016-0486-4</a>","ieee":"I. Bräunlich, C. Mair, M. Bauer, and W. Caseri, “Structural Transitions and Thermochromism of Linear Polynuclear Cobalt(II)-4-Octadecyl-1,2,4-triazole Complexes,” <i>Journal of Inorganic and Organometallic Polymers and Materials</i>, vol. 27, no. 3, pp. 605–611, 2017, doi: <a href=\"https://doi.org/10.1007/s10904-016-0486-4\">10.1007/s10904-016-0486-4</a>.","ama":"Bräunlich I, Mair C, Bauer M, Caseri W. Structural Transitions and Thermochromism of Linear Polynuclear Cobalt(II)-4-Octadecyl-1,2,4-triazole Complexes. <i>Journal of Inorganic and Organometallic Polymers and Materials</i>. 2017;27(3):605-611. doi:<a href=\"https://doi.org/10.1007/s10904-016-0486-4\">10.1007/s10904-016-0486-4</a>","bibtex":"@article{Bräunlich_Mair_Bauer_Caseri_2017, title={Structural Transitions and Thermochromism of Linear Polynuclear Cobalt(II)-4-Octadecyl-1,2,4-triazole Complexes}, volume={27}, DOI={<a href=\"https://doi.org/10.1007/s10904-016-0486-4\">10.1007/s10904-016-0486-4</a>}, number={3}, journal={Journal of Inorganic and Organometallic Polymers and Materials}, publisher={Springer Science and Business Media LLC}, author={Bräunlich, Irene and Mair, Christiane and Bauer, Matthias and Caseri, Walter}, year={2017}, pages={605–611} }","mla":"Bräunlich, Irene, et al. “Structural Transitions and Thermochromism of Linear Polynuclear Cobalt(II)-4-Octadecyl-1,2,4-Triazole Complexes.” <i>Journal of Inorganic and Organometallic Polymers and Materials</i>, vol. 27, no. 3, Springer Science and Business Media LLC, 2017, pp. 605–11, doi:<a href=\"https://doi.org/10.1007/s10904-016-0486-4\">10.1007/s10904-016-0486-4</a>."},"publication_status":"published","date_updated":"2023-01-31T08:28:36Z","intvolume":"        27","title":"Structural Transitions and Thermochromism of Linear Polynuclear Cobalt(II)-4-Octadecyl-1,2,4-triazole Complexes","year":"2017","publication_identifier":{"issn":["1574-1443","1574-1451"]},"author":[{"first_name":"Irene","last_name":"Bräunlich","full_name":"Bräunlich, Irene"},{"full_name":"Mair, Christiane","last_name":"Mair","first_name":"Christiane"},{"first_name":"Matthias","orcid":"0000-0002-9294-6076","last_name":"Bauer","full_name":"Bauer, Matthias","id":"47241"},{"full_name":"Caseri, Walter","last_name":"Caseri","first_name":"Walter"}],"doi":"10.1007/s10904-016-0486-4","language":[{"iso":"eng"}],"publication":"Journal of Inorganic and Organometallic Polymers and Materials","issue":"3","keyword":["Materials Chemistry","Polymers and Plastics"],"type":"journal_article","department":[{"_id":"35"},{"_id":"306"}],"date_created":"2023-01-30T18:50:45Z"},{"date_created":"2023-02-06T12:47:44Z","type":"journal_article","keyword":["Electrochemistry","Spectroscopy","Surfaces and Interfaces","Condensed Matter Physics","General Materials Science"],"department":[{"_id":"314"}],"issue":"24","publication":"Langmuir","language":[{"iso":"eng"}],"doi":"10.1021/acs.langmuir.7b00887","title":"Silica Polymerization from Supersaturated Dilute Aqueous Solutions in the Presence of Alkaline Earth Salts","year":"2017","author":[{"full_name":"Kley, M.","first_name":"M.","last_name":"Kley"},{"last_name":"Kempter","first_name":"A.","full_name":"Kempter, A."},{"last_name":"Boyko","first_name":"V.","full_name":"Boyko, V."},{"first_name":"Klaus","last_name":"Huber","full_name":"Huber, Klaus","id":"237"}],"publication_identifier":{"issn":["0743-7463","1520-5827"]},"date_updated":"2023-02-06T12:48:16Z","publication_status":"published","intvolume":"        33","citation":{"apa":"Kley, M., Kempter, A., Boyko, V., &#38; Huber, K. (2017). Silica Polymerization from Supersaturated Dilute Aqueous Solutions in the Presence of Alkaline Earth Salts. <i>Langmuir</i>, <i>33</i>(24), 6071–6083. <a href=\"https://doi.org/10.1021/acs.langmuir.7b00887\">https://doi.org/10.1021/acs.langmuir.7b00887</a>","ieee":"M. Kley, A. Kempter, V. Boyko, and K. Huber, “Silica Polymerization from Supersaturated Dilute Aqueous Solutions in the Presence of Alkaline Earth Salts,” <i>Langmuir</i>, vol. 33, no. 24, pp. 6071–6083, 2017, doi: <a href=\"https://doi.org/10.1021/acs.langmuir.7b00887\">10.1021/acs.langmuir.7b00887</a>.","chicago":"Kley, M., A. Kempter, V. Boyko, and Klaus Huber. “Silica Polymerization from Supersaturated Dilute Aqueous Solutions in the Presence of Alkaline Earth Salts.” <i>Langmuir</i> 33, no. 24 (2017): 6071–83. <a href=\"https://doi.org/10.1021/acs.langmuir.7b00887\">https://doi.org/10.1021/acs.langmuir.7b00887</a>.","short":"M. Kley, A. Kempter, V. Boyko, K. Huber, Langmuir 33 (2017) 6071–6083.","mla":"Kley, M., et al. “Silica Polymerization from Supersaturated Dilute Aqueous Solutions in the Presence of Alkaline Earth Salts.” <i>Langmuir</i>, vol. 33, no. 24, American Chemical Society (ACS), 2017, pp. 6071–83, doi:<a href=\"https://doi.org/10.1021/acs.langmuir.7b00887\">10.1021/acs.langmuir.7b00887</a>.","ama":"Kley M, Kempter A, Boyko V, Huber K. Silica Polymerization from Supersaturated Dilute Aqueous Solutions in the Presence of Alkaline Earth Salts. <i>Langmuir</i>. 2017;33(24):6071-6083. doi:<a href=\"https://doi.org/10.1021/acs.langmuir.7b00887\">10.1021/acs.langmuir.7b00887</a>","bibtex":"@article{Kley_Kempter_Boyko_Huber_2017, title={Silica Polymerization from Supersaturated Dilute Aqueous Solutions in the Presence of Alkaline Earth Salts}, volume={33}, DOI={<a href=\"https://doi.org/10.1021/acs.langmuir.7b00887\">10.1021/acs.langmuir.7b00887</a>}, number={24}, journal={Langmuir}, publisher={American Chemical Society (ACS)}, author={Kley, M. and Kempter, A. and Boyko, V. and Huber, Klaus}, year={2017}, pages={6071–6083} }"},"page":"6071-6083","_id":"41836","publisher":"American Chemical Society (ACS)","user_id":"237","volume":33,"status":"public"},{"doi":"10.1021/acs.langmuir.7b01634","language":[{"iso":"eng"}],"publication_status":"published","date_updated":"2023-02-06T12:47:05Z","intvolume":"        33","year":"2017","title":"Insight into the Final Step of the Supramolecular Buildup of Eumelanin","publication_identifier":{"issn":["0743-7463","1520-5827"]},"author":[{"full_name":"Büngeler, Anne","first_name":"Anne","last_name":"Büngeler"},{"last_name":"Hämisch","first_name":"Benjamin","full_name":"Hämisch, Benjamin"},{"full_name":"Huber, Klaus","first_name":"Klaus","last_name":"Huber","id":"237"},{"full_name":"Bremser, Wolfgang","first_name":"Wolfgang","last_name":"Bremser"},{"full_name":"Strube, Oliver I.","first_name":"Oliver I.","last_name":"Strube"}],"keyword":["Electrochemistry","Spectroscopy","Surfaces and Interfaces","Condensed Matter Physics","General Materials Science"],"type":"journal_article","department":[{"_id":"314"}],"date_created":"2023-02-06T12:46:40Z","publication":"Langmuir","issue":"27","user_id":"237","volume":33,"page":"6895-6901","publisher":"American Chemical Society (ACS)","_id":"41835","status":"public","citation":{"mla":"Büngeler, Anne, et al. “Insight into the Final Step of the Supramolecular Buildup of Eumelanin.” <i>Langmuir</i>, vol. 33, no. 27, American Chemical Society (ACS), 2017, pp. 6895–901, doi:<a href=\"https://doi.org/10.1021/acs.langmuir.7b01634\">10.1021/acs.langmuir.7b01634</a>.","bibtex":"@article{Büngeler_Hämisch_Huber_Bremser_Strube_2017, title={Insight into the Final Step of the Supramolecular Buildup of Eumelanin}, volume={33}, DOI={<a href=\"https://doi.org/10.1021/acs.langmuir.7b01634\">10.1021/acs.langmuir.7b01634</a>}, number={27}, journal={Langmuir}, publisher={American Chemical Society (ACS)}, author={Büngeler, Anne and Hämisch, Benjamin and Huber, Klaus and Bremser, Wolfgang and Strube, Oliver I.}, year={2017}, pages={6895–6901} }","ama":"Büngeler A, Hämisch B, Huber K, Bremser W, Strube OI. 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Strube. “Insight into the Final Step of the Supramolecular Buildup of Eumelanin.” <i>Langmuir</i> 33, no. 27 (2017): 6895–6901. <a href=\"https://doi.org/10.1021/acs.langmuir.7b01634\">https://doi.org/10.1021/acs.langmuir.7b01634</a>.","short":"A. Büngeler, B. Hämisch, K. Huber, W. Bremser, O.I. Strube, Langmuir 33 (2017) 6895–6901."}},{"abstract":[{"lang":"eng","text":"Dimethylacrylamide-based hydrogels were utilized as porogenic matrices in the synthesis of mesoporous aluminum oxide (γ-Al2O3) with specific BET surface areas up to 360 m2 g–1. Polymers with molecular mass in the range 12000–35000 g mol–1 were synthesized from dimethylacrylamide and various comonomers by free-radical polymerization. Photo-cross-linking of the polymers and impregnation with aluminum nitrate [Al(NO3)3] was carried out in a single step, followed by formation of Al(OH)3/AlO(OH) and subsequent calcination. Calcination led to the formation of mesoporous Al2O3 and simultaneous combustion of the hydrogel. The structural properties of the products were characterized by powder XRD, N2 physisorption analysis, Hg intrusion porosimetry, and thermogravimetric analysis."}],"quality_controlled":"1","publication":"European Journal of Inorganic Chemistry","citation":{"mla":"Weinberger, Christian, et al. “Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina.” <i>European Journal of Inorganic Chemistry</i>, 2017, pp. 1026–31, doi:<a href=\"https://doi.org/10.1002/ejic.201601364\">10.1002/ejic.201601364</a>.","ama":"Weinberger C, Chen Z, Birnbaum W, Kuckling D, Tiemann M. Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina. <i>European Journal of Inorganic Chemistry</i>. Published online 2017:1026-1031. doi:<a href=\"https://doi.org/10.1002/ejic.201601364\">10.1002/ejic.201601364</a>","bibtex":"@article{Weinberger_Chen_Birnbaum_Kuckling_Tiemann_2017, title={Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina}, DOI={<a href=\"https://doi.org/10.1002/ejic.201601364\">10.1002/ejic.201601364</a>}, journal={European Journal of Inorganic Chemistry}, author={Weinberger, Christian and Chen, Zimei and Birnbaum, Wolfgang and Kuckling, Dirk and Tiemann, Michael}, year={2017}, pages={1026–1031} }","apa":"Weinberger, C., Chen, Z., Birnbaum, W., Kuckling, D., &#38; Tiemann, M. (2017). Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina. <i>European Journal of Inorganic Chemistry</i>, 1026–1031. <a href=\"https://doi.org/10.1002/ejic.201601364\">https://doi.org/10.1002/ejic.201601364</a>","ieee":"C. Weinberger, Z. Chen, W. Birnbaum, D. Kuckling, and M. Tiemann, “Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina,” <i>European Journal of Inorganic Chemistry</i>, pp. 1026–1031, 2017, doi: <a href=\"https://doi.org/10.1002/ejic.201601364\">10.1002/ejic.201601364</a>.","short":"C. Weinberger, Z. Chen, W. Birnbaum, D. Kuckling, M. Tiemann, European Journal of Inorganic Chemistry (2017) 1026–1031.","chicago":"Weinberger, Christian, Zimei Chen, Wolfgang Birnbaum, Dirk Kuckling, and Michael Tiemann. “Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina.” <i>European Journal of Inorganic Chemistry</i>, 2017, 1026–31. <a href=\"https://doi.org/10.1002/ejic.201601364\">https://doi.org/10.1002/ejic.201601364</a>."},"type":"journal_article","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"},{"_id":"311"}],"date_created":"2021-10-08T11:05:54Z","publication_status":"published","date_updated":"2023-03-08T10:24:33Z","article_type":"original","title":"Photo-Cross-Linked Polydimethylacrylamide Hydrogels as Porogens for Mesoporous Alumina","year":"2017","status":"public","publication_identifier":{"issn":["1434-1948"]},"author":[{"id":"11848","full_name":"Weinberger, Christian","first_name":"Christian","last_name":"Weinberger"},{"last_name":"Chen","first_name":"Zimei","full_name":"Chen, Zimei"},{"first_name":"Wolfgang","last_name":"Birnbaum","full_name":"Birnbaum, Wolfgang"},{"id":"287","last_name":"Kuckling","first_name":"Dirk","full_name":"Kuckling, Dirk"},{"id":"23547","full_name":"Tiemann, Michael","orcid":"0000-0003-1711-2722","first_name":"Michael","last_name":"Tiemann"}],"user_id":"23547","doi":"10.1002/ejic.201601364","page":"1026-1031","_id":"25915","language":[{"iso":"eng"}]},{"date_created":"2021-10-08T10:53:18Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"},{"_id":"311"}],"type":"journal_article","publication":"Processes","abstract":[{"lang":"eng","text":"Dimethylacrylamide-based hydrogels were utilized as porogenic matrices in the synthesis of mesoporous aluminum oxide (γ-Al2O3) with specific BET surface areas up to 360 m2 g–1. Polymers with molecular mass in the range 12000–35000 g mol–1 were synthesized from dimethylacrylamide and various comonomers by free-radical polymerization. Photo-cross-linking of the polymers and impregnation with aluminum nitrate [Al(NO3)3] was carried out in a single step, followed by formation of Al(OH)3/AlO(OH) and subsequent calcination. Calcination led to the formation of mesoporous Al2O3 and simultaneous combustion of the hydrogel. The structural properties of the products were characterized by powder XRD, N2 physisorption analysis, Hg intrusion porosimetry, and thermogravimetric analysis."}],"language":[{"iso":"eng"}],"article_number":"70","main_file_link":[{"open_access":"1","url":"https://www.mdpi.com/2227-9717/5/4/70/pdf?version=1510132833"}],"doi":"10.3390/pr5040070","publication_identifier":{"issn":["2227-9717"]},"author":[{"first_name":"Zimei","last_name":"Chen","full_name":"Chen, Zimei"},{"first_name":"Christian","last_name":"Weinberger","full_name":"Weinberger, Christian","id":"11848"},{"last_name":"Tiemann","first_name":"Michael","orcid":"0000-0003-1711-2722","full_name":"Tiemann, Michael","id":"23547"},{"id":"287","first_name":"Dirk","last_name":"Kuckling","full_name":"Kuckling, Dirk"}],"year":"2017","title":"Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia","article_type":"original","publication_status":"published","date_updated":"2023-03-08T10:25:25Z","oa":"1","citation":{"chicago":"Chen, Zimei, Christian Weinberger, Michael Tiemann, and Dirk Kuckling. “Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia.” <i>Processes</i>, 2017. <a href=\"https://doi.org/10.3390/pr5040070\">https://doi.org/10.3390/pr5040070</a>.","short":"Z. Chen, C. Weinberger, M. Tiemann, D. Kuckling, Processes (2017).","ieee":"Z. Chen, C. Weinberger, M. Tiemann, and D. Kuckling, “Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia,” <i>Processes</i>, Art. no. 70, 2017, doi: <a href=\"https://doi.org/10.3390/pr5040070\">10.3390/pr5040070</a>.","apa":"Chen, Z., Weinberger, C., Tiemann, M., &#38; Kuckling, D. (2017). Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia. <i>Processes</i>, Article 70. <a href=\"https://doi.org/10.3390/pr5040070\">https://doi.org/10.3390/pr5040070</a>","bibtex":"@article{Chen_Weinberger_Tiemann_Kuckling_2017, title={Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia}, DOI={<a href=\"https://doi.org/10.3390/pr5040070\">10.3390/pr5040070</a>}, number={70}, journal={Processes}, author={Chen, Zimei and Weinberger, Christian and Tiemann, Michael and Kuckling, Dirk}, year={2017} }","ama":"Chen Z, Weinberger C, Tiemann M, Kuckling D. Organic Polymers as Porogenic Structure Matrices for Mesoporous Alumina and Magnesia. <i>Processes</i>. 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Influence of Small Fluorophilic and Lipophilic Organic Molecules on Dipalmitoylphosphatidylcholine Bilayers. <i>J Phys Chem B</i>. 2017;121 (35):8311-8321. doi:<a href=\"https://doi.org/10.1021/acs.jpcb.7b06520\">10.1021/acs.jpcb.7b06520</a>","short":"M. Brehm, G. Saddiq, T. Watermann, D. Sebastiani, J. Phys. Chem. B 121 (35) (2017) 8311–8321.","chicago":"Brehm, Martin, G. Saddiq, T. Watermann, and D. Sebastiani. “Influence of Small Fluorophilic and Lipophilic Organic Molecules on Dipalmitoylphosphatidylcholine Bilayers.” <i>J. Phys. Chem. B</i> 121 (35) (2017): 8311–21. <a href=\"https://doi.org/10.1021/acs.jpcb.7b06520\">https://doi.org/10.1021/acs.jpcb.7b06520</a>.","bibtex":"@article{Brehm_Saddiq_Watermann_Sebastiani_2017, title={Influence of Small Fluorophilic and Lipophilic Organic Molecules on Dipalmitoylphosphatidylcholine Bilayers}, volume={121 (35)}, DOI={<a href=\"https://doi.org/10.1021/acs.jpcb.7b06520\">10.1021/acs.jpcb.7b06520</a>}, journal={J. Phys. Chem. B}, author={Brehm, Martin and Saddiq, G. and Watermann, T. and Sebastiani, D.}, year={2017}, pages={8311–8321} }","apa":"Brehm, M., Saddiq, G., Watermann, T., &#38; Sebastiani, D. (2017). Influence of Small Fluorophilic and Lipophilic Organic Molecules on Dipalmitoylphosphatidylcholine Bilayers. <i>J. Phys. Chem. B</i>, <i>121 (35)</i>, 8311–8321. <a href=\"https://doi.org/10.1021/acs.jpcb.7b06520\">https://doi.org/10.1021/acs.jpcb.7b06520</a>","mla":"Brehm, Martin, et al. “Influence of Small Fluorophilic and Lipophilic Organic Molecules on Dipalmitoylphosphatidylcholine Bilayers.” <i>J. Phys. Chem. B</i>, vol. 121 (35), 2017, pp. 8311–21, doi:<a href=\"https://doi.org/10.1021/acs.jpcb.7b06520\">10.1021/acs.jpcb.7b06520</a>.","ieee":"M. Brehm, G. Saddiq, T. Watermann, and D. Sebastiani, “Influence of Small Fluorophilic and Lipophilic Organic Molecules on Dipalmitoylphosphatidylcholine Bilayers,” <i>J. Phys. Chem. B</i>, vol. 121 (35), pp. 8311–8321, 2017, doi: <a href=\"https://doi.org/10.1021/acs.jpcb.7b06520\">10.1021/acs.jpcb.7b06520</a>."},"publication":"J. Phys. Chem. B","volume":"121 (35)","doi":"10.1021/acs.jpcb.7b06520","user_id":"100167","_id":"44983","language":[{"iso":"eng"}],"page":"8311-8321","date_updated":"2023-05-16T20:41:54Z","author":[{"first_name":"Martin","last_name":"Brehm","full_name":"Brehm, Martin","id":"100167"},{"last_name":"Saddiq","first_name":"G.","full_name":"Saddiq, G."},{"full_name":"Watermann, T.","last_name":"Watermann","first_name":"T."},{"full_name":"Sebastiani, D.","first_name":"D.","last_name":"Sebastiani"}],"title":"Influence of Small Fluorophilic and Lipophilic Organic Molecules on Dipalmitoylphosphatidylcholine Bilayers","year":"2017","status":"public"},{"author":[{"first_name":"Martin","last_name":"Brehm","full_name":"Brehm, Martin","id":"100167"},{"last_name":"Thomas","first_name":"M.","full_name":"Thomas, M."}],"year":"2017","title":"Computing Bulk Phase Raman Optical Activity Spectra from ab initio Molecular Dynamics Simulations","status":"public","date_updated":"2023-05-16T20:42:17Z","_id":"44982","language":[{"iso":"eng"}],"page":"3409-3414","volume":"8 (14)","user_id":"100167","doi":"10.1021/acs.jpclett.7b01616","citation":{"mla":"Brehm, Martin, and M. Thomas. “Computing Bulk Phase Raman Optical Activity Spectra from Ab Initio Molecular Dynamics Simulations.” <i>J. Phys. Chem. Lett.</i>, vol. 8 (14), 2017, pp. 3409–14, doi:<a href=\"https://doi.org/10.1021/acs.jpclett.7b01616\">10.1021/acs.jpclett.7b01616</a>.","ama":"Brehm M, Thomas M. Computing Bulk Phase Raman Optical Activity Spectra from ab initio Molecular Dynamics Simulations. <i>J Phys Chem Lett</i>. 2017;8 (14):3409-3414. doi:<a href=\"https://doi.org/10.1021/acs.jpclett.7b01616\">10.1021/acs.jpclett.7b01616</a>","bibtex":"@article{Brehm_Thomas_2017, title={Computing Bulk Phase Raman Optical Activity Spectra from ab initio Molecular Dynamics Simulations}, volume={8 (14)}, DOI={<a href=\"https://doi.org/10.1021/acs.jpclett.7b01616\">10.1021/acs.jpclett.7b01616</a>}, journal={J. Phys. Chem. Lett.}, author={Brehm, Martin and Thomas, M.}, year={2017}, pages={3409–3414} }","apa":"Brehm, M., &#38; Thomas, M. (2017). Computing Bulk Phase Raman Optical Activity Spectra from ab initio Molecular Dynamics Simulations. <i>J. Phys. Chem. Lett.</i>, <i>8 (14)</i>, 3409–3414. <a href=\"https://doi.org/10.1021/acs.jpclett.7b01616\">https://doi.org/10.1021/acs.jpclett.7b01616</a>","ieee":"M. Brehm and M. Thomas, “Computing Bulk Phase Raman Optical Activity Spectra from ab initio Molecular Dynamics Simulations,” <i>J. Phys. Chem. Lett.</i>, vol. 8 (14), pp. 3409–3414, 2017, doi: <a href=\"https://doi.org/10.1021/acs.jpclett.7b01616\">10.1021/acs.jpclett.7b01616</a>.","chicago":"Brehm, Martin, and M. Thomas. “Computing Bulk Phase Raman Optical Activity Spectra from Ab Initio Molecular Dynamics Simulations.” <i>J. Phys. Chem. Lett.</i> 8 (14) (2017): 3409–14. <a href=\"https://doi.org/10.1021/acs.jpclett.7b01616\">https://doi.org/10.1021/acs.jpclett.7b01616</a>.","short":"M. Brehm, M. Thomas, J. Phys. Chem. Lett. 8 (14) (2017) 3409–3414."},"publication":"J. Phys. Chem. Lett.","extern":"1","date_created":"2023-05-16T20:22:01Z","department":[{"_id":"803"}],"type":"journal_article"},{"extern":"1","citation":{"short":"C. Slawik, C. Rickmeyer, M. Brehm, A. Böhme, G. Schüürmann, Environ. Sci. Technol. 51 (7) (2017) 4018–4026.","chicago":"Slawik, C., C. Rickmeyer, Martin Brehm, A. Böhme, and G. Schüürmann. “Glutathione Adduct Patterns of Michael-Acceptor Carbonyls.” <i>Environ. Sci. Technol.</i> 51 (7) (2017): 4018–26. <a href=\"https://doi.org/10.1021/acs.est.6b04981\">https://doi.org/10.1021/acs.est.6b04981</a>.","apa":"Slawik, C., Rickmeyer, C., Brehm, M., Böhme, A., &#38; Schüürmann, G. (2017). Glutathione Adduct Patterns of Michael-Acceptor Carbonyls. <i>Environ. Sci. Technol.</i>, <i>51 (7)</i>, 4018–4026. <a href=\"https://doi.org/10.1021/acs.est.6b04981\">https://doi.org/10.1021/acs.est.6b04981</a>","ieee":"C. Slawik, C. Rickmeyer, M. Brehm, A. Böhme, and G. Schüürmann, “Glutathione Adduct Patterns of Michael-Acceptor Carbonyls,” <i>Environ. Sci. Technol.</i>, vol. 51 (7), pp. 4018–4026, 2017, doi: <a href=\"https://doi.org/10.1021/acs.est.6b04981\">10.1021/acs.est.6b04981</a>.","ama":"Slawik C, Rickmeyer C, Brehm M, Böhme A, Schüürmann G. Glutathione Adduct Patterns of Michael-Acceptor Carbonyls. <i>Environ Sci Technol</i>. 2017;51 (7):4018-4026. doi:<a href=\"https://doi.org/10.1021/acs.est.6b04981\">10.1021/acs.est.6b04981</a>","bibtex":"@article{Slawik_Rickmeyer_Brehm_Böhme_Schüürmann_2017, title={Glutathione Adduct Patterns of Michael-Acceptor Carbonyls}, volume={51 (7)}, DOI={<a href=\"https://doi.org/10.1021/acs.est.6b04981\">10.1021/acs.est.6b04981</a>}, journal={Environ. Sci. Technol.}, author={Slawik, C. and Rickmeyer, C. and Brehm, Martin and Böhme, A. and Schüürmann, G.}, year={2017}, pages={4018–4026} }","mla":"Slawik, C., et al. “Glutathione Adduct Patterns of Michael-Acceptor Carbonyls.” <i>Environ. Sci. Technol.</i>, vol. 51 (7), 2017, pp. 4018–26, doi:<a href=\"https://doi.org/10.1021/acs.est.6b04981\">10.1021/acs.est.6b04981</a>."},"publication":"Environ. Sci. Technol.","department":[{"_id":"803"}],"type":"journal_article","date_created":"2023-05-16T20:22:01Z","date_updated":"2023-05-16T20:42:06Z","author":[{"full_name":"Slawik, C.","first_name":"C.","last_name":"Slawik"},{"full_name":"Rickmeyer, C.","last_name":"Rickmeyer","first_name":"C."},{"full_name":"Brehm, Martin","first_name":"Martin","last_name":"Brehm","id":"100167"},{"full_name":"Böhme, A.","first_name":"A.","last_name":"Böhme"},{"first_name":"G.","last_name":"Schüürmann","full_name":"Schüürmann, G."}],"status":"public","title":"Glutathione Adduct Patterns of Michael-Acceptor Carbonyls","year":"2017","volume":"51 (7)","user_id":"100167","doi":"10.1021/acs.est.6b04981","_id":"44981","language":[{"iso":"eng"}],"page":"4018-4026"},{"type":"journal_article","department":[{"_id":"803"}],"date_created":"2023-05-16T20:22:02Z","extern":"1","publication":"Adv. Exp. Med. Biol.","citation":{"ieee":"M. Brehm <i>et al.</i>, “An Integrated Data-Driven Strategy for Safe-by-Design Nanoparticles: The FP7 MODERN Project.,” <i>Adv. Exp. Med. Biol.</i>, vol. 947, pp. 257–301, 2017, doi: <a href=\"https://doi.org/10.1007/978-3-319-47754-1_9\">10.1007/978-3-319-47754-1_9</a>.","apa":"Brehm, M., Kafka, A., Bamler, M., Kühne, R., Schüürmann, G., Sikk, L., Burk, J., Burk, P., Tamm, T., Tämm, K., Pokhrel, S., Mädler, L., Kahru, A., Aruoja, V., Sihtmäe, M., Scott-Fordsmand, J., Sorensen, P. B., Escorihuela, L., Roca, C. P., … Rallo, R. (2017). An Integrated Data-Driven Strategy for Safe-by-Design Nanoparticles: The FP7 MODERN Project. <i>Adv. Exp. Med. Biol.</i>, <i>947</i>, 257–301. <a href=\"https://doi.org/10.1007/978-3-319-47754-1_9\">https://doi.org/10.1007/978-3-319-47754-1_9</a>","short":"M. Brehm, A. Kafka, M. Bamler, R. Kühne, G. Schüürmann, L. Sikk, J. Burk, P. Burk, T. Tamm, K. Tämm, S. Pokhrel, L. Mädler, A. Kahru, V. Aruoja, M. Sihtmäe, J. Scott-Fordsmand, P.B. Sorensen, L. Escorihuela, C.P. Roca, A. Fernández, F. Giralt, R. Rallo, Adv. Exp. Med. Biol. 947 (2017) 257–301.","chicago":"Brehm, Martin, A. Kafka, M. Bamler, R. Kühne, G. Schüürmann, L. Sikk, J. Burk, et al. “An Integrated Data-Driven Strategy for Safe-by-Design Nanoparticles: The FP7 MODERN Project.” <i>Adv. Exp. Med. Biol.</i> 947 (2017): 257–301. <a href=\"https://doi.org/10.1007/978-3-319-47754-1_9\">https://doi.org/10.1007/978-3-319-47754-1_9</a>.","mla":"Brehm, Martin, et al. “An Integrated Data-Driven Strategy for Safe-by-Design Nanoparticles: The FP7 MODERN Project.” <i>Adv. Exp. Med. Biol.</i>, vol. 947, 2017, pp. 257–301, doi:<a href=\"https://doi.org/10.1007/978-3-319-47754-1_9\">10.1007/978-3-319-47754-1_9</a>.","bibtex":"@article{Brehm_Kafka_Bamler_Kühne_Schüürmann_Sikk_Burk_Burk_Tamm_Tämm_et al._2017, title={An Integrated Data-Driven Strategy for Safe-by-Design Nanoparticles: The FP7 MODERN Project.}, volume={947}, DOI={<a href=\"https://doi.org/10.1007/978-3-319-47754-1_9\">10.1007/978-3-319-47754-1_9</a>}, journal={Adv. Exp. Med. Biol.}, author={Brehm, Martin and Kafka, A. and Bamler, M. and Kühne, R. and Schüürmann, G. and Sikk, L. and Burk, J. and Burk, P. and Tamm, T. and Tämm, K. and et al.}, year={2017}, pages={257–301} }","ama":"Brehm M, Kafka A, Bamler M, et al. An Integrated Data-Driven Strategy for Safe-by-Design Nanoparticles: The FP7 MODERN Project. <i>Adv Exp Med Biol</i>. 2017;947:257-301. doi:<a href=\"https://doi.org/10.1007/978-3-319-47754-1_9\">10.1007/978-3-319-47754-1_9</a>"},"doi":"10.1007/978-3-319-47754-1_9","user_id":"100167","volume":947,"page":"257-301","_id":"44985","language":[{"iso":"eng"}],"date_updated":"2023-05-16T20:42:55Z","intvolume":"       947","year":"2017","title":"An Integrated Data-Driven Strategy for Safe-by-Design Nanoparticles: The FP7 MODERN Project.","status":"public","author":[{"id":"100167","last_name":"Brehm","first_name":"Martin","full_name":"Brehm, Martin"},{"first_name":"A.","last_name":"Kafka","full_name":"Kafka, A."},{"first_name":"M.","last_name":"Bamler","full_name":"Bamler, M."},{"full_name":"Kühne, R.","last_name":"Kühne","first_name":"R."},{"full_name":"Schüürmann, G.","last_name":"Schüürmann","first_name":"G."},{"last_name":"Sikk","first_name":"L.","full_name":"Sikk, L."},{"first_name":"J.","last_name":"Burk","full_name":"Burk, J."},{"full_name":"Burk, P.","first_name":"P.","last_name":"Burk"},{"full_name":"Tamm, T.","last_name":"Tamm","first_name":"T."},{"first_name":"K.","last_name":"Tämm","full_name":"Tämm, K."},{"full_name":"Pokhrel, S.","first_name":"S.","last_name":"Pokhrel"},{"last_name":"Mädler","first_name":"L.","full_name":"Mädler, L."},{"full_name":"Kahru, A.","first_name":"A.","last_name":"Kahru"},{"first_name":"V.","last_name":"Aruoja","full_name":"Aruoja, V."},{"first_name":"M.","last_name":"Sihtmäe","full_name":"Sihtmäe, M."},{"first_name":"J.","last_name":"Scott-Fordsmand","full_name":"Scott-Fordsmand, J."},{"first_name":"P. B.","last_name":"Sorensen","full_name":"Sorensen, P. B."},{"full_name":"Escorihuela, L.","last_name":"Escorihuela","first_name":"L."},{"full_name":"Roca, C. P.","last_name":"Roca","first_name":"C. P."},{"full_name":"Fernández, A.","first_name":"A.","last_name":"Fernández"},{"full_name":"Giralt, F.","first_name":"F.","last_name":"Giralt"},{"full_name":"Rallo, R.","last_name":"Rallo","first_name":"R."}]},{"citation":{"ieee":"C. Peschel, M. Brehm, and D. Sebastiani, “Polyphilic Interactions as Structural Driving Force Investigated by Molecular Dynamics Simulation (Project 7),” <i>Polymers</i>, vol. 9, no. 9, Art. no. 445, 2017, doi: <a href=\"https://doi.org/10.3390/polym9090445\">10.3390/polym9090445</a>.","apa":"Peschel, C., Brehm, M., &#38; Sebastiani, D. (2017). Polyphilic Interactions as Structural Driving Force Investigated by Molecular Dynamics Simulation (Project 7). <i>Polymers</i>, <i>9</i>(9), Article 445. <a href=\"https://doi.org/10.3390/polym9090445\">https://doi.org/10.3390/polym9090445</a>","chicago":"Peschel, Christopher, Martin Brehm, and Daniel Sebastiani. “Polyphilic Interactions as Structural Driving Force Investigated by Molecular Dynamics Simulation (Project 7).” <i>Polymers</i> 9, no. 9 (2017). <a href=\"https://doi.org/10.3390/polym9090445\">https://doi.org/10.3390/polym9090445</a>.","short":"C. Peschel, M. Brehm, D. Sebastiani, Polymers 9 (2017).","mla":"Peschel, Christopher, et al. “Polyphilic Interactions as Structural Driving Force Investigated by Molecular Dynamics Simulation (Project 7).” <i>Polymers</i>, vol. 9, no. 9, 445, MDPI AG, 2017, doi:<a href=\"https://doi.org/10.3390/polym9090445\">10.3390/polym9090445</a>.","bibtex":"@article{Peschel_Brehm_Sebastiani_2017, title={Polyphilic Interactions as Structural Driving Force Investigated by Molecular Dynamics Simulation (Project 7)}, volume={9}, DOI={<a href=\"https://doi.org/10.3390/polym9090445\">10.3390/polym9090445</a>}, number={9445}, journal={Polymers}, publisher={MDPI AG}, author={Peschel, Christopher and Brehm, Martin and Sebastiani, Daniel}, year={2017} }","ama":"Peschel C, Brehm M, Sebastiani D. Polyphilic Interactions as Structural Driving Force Investigated by Molecular Dynamics Simulation (Project 7). <i>Polymers</i>. 2017;9(9). doi:<a href=\"https://doi.org/10.3390/polym9090445\">10.3390/polym9090445</a>"},"_id":"45183","publisher":"MDPI AG","user_id":"100167","volume":9,"status":"public","date_created":"2023-05-21T15:02:10Z","type":"journal_article","keyword":["Polymers and Plastics","General Chemistry"],"department":[{"_id":"803"}],"issue":"9","publication":"Polymers","extern":"1","abstract":[{"lang":"eng","text":"<jats:p>We investigated the effect of fluorinated molecules on dipalmitoylphosphatidylcholine (DPPC) bilayers by force-field molecular dynamics simulations. In the first step, we developed all-atom force-field parameters for additive molecules in membranes to enable an accurate description of those systems. On the basis of this force field, we performed extensive simulations of various bilayer systems containing different additives. The additive molecules were chosen to be of different size and shape, and they included small molecules such as perfluorinated alcohols, but also more complex molecules. From these simulations, we investigated the structural and dynamic effects of the additives on the membrane properties, as well as the behavior of the additive molecules themselves. Our results are in good agreement with other theoretical and experimental studies, and they contribute to a microscopic understanding of interactions, which might be used to specifically tune membrane properties by additives in the future.</jats:p>"}],"article_number":"445","language":[{"iso":"eng"}],"doi":"10.3390/polym9090445","year":"2017","title":"Polyphilic Interactions as Structural Driving Force Investigated by Molecular Dynamics Simulation (Project 7)","author":[{"full_name":"Peschel, Christopher","last_name":"Peschel","first_name":"Christopher"},{"first_name":"Martin","last_name":"Brehm","full_name":"Brehm, Martin","id":"100167"},{"first_name":"Daniel","last_name":"Sebastiani","full_name":"Sebastiani, Daniel"}],"publication_identifier":{"issn":["2073-4360"]},"publication_status":"published","date_updated":"2023-05-21T15:02:55Z","intvolume":"         9"},{"type":"journal_article","department":[{"_id":"43"},{"_id":"35"},{"_id":"306"}],"date_created":"2020-03-23T10:40:15Z","project":[{"_id":"52","name":"Computing Resources Provided by the Paderborn Center for Parallel Computing"}],"publication":"Inorganic Chemistry","citation":{"mla":"Zimmer, Peter, et al. “The Connection between NHC Ligand Count and Photophysical Properties in Fe(II) Photosensitizers: An Experimental Study.” <i>Inorganic Chemistry</i>, 2017, pp. 360–73, doi:<a href=\"https://doi.org/10.1021/acs.inorgchem.7b02624\">10.1021/acs.inorgchem.7b02624</a>.","bibtex":"@article{Zimmer_Burkhardt_Friedrich_Steube_Neuba_Schepper_Müller_Flörke_Huber_Lochbrunner_et al._2017, title={The Connection between NHC Ligand Count and Photophysical Properties in Fe(II) Photosensitizers: An Experimental Study}, DOI={<a href=\"https://doi.org/10.1021/acs.inorgchem.7b02624\">10.1021/acs.inorgchem.7b02624</a>}, journal={Inorganic Chemistry}, author={Zimmer, Peter and Burkhardt, Lukas and Friedrich, Aleksej and Steube, Jakob and Neuba, Adam and Schepper, Rahel and Müller, Patrick and Flörke, Ulrich and Huber, Marina and Lochbrunner, Stefan and et al.}, year={2017}, pages={360–373} }","ama":"Zimmer P, Burkhardt L, Friedrich A, et al. The Connection between NHC Ligand Count and Photophysical Properties in Fe(II) Photosensitizers: An Experimental Study. <i>Inorganic Chemistry</i>. Published online 2017:360-373. doi:<a href=\"https://doi.org/10.1021/acs.inorgchem.7b02624\">10.1021/acs.inorgchem.7b02624</a>","ieee":"P. Zimmer <i>et al.</i>, “The Connection between NHC Ligand Count and Photophysical Properties in Fe(II) Photosensitizers: An Experimental Study,” <i>Inorganic Chemistry</i>, pp. 360–373, 2017, doi: <a href=\"https://doi.org/10.1021/acs.inorgchem.7b02624\">10.1021/acs.inorgchem.7b02624</a>.","apa":"Zimmer, P., Burkhardt, L., Friedrich, A., Steube, J., Neuba, A., Schepper, R., Müller, P., Flörke, U., Huber, M., Lochbrunner, S., &#38; Bauer, M. (2017). The Connection between NHC Ligand Count and Photophysical Properties in Fe(II) Photosensitizers: An Experimental Study. <i>Inorganic Chemistry</i>, 360–373. <a href=\"https://doi.org/10.1021/acs.inorgchem.7b02624\">https://doi.org/10.1021/acs.inorgchem.7b02624</a>","short":"P. Zimmer, L. Burkhardt, A. Friedrich, J. Steube, A. Neuba, R. Schepper, P. Müller, U. Flörke, M. Huber, S. Lochbrunner, M. Bauer, Inorganic Chemistry (2017) 360–373.","chicago":"Zimmer, Peter, Lukas Burkhardt, Aleksej Friedrich, Jakob Steube, Adam Neuba, Rahel Schepper, Patrick Müller, et al. “The Connection between NHC Ligand Count and Photophysical Properties in Fe(II) Photosensitizers: An Experimental Study.” <i>Inorganic Chemistry</i>, 2017, 360–73. <a href=\"https://doi.org/10.1021/acs.inorgchem.7b02624\">https://doi.org/10.1021/acs.inorgchem.7b02624</a>."},"doi":"10.1021/acs.inorgchem.7b02624","user_id":"48467","page":"360-373","_id":"16317","language":[{"iso":"eng"}],"date_updated":"2023-08-09T12:52:44Z","publication_status":"published","title":"The Connection between NHC Ligand Count and Photophysical Properties in Fe(II) Photosensitizers: An Experimental Study","status":"public","year":"2017","author":[{"full_name":"Zimmer, Peter","last_name":"Zimmer","first_name":"Peter"},{"id":"54038","first_name":"Lukas","last_name":"Burkhardt","orcid":"0000-0003-0747-9811","full_name":"Burkhardt, Lukas"},{"last_name":"Friedrich","first_name":"Aleksej","full_name":"Friedrich, Aleksej"},{"orcid":"0000-0003-3178-4429","last_name":"Steube","first_name":"Jakob","full_name":"Steube, Jakob","id":"40342"},{"first_name":"Adam","last_name":"Neuba","full_name":"Neuba, Adam"},{"full_name":"Schepper, Rahel","last_name":"Schepper","first_name":"Rahel"},{"id":"54037","full_name":"Müller, Patrick","last_name":"Müller","orcid":"0000-0003-1103-4073","first_name":"Patrick"},{"full_name":"Flörke, Ulrich","last_name":"Flörke","first_name":"Ulrich"},{"full_name":"Huber, Marina","first_name":"Marina","last_name":"Huber"},{"full_name":"Lochbrunner, Stefan","last_name":"Lochbrunner","first_name":"Stefan"},{"full_name":"Bauer, Matthias","orcid":"0000-0002-9294-6076","first_name":"Matthias","last_name":"Bauer","id":"47241"}],"publication_identifier":{"issn":["0020-1669","1520-510X"]}},{"doi":"10.1002/ejic.201700064","user_id":"48467","page":"1504-1509","language":[{"iso":"eng"}],"_id":"16319","date_updated":"2023-08-09T12:53:31Z","publication_status":"published","status":"public","title":"N-Heterocyclic Carbene Complexes of Iron as Photosensitizers for Light-Induced Water Reduction","year":"2017","publication_identifier":{"issn":["1434-1948"]},"author":[{"full_name":"Zimmer, Peter","first_name":"Peter","last_name":"Zimmer"},{"id":"54037","full_name":"Müller, Patrick","first_name":"Patrick","orcid":"0000-0003-1103-4073","last_name":"Müller"},{"id":"54038","full_name":"Burkhardt, Lukas","orcid":"0000-0003-0747-9811","first_name":"Lukas","last_name":"Burkhardt"},{"first_name":"Rahel","last_name":"Schepper","full_name":"Schepper, Rahel"},{"full_name":"Neuba, Adam","first_name":"Adam","last_name":"Neuba"},{"id":"40342","last_name":"Steube","orcid":"0000-0003-3178-4429","first_name":"Jakob","full_name":"Steube, Jakob"},{"full_name":"Dietrich, Fabian","first_name":"Fabian","last_name":"Dietrich"},{"full_name":"Flörke, Ulrich","last_name":"Flörke","first_name":"Ulrich"},{"full_name":"Mangold, Stefan","last_name":"Mangold","first_name":"Stefan"},{"first_name":"Markus","last_name":"Gerhards","full_name":"Gerhards, Markus"},{"full_name":"Bauer, Matthias","first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","id":"47241"}],"type":"journal_article","department":[{"_id":"43"},{"_id":"306"},{"_id":"304"},{"_id":"35"}],"date_created":"2020-03-23T10:40:43Z","publication":"European Journal of Inorganic Chemistry","citation":{"apa":"Zimmer, P., Müller, P., Burkhardt, L., Schepper, R., Neuba, A., Steube, J., Dietrich, F., Flörke, U., Mangold, S., Gerhards, M., &#38; Bauer, M. (2017). N-Heterocyclic Carbene Complexes of Iron as Photosensitizers for Light-Induced Water Reduction. <i>European Journal of Inorganic Chemistry</i>, 1504–1509. <a href=\"https://doi.org/10.1002/ejic.201700064\">https://doi.org/10.1002/ejic.201700064</a>","mla":"Zimmer, Peter, et al. “N-Heterocyclic Carbene Complexes of Iron as Photosensitizers for Light-Induced Water Reduction.” <i>European Journal of Inorganic Chemistry</i>, 2017, pp. 1504–09, doi:<a href=\"https://doi.org/10.1002/ejic.201700064\">10.1002/ejic.201700064</a>.","ieee":"P. Zimmer <i>et al.</i>, “N-Heterocyclic Carbene Complexes of Iron as Photosensitizers for Light-Induced Water Reduction,” <i>European Journal of Inorganic Chemistry</i>, pp. 1504–1509, 2017, doi: <a href=\"https://doi.org/10.1002/ejic.201700064\">10.1002/ejic.201700064</a>.","ama":"Zimmer P, Müller P, Burkhardt L, et al. N-Heterocyclic Carbene Complexes of Iron as Photosensitizers for Light-Induced Water Reduction. <i>European Journal of Inorganic Chemistry</i>. Published online 2017:1504-1509. doi:<a href=\"https://doi.org/10.1002/ejic.201700064\">10.1002/ejic.201700064</a>","short":"P. Zimmer, P. Müller, L. Burkhardt, R. Schepper, A. Neuba, J. Steube, F. Dietrich, U. Flörke, S. Mangold, M. Gerhards, M. Bauer, European Journal of Inorganic Chemistry (2017) 1504–1509.","chicago":"Zimmer, Peter, Patrick Müller, Lukas Burkhardt, Rahel Schepper, Adam Neuba, Jakob Steube, Fabian Dietrich, et al. “N-Heterocyclic Carbene Complexes of Iron as Photosensitizers for Light-Induced Water Reduction.” <i>European Journal of Inorganic Chemistry</i>, 2017, 1504–9. <a href=\"https://doi.org/10.1002/ejic.201700064\">https://doi.org/10.1002/ejic.201700064</a>.","bibtex":"@article{Zimmer_Müller_Burkhardt_Schepper_Neuba_Steube_Dietrich_Flörke_Mangold_Gerhards_et al._2017, title={N-Heterocyclic Carbene Complexes of Iron as Photosensitizers for Light-Induced Water Reduction}, DOI={<a href=\"https://doi.org/10.1002/ejic.201700064\">10.1002/ejic.201700064</a>}, journal={European Journal of Inorganic Chemistry}, author={Zimmer, Peter and Müller, Patrick and Burkhardt, Lukas and Schepper, Rahel and Neuba, Adam and Steube, Jakob and Dietrich, Fabian and Flörke, Ulrich and Mangold, Stefan and Gerhards, Markus and et al.}, year={2017}, pages={1504–1509} }"}},{"citation":{"ama":"Longwitz L, Steinbauer J, Spannenberg A, Werner T. Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions. <i>ACS Catalysis</i>. 2017;8(1):665-672. doi:<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>","bibtex":"@article{Longwitz_Steinbauer_Spannenberg_Werner_2017, title={Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions}, volume={8}, DOI={<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>}, number={1}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Longwitz, Lars and Steinbauer, Johannes and Spannenberg, Anke and Werner, Thomas}, year={2017}, pages={665–672} }","mla":"Longwitz, Lars, et al. “Calcium-Based Catalytic System for the Synthesis of Bio-Derived Cyclic Carbonates under Mild Conditions.” <i>ACS Catalysis</i>, vol. 8, no. 1, American Chemical Society (ACS), 2017, pp. 665–72, doi:<a href=\"https://doi.org/10.1021/acscatal.7b03367\">10.1021/acscatal.7b03367</a>.","short":"L. 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Li, T. Werner, Organic Letters 19 (2017) 2568–2571.","apa":"Li, W., &#38; Werner, T. (2017). B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles. <i>Organic Letters</i>, <i>19</i>(10), 2568–2571. <a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">https://doi.org/10.1021/acs.orglett.7b00720</a>","ieee":"W. Li and T. Werner, “B(C6F5)3-Catalyzed Michael Reactions: Aromatic C–H as Nucleophiles,” <i>Organic Letters</i>, vol. 19, no. 10, pp. 2568–2571, 2017, doi: <a href=\"https://doi.org/10.1021/acs.orglett.7b00720\">10.1021/acs.orglett.7b00720</a>.","ama":"Li W, Werner T. 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Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides. <i>Green Chemistry</i>. 2017;19(18):4435-4445. doi:<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>","bibtex":"@article{Steinbauer_Longwitz_Frank_Epping_Kragl_Werner_2017, title={Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides}, volume={19}, DOI={<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>}, number={18}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Steinbauer, J. and Longwitz, L. and Frank, M. and Epping, J. and Kragl, U. and Werner, Thomas}, year={2017}, pages={4435–4445} }","mla":"Steinbauer, J., et al. “Immobilized Bifunctional Phosphonium Salts as Recyclable Organocatalysts in the Cycloaddition of CO<sub>2</sub> and Epoxides.” <i>Green Chemistry</i>, vol. 19, no. 18, Royal Society of Chemistry (RSC), 2017, pp. 4435–45, doi:<a href=\"https://doi.org/10.1039/c7gc01782k\">10.1039/c7gc01782k</a>.","chicago":"Steinbauer, J., L. Longwitz, M. Frank, J. Epping, U. Kragl, and Thomas Werner. “Immobilized Bifunctional Phosphonium Salts as Recyclable Organocatalysts in the Cycloaddition of CO<sub>2</sub> and Epoxides.” <i>Green Chemistry</i> 19, no. 18 (2017): 4435–45. <a href=\"https://doi.org/10.1039/c7gc01782k\">https://doi.org/10.1039/c7gc01782k</a>.","short":"J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, T. Werner, Green Chemistry 19 (2017) 4435–4445.","apa":"Steinbauer, J., Longwitz, L., Frank, M., Epping, J., Kragl, U., &#38; Werner, T. (2017). Immobilized bifunctional phosphonium salts as recyclable organocatalysts in the cycloaddition of CO<sub>2</sub> and epoxides. <i>Green Chemistry</i>, <i>19</i>(18), 4435–4445. <a href=\"https://doi.org/10.1039/c7gc01782k\">https://doi.org/10.1039/c7gc01782k</a>","ieee":"J. Steinbauer, L. Longwitz, M. Frank, J. Epping, U. Kragl, and T. 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Spannenberg, and Thomas Werner. “An in Situ Formed Ca<sup>2+</sup>–Crown Ether Complex and Its Use in CO<sub>2</sub>-Fixation Reactions with Terminal and Internal Epoxides.” <i>Green Chemistry</i> 19, no. 16 (2017): 3769–79. <a href=\"https://doi.org/10.1039/c7gc01114h\">https://doi.org/10.1039/c7gc01114h</a>.","short":"J. Steinbauer, A. Spannenberg, T. Werner, Green Chemistry 19 (2017) 3769–3779.","ama":"Steinbauer J, Spannenberg A, Werner T. An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides. <i>Green Chemistry</i>. 2017;19(16):3769-3779. doi:<a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>","bibtex":"@article{Steinbauer_Spannenberg_Werner_2017, title={An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides}, volume={19}, DOI={<a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>}, number={16}, journal={Green Chemistry}, publisher={Royal Society of Chemistry (RSC)}, author={Steinbauer, J. and Spannenberg, A. and Werner, Thomas}, year={2017}, pages={3769–3779} }","apa":"Steinbauer, J., Spannenberg, A., &#38; Werner, T. (2017). An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides. <i>Green Chemistry</i>, <i>19</i>(16), 3769–3779. <a href=\"https://doi.org/10.1039/c7gc01114h\">https://doi.org/10.1039/c7gc01114h</a>","mla":"Steinbauer, J., et al. “An in Situ Formed Ca<sup>2+</sup>–Crown Ether Complex and Its Use in CO<sub>2</sub>-Fixation Reactions with Terminal and Internal Epoxides.” <i>Green Chemistry</i>, vol. 19, no. 16, Royal Society of Chemistry (RSC), 2017, pp. 3769–79, doi:<a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>.","ieee":"J. Steinbauer, A. Spannenberg, and T. Werner, “An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides,” <i>Green Chemistry</i>, vol. 19, no. 16, pp. 3769–3779, 2017, doi: <a href=\"https://doi.org/10.1039/c7gc01114h\">10.1039/c7gc01114h</a>."},"intvolume":"        19","date_updated":"2025-11-10T09:18:18Z","publication_status":"published","publication_identifier":{"issn":["1463-9262","1463-9270"]},"author":[{"first_name":"J.","last_name":"Steinbauer","full_name":"Steinbauer, J."},{"full_name":"Spannenberg, A.","last_name":"Spannenberg","first_name":"A."},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"year":"2017","title":"An in situ formed Ca<sup>2+</sup>–crown ether complex and its use in CO<sub>2</sub>-fixation reactions with terminal and internal epoxides","doi":"10.1039/c7gc01114h","language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"<p>Calcium punched beyond its weight: An <italic>in situ</italic> formed Ca<sup>2+</sup>–crown ether complex showed unprecedented efficiency in cyclic carbonate synthesis.</p>"}],"extern":"1","publication":"Green Chemistry","issue":"16","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","T3","CSSD"],"date_created":"2023-01-22T20:59:12Z"},{"language":[{"iso":"eng"}],"article_number":"50","doi":"10.1007/s41061-017-0136-5","author":[{"full_name":"Büttner, Hendrik","last_name":"Büttner","first_name":"Hendrik"},{"full_name":"Longwitz, Lars","first_name":"Lars","last_name":"Longwitz"},{"full_name":"Steinbauer, Johannes","first_name":"Johannes","last_name":"Steinbauer"},{"full_name":"Wulf, Christoph","last_name":"Wulf","first_name":"Christoph"},{"full_name":"Werner, Thomas","last_name":"Werner","first_name":"Thomas","orcid":"0000-0001-9025-3244","id":"89271"}],"publication_identifier":{"issn":["2365-0869","2364-8961"]},"year":"2017","title":"Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2","intvolume":"       375","publication_status":"published","date_updated":"2025-11-10T09:17:38Z","date_created":"2023-01-22T20:59:56Z","department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"type":"journal_article","keyword":["T1","CSSD"],"issue":"3","publication":"Topics in Current Chemistry","extern":"1","publisher":"Springer Science and Business Media LLC","_id":"37977","volume":375,"user_id":"89271","status":"public","citation":{"bibtex":"@article{Büttner_Longwitz_Steinbauer_Wulf_Werner_2017, title={Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2}, volume={375}, DOI={<a href=\"https://doi.org/10.1007/s41061-017-0136-5\">10.1007/s41061-017-0136-5</a>}, number={350}, journal={Topics in Current Chemistry}, publisher={Springer Science and Business Media LLC}, author={Büttner, Hendrik and Longwitz, Lars and Steinbauer, Johannes and Wulf, Christoph and Werner, Thomas}, year={2017} }","ama":"Büttner H, Longwitz L, Steinbauer J, Wulf C, Werner T. Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2. <i>Topics in Current Chemistry</i>. 2017;375(3). doi:<a href=\"https://doi.org/10.1007/s41061-017-0136-5\">10.1007/s41061-017-0136-5</a>","mla":"Büttner, Hendrik, et al. “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2.” <i>Topics in Current Chemistry</i>, vol. 375, no. 3, 50, Springer Science and Business Media LLC, 2017, doi:<a href=\"https://doi.org/10.1007/s41061-017-0136-5\">10.1007/s41061-017-0136-5</a>.","chicago":"Büttner, Hendrik, Lars Longwitz, Johannes Steinbauer, Christoph Wulf, and Thomas Werner. “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2.” <i>Topics in Current Chemistry</i> 375, no. 3 (2017). <a href=\"https://doi.org/10.1007/s41061-017-0136-5\">https://doi.org/10.1007/s41061-017-0136-5</a>.","short":"H. Büttner, L. Longwitz, J. Steinbauer, C. Wulf, T. Werner, Topics in Current Chemistry 375 (2017).","ieee":"H. Büttner, L. Longwitz, J. Steinbauer, C. Wulf, and T. Werner, “Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2,” <i>Topics in Current Chemistry</i>, vol. 375, no. 3, Art. no. 50, 2017, doi: <a href=\"https://doi.org/10.1007/s41061-017-0136-5\">10.1007/s41061-017-0136-5</a>.","apa":"Büttner, H., Longwitz, L., Steinbauer, J., Wulf, C., &#38; Werner, T. (2017). Recent Developments in the Synthesis of Cyclic Carbonates from Epoxides and CO2. <i>Topics in Current Chemistry</i>, <i>375</i>(3), Article 50. <a href=\"https://doi.org/10.1007/s41061-017-0136-5\">https://doi.org/10.1007/s41061-017-0136-5</a>"}},{"language":[{"iso":"eng"}],"doi":"10.1021/acs.orglett.7b02701","year":"2017","title":"B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds","publication_identifier":{"issn":["1523-7060","1523-7052"]},"author":[{"full_name":"Li, Wu","first_name":"Wu","last_name":"Li"},{"last_name":"Wang","first_name":"Ming-Ming","full_name":"Wang, Ming-Ming"},{"full_name":"Hu, Yuya","last_name":"Hu","first_name":"Yuya"},{"first_name":"Thomas","last_name":"Werner","orcid":"0000-0001-9025-3244","full_name":"Werner, Thomas","id":"89271"}],"publication_status":"published","date_updated":"2025-11-10T09:18:33Z","intvolume":"        19","date_created":"2023-01-22T20:57:15Z","type":"journal_article","keyword":["CSSD"],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"issue":"21","publication":"Organic Letters","extern":"1","page":"5768-5771","publisher":"American Chemical Society (ACS)","_id":"37972","user_id":"89271","volume":19,"status":"public","citation":{"mla":"Li, Wu, et al. “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” <i>Organic Letters</i>, vol. 19, no. 21, American Chemical Society (ACS), 2017, pp. 5768–71, doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>.","bibtex":"@article{Li_Wang_Hu_Werner_2017, title={B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds}, volume={19}, DOI={<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>}, number={21}, journal={Organic Letters}, publisher={American Chemical Society (ACS)}, author={Li, Wu and Wang, Ming-Ming and Hu, Yuya and Werner, Thomas}, year={2017}, pages={5768–5771} }","ama":"Li W, Wang M-M, Hu Y, Werner T. B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. <i>Organic Letters</i>. 2017;19(21):5768-5771. doi:<a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>","ieee":"W. Li, M.-M. Wang, Y. Hu, and T. Werner, “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds,” <i>Organic Letters</i>, vol. 19, no. 21, pp. 5768–5771, 2017, doi: <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">10.1021/acs.orglett.7b02701</a>.","apa":"Li, W., Wang, M.-M., Hu, Y., &#38; Werner, T. (2017). B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds. <i>Organic Letters</i>, <i>19</i>(21), 5768–5771. <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">https://doi.org/10.1021/acs.orglett.7b02701</a>","chicago":"Li, Wu, Ming-Ming Wang, Yuya Hu, and Thomas Werner. “B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub>-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds.” <i>Organic Letters</i> 19, no. 21 (2017): 5768–71. <a href=\"https://doi.org/10.1021/acs.orglett.7b02701\">https://doi.org/10.1021/acs.orglett.7b02701</a>.","short":"W. Li, M.-M. Wang, Y. Hu, T. Werner, Organic Letters 19 (2017) 5768–5771."}}]