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Carl, S. Prévost, R. Schweins, J.E. Houston, I. Morfin, K. Huber, Macromolecules 52 (2019) 8759–8770.","apa":"Carl, N., Prévost, S., Schweins, R., Houston, J. E., Morfin, I., &#38; Huber, K. (2019). Invertible Micelles Based on Ion-Specific Interactions of Sr<sup>2+</sup> and Ba<sup>2+</sup> with Double Anionic Block Copolyelectrolytes. <i>Macromolecules</i>, <i>52</i>(22), 8759–8770. <a href=\"https://doi.org/10.1021/acs.macromol.9b01924\">https://doi.org/10.1021/acs.macromol.9b01924</a>","ama":"Carl N, Prévost S, Schweins R, Houston JE, Morfin I, Huber K. Invertible Micelles Based on Ion-Specific Interactions of Sr<sup>2+</sup> and Ba<sup>2+</sup> with Double Anionic Block Copolyelectrolytes. <i>Macromolecules</i>. 2019;52(22):8759-8770. doi:<a href=\"https://doi.org/10.1021/acs.macromol.9b01924\">10.1021/acs.macromol.9b01924</a>","chicago":"Carl, Nico, Sylvain Prévost, Ralf Schweins, Judith E. Houston, Isabelle Morfin, and Klaus Huber. “Invertible Micelles Based on Ion-Specific Interactions of Sr<sup>2+</sup> and Ba<sup>2+</sup> with Double Anionic Block Copolyelectrolytes.” <i>Macromolecules</i> 52, no. 22 (2019): 8759–70. <a href=\"https://doi.org/10.1021/acs.macromol.9b01924\">https://doi.org/10.1021/acs.macromol.9b01924</a>.","ieee":"N. Carl, S. Prévost, R. Schweins, J. E. Houston, I. Morfin, and K. Huber, “Invertible Micelles Based on Ion-Specific Interactions of Sr<sup>2+</sup> and Ba<sup>2+</sup> with Double Anionic Block Copolyelectrolytes,” <i>Macromolecules</i>, vol. 52, no. 22, pp. 8759–8770, 2019, doi: <a href=\"https://doi.org/10.1021/acs.macromol.9b01924\">10.1021/acs.macromol.9b01924</a>."},"publication_status":"published","year":"2019","publication_identifier":{"issn":["0024-9297","1520-5835"]},"language":[{"iso":"eng"}],"status":"public","date_created":"2023-02-06T12:21:49Z","publisher":"American Chemical Society (ACS)","date_updated":"2023-02-06T12:22:24Z","_id":"41825"},{"publication":"Macromolecular Rapid Communications","type":"journal_article","volume":40,"issue":"7","article_number":"1800674","title":"Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films","doi":"10.1002/marc.201800674","user_id":"94","keyword":["Materials Chemistry","Polymers and Plastics","Organic Chemistry"],"publisher":"Wiley","date_created":"2022-07-28T09:41:44Z","status":"public","publication_identifier":{"issn":["1022-1336","1521-3927"]},"year":"2018","language":[{"iso":"eng"}],"_id":"32444","date_updated":"2022-07-28T09:44:55Z","author":[{"first_name":"Jie","full_name":"Li, Jie","last_name":"Li"},{"first_name":"Xiaoqian","full_name":"Yu, Xiaoqian","last_name":"Yu"},{"first_name":"Artjom","full_name":"Herberg, Artjom","last_name":"Herberg","id":"94"},{"full_name":"Kuckling, Dirk","first_name":"Dirk","id":"287","last_name":"Kuckling"}],"article_type":"original","intvolume":"        40","publication_status":"published","citation":{"ieee":"J. Li, X. Yu, A. Herberg, and D. Kuckling, “Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films,” <i>Macromolecular Rapid Communications</i>, vol. 40, no. 7, Art. no. 1800674, 2018, doi: <a href=\"https://doi.org/10.1002/marc.201800674\">10.1002/marc.201800674</a>.","chicago":"Li, Jie, Xiaoqian Yu, Artjom Herberg, and Dirk Kuckling. “Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films.” <i>Macromolecular Rapid Communications</i> 40, no. 7 (2018). <a href=\"https://doi.org/10.1002/marc.201800674\">https://doi.org/10.1002/marc.201800674</a>.","ama":"Li J, Yu X, Herberg A, Kuckling D. Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films. <i>Macromolecular Rapid Communications</i>. 2018;40(7). doi:<a href=\"https://doi.org/10.1002/marc.201800674\">10.1002/marc.201800674</a>","apa":"Li, J., Yu, X., Herberg, A., &#38; Kuckling, D. (2018). Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films. <i>Macromolecular Rapid Communications</i>, <i>40</i>(7), Article 1800674. <a href=\"https://doi.org/10.1002/marc.201800674\">https://doi.org/10.1002/marc.201800674</a>","short":"J. Li, X. Yu, A. Herberg, D. Kuckling, Macromolecular Rapid Communications 40 (2018).","bibtex":"@article{Li_Yu_Herberg_Kuckling_2018, title={Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films}, volume={40}, DOI={<a href=\"https://doi.org/10.1002/marc.201800674\">10.1002/marc.201800674</a>}, number={71800674}, journal={Macromolecular Rapid Communications}, publisher={Wiley}, author={Li, Jie and Yu, Xiaoqian and Herberg, Artjom and Kuckling, Dirk}, year={2018} }","mla":"Li, Jie, et al. “Biomolecule Sensor Based on Azlactone‐Modified Hydrogel Films.” <i>Macromolecular Rapid Communications</i>, vol. 40, no. 7, 1800674, Wiley, 2018, doi:<a href=\"https://doi.org/10.1002/marc.201800674\">10.1002/marc.201800674</a>."},"department":[{"_id":"163"}]},{"date_updated":"2023-01-07T10:33:24Z","_id":"35330","status":"public","publication_identifier":{"issn":["2310-2861"]},"year":"2018","language":[{"iso":"eng"}],"publisher":"MDPI AG","date_created":"2023-01-06T12:51:42Z","department":[{"_id":"2"},{"_id":"315"}],"publication_status":"published","citation":{"ama":"Steck K, Schmidt C, Stubenrauch C. The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water—Surfactant—12-HOA System: Gelator and Co-Surfactant. <i>Gels</i>. 2018;4(3). doi:<a href=\"https://doi.org/10.3390/gels4030078\">10.3390/gels4030078</a>","apa":"Steck, K., Schmidt, C., &#38; Stubenrauch, C. (2018). The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water—Surfactant—12-HOA System: Gelator and Co-Surfactant. <i>Gels</i>, <i>4</i>(3), Article 78. <a href=\"https://doi.org/10.3390/gels4030078\">https://doi.org/10.3390/gels4030078</a>","chicago":"Steck, Katja, Claudia Schmidt, and Cosima Stubenrauch. “The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water—Surfactant—12-HOA System: Gelator and Co-Surfactant.” <i>Gels</i> 4, no. 3 (2018). <a href=\"https://doi.org/10.3390/gels4030078\">https://doi.org/10.3390/gels4030078</a>.","ieee":"K. Steck, C. Schmidt, and C. Stubenrauch, “The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water—Surfactant—12-HOA System: Gelator and Co-Surfactant,” <i>Gels</i>, vol. 4, no. 3, Art. no. 78, 2018, doi: <a href=\"https://doi.org/10.3390/gels4030078\">10.3390/gels4030078</a>.","mla":"Steck, Katja, et al. “The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water—Surfactant—12-HOA System: Gelator and Co-Surfactant.” <i>Gels</i>, vol. 4, no. 3, 78, MDPI AG, 2018, doi:<a href=\"https://doi.org/10.3390/gels4030078\">10.3390/gels4030078</a>.","bibtex":"@article{Steck_Schmidt_Stubenrauch_2018, title={The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water—Surfactant—12-HOA System: Gelator and Co-Surfactant}, volume={4}, DOI={<a href=\"https://doi.org/10.3390/gels4030078\">10.3390/gels4030078</a>}, number={378}, journal={Gels}, publisher={MDPI AG}, author={Steck, Katja and Schmidt, Claudia and Stubenrauch, Cosima}, year={2018} }","short":"K. Steck, C. Schmidt, C. Stubenrauch, Gels 4 (2018)."},"intvolume":"         4","author":[{"last_name":"Steck","full_name":"Steck, Katja","first_name":"Katja"},{"last_name":"Schmidt","id":"466","first_name":"Claudia","full_name":"Schmidt, Claudia","orcid":"0000-0003-3179-9997"},{"last_name":"Stubenrauch","full_name":"Stubenrauch, Cosima","first_name":"Cosima"}],"article_type":"original","issue":"3","article_number":"78","volume":4,"type":"journal_article","publication":"Gels","quality_controlled":"1","user_id":"466","keyword":["Polymers and Plastics","Organic Chemistry","Biomaterials","Bioengineering"],"abstract":[{"text":"<jats:p>Gelled lyotropic liquid crystals can be formed by adding a gelator to a mixture of surfactant and solvent. If the gel network and the liquid-crystalline phase coexist without influencing each other, the self-assembly is called orthogonal. In this study, the influence of the organogelator 12-hydroxyoctadecanoic acid (12-HOA) on the lamellar and hexagonal liquid crystalline phases of the binary system H2O–C12E7 (heptaethylene glycol monododecyl ether) is investigated. More precisely, we added 12-HOA at mass fractions from 0.015 to 0.05 and studied the resulting phase diagram of the system H2O–C12E7 by visual observation of birefringence and by 2H NMR spectroscopy. In addition, the dynamic shear moduli of the samples were measured in order to examine their gel character. The results show that 12-HOA is partly acting as co-surfactant, manifested by the destabilization of the hexagonal phase and the stabilization of the lamellar phase. The higher the total surfactant concentration, the more 12-HOA is incorporated in the surfactant layer. Accordingly, its gelation capacity is substantially reduced in the surfactant solution compared to the system 12-HOA–n-decane, and large amounts of gelator are required for gels to form, especially in the lamellar phase.</jats:p>","lang":"eng"}],"doi":"10.3390/gels4030078","title":"The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water—Surfactant—12-HOA System: Gelator and Co-Surfactant"},{"department":[{"_id":"35"},{"_id":"306"}],"citation":{"apa":"Garai, A., Sobottka, S., Schepper, R., Sinha, W., Bauer, M., Sarkar, B., &#38; Kar, S. (2018). Chromium Complexes with Oxido and Corrolato Ligands: Metal-Based Redox Processes versus Ligand Non-Innocence. <i>Chemistry - A European Journal</i>, <i>24</i>(48), 12613–12622. <a href=\"https://doi.org/10.1002/chem.201801452\">https://doi.org/10.1002/chem.201801452</a>","ama":"Garai A, Sobottka S, Schepper R, et al. Chromium Complexes with Oxido and Corrolato Ligands: Metal-Based Redox Processes versus Ligand Non-Innocence. <i>Chemistry - A European Journal</i>. 2018;24(48):12613-12622. doi:<a href=\"https://doi.org/10.1002/chem.201801452\">10.1002/chem.201801452</a>","chicago":"Garai, Antara, Sebastian Sobottka, Rahel Schepper, Woormileela Sinha, Matthias Bauer, Biprajit Sarkar, and Sanjib Kar. “Chromium Complexes with Oxido and Corrolato Ligands: Metal-Based Redox Processes versus Ligand Non-Innocence.” <i>Chemistry - A European Journal</i> 24, no. 48 (2018): 12613–22. <a href=\"https://doi.org/10.1002/chem.201801452\">https://doi.org/10.1002/chem.201801452</a>.","ieee":"A. Garai <i>et al.</i>, “Chromium Complexes with Oxido and Corrolato Ligands: Metal-Based Redox Processes versus Ligand Non-Innocence,” <i>Chemistry - A European Journal</i>, vol. 24, no. 48, pp. 12613–12622, 2018, doi: <a href=\"https://doi.org/10.1002/chem.201801452\">10.1002/chem.201801452</a>.","mla":"Garai, Antara, et al. “Chromium Complexes with Oxido and Corrolato Ligands: Metal-Based Redox Processes versus Ligand Non-Innocence.” <i>Chemistry - A European Journal</i>, vol. 24, no. 48, Wiley, 2018, pp. 12613–22, doi:<a href=\"https://doi.org/10.1002/chem.201801452\">10.1002/chem.201801452</a>.","bibtex":"@article{Garai_Sobottka_Schepper_Sinha_Bauer_Sarkar_Kar_2018, title={Chromium Complexes with Oxido and Corrolato Ligands: Metal-Based Redox Processes versus Ligand Non-Innocence}, volume={24}, DOI={<a href=\"https://doi.org/10.1002/chem.201801452\">10.1002/chem.201801452</a>}, number={48}, journal={Chemistry - A European Journal}, publisher={Wiley}, author={Garai, Antara and Sobottka, Sebastian and Schepper, Rahel and Sinha, Woormileela and Bauer, Matthias and Sarkar, Biprajit and Kar, Sanjib}, year={2018}, pages={12613–12622} }","short":"A. Garai, S. Sobottka, R. Schepper, W. Sinha, M. Bauer, B. Sarkar, S. Kar, Chemistry - A European Journal 24 (2018) 12613–12622."},"publication_status":"published","intvolume":"        24","author":[{"last_name":"Garai","full_name":"Garai, Antara","first_name":"Antara"},{"last_name":"Sobottka","full_name":"Sobottka, Sebastian","first_name":"Sebastian"},{"last_name":"Schepper","first_name":"Rahel","full_name":"Schepper, Rahel"},{"full_name":"Sinha, Woormileela","first_name":"Woormileela","last_name":"Sinha"},{"orcid":"0000-0002-9294-6076","first_name":"Matthias","full_name":"Bauer, Matthias","id":"47241","last_name":"Bauer"},{"full_name":"Sarkar, Biprajit","first_name":"Biprajit","last_name":"Sarkar"},{"last_name":"Kar","full_name":"Kar, Sanjib","first_name":"Sanjib"}],"date_updated":"2023-01-31T08:15:57Z","_id":"41042","publication_identifier":{"issn":["0947-6539"]},"year":"2018","language":[{"iso":"eng"}],"status":"public","date_created":"2023-01-30T18:44:13Z","publisher":"Wiley","user_id":"27611","keyword":["General Chemistry","Catalysis","Organic Chemistry"],"doi":"10.1002/chem.201801452","title":"Chromium Complexes with Oxido and Corrolato Ligands: Metal-Based Redox Processes versus Ligand Non-Innocence","issue":"48","page":"12613-12622","volume":24,"type":"journal_article","publication":"Chemistry - A European Journal"},{"doi":"10.1002/chem.201802694","title":"Diferrate [Fe<sub>2</sub>(CO)<sub>6</sub>(μ-CO){μ-P(aryl)<sub>2</sub>}]<sup>−</sup> as Self-Assembling Iron/Phosphor-Based Catalyst for the Hydrogen Evolution Reaction in Photocatalytic Proton Reduction-Spectroscopic Insights","keyword":["General Chemistry","Catalysis","Organic Chemistry"],"user_id":"48467","type":"journal_article","publication":"Chemistry - A European Journal","issue":"60","page":"16052-16065","volume":24,"intvolume":"        24","author":[{"last_name":"Fischer","first_name":"Steffen","full_name":"Fischer, Steffen"},{"full_name":"Rösel, Arend","first_name":"Arend","last_name":"Rösel"},{"last_name":"Kammer","first_name":"Anja","full_name":"Kammer, Anja"},{"first_name":"Enrico","full_name":"Barsch, Enrico","last_name":"Barsch"},{"full_name":"Schoch, Roland","first_name":"Roland","id":"48467","last_name":"Schoch","orcid":"0000-0003-2061-7289"},{"full_name":"Junge, Henrik","first_name":"Henrik","last_name":"Junge"},{"full_name":"Bauer, Matthias","first_name":"Matthias","last_name":"Bauer","id":"47241","orcid":"0000-0002-9294-6076"},{"full_name":"Beller, Matthias","first_name":"Matthias","last_name":"Beller"},{"last_name":"Ludwig","first_name":"Ralf","full_name":"Ludwig, Ralf"}],"department":[{"_id":"35"},{"_id":"306"}],"citation":{"ama":"Fischer S, Rösel A, Kammer A, et al. Diferrate [Fe<sub>2</sub>(CO)<sub>6</sub>(μ-CO){μ-P(aryl)<sub>2</sub>}]<sup>−</sup> as Self-Assembling Iron/Phosphor-Based Catalyst for the Hydrogen Evolution Reaction in Photocatalytic Proton Reduction-Spectroscopic Insights. <i>Chemistry - A European Journal</i>. 2018;24(60):16052-16065. doi:<a href=\"https://doi.org/10.1002/chem.201802694\">10.1002/chem.201802694</a>","apa":"Fischer, S., Rösel, A., Kammer, A., Barsch, E., Schoch, R., Junge, H., Bauer, M., Beller, M., &#38; Ludwig, R. (2018). Diferrate [Fe<sub>2</sub>(CO)<sub>6</sub>(μ-CO){μ-P(aryl)<sub>2</sub>}]<sup>−</sup> as Self-Assembling Iron/Phosphor-Based Catalyst for the Hydrogen Evolution Reaction in Photocatalytic Proton Reduction-Spectroscopic Insights. <i>Chemistry - A European Journal</i>, <i>24</i>(60), 16052–16065. <a href=\"https://doi.org/10.1002/chem.201802694\">https://doi.org/10.1002/chem.201802694</a>","chicago":"Fischer, Steffen, Arend Rösel, Anja Kammer, Enrico Barsch, Roland Schoch, Henrik Junge, Matthias Bauer, Matthias Beller, and Ralf Ludwig. “Diferrate [Fe<sub>2</sub>(CO)<sub>6</sub>(μ-CO){μ-P(Aryl)<sub>2</sub>}]<sup>−</sup> as Self-Assembling Iron/Phosphor-Based Catalyst for the Hydrogen Evolution Reaction in Photocatalytic Proton Reduction-Spectroscopic Insights.” <i>Chemistry - A European Journal</i> 24, no. 60 (2018): 16052–65. <a href=\"https://doi.org/10.1002/chem.201802694\">https://doi.org/10.1002/chem.201802694</a>.","ieee":"S. Fischer <i>et al.</i>, “Diferrate [Fe<sub>2</sub>(CO)<sub>6</sub>(μ-CO){μ-P(aryl)<sub>2</sub>}]<sup>−</sup> as Self-Assembling Iron/Phosphor-Based Catalyst for the Hydrogen Evolution Reaction in Photocatalytic Proton Reduction-Spectroscopic Insights,” <i>Chemistry - A European Journal</i>, vol. 24, no. 60, pp. 16052–16065, 2018, doi: <a href=\"https://doi.org/10.1002/chem.201802694\">10.1002/chem.201802694</a>.","mla":"Fischer, Steffen, et al. “Diferrate [Fe<sub>2</sub>(CO)<sub>6</sub>(μ-CO){μ-P(Aryl)<sub>2</sub>}]<sup>−</sup> as Self-Assembling Iron/Phosphor-Based Catalyst for the Hydrogen Evolution Reaction in Photocatalytic Proton Reduction-Spectroscopic Insights.” <i>Chemistry - A European Journal</i>, vol. 24, no. 60, Wiley, 2018, pp. 16052–65, doi:<a href=\"https://doi.org/10.1002/chem.201802694\">10.1002/chem.201802694</a>.","bibtex":"@article{Fischer_Rösel_Kammer_Barsch_Schoch_Junge_Bauer_Beller_Ludwig_2018, title={Diferrate [Fe<sub>2</sub>(CO)<sub>6</sub>(μ-CO){μ-P(aryl)<sub>2</sub>}]<sup>−</sup> as Self-Assembling Iron/Phosphor-Based Catalyst for the Hydrogen Evolution Reaction in Photocatalytic Proton Reduction-Spectroscopic Insights}, volume={24}, DOI={<a href=\"https://doi.org/10.1002/chem.201802694\">10.1002/chem.201802694</a>}, number={60}, journal={Chemistry - A European Journal}, publisher={Wiley}, author={Fischer, Steffen and Rösel, Arend and Kammer, Anja and Barsch, Enrico and Schoch, Roland and Junge, Henrik and Bauer, Matthias and Beller, Matthias and Ludwig, Ralf}, year={2018}, pages={16052–16065} }","short":"S. Fischer, A. Rösel, A. Kammer, E. Barsch, R. Schoch, H. Junge, M. Bauer, M. Beller, R. Ludwig, Chemistry - A European Journal 24 (2018) 16052–16065."},"publication_status":"published","language":[{"iso":"eng"}],"publication_identifier":{"issn":["0947-6539"]},"year":"2018","status":"public","date_created":"2023-01-30T18:39:34Z","publisher":"Wiley","date_updated":"2023-01-31T07:57:14Z","_id":"41037"},{"department":[{"_id":"35"},{"_id":"306"}],"publication_status":"published","citation":{"short":"M. Bauer, M. Tünnermann, P. Rehsies, U. Flörke, Synlett 29 (2018) 2638–2642.","bibtex":"@article{Bauer_Tünnermann_Rehsies_Flörke_2018, title={A Straightforward Synthesis to Novel 1,10-Phenanthrolines with Fused Thiophene Structure}, volume={29}, DOI={<a href=\"https://doi.org/10.1055/s-0037-1611022\">10.1055/s-0037-1611022</a>}, number={20}, journal={Synlett}, publisher={Georg Thieme Verlag KG}, author={Bauer, Matthias and Tünnermann, Maike and Rehsies, Pia and Flörke, Ulrich}, year={2018}, pages={2638–2642} }","mla":"Bauer, Matthias, et al. “A Straightforward Synthesis to Novel 1,10-Phenanthrolines with Fused Thiophene Structure.” <i>Synlett</i>, vol. 29, no. 20, Georg Thieme Verlag KG, 2018, pp. 2638–42, doi:<a href=\"https://doi.org/10.1055/s-0037-1611022\">10.1055/s-0037-1611022</a>.","ieee":"M. Bauer, M. Tünnermann, P. Rehsies, and U. Flörke, “A Straightforward Synthesis to Novel 1,10-Phenanthrolines with Fused Thiophene Structure,” <i>Synlett</i>, vol. 29, no. 20, pp. 2638–2642, 2018, doi: <a href=\"https://doi.org/10.1055/s-0037-1611022\">10.1055/s-0037-1611022</a>.","chicago":"Bauer, Matthias, Maike Tünnermann, Pia Rehsies, and Ulrich Flörke. “A Straightforward Synthesis to Novel 1,10-Phenanthrolines with Fused Thiophene Structure.” <i>Synlett</i> 29, no. 20 (2018): 2638–42. <a href=\"https://doi.org/10.1055/s-0037-1611022\">https://doi.org/10.1055/s-0037-1611022</a>.","apa":"Bauer, M., Tünnermann, M., Rehsies, P., &#38; Flörke, U. (2018). A Straightforward Synthesis to Novel 1,10-Phenanthrolines with Fused Thiophene Structure. <i>Synlett</i>, <i>29</i>(20), 2638–2642. <a href=\"https://doi.org/10.1055/s-0037-1611022\">https://doi.org/10.1055/s-0037-1611022</a>","ama":"Bauer M, Tünnermann M, Rehsies P, Flörke U. A Straightforward Synthesis to Novel 1,10-Phenanthrolines with Fused Thiophene Structure. <i>Synlett</i>. 2018;29(20):2638-2642. doi:<a href=\"https://doi.org/10.1055/s-0037-1611022\">10.1055/s-0037-1611022</a>"},"intvolume":"        29","author":[{"orcid":"0000-0002-9294-6076","first_name":"Matthias","full_name":"Bauer, Matthias","id":"47241","last_name":"Bauer"},{"first_name":"Maike","full_name":"Tünnermann, Maike","last_name":"Tünnermann"},{"full_name":"Rehsies, Pia","first_name":"Pia","last_name":"Rehsies"},{"last_name":"Flörke","first_name":"Ulrich","full_name":"Flörke, Ulrich"}],"date_updated":"2023-01-31T08:27:16Z","_id":"41036","status":"public","language":[{"iso":"eng"}],"year":"2018","publication_identifier":{"issn":["0936-5214","1437-2096"]},"publisher":"Georg Thieme Verlag KG","date_created":"2023-01-30T18:26:29Z","keyword":["Organic Chemistry"],"user_id":"27611","abstract":[{"lang":"eng","text":"<jats:p>We report here a straightforward synthesis for a series of new structures with fused 1,10-phenanthroline-thiophene connection. They are synthesized with a modified Hinsberg thiophene procedure, followed by successive modification to yield several 5,7-disubstituted thieno[3,4-f][1,10]phenanthrolines, most notable thiophene-substituted compounds that could be potentially of use for organic electronics ­applications. For some selected examples, crystal structures were ­obtained, showing a nearly coplanar arrangement around the fused connection, also beneficial for an effective electron transfer in organic electronics or solar cells.</jats:p>"}],"doi":"10.1055/s-0037-1611022","title":"A Straightforward Synthesis to Novel 1,10-Phenanthrolines with Fused Thiophene Structure","issue":"20","volume":29,"page":"2638-2642","type":"journal_article","publication":"Synlett"},{"intvolume":"      2018","author":[{"full_name":"Hu, Yuya","first_name":"Yuya","last_name":"Hu"},{"last_name":"Yin","first_name":"Zhiping","full_name":"Yin, Zhiping"},{"last_name":"Werner","id":"89271","full_name":"Werner, Thomas","first_name":"Thomas","orcid":"0000-0001-9025-3244"},{"last_name":"Spannenberg","first_name":"Anke","full_name":"Spannenberg, Anke"},{"last_name":"Wu","first_name":"Xiao-Feng","full_name":"Wu, Xiao-Feng"}],"department":[{"_id":"35"},{"_id":"2"},{"_id":"657"}],"publication_status":"published","citation":{"mla":"Hu, Yuya, et al. “1,8-Diazabicyclo[5.4.0]Undec-7-Ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur.” <i>European Journal of Organic Chemistry</i>, vol. 2018, no. 10, Wiley, 2018, pp. 1274–76, doi:<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>.","bibtex":"@article{Hu_Yin_Werner_Spannenberg_Wu_2018, title={1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur}, volume={2018}, DOI={<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>}, number={10}, journal={European Journal of Organic Chemistry}, publisher={Wiley}, author={Hu, Yuya and Yin, Zhiping and Werner, Thomas and Spannenberg, Anke and Wu, Xiao-Feng}, year={2018}, pages={1274–1276} }","short":"Y. Hu, Z. Yin, T. Werner, A. Spannenberg, X.-F. Wu, European Journal of Organic Chemistry 2018 (2018) 1274–1276.","ama":"Hu Y, Yin Z, Werner T, Spannenberg A, Wu X-F. 1,8-Diazabicyclo[5.4.0]undec-7-ene-Catalyzed Carbonylative Cyclization of Propargylic Alcohols with Elemental Sulfur. <i>European Journal of Organic Chemistry</i>. 2018;2018(10):1274-1276. doi:<a href=\"https://doi.org/10.1002/ejoc.201701813\">10.1002/ejoc.201701813</a>","apa":"Hu, Y., Yin, Z., Werner, T., Spannenberg, A., &#38; Wu, X.-F. 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