[{"publication":"Chemical Communications","abstract":[{"lang":"eng","text":"Combining strong σ-donating N-heterocyclic carbene ligands and π-accepting pyridine ligands with a high octahedricity in rigid iron(II) complexes increases the 3MLCT lifetime from 0.15 ps in the prototypical [Fe(tpy)2]2+ complex to 9.2 ps in [Fe(dpmi)2]2+12+. The tripodal CNN ligand dpmi (di(pyridine-2-yl)(3-methylimidazol-2-yl)methane) forms six-membered chelate rings with the iron(II) centre leading to close to 90° bite angles and enhanced iron-ligand orbital overlap"}],"language":[{"iso":"eng"}],"keyword":["Materials Chemistry","Metals and Alloys","Surfaces","Coatings and Films","General Chemistry","Ceramics and Composites","Electronic","Optical and Magnetic Materials","Catalysis"],"issue":"61","year":"2021","date_created":"2023-01-30T16:49:33Z","publisher":"Royal Society of Chemistry (RSC)","title":"Higher MLCT lifetime of carbene iron(ii) complexes by chelate ring expansion","type":"journal_article","status":"public","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"_id":"41003","article_type":"original","publication_status":"published","publication_identifier":{"issn":["1359-7345","1364-548X"]},"citation":{"apa":"Reuter, T., Kruse, A., Schoch, R., Lochbrunner, S., Bauer, M., & Heinze, K. (2021). Higher MLCT lifetime of carbene iron(<scp>ii</scp>) complexes by chelate ring expansion. Chemical Communications, 57(61), 7541–7544. https://doi.org/10.1039/d1cc02173g","bibtex":"@article{Reuter_Kruse_Schoch_Lochbrunner_Bauer_Heinze_2021, title={Higher MLCT lifetime of carbene iron(<scp>ii</scp>) complexes by chelate ring expansion}, volume={57}, DOI={10.1039/d1cc02173g}, number={61}, journal={Chemical Communications}, publisher={Royal Society of Chemistry (RSC)}, author={Reuter, Thomas and Kruse, Ayla and Schoch, Roland and Lochbrunner, Stefan and Bauer, Matthias and Heinze, Katja}, year={2021}, pages={7541–7544} }","mla":"Reuter, Thomas, et al. “Higher MLCT Lifetime of Carbene Iron(<scp>ii</Scp>) Complexes by Chelate Ring Expansion.” Chemical Communications, vol. 57, no. 61, Royal Society of Chemistry (RSC), 2021, pp. 7541–44, doi:10.1039/d1cc02173g.","short":"T. Reuter, A. Kruse, R. Schoch, S. Lochbrunner, M. Bauer, K. Heinze, Chemical Communications 57 (2021) 7541–7544.","ieee":"T. Reuter, A. Kruse, R. Schoch, S. Lochbrunner, M. Bauer, and K. Heinze, “Higher MLCT lifetime of carbene iron(<scp>ii</scp>) complexes by chelate ring expansion,” Chemical Communications, vol. 57, no. 61, pp. 7541–7544, 2021, doi: 10.1039/d1cc02173g.","chicago":"Reuter, Thomas, Ayla Kruse, Roland Schoch, Stefan Lochbrunner, Matthias Bauer, and Katja Heinze. “Higher MLCT Lifetime of Carbene Iron(<scp>ii</Scp>) Complexes by Chelate Ring Expansion.” Chemical Communications 57, no. 61 (2021): 7541–44. https://doi.org/10.1039/d1cc02173g.","ama":"Reuter T, Kruse A, Schoch R, Lochbrunner S, Bauer M, Heinze K. Higher MLCT lifetime of carbene iron(<scp>ii</scp>) complexes by chelate ring expansion. Chemical Communications. 2021;57(61):7541-7544. doi:10.1039/d1cc02173g"},"intvolume":" 57","page":"7541-7544","author":[{"last_name":"Reuter","full_name":"Reuter, Thomas","first_name":"Thomas"},{"first_name":"Ayla","full_name":"Kruse, Ayla","last_name":"Kruse"},{"last_name":"Schoch","orcid":"0000-0003-2061-7289","id":"48467","full_name":"Schoch, Roland","first_name":"Roland"},{"last_name":"Lochbrunner","full_name":"Lochbrunner, Stefan","first_name":"Stefan"},{"first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","id":"47241","full_name":"Bauer, Matthias"},{"first_name":"Katja","last_name":"Heinze","full_name":"Heinze, Katja"}],"volume":57,"date_updated":"2023-01-31T08:06:16Z","doi":"10.1039/d1cc02173g"},{"status":"public","type":"journal_article","article_type":"review","_id":"40997","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"citation":{"ama":"Dierks P, Vukadinovic Y, Bauer M. Photoactive iron complexes: more sustainable, but still a challenge. Inorganic Chemistry Frontiers. 2021;9(2):206-220. doi:10.1039/d1qi01112j","ieee":"P. Dierks, Y. Vukadinovic, and M. Bauer, “Photoactive iron complexes: more sustainable, but still a challenge,” Inorganic Chemistry Frontiers, vol. 9, no. 2, pp. 206–220, 2021, doi: 10.1039/d1qi01112j.","chicago":"Dierks, Philipp, Yannik Vukadinovic, and Matthias Bauer. “Photoactive Iron Complexes: More Sustainable, but Still a Challenge.” Inorganic Chemistry Frontiers 9, no. 2 (2021): 206–20. https://doi.org/10.1039/d1qi01112j.","mla":"Dierks, Philipp, et al. “Photoactive Iron Complexes: More Sustainable, but Still a Challenge.” Inorganic Chemistry Frontiers, vol. 9, no. 2, Royal Society of Chemistry (RSC), 2021, pp. 206–20, doi:10.1039/d1qi01112j.","bibtex":"@article{Dierks_Vukadinovic_Bauer_2021, title={Photoactive iron complexes: more sustainable, but still a challenge}, volume={9}, DOI={10.1039/d1qi01112j}, number={2}, journal={Inorganic Chemistry Frontiers}, publisher={Royal Society of Chemistry (RSC)}, author={Dierks, Philipp and Vukadinovic, Yannik and Bauer, Matthias}, year={2021}, pages={206–220} }","short":"P. Dierks, Y. Vukadinovic, M. Bauer, Inorganic Chemistry Frontiers 9 (2021) 206–220.","apa":"Dierks, P., Vukadinovic, Y., & Bauer, M. (2021). Photoactive iron complexes: more sustainable, but still a challenge. Inorganic Chemistry Frontiers, 9(2), 206–220. https://doi.org/10.1039/d1qi01112j"},"page":"206-220","intvolume":" 9","publication_status":"published","publication_identifier":{"issn":["2052-1553"]},"doi":"10.1039/d1qi01112j","date_updated":"2023-01-31T08:04:56Z","author":[{"full_name":"Dierks, Philipp","last_name":"Dierks","first_name":"Philipp"},{"full_name":"Vukadinovic, Yannik","last_name":"Vukadinovic","first_name":"Yannik"},{"first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","id":"47241","full_name":"Bauer, Matthias"}],"volume":9,"abstract":[{"text":"On transition metals such as iron rests lots of hope to replace precious metal catalysts in the field of photochemistry for a more sustainable future. Indeed, significant progress has been made in recent years in terms of lifetime extension and emerging applications in catalysis. For this reason, recent synthetic strategies of new photoactive iron compounds, which have proved to show particularly promising properties, are reviewed here. The lifetime of the excited state serves as a key parameter for comparison with the standard ruthenium complex, [Ru(bpy)3]2+, to discuss the potential and performance of the iron complexes. This approach is complemented by a more holistic examination of the sustainability of such a substitution strategy in order to answer the question: when or at which point can we assume that iron represents a more sustainable alternative for noble metals in photochemical applications?","lang":"eng"}],"publication":"Inorganic Chemistry Frontiers","keyword":["Inorganic Chemistry"],"language":[{"iso":"eng"}],"year":"2021","issue":"2","title":"Photoactive iron complexes: more sustainable, but still a challenge","publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-30T16:47:45Z"},{"doi":"10.1002/anie.202110821","title":"Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis","date_created":"2023-01-30T16:48:53Z","author":[{"full_name":"Ghosh, Pradip","last_name":"Ghosh","first_name":"Pradip"},{"orcid":"0000-0003-2061-7289","last_name":"Schoch","id":"48467","full_name":"Schoch, Roland","first_name":"Roland"},{"id":"47241","full_name":"Bauer, Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","first_name":"Matthias"},{"full_name":"Jacobi von Wangelin, Axel","last_name":"Jacobi von Wangelin","first_name":"Axel"}],"volume":61,"publisher":"Wiley","date_updated":"2023-01-31T08:05:26Z","citation":{"mla":"Ghosh, Pradip, et al. “Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis.” Angewandte Chemie International Edition, vol. 61, no. 1, Wiley, 2021, doi:10.1002/anie.202110821.","short":"P. Ghosh, R. Schoch, M. Bauer, A. Jacobi von Wangelin, Angewandte Chemie International Edition 61 (2021).","bibtex":"@article{Ghosh_Schoch_Bauer_Jacobi von Wangelin_2021, title={Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis}, volume={61}, DOI={10.1002/anie.202110821}, number={1}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Ghosh, Pradip and Schoch, Roland and Bauer, Matthias and Jacobi von Wangelin, Axel}, year={2021} }","apa":"Ghosh, P., Schoch, R., Bauer, M., & Jacobi von Wangelin, A. (2021). Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis. Angewandte Chemie International Edition, 61(1). https://doi.org/10.1002/anie.202110821","chicago":"Ghosh, Pradip, Roland Schoch, Matthias Bauer, and Axel Jacobi von Wangelin. “Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis.” Angewandte Chemie International Edition 61, no. 1 (2021). https://doi.org/10.1002/anie.202110821.","ieee":"P. Ghosh, R. Schoch, M. Bauer, and A. Jacobi von Wangelin, “Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis,” Angewandte Chemie International Edition, vol. 61, no. 1, 2021, doi: 10.1002/anie.202110821.","ama":"Ghosh P, Schoch R, Bauer M, Jacobi von Wangelin A. Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis. Angewandte Chemie International Edition. 2021;61(1). doi:10.1002/anie.202110821"},"intvolume":" 61","year":"2021","issue":"1","publication_status":"published","publication_identifier":{"issn":["1433-7851","1521-3773"]},"language":[{"iso":"eng"}],"article_type":"original","keyword":["General Chemistry","Catalysis"],"user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"_id":"41000","status":"public","abstract":[{"lang":"eng","text":"Metal-catalyzed C−H activations are environmentally and economically attractive synthetic strategies for the construction of functional molecules as they obviate the need for pre-functionalized substrates and minimize waste generation. Great challenges reside in the control of selectivities, the utilization of unbiased hydrocarbons, and the operation of atom-economical dehydrocoupling mechanisms. An especially mild borylation of benzylic CH bonds was developed with the ligand-free pre-catalyst Co[N(SiMe3)2]2 and the bench-stable and inexpensive borylation reagent B2pin2 that produces H2 as the only by-product. A full set of kinetic, spectroscopic, and preparative mechanistic studies are indicative of a tandem catalysis mechanism of CH-borylation and dehydrocoupling via molecular CoI catalysts."}],"type":"journal_article","publication":"Angewandte Chemie International Edition"},{"user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"_id":"41013","article_type":"original","type":"journal_article","status":"public","author":[{"last_name":"Wissel","full_name":"Wissel, Kerstin","first_name":"Kerstin"},{"id":"48467","full_name":"Schoch, Roland","orcid":"0000-0003-2061-7289","last_name":"Schoch","first_name":"Roland"},{"first_name":"Tobias","last_name":"Vogel","full_name":"Vogel, Tobias"},{"last_name":"Donzelli","full_name":"Donzelli, Manuel","first_name":"Manuel"},{"last_name":"Matveeva","full_name":"Matveeva, Galina","first_name":"Galina"},{"full_name":"Kolb, Ute","last_name":"Kolb","first_name":"Ute"},{"full_name":"Bauer, Matthias","id":"47241","last_name":"Bauer","orcid":"0000-0002-9294-6076","first_name":"Matthias"},{"last_name":"Slater","full_name":"Slater, Peter R.","first_name":"Peter R."},{"full_name":"Clemens, Oliver","last_name":"Clemens","first_name":"Oliver"}],"volume":33,"date_updated":"2023-01-31T08:07:28Z","doi":"10.1021/acs.chemmater.0c01762","publication_status":"published","publication_identifier":{"issn":["0897-4756","1520-5002"]},"citation":{"apa":"Wissel, K., Schoch, R., Vogel, T., Donzelli, M., Matveeva, G., Kolb, U., Bauer, M., Slater, P. R., & Clemens, O. (2021). Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La2NiO3F2 within Fluoride-Ion Batteries. Chemistry of Materials, 33(2), 499–512. https://doi.org/10.1021/acs.chemmater.0c01762","mla":"Wissel, Kerstin, et al. “Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La2NiO3F2 within Fluoride-Ion Batteries.” Chemistry of Materials, vol. 33, no. 2, American Chemical Society (ACS), 2021, pp. 499–512, doi:10.1021/acs.chemmater.0c01762.","bibtex":"@article{Wissel_Schoch_Vogel_Donzelli_Matveeva_Kolb_Bauer_Slater_Clemens_2021, title={Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La2NiO3F2 within Fluoride-Ion Batteries}, volume={33}, DOI={10.1021/acs.chemmater.0c01762}, number={2}, journal={Chemistry of Materials}, publisher={American Chemical Society (ACS)}, author={Wissel, Kerstin and Schoch, Roland and Vogel, Tobias and Donzelli, Manuel and Matveeva, Galina and Kolb, Ute and Bauer, Matthias and Slater, Peter R. and Clemens, Oliver}, year={2021}, pages={499–512} }","short":"K. Wissel, R. Schoch, T. Vogel, M. Donzelli, G. Matveeva, U. Kolb, M. Bauer, P.R. Slater, O. Clemens, Chemistry of Materials 33 (2021) 499–512.","ama":"Wissel K, Schoch R, Vogel T, et al. Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La2NiO3F2 within Fluoride-Ion Batteries. Chemistry of Materials. 2021;33(2):499-512. doi:10.1021/acs.chemmater.0c01762","ieee":"K. Wissel et al., “Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La2NiO3F2 within Fluoride-Ion Batteries,” Chemistry of Materials, vol. 33, no. 2, pp. 499–512, 2021, doi: 10.1021/acs.chemmater.0c01762.","chicago":"Wissel, Kerstin, Roland Schoch, Tobias Vogel, Manuel Donzelli, Galina Matveeva, Ute Kolb, Matthias Bauer, Peter R. Slater, and Oliver Clemens. “Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La2NiO3F2 within Fluoride-Ion Batteries.” Chemistry of Materials 33, no. 2 (2021): 499–512. https://doi.org/10.1021/acs.chemmater.0c01762."},"intvolume":" 33","page":"499-512","language":[{"iso":"eng"}],"keyword":["Materials Chemistry","General Chemical Engineering","General Chemistry"],"publication":"Chemistry of Materials","abstract":[{"text":"Within this article, it is shown that an electrochemical defluorination and additional fluorination of Ruddlesden–Popper-type La2NiO3F2 is possible within all-solid-state fluoride-ion batteries. Structural changes within the reduced and oxidized phases have been examined by X-ray diffraction studies at different states of charging and discharging. The synthesis of the oxidized phase La2NiO3F2+x proved to be successful by structural analysis using both X-ray powder diffraction and automated electron diffraction tomography techniques. The structural reversibility on re-fluorinating and re-defluorinating is also demonstrated. Moreover, the influence of different sequences of consecutive reduction and oxidation steps on the formed phases has been investigated. The observed structural changes have been compared to changes in phases obtained via other topochemical modification approaches such as hydride-based reduction and oxidative fluorination using F2 gas, highlighting the potential of such electrochemical reactions as alternative synthesis routes. Furthermore, the electrochemical routes represent safe and controllable synthesis approaches for novel phases, which cannot be synthesized via other topochemical methods. Additionally, side reactions, occurring alongside the desired electrochemical reactions, have been addressed and the cycling performance has been studied.","lang":"eng"}],"date_created":"2023-01-30T17:01:00Z","publisher":"American Chemical Society (ACS)","title":"Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La2NiO3F2 within Fluoride-Ion Batteries","issue":"2","year":"2021"},{"publication":"Angewandte Chemie International Edition","abstract":[{"text":"We present the η3-coordination of the 2-phosphaethynthiolate anion in the complex (PN)2La(SCP) (2) [PN=N-(2-(diisopropylphosphanyl)-4-methylphenyl)-2,4,6-trimethylanilide)]. Structural comparison with dinuclear thiocyanate-bridged (PN)2La(μ-1,3-SCN)2La(PN)2 (3) and azide-bridged (PN)2La(μ-1,3-N3)2La(PN)2 (4) complexes indicates that the [SCP]− coordination mode is mainly governed by electronic, rather than steric factors. Quantum mechanical investigations reveal large contributions of the antibonding π*-orbital of the [SCP]− ligand to the LUMO of complex 2, rendering it the ideal precursor for the first functionalization of the [SCP]− anion. Complex 2 was therefore reacted with CAACs which induced a selective rearrangement of the [SCP]− ligand to form the first CAAC stabilized group 15–group 16 fulminate-type complexes (PN)2La{SPC(RCAAC)} (5 a,b, R=Ad, Me). A detailed reaction mechanism for the SCP-to-SPC isomerization is proposed based on DFT calculations.","lang":"eng"}],"language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis"],"issue":"17","year":"2021","date_created":"2023-01-30T17:00:21Z","publisher":"Wiley","title":"η 3 ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**","type":"journal_article","status":"public","department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","_id":"41010","article_type":"original","publication_identifier":{"issn":["1433-7851","1521-3773"]},"publication_status":"published","intvolume":" 60","page":"9534-9539","citation":{"apa":"Watt, F. A., Burkhardt, L., Schoch, R., Mitzinger, S., Bauer, M., Weigend, F., Goicoechea, J. M., Tambornino, F., & Hohloch, S. (2021). η 3 ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**. Angewandte Chemie International Edition, 60(17), 9534–9539. https://doi.org/10.1002/anie.202100559","mla":"Watt, Fabian A., et al. “η 3 ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**.” Angewandte Chemie International Edition, vol. 60, no. 17, Wiley, 2021, pp. 9534–39, doi:10.1002/anie.202100559.","short":"F.A. Watt, L. Burkhardt, R. Schoch, S. Mitzinger, M. Bauer, F. Weigend, J.M. Goicoechea, F. Tambornino, S. Hohloch, Angewandte Chemie International Edition 60 (2021) 9534–9539.","bibtex":"@article{Watt_Burkhardt_Schoch_Mitzinger_Bauer_Weigend_Goicoechea_Tambornino_Hohloch_2021, title={η 3 ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**}, volume={60}, DOI={10.1002/anie.202100559}, number={17}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Watt, Fabian A. and Burkhardt, Lukas and Schoch, Roland and Mitzinger, Stefan and Bauer, Matthias and Weigend, Florian and Goicoechea, Jose M. and Tambornino, Frank and Hohloch, Stephan}, year={2021}, pages={9534–9539} }","ieee":"F. A. Watt et al., “η 3 ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**,” Angewandte Chemie International Edition, vol. 60, no. 17, pp. 9534–9539, 2021, doi: 10.1002/anie.202100559.","chicago":"Watt, Fabian A., Lukas Burkhardt, Roland Schoch, Stefan Mitzinger, Matthias Bauer, Florian Weigend, Jose M. Goicoechea, Frank Tambornino, and Stephan Hohloch. “η 3 ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**.” Angewandte Chemie International Edition 60, no. 17 (2021): 9534–39. https://doi.org/10.1002/anie.202100559.","ama":"Watt FA, Burkhardt L, Schoch R, et al. η 3 ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**. Angewandte Chemie International Edition. 2021;60(17):9534-9539. doi:10.1002/anie.202100559"},"volume":60,"author":[{"first_name":"Fabian A.","last_name":"Watt","full_name":"Watt, Fabian A."},{"first_name":"Lukas","full_name":"Burkhardt, Lukas","last_name":"Burkhardt"},{"first_name":"Roland","full_name":"Schoch, Roland","id":"48467","last_name":"Schoch","orcid":"0000-0003-2061-7289"},{"full_name":"Mitzinger, Stefan","last_name":"Mitzinger","first_name":"Stefan"},{"first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","id":"47241","full_name":"Bauer, Matthias"},{"first_name":"Florian","full_name":"Weigend, Florian","last_name":"Weigend"},{"last_name":"Goicoechea","full_name":"Goicoechea, Jose M.","first_name":"Jose M."},{"first_name":"Frank","last_name":"Tambornino","full_name":"Tambornino, Frank"},{"full_name":"Hohloch, Stephan","last_name":"Hohloch","first_name":"Stephan"}],"date_updated":"2023-01-31T08:06:50Z","doi":"10.1002/anie.202100559"},{"date_updated":"2023-01-31T08:07:16Z","volume":60,"author":[{"full_name":"Winkler, Mario","last_name":"Winkler","first_name":"Mario"},{"first_name":"Marc","last_name":"Schnierle","full_name":"Schnierle, Marc"},{"first_name":"Felix","full_name":"Ehrlich, Felix","last_name":"Ehrlich"},{"full_name":"Mehnert, Kim-Isabelle","last_name":"Mehnert","first_name":"Kim-Isabelle"},{"full_name":"Hunger, David","last_name":"Hunger","first_name":"David"},{"first_name":"Alena M.","full_name":"Sheveleva, Alena M.","last_name":"Sheveleva"},{"full_name":"Burkhardt, Lukas","last_name":"Burkhardt","first_name":"Lukas"},{"first_name":"Matthias","orcid":"0000-0002-9294-6076","last_name":"Bauer","full_name":"Bauer, Matthias","id":"47241"},{"first_name":"Floriana","last_name":"Tuna","full_name":"Tuna, Floriana"},{"last_name":"Ringenberg","full_name":"Ringenberg, Mark R.","first_name":"Mark R."},{"last_name":"van Slageren","full_name":"van Slageren, Joris","first_name":"Joris"}],"doi":"10.1021/acs.inorgchem.0c03259","publication_identifier":{"issn":["0020-1669","1520-510X"]},"publication_status":"published","page":"2856-2865","intvolume":" 60","citation":{"chicago":"Winkler, Mario, Marc Schnierle, Felix Ehrlich, Kim-Isabelle Mehnert, David Hunger, Alena M. Sheveleva, Lukas Burkhardt, et al. “Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(Dppf)Fe(CO) 3]+/0.” Inorganic Chemistry 60, no. 5 (2021): 2856–65. https://doi.org/10.1021/acs.inorgchem.0c03259.","ieee":"M. Winkler et al., “Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) 3]+/0,” Inorganic Chemistry, vol. 60, no. 5, pp. 2856–2865, 2021, doi: 10.1021/acs.inorgchem.0c03259.","ama":"Winkler M, Schnierle M, Ehrlich F, et al. Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) 3]+/0. Inorganic Chemistry. 2021;60(5):2856-2865. doi:10.1021/acs.inorgchem.0c03259","apa":"Winkler, M., Schnierle, M., Ehrlich, F., Mehnert, K.-I., Hunger, D., Sheveleva, A. M., Burkhardt, L., Bauer, M., Tuna, F., Ringenberg, M. R., & van Slageren, J. (2021). Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) 3]+/0. Inorganic Chemistry, 60(5), 2856–2865. https://doi.org/10.1021/acs.inorgchem.0c03259","short":"M. Winkler, M. Schnierle, F. Ehrlich, K.-I. Mehnert, D. Hunger, A.M. Sheveleva, L. Burkhardt, M. Bauer, F. Tuna, M.R. Ringenberg, J. van Slageren, Inorganic Chemistry 60 (2021) 2856–2865.","mla":"Winkler, Mario, et al. “Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(Dppf)Fe(CO) 3]+/0.” Inorganic Chemistry, vol. 60, no. 5, American Chemical Society (ACS), 2021, pp. 2856–65, doi:10.1021/acs.inorgchem.0c03259.","bibtex":"@article{Winkler_Schnierle_Ehrlich_Mehnert_Hunger_Sheveleva_Burkhardt_Bauer_Tuna_Ringenberg_et al._2021, title={Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) 3]+/0}, volume={60}, DOI={10.1021/acs.inorgchem.0c03259}, number={5}, journal={Inorganic Chemistry}, publisher={American Chemical Society (ACS)}, author={Winkler, Mario and Schnierle, Marc and Ehrlich, Felix and Mehnert, Kim-Isabelle and Hunger, David and Sheveleva, Alena M. and Burkhardt, Lukas and Bauer, Matthias and Tuna, Floriana and Ringenberg, Mark R. and et al.}, year={2021}, pages={2856–2865} }"},"_id":"41012","department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","article_type":"original","type":"journal_article","status":"public","publisher":"American Chemical Society (ACS)","date_created":"2023-01-30T17:00:49Z","title":"Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) 3]+/0","issue":"5","year":"2021","keyword":["Inorganic Chemistry","Physical and Theoretical Chemistry"],"language":[{"iso":"eng"}],"publication":"Inorganic Chemistry","abstract":[{"lang":"eng","text":"Here we explore the electronic structure of the diiron complex [(dppf)Fe(CO)3]0/+ [10/+; dppf = 1,1′-bis(diphenylphosphino)ferrocene] in two oxidation states by an advanced multitechnique experimental approach. A combination of magnetic circular dichroism, X-ray absorption and emission, high-frequency electron paramagnetic resonance (EPR), and Mössbauer spectroscopies is used to establish that oxidation of 10 occurs on the carbonyl iron ion, resulting in a low-spin iron(I) ion. It is shown that an unequivocal result is obtained by combining several methods. Compound 1+ displays slow spin dynamics, which is used here to study its geometric structure by means of pulsed EPR methods. Surprisingly, these data show an association of the tetrakis[3,5-bis(trifluoromethylphenyl)]borate counterion with 1+."}]},{"article_type":"original","_id":"41011","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"status":"public","type":"journal_article","doi":"10.1002/open.202000307","date_updated":"2023-01-31T08:07:01Z","author":[{"last_name":"Chakraborty","full_name":"Chakraborty, Uttam","first_name":"Uttam"},{"first_name":"Patrick","last_name":"Bügel","full_name":"Bügel, Patrick"},{"last_name":"Fritsch","full_name":"Fritsch, Lorena","id":"44418","first_name":"Lorena"},{"first_name":"Florian","full_name":"Weigend, Florian","last_name":"Weigend"},{"first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","id":"47241","full_name":"Bauer, Matthias"},{"first_name":"Axel","last_name":"Jacobi von Wangelin","full_name":"Jacobi von Wangelin, Axel"}],"volume":10,"citation":{"ama":"Chakraborty U, Bügel P, Fritsch L, Weigend F, Bauer M, Jacobi von Wangelin A. Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles. ChemistryOpen. 2021;10(2):265-271. doi:10.1002/open.202000307","ieee":"U. Chakraborty, P. Bügel, L. Fritsch, F. Weigend, M. Bauer, and A. Jacobi von Wangelin, “Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles,” ChemistryOpen, vol. 10, no. 2, pp. 265–271, 2021, doi: 10.1002/open.202000307.","chicago":"Chakraborty, Uttam, Patrick Bügel, Lorena Fritsch, Florian Weigend, Matthias Bauer, and Axel Jacobi von Wangelin. “Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles.” ChemistryOpen 10, no. 2 (2021): 265–71. https://doi.org/10.1002/open.202000307.","apa":"Chakraborty, U., Bügel, P., Fritsch, L., Weigend, F., Bauer, M., & Jacobi von Wangelin, A. (2021). Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles. ChemistryOpen, 10(2), 265–271. https://doi.org/10.1002/open.202000307","short":"U. Chakraborty, P. Bügel, L. Fritsch, F. Weigend, M. Bauer, A. Jacobi von Wangelin, ChemistryOpen 10 (2021) 265–271.","bibtex":"@article{Chakraborty_Bügel_Fritsch_Weigend_Bauer_Jacobi von Wangelin_2021, title={Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles}, volume={10}, DOI={10.1002/open.202000307}, number={2}, journal={ChemistryOpen}, publisher={Wiley}, author={Chakraborty, Uttam and Bügel, Patrick and Fritsch, Lorena and Weigend, Florian and Bauer, Matthias and Jacobi von Wangelin, Axel}, year={2021}, pages={265–271} }","mla":"Chakraborty, Uttam, et al. “Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles.” ChemistryOpen, vol. 10, no. 2, Wiley, 2021, pp. 265–71, doi:10.1002/open.202000307."},"intvolume":" 10","page":"265-271","publication_status":"published","publication_identifier":{"issn":["2191-1363","2191-1363"]},"keyword":["General Chemistry"],"language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"The controlled assembly of well-defined planar nanoclusters from molecular precursors is synthetically challenging and often plagued by the predominant formation of 3D-structures and nanoparticles. Herein, we report planar iron hydride nanoclusters from reactions of main group element hydrides with iron(II) bis(hexamethyldisilazide). The structures and properties of isolated Fe4, Fe6, and Fe7 nanoplatelets and calculated intermediates enable an unprecedented insight into the underlying building principle and growth mechanism of iron clusters, metal monolayers, and nanoparticles."}],"publication":"ChemistryOpen","title":"Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles","publisher":"Wiley","date_created":"2023-01-30T17:00:36Z","year":"2021","issue":"2"},{"article_number":"110330","article_type":"original","language":[{"iso":"eng"}],"_id":"25894","user_id":"23547","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"}],"abstract":[{"lang":"eng","text":"Powder X-ray diffraction (XRD) patterns of ordered mesoporous CMK-8 and CMK-9 carbon materials are simulated by geometric modeling. The materials are amorphous at the atomic length scale but exhibit highly symmetric gyroidal structures at the nanometer scale, corresponding to regular, continuous nanopore systems with cubic symmetry. Their structures lead to characteristic low-angle XRD signatures. We introduce a model based on geometrical considerations to simulate CMK-8 and CMK-9 structures with variable volume fraction of carbon (vs. pore volume, i.e., variable 'pore wall thickness'). In addition, we also simulate carbon materials with variable amounts of guest species (e.g., sulfur) residing in their pores. The corresponding XRD patterns are calculated. The carbon volume fraction turns out to have a significant impact on the relative diffraction peak intensities, especially in case of CMK-9 carbon that features a bimodal porosity. Likewise, the presence of guest species in the pores may also strongly affect the relative peak intensities. Our study suggests that careful evaluation of experimental low-angle XRD patterns of (real) CMK-8 or CMK-9 materials offers an opportunity to obtain detailed information about the nanostructural properties in addition to the mere identification of the pore systems geometry."}],"status":"public","type":"journal_article","publication":"Microporous and Mesoporous Materials","title":"Modeling of gyroidal mesoporous CMK-8 and CMK-9 carbon nanostructures and their X-Ray diffraction patterns","doi":"10.1016/j.micromeso.2020.110330","date_updated":"2023-03-07T10:44:44Z","date_created":"2021-10-08T10:02:31Z","author":[{"first_name":"Bertram","last_name":"Schwind","full_name":"Schwind, Bertram"},{"full_name":"Smått, Jan-Henrik","last_name":"Smått","first_name":"Jan-Henrik"},{"first_name":"Michael","full_name":"Tiemann, Michael","id":"23547","orcid":"0000-0003-1711-2722","last_name":"Tiemann"},{"first_name":"Christian","id":"11848","full_name":"Weinberger, Christian","last_name":"Weinberger"}],"year":"2021","citation":{"chicago":"Schwind, Bertram, Jan-Henrik Smått, Michael Tiemann, and Christian Weinberger. “Modeling of Gyroidal Mesoporous CMK-8 and CMK-9 Carbon Nanostructures and Their X-Ray Diffraction Patterns.” Microporous and Mesoporous Materials, 2021. https://doi.org/10.1016/j.micromeso.2020.110330.","ieee":"B. Schwind, J.-H. Smått, M. Tiemann, and C. Weinberger, “Modeling of gyroidal mesoporous CMK-8 and CMK-9 carbon nanostructures and their X-Ray diffraction patterns,” Microporous and Mesoporous Materials, Art. no. 110330, 2021, doi: 10.1016/j.micromeso.2020.110330.","ama":"Schwind B, Smått J-H, Tiemann M, Weinberger C. Modeling of gyroidal mesoporous CMK-8 and CMK-9 carbon nanostructures and their X-Ray diffraction patterns. Microporous and Mesoporous Materials. Published online 2021. doi:10.1016/j.micromeso.2020.110330","mla":"Schwind, Bertram, et al. “Modeling of Gyroidal Mesoporous CMK-8 and CMK-9 Carbon Nanostructures and Their X-Ray Diffraction Patterns.” Microporous and Mesoporous Materials, 110330, 2021, doi:10.1016/j.micromeso.2020.110330.","short":"B. Schwind, J.-H. Smått, M. Tiemann, C. Weinberger, Microporous and Mesoporous Materials (2021).","bibtex":"@article{Schwind_Smått_Tiemann_Weinberger_2021, title={Modeling of gyroidal mesoporous CMK-8 and CMK-9 carbon nanostructures and their X-Ray diffraction patterns}, DOI={10.1016/j.micromeso.2020.110330}, number={110330}, journal={Microporous and Mesoporous Materials}, author={Schwind, Bertram and Smått, Jan-Henrik and Tiemann, Michael and Weinberger, Christian}, year={2021} }","apa":"Schwind, B., Smått, J.-H., Tiemann, M., & Weinberger, C. (2021). Modeling of gyroidal mesoporous CMK-8 and CMK-9 carbon nanostructures and their X-Ray diffraction patterns. Microporous and Mesoporous Materials, Article 110330. https://doi.org/10.1016/j.micromeso.2020.110330"},"publication_status":"published","quality_controlled":"1","publication_identifier":{"issn":["1387-1811"]}},{"citation":{"short":"T. de los Arcos, H. Müller, F. Wang, V.R. Damerla, C. Hoppe, C. Weinberger, M. Tiemann, G. Grundmeier, Vibrational Spectroscopy (2021).","bibtex":"@article{de los Arcos_Müller_Wang_Damerla_Hoppe_Weinberger_Tiemann_Grundmeier_2021, title={Review of infrared spectroscopy techniques for the determination of internal structure in thin SiO2 films}, DOI={10.1016/j.vibspec.2021.103256}, number={103256}, journal={Vibrational Spectroscopy}, author={de los Arcos, Teresa and Müller, Hendrik and Wang, Fuzeng and Damerla, Varun Raj and Hoppe, Christian and Weinberger, Christian and Tiemann, Michael and Grundmeier, Guido}, year={2021} }","mla":"de los Arcos, Teresa, et al. “Review of Infrared Spectroscopy Techniques for the Determination of Internal Structure in Thin SiO2 Films.” Vibrational Spectroscopy, 103256, 2021, doi:10.1016/j.vibspec.2021.103256.","apa":"de los Arcos, T., Müller, H., Wang, F., Damerla, V. R., Hoppe, C., Weinberger, C., Tiemann, M., & Grundmeier, G. (2021). Review of infrared spectroscopy techniques for the determination of internal structure in thin SiO2 films. Vibrational Spectroscopy, Article 103256. https://doi.org/10.1016/j.vibspec.2021.103256","ama":"de los Arcos T, Müller H, Wang F, et al. Review of infrared spectroscopy techniques for the determination of internal structure in thin SiO2 films. Vibrational Spectroscopy. Published online 2021. doi:10.1016/j.vibspec.2021.103256","chicago":"Arcos, Teresa de los, Hendrik Müller, Fuzeng Wang, Varun Raj Damerla, Christian Hoppe, Christian Weinberger, Michael Tiemann, and Guido Grundmeier. “Review of Infrared Spectroscopy Techniques for the Determination of Internal Structure in Thin SiO2 Films.” Vibrational Spectroscopy, 2021. https://doi.org/10.1016/j.vibspec.2021.103256.","ieee":"T. de los Arcos et al., “Review of infrared spectroscopy techniques for the determination of internal structure in thin SiO2 films,” Vibrational Spectroscopy, Art. no. 103256, 2021, doi: 10.1016/j.vibspec.2021.103256."},"year":"2021","quality_controlled":"1","publication_identifier":{"issn":["0924-2031"]},"publication_status":"published","doi":"10.1016/j.vibspec.2021.103256","title":"Review of infrared spectroscopy techniques for the determination of internal structure in thin SiO2 films","author":[{"first_name":"Teresa","last_name":"de los Arcos","full_name":"de los Arcos, Teresa"},{"full_name":"Müller, Hendrik","last_name":"Müller","first_name":"Hendrik"},{"last_name":"Wang","full_name":"Wang, Fuzeng","first_name":"Fuzeng"},{"first_name":"Varun Raj","last_name":"Damerla","full_name":"Damerla, Varun Raj"},{"last_name":"Hoppe","full_name":"Hoppe, Christian","first_name":"Christian"},{"full_name":"Weinberger, Christian","id":"11848","last_name":"Weinberger","first_name":"Christian"},{"first_name":"Michael","full_name":"Tiemann, Michael","id":"23547","orcid":"0000-0003-1711-2722","last_name":"Tiemann"},{"first_name":"Guido","full_name":"Grundmeier, Guido","id":"194","last_name":"Grundmeier"}],"date_created":"2021-10-08T10:09:45Z","date_updated":"2023-03-07T10:44:06Z","status":"public","abstract":[{"text":"A comparison of infrared spectroscopic analytical approaches was made in order to assess their applicability for internal structure characterization of SiO2 thin films. Markers for porosity and/or disorder based on the analysis of the asymmetric stretching absorption band of SiO2 between 900−1350 cm−1 were discussed. The shape of this band, which shows a well-defined LO–TO splitting, depends not only on the inherent characteristics of the film under analysis but also on the particular geometry of the IR experiment and the specific surface selection rules of the substrate. Three types of SiO2 thin films with clearly defined porosity ranging from dense films to mesoporous films were investigated by transmission (at different incidence angles), direct specular reflection (at different angles), and diffuse reflection. Two different types of substrate, metallic and semiconducting, were used. The combined effect of substrate and specific technique in the final shape of the band, was discussed, and the efficacy for their applicability to the determination of porosity in thin SiO2 films was critically evaluated.","lang":"eng"}],"publication":"Vibrational Spectroscopy","type":"journal_article","language":[{"iso":"eng"}],"article_type":"original","article_number":"103256","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"},{"_id":"302"}],"user_id":"23547","_id":"25897"},{"date_created":"2021-10-08T10:01:21Z","author":[{"first_name":"Michael","last_name":"Tiemann","orcid":"0000-0003-1711-2722","id":"23547","full_name":"Tiemann, Michael"},{"first_name":"Christian","last_name":"Weinberger","id":"11848","full_name":"Weinberger, Christian"}],"date_updated":"2023-03-07T10:45:40Z","oa":"1","doi":"10.1002/admi.202001153","main_file_link":[{"open_access":"1","url":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admi.202001153"}],"title":"Selective Modification of Hierarchical Pores and Surfaces in Nanoporous Materials","publication_identifier":{"issn":["2196-7350","2196-7350"]},"quality_controlled":"1","publication_status":"published","citation":{"apa":"Tiemann, M., & Weinberger, C. (2021). Selective Modification of Hierarchical Pores and Surfaces in Nanoporous Materials. Advanced Materials Interfaces, Article 2001153. https://doi.org/10.1002/admi.202001153","mla":"Tiemann, Michael, and Christian Weinberger. “Selective Modification of Hierarchical Pores and Surfaces in Nanoporous Materials.” Advanced Materials Interfaces, 2001153, 2021, doi:10.1002/admi.202001153.","bibtex":"@article{Tiemann_Weinberger_2021, title={Selective Modification of Hierarchical Pores and Surfaces in Nanoporous Materials}, DOI={10.1002/admi.202001153}, number={2001153}, journal={Advanced Materials Interfaces}, author={Tiemann, Michael and Weinberger, Christian}, year={2021} }","short":"M. Tiemann, C. Weinberger, Advanced Materials Interfaces (2021).","ieee":"M. Tiemann and C. Weinberger, “Selective Modification of Hierarchical Pores and Surfaces in Nanoporous Materials,” Advanced Materials Interfaces, Art. no. 2001153, 2021, doi: 10.1002/admi.202001153.","chicago":"Tiemann, Michael, and Christian Weinberger. “Selective Modification of Hierarchical Pores and Surfaces in Nanoporous Materials.” Advanced Materials Interfaces, 2021. https://doi.org/10.1002/admi.202001153.","ama":"Tiemann M, Weinberger C. Selective Modification of Hierarchical Pores and Surfaces in Nanoporous Materials. Advanced Materials Interfaces. Published online 2021. doi:10.1002/admi.202001153"},"year":"2021","department":[{"_id":"35"},{"_id":"2"},{"_id":"307"}],"user_id":"23547","_id":"25893","language":[{"iso":"eng"}],"article_type":"review","article_number":"2001153","publication":"Advanced Materials Interfaces","type":"journal_article","status":"public","abstract":[{"text":"Tailor-made ordered mesoporous materials bear great potential in numerous fields of application where large interfaces are required. However, the inherent surfacechemical properties of conventional materials, such as silica, carbon or organosilica, poses some limitations with respect to their application. Surface manipulation by functionalization with chemically more reactive groups is one way to improve materials for their desired purpose. Another approach is the design of high surface-area composite materials. The surface manipulation, either by functionalization or by introducing guest species, can be performed selectively. This means that when several distinct, i.e. , hierarchical, types of surfaces or pore systems exist in a material, each of them may be chosen for manipulation. Several strategies can be identified to achieve this goal. Molecules or molecule assemblies can be utilized to temporarily protect pores or surfaces (soft protection), while manipulation occurs at the accessible sites. This approach is a recurring motive in this review and can also be applied to rigid template matrices (hard protection). Furthermore, the size of functionalization agents (size protection) and their reactivity/diffusion (kinetic protection) into the pores can also be utilized to achieve selectivity. In addition, challenges in the synthesis and characterization of selectively manipulated ordered mesoporous materials are discussed.","lang":"eng"}]},{"publication":"Journal of Aerosol Science","type":"journal_article","abstract":[{"lang":"eng","text":"In this report, a flame spray pyrolysis setup has been examined with various in situ extraction methods of particle samples along the flame axis. First, two precursor formulations leading to the formation of iron oxide nanoparticles were used in a standardized SpraySyn burner system, and the final particle outcome was characterized by a broad range of established powder characterization techniques (TEM/HRTEM, SAXS, XRD, BET). The characterization of the powder products evidenced that mostly homogeneous gas-to-particle conversion takes place when applying an acidic precursor solution, whereas the absence of the acid leads to a dominant droplet-to-particle pathway. Our study indicates that a droplet-to-particle-pathway could be present even when processing the acidic formulation. However, even if a secondary pathway might take place in this case as well, it is not dominant and nearly negligible. Subsequently, the in situ particle structure evolution was investigated for the dominant gas-to-particle pathway, and particles were extracted along the flame axis for online SMPS and offline TEM/HRTEM analysis. Due to the highly reactive conditions within the flame (high temperatures, turbulent flow field, high particle number concentrations), the extraction of representative samples from spray flames is challenging. In order to handle the reactive conditions, two extraction techniques were tailored in this report. To extract an aerosol sample within the flame for SMPS measurement, a Hole in a Tube probe was adjusted. Thus, the mobility particle diameter as well as the corresponding distribution widths were obtained at different heights above the burner along the flame axis. For TEM/HRTEM image analysis, particle samples were collected thermophoretically by means of a tailored shutter system. Since all sampling grids were protected until reaching the flame axis and due to the low sampling time, momentary captures of local particle structures could be extracted precisely. The particle morphologies have clearly shown an evolution from spherical and paired particles in the flame center to fractal and compact agglomerates at later synthesis stages."}],"status":"public","_id":"25896","department":[{"_id":"9"},{"_id":"35"},{"_id":"2"},{"_id":"307"}],"user_id":"23547","article_number":"105722","article_type":"original","language":[{"iso":"eng"}],"quality_controlled":"1","publication_identifier":{"issn":["0021-8502"]},"publication_status":"published","year":"2021","citation":{"bibtex":"@article{Tischendorf_Simmler_Weinberger_Bieber_Reddemann_Fröde_Lindner_Pitsch_Kneer_Tiemann_et al._2021, title={Examination of the evolution of iron oxide nanoparticles in flame spray pyrolysis by tailored in situ particle sampling techniques}, DOI={10.1016/j.jaerosci.2020.105722}, number={105722}, journal={Journal of Aerosol Science}, author={Tischendorf, R. and Simmler, M. and Weinberger, Christian and Bieber, M. and Reddemann, M. and Fröde, F. and Lindner, J. and Pitsch, H. and Kneer, R. and Tiemann, Michael and et al.}, year={2021} }","mla":"Tischendorf, R., et al. “Examination of the Evolution of Iron Oxide Nanoparticles in Flame Spray Pyrolysis by Tailored in Situ Particle Sampling Techniques.” Journal of Aerosol Science, 105722, 2021, doi:10.1016/j.jaerosci.2020.105722.","short":"R. Tischendorf, M. Simmler, C. Weinberger, M. Bieber, M. Reddemann, F. Fröde, J. Lindner, H. Pitsch, R. Kneer, M. Tiemann, H. Nirschl, H.-J. Schmid, Journal of Aerosol Science (2021).","apa":"Tischendorf, R., Simmler, M., Weinberger, C., Bieber, M., Reddemann, M., Fröde, F., Lindner, J., Pitsch, H., Kneer, R., Tiemann, M., Nirschl, H., & Schmid, H.-J. (2021). Examination of the evolution of iron oxide nanoparticles in flame spray pyrolysis by tailored in situ particle sampling techniques. Journal of Aerosol Science, Article 105722. https://doi.org/10.1016/j.jaerosci.2020.105722","ama":"Tischendorf R, Simmler M, Weinberger C, et al. Examination of the evolution of iron oxide nanoparticles in flame spray pyrolysis by tailored in situ particle sampling techniques. Journal of Aerosol Science. Published online 2021. doi:10.1016/j.jaerosci.2020.105722","ieee":"R. Tischendorf et al., “Examination of the evolution of iron oxide nanoparticles in flame spray pyrolysis by tailored in situ particle sampling techniques,” Journal of Aerosol Science, Art. no. 105722, 2021, doi: 10.1016/j.jaerosci.2020.105722.","chicago":"Tischendorf, R., M. Simmler, Christian Weinberger, M. Bieber, M. Reddemann, F. Fröde, J. Lindner, et al. “Examination of the Evolution of Iron Oxide Nanoparticles in Flame Spray Pyrolysis by Tailored in Situ Particle Sampling Techniques.” Journal of Aerosol Science, 2021. https://doi.org/10.1016/j.jaerosci.2020.105722."},"date_updated":"2023-03-08T08:07:30Z","author":[{"full_name":"Tischendorf, R.","last_name":"Tischendorf","first_name":"R."},{"last_name":"Simmler","full_name":"Simmler, M.","first_name":"M."},{"first_name":"Christian","id":"11848","full_name":"Weinberger, Christian","last_name":"Weinberger"},{"first_name":"M.","full_name":"Bieber, M.","last_name":"Bieber"},{"full_name":"Reddemann, M.","last_name":"Reddemann","first_name":"M."},{"first_name":"F.","last_name":"Fröde","full_name":"Fröde, F."},{"last_name":"Lindner","full_name":"Lindner, J.","first_name":"J."},{"full_name":"Pitsch, H.","last_name":"Pitsch","first_name":"H."},{"first_name":"R.","full_name":"Kneer, R.","last_name":"Kneer"},{"full_name":"Tiemann, Michael","id":"23547","orcid":"0000-0003-1711-2722","last_name":"Tiemann","first_name":"Michael"},{"first_name":"H.","last_name":"Nirschl","full_name":"Nirschl, H."},{"last_name":"Schmid","full_name":"Schmid, H.-J.","first_name":"H.-J."}],"date_created":"2021-10-08T10:07:18Z","title":"Examination of the evolution of iron oxide nanoparticles in flame spray pyrolysis by tailored in situ particle sampling techniques","doi":"10.1016/j.jaerosci.2020.105722"},{"publication_status":"published","publication_identifier":{"issn":["1552-4973","1552-4981"]},"citation":{"mla":"Garcia Diosa, Jaime Andres, et al. “TiO2 Nanoparticle Coatings on Glass Surfaces for the Selective Trapping of Leukemia Cells from Peripheral Blood.” Journal of Biomedical Materials Research Part B: Applied Biomaterials, vol. 109, 2021, pp. 2142–2153, doi:10.1002/jbm.b.34862.","bibtex":"@article{Garcia Diosa_Gonzalez Orive_Weinberger_Schwiderek_Knust_Tiemann_Grundmeier_Keller_Camargo Amado_2021, title={TiO2 nanoparticle coatings on glass surfaces for the selective trapping of leukemia cells from peripheral blood}, volume={109}, DOI={10.1002/jbm.b.34862}, journal={Journal of Biomedical Materials Research Part B: Applied Biomaterials}, author={Garcia Diosa, Jaime Andres and Gonzalez Orive, Alejandro and Weinberger, Christian and Schwiderek, Sabrina and Knust, Steffen and Tiemann, Michael and Grundmeier, Guido and Keller, Adrian and Camargo Amado, Ruben Jesus}, year={2021}, pages={2142–2153} }","short":"J.A. Garcia Diosa, A. Gonzalez Orive, C. Weinberger, S. Schwiderek, S. Knust, M. Tiemann, G. Grundmeier, A. Keller, R.J. Camargo Amado, Journal of Biomedical Materials Research Part B: Applied Biomaterials 109 (2021) 2142–2153.","apa":"Garcia Diosa, J. A., Gonzalez Orive, A., Weinberger, C., Schwiderek, S., Knust, S., Tiemann, M., Grundmeier, G., Keller, A., & Camargo Amado, R. J. (2021). TiO2 nanoparticle coatings on glass surfaces for the selective trapping of leukemia cells from peripheral blood. Journal of Biomedical Materials Research Part B: Applied Biomaterials, 109, 2142–2153. https://doi.org/10.1002/jbm.b.34862","ama":"Garcia Diosa JA, Gonzalez Orive A, Weinberger C, et al. TiO2 nanoparticle coatings on glass surfaces for the selective trapping of leukemia cells from peripheral blood. Journal of Biomedical Materials Research Part B: Applied Biomaterials. 2021;109:2142–2153. doi:10.1002/jbm.b.34862","ieee":"J. A. Garcia Diosa et al., “TiO2 nanoparticle coatings on glass surfaces for the selective trapping of leukemia cells from peripheral blood,” Journal of Biomedical Materials Research Part B: Applied Biomaterials, vol. 109, pp. 2142–2153, 2021, doi: 10.1002/jbm.b.34862.","chicago":"Garcia Diosa, Jaime Andres, Alejandro Gonzalez Orive, Christian Weinberger, Sabrina Schwiderek, Steffen Knust, Michael Tiemann, Guido Grundmeier, Adrian Keller, and Ruben Jesus Camargo Amado. “TiO2 Nanoparticle Coatings on Glass Surfaces for the Selective Trapping of Leukemia Cells from Peripheral Blood.” Journal of Biomedical Materials Research Part B: Applied Biomaterials 109 (2021): 2142–2153. https://doi.org/10.1002/jbm.b.34862."},"intvolume":" 109","page":"2142–2153","date_updated":"2023-03-08T08:10:25Z","author":[{"first_name":"Jaime Andres","full_name":"Garcia Diosa, Jaime Andres","last_name":"Garcia Diosa"},{"first_name":"Alejandro","last_name":"Gonzalez Orive","full_name":"Gonzalez Orive, Alejandro"},{"first_name":"Christian","last_name":"Weinberger","id":"11848","full_name":"Weinberger, Christian"},{"last_name":"Schwiderek","full_name":"Schwiderek, Sabrina","first_name":"Sabrina"},{"full_name":"Knust, Steffen","last_name":"Knust","first_name":"Steffen"},{"full_name":"Tiemann, Michael","id":"23547","last_name":"Tiemann","orcid":"0000-0003-1711-2722","first_name":"Michael"},{"first_name":"Guido","last_name":"Grundmeier","full_name":"Grundmeier, Guido","id":"194"},{"orcid":"0000-0001-7139-3110","last_name":"Keller","full_name":"Keller, Adrian","id":"48864","first_name":"Adrian"},{"last_name":"Camargo Amado","full_name":"Camargo Amado, Ruben Jesus","first_name":"Ruben Jesus"}],"volume":109,"doi":"10.1002/jbm.b.34862","type":"journal_article","status":"public","_id":"22635","user_id":"23547","department":[{"_id":"302"},{"_id":"307"},{"_id":"35"},{"_id":"2"}],"article_type":"original","quality_controlled":"1","year":"2021","date_created":"2021-07-08T11:34:21Z","title":"TiO2 nanoparticle coatings on glass surfaces for the selective trapping of leukemia cells from peripheral blood","publication":"Journal of Biomedical Materials Research Part B: Applied Biomaterials","abstract":[{"text":"Photodynamic therapy (PDT) using TiO2 nanoparticles has become an important alternative treatment for different types of cancer due to their high photocatalytic activity and high absorption of UV-A light. To potentiate this treatment, we have coated commercial glass plates with TiO2 nanoparticles prepared by the sol–gel method (TiO2-m), which exhibit a remarkable selectivity for the irreversible trapping of cancer cells. The physicochemical properties of the deposited TiO2-m nanoparticle coatings have been characterized by a number of complementary surface-analytical techniques and their interaction with leukemia and healthy blood cells were investigated. Scanning electron and atomic force microscopy verify the formation of a compact layer of TiO2-m nanoparticles. The particles are predominantly in the anatase phase and have hydroxyl-terminated surfaces as revealed by Raman, X-ray photoelectron, and infrared spectroscopy, as well as X-ray diffraction. We find that lymphoblastic leukemia cells adhere to the TiO2-m coating and undergo amoeboid-like migration, whereas lymphocytic cells show distinctly weaker interactions with the coating. This evidences the potential of this nanomaterial coating to selectively trap cancer cells and renders it a promising candidate for the development of future prototypes of PDT devices for the treatment of leukemia and other types of cancers with non-adherent cells.","lang":"eng"}],"language":[{"iso":"eng"}]},{"publication_status":"published","publication_identifier":{"issn":["1477-9226","1477-9234"]},"quality_controlled":"1","year":"2021","citation":{"short":"F. Steinke, A. Javed, S. Wöhlbrandt, M. Tiemann, N. Stock, Dalton Transactions (2021) 13572–13579.","mla":"Steinke, Felix, et al. “New Isoreticular Phosphonate MOFs Based on a Tetratopic Linker.” Dalton Transactions, 2021, pp. 13572–79, doi:10.1039/d1dt02610k.","bibtex":"@article{Steinke_Javed_Wöhlbrandt_Tiemann_Stock_2021, title={New isoreticular phosphonate MOFs based on a tetratopic linker}, DOI={10.1039/d1dt02610k}, journal={Dalton Transactions}, author={Steinke, Felix and Javed, Ali and Wöhlbrandt, Stephan and Tiemann, Michael and Stock, Norbert}, year={2021}, pages={13572–13579} }","apa":"Steinke, F., Javed, A., Wöhlbrandt, S., Tiemann, M., & Stock, N. (2021). New isoreticular phosphonate MOFs based on a tetratopic linker. Dalton Transactions, 13572–13579. https://doi.org/10.1039/d1dt02610k","chicago":"Steinke, Felix, Ali Javed, Stephan Wöhlbrandt, Michael Tiemann, and Norbert Stock. “New Isoreticular Phosphonate MOFs Based on a Tetratopic Linker.” Dalton Transactions, 2021, 13572–79. https://doi.org/10.1039/d1dt02610k.","ieee":"F. Steinke, A. Javed, S. Wöhlbrandt, M. Tiemann, and N. Stock, “New isoreticular phosphonate MOFs based on a tetratopic linker,” Dalton Transactions, pp. 13572–13579, 2021, doi: 10.1039/d1dt02610k.","ama":"Steinke F, Javed A, Wöhlbrandt S, Tiemann M, Stock N. New isoreticular phosphonate MOFs based on a tetratopic linker. Dalton Transactions. Published online 2021:13572-13579. doi:10.1039/d1dt02610k"},"page":"13572-13579","date_updated":"2023-03-08T08:08:22Z","date_created":"2021-10-08T09:57:34Z","author":[{"first_name":"Felix","full_name":"Steinke, Felix","last_name":"Steinke"},{"full_name":"Javed, Ali","last_name":"Javed","first_name":"Ali"},{"first_name":"Stephan","last_name":"Wöhlbrandt","full_name":"Wöhlbrandt, Stephan"},{"last_name":"Tiemann","orcid":"0000-0003-1711-2722","id":"23547","full_name":"Tiemann, Michael","first_name":"Michael"},{"first_name":"Norbert","full_name":"Stock, Norbert","last_name":"Stock"}],"title":"New isoreticular phosphonate MOFs based on a tetratopic linker","doi":"10.1039/d1dt02610k","type":"journal_article","publication":"Dalton Transactions","abstract":[{"lang":"eng","text":"The tetratopic linker 1,1,2,2-tetrakis(4-phosphonophenyl)ethylene (H8TPPE) was used to synthesize the three new porous metal–organic frameworks of composition [M2(H2O)2(H2TPPE)]·xH2O (M = Al3+, Ga3+, Fe3+), denoted as M-CAU-53 under hydrothermal reaction conditions, using the corresponding metal nitrates as starting materials. The crystal structures of the compounds were determined ab initio from powder X-ray diffraction data, revealing small structural differences. Proton conductivity measurements were carried out, indicating different conductivity mechanisms. The differences in proton conductivity could be linked to the individual structures. In addition, a thorough characterization via thermogravimetry, elemental analysis, IR-spectroscopy as well as N2- and H2O-sorption is given."}],"status":"public","_id":"25892","user_id":"23547","department":[{"_id":"2"},{"_id":"307"}],"article_type":"original","language":[{"iso":"eng"}]},{"status":"public","abstract":[{"lang":"eng","text":"Two closely related FeII complexes with 2,6-bis(1-ethyl-1H-1,2,3-triazol-4yl)pyridine and 2,6-bis(1,2,3-triazol-5-ylidene)pyridine ligands are presented to gain new insights into the photophysics of bis(tridentate) iron(II) complexes. The [Fe(N^N^N)2]2+ pseudoisomer sensitizes singlet oxygen through a MC state with nanosecond lifetime after MLCT excitation, while the bis(tridentate) [Fe(C^N^C)2]2+ pseudoisomer possesses a similar 3MLCT lifetime as the tris(bidentate) [Fe(C^C)2(N^N)]2+ complexes with four mesoionic carbenes."}],"type":"journal_article","publication":"Chemical Communications","language":[{"iso":"eng"}],"article_type":"original","keyword":["Materials Chemistry","Metals and Alloys","Surfaces","Coatings and Films","General Chemistry","Ceramics and Composite","Metallkomplexe","Optical and Magnetic Materials","Catalysis"],"user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"_id":"41007","citation":{"chicago":"Dierks, Philipp, Ayla Kruse, Olga S. Bokareva, Mohammed J. Al-Marri, Jens Kalmbach, Marc Baltrun, Adam Neuba, et al. “Distinct Photodynamics of κ-N and κ-C Pseudoisomeric Iron(Ii) Complexes.” Chemical Communications 57, no. 54 (2021): 6640–43. https://doi.org/10.1039/d1cc01716k.","ieee":"P. Dierks et al., “Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes,” Chemical Communications, vol. 57, no. 54, pp. 6640–6643, 2021, doi: 10.1039/d1cc01716k.","ama":"Dierks P, Kruse A, Bokareva OS, et al. Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes. Chemical Communications. 2021;57(54):6640-6643. doi:10.1039/d1cc01716k","apa":"Dierks, P., Kruse, A., Bokareva, O. S., Al-Marri, M. J., Kalmbach, J., Baltrun, M., Neuba, A., Schoch, R., Hohloch, S., Heinze, K., Seitz, M., Kühn, O., Lochbrunner, S., & Bauer, M. (2021). Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes. Chemical Communications, 57(54), 6640–6643. https://doi.org/10.1039/d1cc01716k","short":"P. Dierks, A. Kruse, O.S. Bokareva, M.J. Al-Marri, J. Kalmbach, M. Baltrun, A. Neuba, R. Schoch, S. Hohloch, K. Heinze, M. Seitz, O. Kühn, S. Lochbrunner, M. Bauer, Chemical Communications 57 (2021) 6640–6643.","bibtex":"@article{Dierks_Kruse_Bokareva_Al-Marri_Kalmbach_Baltrun_Neuba_Schoch_Hohloch_Heinze_et al._2021, title={Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes}, volume={57}, DOI={10.1039/d1cc01716k}, number={54}, journal={Chemical Communications}, publisher={Royal Society of Chemistry (RSC)}, author={Dierks, Philipp and Kruse, Ayla and Bokareva, Olga S. and Al-Marri, Mohammed J. and Kalmbach, Jens and Baltrun, Marc and Neuba, Adam and Schoch, Roland and Hohloch, Stephan and Heinze, Katja and et al.}, year={2021}, pages={6640–6643} }","mla":"Dierks, Philipp, et al. “Distinct Photodynamics of κ-N and κ-C Pseudoisomeric Iron(Ii) Complexes.” Chemical Communications, vol. 57, no. 54, Royal Society of Chemistry (RSC), 2021, pp. 6640–43, doi:10.1039/d1cc01716k."},"page":"6640-6643","intvolume":" 57","year":"2021","issue":"54","publication_status":"published","publication_identifier":{"issn":["1359-7345","1364-548X"]},"doi":"10.1039/d1cc01716k","title":"Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes","author":[{"full_name":"Dierks, Philipp","last_name":"Dierks","first_name":"Philipp"},{"first_name":"Ayla","last_name":"Kruse","full_name":"Kruse, Ayla"},{"first_name":"Olga S.","full_name":"Bokareva, Olga S.","last_name":"Bokareva"},{"first_name":"Mohammed J.","last_name":"Al-Marri","full_name":"Al-Marri, Mohammed J."},{"full_name":"Kalmbach, Jens","last_name":"Kalmbach","first_name":"Jens"},{"first_name":"Marc","last_name":"Baltrun","full_name":"Baltrun, Marc"},{"first_name":"Adam","last_name":"Neuba","full_name":"Neuba, Adam"},{"first_name":"Roland","orcid":"0000-0003-2061-7289","last_name":"Schoch","full_name":"Schoch, Roland","id":"48467"},{"last_name":"Hohloch","full_name":"Hohloch, Stephan","first_name":"Stephan"},{"last_name":"Heinze","full_name":"Heinze, Katja","first_name":"Katja"},{"first_name":"Michael","last_name":"Seitz","full_name":"Seitz, Michael"},{"last_name":"Kühn","full_name":"Kühn, Oliver","first_name":"Oliver"},{"last_name":"Lochbrunner","full_name":"Lochbrunner, Stefan","first_name":"Stefan"},{"first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","full_name":"Bauer, Matthias","id":"47241"}],"date_created":"2023-01-30T16:59:55Z","volume":57,"date_updated":"2024-10-11T08:42:44Z","publisher":"Royal Society of Chemistry (RSC)"},{"author":[{"full_name":"Vukadinovic, Yannik","last_name":"Vukadinovic","first_name":"Yannik"},{"full_name":"Burkhardt, Lukas","last_name":"Burkhardt","first_name":"Lukas"},{"first_name":"Ayla","last_name":"Päpcke","full_name":"Päpcke, Ayla"},{"first_name":"Anabel","full_name":"Miletic, Anabel","last_name":"Miletic"},{"last_name":"Fritsch","full_name":"Fritsch, Lorena","first_name":"Lorena"},{"first_name":"Björn","last_name":"Altenburger","full_name":"Altenburger, Björn"},{"first_name":"Roland","last_name":"Schoch","full_name":"Schoch, Roland"},{"full_name":"Neuba, Adam","last_name":"Neuba","first_name":"Adam"},{"full_name":"Lochbrunner, Stefan","last_name":"Lochbrunner","first_name":"Stefan"},{"first_name":"Matthias","full_name":"Bauer, Matthias","last_name":"Bauer"}],"date_created":"2020-08-28T09:08:09Z","date_updated":"2022-01-06T06:53:36Z","doi":"10.1021/acs.inorgchem.0c00393","title":"When Donors Turn into Acceptors: Ground and Excited State Properties of FeII Complexes with Amine-Substituted Tridentate Bis-imidazole-2-ylidene Pyridine Ligands","publication_identifier":{"issn":["0020-1669","1520-510X"]},"publication_status":"published","page":"8762-8774","citation":{"ama":"Vukadinovic Y, Burkhardt L, Päpcke A, et al. When Donors Turn into Acceptors: Ground and Excited State Properties of FeII Complexes with Amine-Substituted Tridentate Bis-imidazole-2-ylidene Pyridine Ligands. Inorganic Chemistry. 2020:8762-8774. doi:10.1021/acs.inorgchem.0c00393","chicago":"Vukadinovic, Yannik, Lukas Burkhardt, Ayla Päpcke, Anabel Miletic, Lorena Fritsch, Björn Altenburger, Roland Schoch, Adam Neuba, Stefan Lochbrunner, and Matthias Bauer. “When Donors Turn into Acceptors: Ground and Excited State Properties of FeII Complexes with Amine-Substituted Tridentate Bis-Imidazole-2-Ylidene Pyridine Ligands.” Inorganic Chemistry, 2020, 8762–74. https://doi.org/10.1021/acs.inorgchem.0c00393.","ieee":"Y. Vukadinovic et al., “When Donors Turn into Acceptors: Ground and Excited State Properties of FeII Complexes with Amine-Substituted Tridentate Bis-imidazole-2-ylidene Pyridine Ligands,” Inorganic Chemistry, pp. 8762–8774, 2020.","short":"Y. Vukadinovic, L. Burkhardt, A. Päpcke, A. Miletic, L. Fritsch, B. Altenburger, R. Schoch, A. Neuba, S. Lochbrunner, M. Bauer, Inorganic Chemistry (2020) 8762–8774.","bibtex":"@article{Vukadinovic_Burkhardt_Päpcke_Miletic_Fritsch_Altenburger_Schoch_Neuba_Lochbrunner_Bauer_2020, title={When Donors Turn into Acceptors: Ground and Excited State Properties of FeII Complexes with Amine-Substituted Tridentate Bis-imidazole-2-ylidene Pyridine Ligands}, DOI={10.1021/acs.inorgchem.0c00393}, journal={Inorganic Chemistry}, author={Vukadinovic, Yannik and Burkhardt, Lukas and Päpcke, Ayla and Miletic, Anabel and Fritsch, Lorena and Altenburger, Björn and Schoch, Roland and Neuba, Adam and Lochbrunner, Stefan and Bauer, Matthias}, year={2020}, pages={8762–8774} }","mla":"Vukadinovic, Yannik, et al. “When Donors Turn into Acceptors: Ground and Excited State Properties of FeII Complexes with Amine-Substituted Tridentate Bis-Imidazole-2-Ylidene Pyridine Ligands.” Inorganic Chemistry, 2020, pp. 8762–74, doi:10.1021/acs.inorgchem.0c00393.","apa":"Vukadinovic, Y., Burkhardt, L., Päpcke, A., Miletic, A., Fritsch, L., Altenburger, B., … Bauer, M. (2020). When Donors Turn into Acceptors: Ground and Excited State Properties of FeII Complexes with Amine-Substituted Tridentate Bis-imidazole-2-ylidene Pyridine Ligands. Inorganic Chemistry, 8762–8774. https://doi.org/10.1021/acs.inorgchem.0c00393"},"year":"2020","department":[{"_id":"35"},{"_id":"306"}],"user_id":"54038","_id":"18534","language":[{"iso":"eng"}],"publication":"Inorganic Chemistry","type":"journal_article","status":"public"},{"year":"2020","issue":"17","title":"Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions","publisher":"American Chemical Society (ACS)","date_created":"2023-01-30T17:37:18Z","publication":"Organometallics","keyword":["Inorganic Chemistry","Organic Chemistry","Physical and Theoretical Chemistry"],"language":[{"iso":"eng"}],"intvolume":" 39","page":"3131-3145","citation":{"ama":"Kirchhof M, Gugeler K, Fischer FR, et al. Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions. Organometallics. 2020;39(17):3131-3145. doi:10.1021/acs.organomet.0c00310","chicago":"Kirchhof, Manuel, Katrin Gugeler, Felix Richard Fischer, Michał Nowakowski, Alina Bauer, Sonia Alvarez-Barcia, Karina Abitaev, et al. “Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions.” Organometallics 39, no. 17 (2020): 3131–45. https://doi.org/10.1021/acs.organomet.0c00310.","ieee":"M. Kirchhof et al., “Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions,” Organometallics, vol. 39, no. 17, pp. 3131–3145, 2020, doi: 10.1021/acs.organomet.0c00310.","short":"M. Kirchhof, K. Gugeler, F.R. Fischer, M. Nowakowski, A. Bauer, S. Alvarez-Barcia, K. Abitaev, M. Schnierle, Y. Qawasmi, W. Frey, A. Baro, D.P. Estes, T. Sottmann, M.R. Ringenberg, B. Plietker, M. Bauer, J. Kästner, S. Laschat, Organometallics 39 (2020) 3131–3145.","mla":"Kirchhof, Manuel, et al. “Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions.” Organometallics, vol. 39, no. 17, American Chemical Society (ACS), 2020, pp. 3131–45, doi:10.1021/acs.organomet.0c00310.","bibtex":"@article{Kirchhof_Gugeler_Fischer_Nowakowski_Bauer_Alvarez-Barcia_Abitaev_Schnierle_Qawasmi_Frey_et al._2020, title={Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions}, volume={39}, DOI={10.1021/acs.organomet.0c00310}, number={17}, journal={Organometallics}, publisher={American Chemical Society (ACS)}, author={Kirchhof, Manuel and Gugeler, Katrin and Fischer, Felix Richard and Nowakowski, Michał and Bauer, Alina and Alvarez-Barcia, Sonia and Abitaev, Karina and Schnierle, Marc and Qawasmi, Yaseen and Frey, Wolfgang and et al.}, year={2020}, pages={3131–3145} }","apa":"Kirchhof, M., Gugeler, K., Fischer, F. R., Nowakowski, M., Bauer, A., Alvarez-Barcia, S., Abitaev, K., Schnierle, M., Qawasmi, Y., Frey, W., Baro, A., Estes, D. P., Sottmann, T., Ringenberg, M. R., Plietker, B., Bauer, M., Kästner, J., & Laschat, S. (2020). Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions. Organometallics, 39(17), 3131–3145. https://doi.org/10.1021/acs.organomet.0c00310"},"publication_identifier":{"issn":["0276-7333","1520-6041"]},"publication_status":"published","doi":"10.1021/acs.organomet.0c00310","date_updated":"2024-05-07T11:41:01Z","volume":39,"author":[{"full_name":"Kirchhof, Manuel","last_name":"Kirchhof","first_name":"Manuel"},{"first_name":"Katrin","full_name":"Gugeler, Katrin","last_name":"Gugeler"},{"last_name":"Fischer","full_name":"Fischer, Felix Richard","first_name":"Felix Richard"},{"orcid":"0000-0002-3734-7011","last_name":"Nowakowski","full_name":"Nowakowski, Michał","id":"78878","first_name":"Michał"},{"last_name":"Bauer","full_name":"Bauer, Alina","first_name":"Alina"},{"last_name":"Alvarez-Barcia","full_name":"Alvarez-Barcia, Sonia","first_name":"Sonia"},{"full_name":"Abitaev, Karina","last_name":"Abitaev","first_name":"Karina"},{"full_name":"Schnierle, Marc","last_name":"Schnierle","first_name":"Marc"},{"full_name":"Qawasmi, Yaseen","last_name":"Qawasmi","first_name":"Yaseen"},{"full_name":"Frey, Wolfgang","last_name":"Frey","first_name":"Wolfgang"},{"last_name":"Baro","full_name":"Baro, Angelika","first_name":"Angelika"},{"first_name":"Deven P.","full_name":"Estes, Deven P.","last_name":"Estes"},{"first_name":"Thomas","full_name":"Sottmann, Thomas","last_name":"Sottmann"},{"first_name":"Mark R.","last_name":"Ringenberg","full_name":"Ringenberg, Mark R."},{"first_name":"Bernd","full_name":"Plietker, Bernd","last_name":"Plietker"},{"id":"47241","full_name":"Bauer, Matthias","orcid":"0000-0002-9294-6076","last_name":"Bauer","first_name":"Matthias"},{"full_name":"Kästner, Johannes","last_name":"Kästner","first_name":"Johannes"},{"full_name":"Laschat, Sabine","last_name":"Laschat","first_name":"Sabine"}],"status":"public","type":"journal_article","_id":"41022","department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467"},{"status":"public","publication":"ACS Catalysis","type":"journal_article","language":[{"iso":"eng"}],"keyword":["Catalysis","General Chemistry"],"department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","_id":"41015","intvolume":" 10","page":"14810-14823","citation":{"ama":"Benedikter M, Musso J, Kesharwani MK, et al. 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