[{"publication":"Angewandte Chemie International Edition","type":"journal_article","status":"public","department":[{"_id":"15"},{"_id":"170"},{"_id":"705"},{"_id":"35"},{"_id":"230"}],"user_id":"16199","_id":"35077","language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis"],"article_number":"e202213229","issue":"9","publication_identifier":{"issn":["1433-7851","1521-3773"]},"publication_status":"published","intvolume":" 62","citation":{"ieee":"Q. Liang, X. Ma, T. Long, J. Yao, Q. Liao, and H. Fu, “Circularly Polarized Lasing from a Microcavity Filled with Achiral Single‐Crystalline Microribbons,” Angewandte Chemie International Edition, vol. 62, no. 9, Art. no. e202213229, 2023, doi: 10.1002/anie.202213229.","chicago":"Liang, Qian, Xuekai Ma, Teng Long, Jiannian Yao, Qing Liao, and Hongbing Fu. “Circularly Polarized Lasing from a Microcavity Filled with Achiral Single‐Crystalline Microribbons.” Angewandte Chemie International Edition 62, no. 9 (2023). https://doi.org/10.1002/anie.202213229.","ama":"Liang Q, Ma X, Long T, Yao J, Liao Q, Fu H. Circularly Polarized Lasing from a Microcavity Filled with Achiral Single‐Crystalline Microribbons. Angewandte Chemie International Edition. 2023;62(9). doi:10.1002/anie.202213229","short":"Q. Liang, X. Ma, T. Long, J. Yao, Q. Liao, H. Fu, Angewandte Chemie International Edition 62 (2023).","bibtex":"@article{Liang_Ma_Long_Yao_Liao_Fu_2023, title={Circularly Polarized Lasing from a Microcavity Filled with Achiral Single‐Crystalline Microribbons}, volume={62}, DOI={10.1002/anie.202213229}, number={9e202213229}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Liang, Qian and Ma, Xuekai and Long, Teng and Yao, Jiannian and Liao, Qing and Fu, Hongbing}, year={2023} }","mla":"Liang, Qian, et al. “Circularly Polarized Lasing from a Microcavity Filled with Achiral Single‐Crystalline Microribbons.” Angewandte Chemie International Edition, vol. 62, no. 9, e202213229, Wiley, 2023, doi:10.1002/anie.202213229.","apa":"Liang, Q., Ma, X., Long, T., Yao, J., Liao, Q., & Fu, H. (2023). Circularly Polarized Lasing from a Microcavity Filled with Achiral Single‐Crystalline Microribbons. Angewandte Chemie International Edition, 62(9), Article e202213229. https://doi.org/10.1002/anie.202213229"},"year":"2023","volume":62,"date_created":"2023-01-02T08:54:29Z","author":[{"first_name":"Qian","last_name":"Liang","full_name":"Liang, Qian"},{"first_name":"Xuekai","last_name":"Ma","full_name":"Ma, Xuekai","id":"59416"},{"first_name":"Teng","full_name":"Long, Teng","last_name":"Long"},{"first_name":"Jiannian","full_name":"Yao, Jiannian","last_name":"Yao"},{"first_name":"Qing","last_name":"Liao","full_name":"Liao, Qing"},{"first_name":"Hongbing","full_name":"Fu, Hongbing","last_name":"Fu"}],"publisher":"Wiley","date_updated":"2025-12-05T13:51:12Z","doi":"10.1002/anie.202213229","title":"Circularly Polarized Lasing from a Microcavity Filled with Achiral Single‐Crystalline Microribbons"},{"user_id":"48864","department":[{"_id":"302"}],"_id":"30209","status":"public","type":"journal_article","doi":"10.3390/ijms23052817","author":[{"full_name":"Hanke, Marcel","last_name":"Hanke","first_name":"Marcel"},{"first_name":"Niklas","full_name":"Hansen, Niklas","last_name":"Hansen"},{"full_name":"Chen, Ruiping","last_name":"Chen","first_name":"Ruiping"},{"full_name":"Grundmeier, Guido","last_name":"Grundmeier","first_name":"Guido"},{"last_name":"Fahmy","full_name":"Fahmy, Karim","first_name":"Karim"},{"last_name":"Keller","full_name":"Keller, Adrian","first_name":"Adrian"}],"volume":23,"date_updated":"2022-03-07T07:29:27Z","citation":{"chicago":"Hanke, Marcel, Niklas Hansen, Ruiping Chen, Guido Grundmeier, Karim Fahmy, and Adrian Keller. “Salting-Out of DNA Origami Nanostructures by Ammonium Sulfate.” International Journal of Molecular Sciences 23, no. 5 (2022): 2817. https://doi.org/10.3390/ijms23052817.","ieee":"M. Hanke, N. Hansen, R. Chen, G. Grundmeier, K. Fahmy, and A. Keller, “Salting-Out of DNA Origami Nanostructures by Ammonium Sulfate,” International Journal of Molecular Sciences, vol. 23, no. 5, p. 2817, 2022, doi: 10.3390/ijms23052817.","ama":"Hanke M, Hansen N, Chen R, Grundmeier G, Fahmy K, Keller A. Salting-Out of DNA Origami Nanostructures by Ammonium Sulfate. International Journal of Molecular Sciences. 2022;23(5):2817. doi:10.3390/ijms23052817","apa":"Hanke, M., Hansen, N., Chen, R., Grundmeier, G., Fahmy, K., & Keller, A. (2022). Salting-Out of DNA Origami Nanostructures by Ammonium Sulfate. International Journal of Molecular Sciences, 23(5), 2817. https://doi.org/10.3390/ijms23052817","bibtex":"@article{Hanke_Hansen_Chen_Grundmeier_Fahmy_Keller_2022, title={Salting-Out of DNA Origami Nanostructures by Ammonium Sulfate}, volume={23}, DOI={10.3390/ijms23052817}, number={5}, journal={International Journal of Molecular Sciences}, publisher={MDPI AG}, author={Hanke, Marcel and Hansen, Niklas and Chen, Ruiping and Grundmeier, Guido and Fahmy, Karim and Keller, Adrian}, year={2022}, pages={2817} }","short":"M. Hanke, N. Hansen, R. Chen, G. Grundmeier, K. Fahmy, A. Keller, International Journal of Molecular Sciences 23 (2022) 2817.","mla":"Hanke, Marcel, et al. “Salting-Out of DNA Origami Nanostructures by Ammonium Sulfate.” International Journal of Molecular Sciences, vol. 23, no. 5, MDPI AG, 2022, p. 2817, doi:10.3390/ijms23052817."},"page":"2817","intvolume":" 23","publication_status":"published","publication_identifier":{"issn":["1422-0067"]},"language":[{"iso":"eng"}],"keyword":["Inorganic Chemistry","Organic Chemistry","Physical and Theoretical Chemistry","Computer Science Applications","Spectroscopy","Molecular Biology","General Medicine","Catalysis"],"abstract":[{"text":"DNA origami technology enables the folding of DNA strands into complex nanoscale shapes whose properties and interactions with molecular species often deviate significantly from that of genomic DNA. Here, we investigate the salting-out of different DNA origami shapes by the kosmotropic salt ammonium sulfate that is routinely employed in protein precipitation. We find that centrifugation in the presence of 3 M ammonium sulfate results in notable precipitation of DNA origami nanostructures but not of double-stranded genomic DNA. The precipitated DNA origami nanostructures can be resuspended in ammonium sulfate-free buffer without apparent formation of aggregates or loss of structural integrity. Even though quasi-1D six-helix bundle DNA origami are slightly less susceptible toward salting-out than more compact DNA origami triangles and 24-helix bundles, precipitation and recovery yields appear to be mostly independent of DNA origami shape and superstructure. Exploiting the specificity of ammonium sulfate salting-out for DNA origami nanostructures, we further apply this method to separate DNA origami triangles from genomic DNA fragments in a complex mixture. Our results thus demonstrate the possibility of concentrating and purifying DNA origami nanostructures by ammonium sulfate-induced salting-out.","lang":"eng"}],"publication":"International Journal of Molecular Sciences","title":"Salting-Out of DNA Origami Nanostructures by Ammonium Sulfate","date_created":"2022-03-07T07:28:02Z","publisher":"MDPI AG","year":"2022","issue":"5"},{"publication_status":"published","publication_identifier":{"issn":["1422-0067"]},"issue":"15","year":"2022","citation":{"bibtex":"@article{Hanke_Hansen_Tomm_Grundmeier_Keller_2022, title={Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate}, volume={23}, DOI={10.3390/ijms23158547}, number={15}, journal={International Journal of Molecular Sciences}, publisher={MDPI AG}, author={Hanke, Marcel and Hansen, Niklas and Tomm, Emilia and Grundmeier, Guido and Keller, Adrian}, year={2022}, pages={8547} }","short":"M. Hanke, N. Hansen, E. Tomm, G. Grundmeier, A. Keller, International Journal of Molecular Sciences 23 (2022) 8547.","mla":"Hanke, Marcel, et al. “Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate.” International Journal of Molecular Sciences, vol. 23, no. 15, MDPI AG, 2022, p. 8547, doi:10.3390/ijms23158547.","apa":"Hanke, M., Hansen, N., Tomm, E., Grundmeier, G., & Keller, A. (2022). Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate. International Journal of Molecular Sciences, 23(15), 8547. https://doi.org/10.3390/ijms23158547","ama":"Hanke M, Hansen N, Tomm E, Grundmeier G, Keller A. Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate. International Journal of Molecular Sciences. 2022;23(15):8547. doi:10.3390/ijms23158547","ieee":"M. Hanke, N. Hansen, E. Tomm, G. Grundmeier, and A. Keller, “Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate,” International Journal of Molecular Sciences, vol. 23, no. 15, p. 8547, 2022, doi: 10.3390/ijms23158547.","chicago":"Hanke, Marcel, Niklas Hansen, Emilia Tomm, Guido Grundmeier, and Adrian Keller. “Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate.” International Journal of Molecular Sciences 23, no. 15 (2022): 8547. https://doi.org/10.3390/ijms23158547."},"page":"8547","intvolume":" 23","publisher":"MDPI AG","date_updated":"2022-08-08T06:40:14Z","date_created":"2022-08-08T06:39:20Z","author":[{"last_name":"Hanke","full_name":"Hanke, Marcel","first_name":"Marcel"},{"full_name":"Hansen, Niklas","last_name":"Hansen","first_name":"Niklas"},{"full_name":"Tomm, Emilia","last_name":"Tomm","first_name":"Emilia"},{"last_name":"Grundmeier","id":"194","full_name":"Grundmeier, Guido","first_name":"Guido"},{"first_name":"Adrian","id":"48864","full_name":"Keller, Adrian","orcid":"0000-0001-7139-3110","last_name":"Keller"}],"volume":23,"title":"Time-Dependent DNA Origami Denaturation by Guanidinium Chloride, Guanidinium Sulfate, and Guanidinium Thiocyanate","doi":"10.3390/ijms23158547","type":"journal_article","publication":"International Journal of Molecular Sciences","abstract":[{"lang":"eng","text":"Guanidinium (Gdm) undergoes interactions with both hydrophilic and hydrophobic groups and, thus, is a highly potent denaturant of biomolecular structure. However, our molecular understanding of the interaction of Gdm with proteins and DNA is still rather limited. Here, we investigated the denaturation of DNA origami nanostructures by three Gdm salts, i.e., guanidinium chloride (GdmCl), guanidinium sulfate (Gdm2SO4), and guanidinium thiocyanate (GdmSCN), at different temperatures and in dependence of incubation time. Using DNA origami nanostructures as sensors that translate small molecular transitions into nanostructural changes, the denaturing effects of the Gdm salts were directly visualized by atomic force microscopy. GdmSCN was the most potent DNA denaturant, which caused complete DNA origami denaturation at 50 °C already at a concentration of 2 M. Under such harsh conditions, denaturation occurred within the first 15 min of Gdm exposure, whereas much slower kinetics were observed for the more weakly denaturing salt Gdm2SO4 at 25 °C. Lastly, we observed a novel non-monotonous temperature dependence of DNA origami denaturation in Gdm2SO4 with the fraction of intact nanostructures having an intermediate minimum at about 40 °C. Our results, thus, provide further insights into the highly complex Gdm–DNA interaction and underscore the importance of the counteranion species."}],"status":"public","_id":"32589","user_id":"48864","department":[{"_id":"302"}],"keyword":["Inorganic Chemistry","Organic Chemistry","Physical and Theoretical Chemistry","Computer Science Applications","Spectroscopy","Molecular Biology","General Medicine","Catalysis"],"language":[{"iso":"eng"}]},{"publication":"ACS Applied Polymer Materials","abstract":[{"lang":"eng","text":"Poly(quinuclidin-3-yl methacrylate-co-divinylbenzene) microparticles having porous as well as nonporous morphology and varying contents of quinuclidine functionality were synthesized by distillation–precipitation polymerization. Further, the synthesized microparticles were explored to catalyze the Baylis–Hillman reaction between 4-nitrobenzaldehyde and acrylonitrile. Porous and nonporous microparticles functionalized with a catalytic moiety with a loading of 70% (labeled as P70 and NP70) were employed to optimize reaction parameters such as water content, solvent, and temperature for the Baylis–Hillman reaction between 4-nitrobenzaldehyde and acrylonitrile. Using optimal conditions, the catalytic efficiency of porous and nonporous microparticles at different feed compositions was determined. Porous microparticles containing 70% of quinuclidine (P70) displayed 100% conversion within 16 h at 50 °C, while nonporous microparticles containing 70% of quinuclidine (NP70) displayed a relatively less catalytic conversion, which is attributed to their lower surface area. Furthermore, the catalytic activity of porous microparticles containing 70% of quinuclidine (P70) for the Baylis–Hillman reaction involving a variety of aryl aldehyde derivatives was determined, where the microparticles displayed impressive catalytic efficiency. In addition, the reusability of the microparticles functionalized with a catalytic moiety was evaluated for five cycles of catalytic reaction."}],"keyword":["distillation−precipitation polymerization","porous microparticles","heterogeneous catalysis Baylis−Hillman reaction","reusable catalyst"],"language":[{"iso":"eng"}],"issue":"12","year":"2022","publisher":"American Chemical Society (ACS)","date_created":"2023-01-10T08:07:12Z","title":"Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction","type":"journal_article","status":"public","_id":"35645","user_id":"94","department":[{"_id":"163"}],"article_type":"original","publication_status":"published","publication_identifier":{"issn":["2637-6105","2637-6105"]},"citation":{"ama":"Kumar A, Kuckling D, Nebhani L. Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction. ACS Applied Polymer Materials. 2022;4(12):8996-9005. doi:10.1021/acsapm.2c01330","ieee":"A. Kumar, D. Kuckling, and L. Nebhani, “Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction,” ACS Applied Polymer Materials, vol. 4, no. 12, pp. 8996–9005, 2022, doi: 10.1021/acsapm.2c01330.","chicago":"Kumar, Amit, Dirk Kuckling, and Leena Nebhani. “Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction.” ACS Applied Polymer Materials 4, no. 12 (2022): 8996–9005. https://doi.org/10.1021/acsapm.2c01330.","mla":"Kumar, Amit, et al. “Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction.” ACS Applied Polymer Materials, vol. 4, no. 12, American Chemical Society (ACS), 2022, pp. 8996–9005, doi:10.1021/acsapm.2c01330.","short":"A. Kumar, D. Kuckling, L. Nebhani, ACS Applied Polymer Materials 4 (2022) 8996–9005.","bibtex":"@article{Kumar_Kuckling_Nebhani_2022, title={Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction}, volume={4}, DOI={10.1021/acsapm.2c01330}, number={12}, journal={ACS Applied Polymer Materials}, publisher={American Chemical Society (ACS)}, author={Kumar, Amit and Kuckling, Dirk and Nebhani, Leena}, year={2022}, pages={8996–9005} }","apa":"Kumar, A., Kuckling, D., & Nebhani, L. (2022). Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction. ACS Applied Polymer Materials, 4(12), 8996–9005. https://doi.org/10.1021/acsapm.2c01330"},"page":"8996-9005","intvolume":" 4","date_updated":"2023-01-10T08:12:15Z","author":[{"first_name":"Amit","full_name":"Kumar, Amit","last_name":"Kumar"},{"first_name":"Dirk","last_name":"Kuckling","full_name":"Kuckling, Dirk","id":"287"},{"first_name":"Leena","last_name":"Nebhani","full_name":"Nebhani, Leena"}],"volume":4,"main_file_link":[{"url":"https://pubs.acs.org/doi/10.1021/acsapm.2c01330"}],"doi":"10.1021/acsapm.2c01330"},{"publication":"ChemCatChem","type":"journal_article","status":"public","abstract":[{"lang":"eng","text":"Increasing the metal-to-ligand charge transfer (MLCT) excited state lifetime of polypyridine iron(II) complexes can be achieved by lowering the ligand's π* orbital energy and by increasing the ligand field splitting. In the homo- and heteroleptic complexes [Fe(cpmp)2]2+ (12+) and [Fe(cpmp)(ddpd)]2+ (22+) with the tridentate ligands 6,2’’-carboxypyridyl-2,2’-methylamine-pyridyl-pyridine (cpmp) and N,N’-dimethyl-N,N’-di-pyridin-2-ylpyridine-2,6-diamine (ddpd) two or one dipyridyl ketone moieties provide low energy π* acceptor orbitals. A good metal-ligand orbital overlap to increase the ligand field splitting is achieved by optimizing the octahedricity through CO and NMe units between the coordinating pyridines which enable the formation of six-membered chelate rings. The push-pull ligand cpmp provides intra-ligand and ligand-to-ligand charge transfer (ILCT, LL'CT) excited states in addition to MLCT excited states. Ground and excited state properties of 12+ and 22+ were accessed by X-ray diffraction analyses, resonance Raman spectroscopy, (spectro)electrochemistry, EPR spectroscopy, X-ray emission spectroscopy, static and time-resolved IR and UV/Vis/NIR absorption spectroscopy as well as quantum chemical calculations."}],"department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","_id":"40988","language":[{"iso":"eng"}],"keyword":["Inorganic Chemistry","Organic Chemistry","Physical and Theoretical Chemistry","Catalysis"],"issue":"8","publication_identifier":{"issn":["1867-3880","1867-3899"]},"publication_status":"published","intvolume":" 14","citation":{"ama":"Weber S, Zimmermann RT, Bremer J, et al. Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3 Reference Catalyst for CO2 Methanation. ChemCatChem. 2022;14(8). doi:10.1002/cctc.202101878","ieee":"S. Weber et al., “Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3 Reference Catalyst for CO2 Methanation,” ChemCatChem, vol. 14, no. 8, 2022, doi: 10.1002/cctc.202101878.","chicago":"Weber, Sebastian, Ronny T. Zimmermann, Jens Bremer, Ken L. Abel, David Poppitz, Nils Prinz, Jan Ilsemann, et al. “Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3 Reference Catalyst for CO2 Methanation.” ChemCatChem 14, no. 8 (2022). https://doi.org/10.1002/cctc.202101878.","apa":"Weber, S., Zimmermann, R. T., Bremer, J., Abel, K. L., Poppitz, D., Prinz, N., Ilsemann, J., Wendholt, S., Yang, Q., Pashminehazar, R., Monaco, F., Cloetens, P., Huang, X., Kübel, C., Kondratenko, E., Bauer, M., Bäumer, M., Zobel, M., Gläser, R., … Sheppard, T. L. (2022). Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3 Reference Catalyst for CO2 Methanation. ChemCatChem, 14(8). https://doi.org/10.1002/cctc.202101878","mla":"Weber, Sebastian, et al. “Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3 Reference Catalyst for CO2 Methanation.” ChemCatChem, vol. 14, no. 8, Wiley, 2022, doi:10.1002/cctc.202101878.","short":"S. Weber, R.T. Zimmermann, J. Bremer, K.L. Abel, D. Poppitz, N. Prinz, J. Ilsemann, S. Wendholt, Q. Yang, R. Pashminehazar, F. Monaco, P. Cloetens, X. Huang, C. Kübel, E. Kondratenko, M. Bauer, M. Bäumer, M. Zobel, R. Gläser, K. Sundmacher, T.L. Sheppard, ChemCatChem 14 (2022).","bibtex":"@article{Weber_Zimmermann_Bremer_Abel_Poppitz_Prinz_Ilsemann_Wendholt_Yang_Pashminehazar_et al._2022, title={Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3 Reference Catalyst for CO2 Methanation}, volume={14}, DOI={10.1002/cctc.202101878}, number={8}, journal={ChemCatChem}, publisher={Wiley}, author={Weber, Sebastian and Zimmermann, Ronny T. and Bremer, Jens and Abel, Ken L. and Poppitz, David and Prinz, Nils and Ilsemann, Jan and Wendholt, Sven and Yang, Qingxin and Pashminehazar, Reihaneh and et al.}, year={2022} }"},"year":"2022","volume":14,"author":[{"last_name":"Weber","full_name":"Weber, Sebastian","first_name":"Sebastian"},{"last_name":"Zimmermann","full_name":"Zimmermann, Ronny T.","first_name":"Ronny T."},{"last_name":"Bremer","full_name":"Bremer, Jens","first_name":"Jens"},{"first_name":"Ken L.","last_name":"Abel","full_name":"Abel, Ken L."},{"full_name":"Poppitz, David","last_name":"Poppitz","first_name":"David"},{"first_name":"Nils","full_name":"Prinz, Nils","last_name":"Prinz"},{"last_name":"Ilsemann","full_name":"Ilsemann, Jan","first_name":"Jan"},{"full_name":"Wendholt, Sven","last_name":"Wendholt","first_name":"Sven"},{"full_name":"Yang, Qingxin","last_name":"Yang","first_name":"Qingxin"},{"first_name":"Reihaneh","full_name":"Pashminehazar, Reihaneh","last_name":"Pashminehazar"},{"last_name":"Monaco","full_name":"Monaco, Federico","first_name":"Federico"},{"last_name":"Cloetens","full_name":"Cloetens, Peter","first_name":"Peter"},{"first_name":"Xiaohui","full_name":"Huang, Xiaohui","last_name":"Huang"},{"first_name":"Christian","last_name":"Kübel","full_name":"Kübel, Christian"},{"full_name":"Kondratenko, Evgenii","last_name":"Kondratenko","first_name":"Evgenii"},{"first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","full_name":"Bauer, Matthias","id":"47241"},{"first_name":"Marcus","last_name":"Bäumer","full_name":"Bäumer, Marcus"},{"last_name":"Zobel","full_name":"Zobel, Mirijam","first_name":"Mirijam"},{"last_name":"Gläser","full_name":"Gläser, Roger","first_name":"Roger"},{"last_name":"Sundmacher","full_name":"Sundmacher, Kai","first_name":"Kai"},{"last_name":"Sheppard","full_name":"Sheppard, Thomas L.","first_name":"Thomas L."}],"date_created":"2023-01-30T16:25:02Z","publisher":"Wiley","date_updated":"2024-05-08T13:03:51Z","doi":"10.1002/cctc.202101878","title":"Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3 Reference Catalyst for CO2 Methanation"},{"keyword":["General Chemistry","Catalysis","Organic Chemistry"],"language":[{"iso":"eng"}],"_id":"35703","user_id":"53339","department":[{"_id":"2"},{"_id":"389"}],"status":"public","type":"journal_article","publication":"Chemistry – A European Journal","title":"Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022)","doi":"10.1002/chem.202200982","publisher":"Wiley","date_updated":"2023-01-23T12:47:43Z","author":[{"last_name":"Hou","full_name":"Hou, Peng","first_name":"Peng"},{"last_name":"Peschtrich","full_name":"Peschtrich, Sebastian","first_name":"Sebastian"},{"first_name":"Nils","full_name":"Huber, Nils","last_name":"Huber"},{"full_name":"Feuerstein, Wolfram","last_name":"Feuerstein","first_name":"Wolfram"},{"full_name":"Bihlmeier, Angela","last_name":"Bihlmeier","first_name":"Angela"},{"full_name":"Krummenacher, Ivo","last_name":"Krummenacher","first_name":"Ivo"},{"first_name":"Roland","last_name":"Schoch","full_name":"Schoch, Roland"},{"first_name":"Wim","full_name":"Klopper, Wim","last_name":"Klopper"},{"last_name":"Breher","full_name":"Breher, Frank","first_name":"Frank"},{"last_name":"Paradies","orcid":"0000-0002-3698-668X","id":"53339","full_name":"Paradies, Jan","first_name":"Jan"}],"date_created":"2023-01-10T09:10:15Z","volume":28,"year":"2022","citation":{"ama":"Hou P, Peschtrich S, Huber N, et al. Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022). Chemistry – A European Journal. 2022;28(23). doi:10.1002/chem.202200982","ieee":"P. Hou et al., “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022),” Chemistry – A European Journal, vol. 28, no. 23, 2022, doi: 10.1002/chem.202200982.","chicago":"Hou, Peng, Sebastian Peschtrich, Nils Huber, Wolfram Feuerstein, Angela Bihlmeier, Ivo Krummenacher, Roland Schoch, Wim Klopper, Frank Breher, and Jan Paradies. “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022).” Chemistry – A European Journal 28, no. 23 (2022). https://doi.org/10.1002/chem.202200982.","bibtex":"@article{Hou_Peschtrich_Huber_Feuerstein_Bihlmeier_Krummenacher_Schoch_Klopper_Breher_Paradies_2022, title={Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022)}, volume={28}, DOI={10.1002/chem.202200982}, number={23}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Hou, Peng and Peschtrich, Sebastian and Huber, Nils and Feuerstein, Wolfram and Bihlmeier, Angela and Krummenacher, Ivo and Schoch, Roland and Klopper, Wim and Breher, Frank and Paradies, Jan}, year={2022} }","short":"P. Hou, S. Peschtrich, N. Huber, W. Feuerstein, A. Bihlmeier, I. Krummenacher, R. Schoch, W. Klopper, F. Breher, J. Paradies, Chemistry – A European Journal 28 (2022).","mla":"Hou, Peng, et al. “Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022).” Chemistry – A European Journal, vol. 28, no. 23, Wiley, 2022, doi:10.1002/chem.202200982.","apa":"Hou, P., Peschtrich, S., Huber, N., Feuerstein, W., Bihlmeier, A., Krummenacher, I., Schoch, R., Klopper, W., Breher, F., & Paradies, J. (2022). Cover Feature: Impact of Heterocycle Annulation on NIR Absorbance in Quinoid Thioacene Derivatives (Chem. Eur. J. 23/2022). 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(2022). Pseudo‐Octahedral Iron(II) Complexes with Near‐Degenerate Charge Transfer and Ligand Field States at the Franck‐Condon Geometry. Chemistry – A European Journal, 28(57). https://doi.org/10.1002/chem.202201858","short":"J. Moll, R. Naumann, L. Sorge, C. Förster, N. Gessner, L. Burkhardt, N. Ugur, P. Nuernberger, W. Seidel, C. Ramanan, M. Bauer, K. Heinze, Chemistry – A European Journal 28 (2022).","bibtex":"@article{Moll_Naumann_Sorge_Förster_Gessner_Burkhardt_Ugur_Nuernberger_Seidel_Ramanan_et al._2022, title={Pseudo‐Octahedral Iron(II) Complexes with Near‐Degenerate Charge Transfer and Ligand Field States at the Franck‐Condon Geometry}, volume={28}, DOI={10.1002/chem.202201858}, number={57}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Moll, Johannes and Naumann, Robert and Sorge, Lukas and Förster, Christoph and Gessner, Niklas and Burkhardt, Lukas and Ugur, Naz and Nuernberger, Patrick and Seidel, Wolfram and Ramanan, Charusheela and et al.}, year={2022} }","mla":"Moll, Johannes, et al. “Pseudo‐Octahedral Iron(II) Complexes with Near‐Degenerate Charge Transfer and Ligand Field States at the Franck‐Condon Geometry.” Chemistry – A European Journal, vol. 28, no. 57, Wiley, 2022, doi:10.1002/chem.202201858.","ama":"Moll J, Naumann R, Sorge L, et al. Pseudo‐Octahedral Iron(II) Complexes with Near‐Degenerate Charge Transfer and Ligand Field States at the Franck‐Condon Geometry. Chemistry – A European Journal. 2022;28(57). doi:10.1002/chem.202201858","chicago":"Moll, Johannes, Robert Naumann, Lukas Sorge, Christoph Förster, Niklas Gessner, Lukas Burkhardt, Naz Ugur, et al. “Pseudo‐Octahedral Iron(II) Complexes with Near‐Degenerate Charge Transfer and Ligand Field States at the Franck‐Condon Geometry.” Chemistry – A European Journal 28, no. 57 (2022). https://doi.org/10.1002/chem.202201858.","ieee":"J. Moll et al., “Pseudo‐Octahedral Iron(II) Complexes with Near‐Degenerate Charge Transfer and Ligand Field States at the Franck‐Condon Geometry,” Chemistry – A European Journal, vol. 28, no. 57, 2022, doi: 10.1002/chem.202201858."},"_id":"40985","department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","keyword":["General Chemistry","Catalysis","Organic Chemistry"],"language":[{"iso":"eng"}],"publication":"Chemistry – A European Journal","type":"journal_article","status":"public"},{"publication_identifier":{"issn":["1867-3880","1867-3899"]},"publication_status":"published","issue":"8","year":"2022","intvolume":" 14","citation":{"mla":"Weber, Sebastian, et al. “Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3Reference Catalyst for CO2Methanation.” ChemCatChem, vol. 14, no. 8, Wiley, 2022, doi:10.1002/cctc.202101878.","bibtex":"@article{Weber_Zimmermann_Bremer_Abel_Poppitz_Prinz_Ilsemann_Strübbe_Yang_Pashminehazar_et al._2022, title={Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3Reference Catalyst for CO2Methanation}, volume={14}, DOI={10.1002/cctc.202101878}, number={8}, journal={ChemCatChem}, publisher={Wiley}, author={Weber, Sebastian and Zimmermann, Ronny T. and Bremer, Jens and Abel, Ken L. and Poppitz, David and Prinz, Nils and Ilsemann, Jan and Strübbe, Sven and Yang, Qingxin and Pashminehazar, Reihaneh and et al.}, year={2022} }","short":"S. Weber, R.T. Zimmermann, J. Bremer, K.L. Abel, D. Poppitz, N. Prinz, J. Ilsemann, S. Strübbe, Q. Yang, R. Pashminehazar, F. Monaco, P. Cloetens, X. Huang, C. Kübel, E. Kondratenko, M. Bauer, M. Bäumer, M. Zobel, R. Gläser, K. Sundmacher, T.L. Sheppard, ChemCatChem 14 (2022).","apa":"Weber, S., Zimmermann, R. T., Bremer, J., Abel, K. L., Poppitz, D., Prinz, N., Ilsemann, J., Strübbe, S., Yang, Q., Pashminehazar, R., Monaco, F., Cloetens, P., Huang, X., Kübel, C., Kondratenko, E., Bauer, M., Bäumer, M., Zobel, M., Gläser, R., … Sheppard, T. L. (2022). Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3Reference Catalyst for CO2Methanation. ChemCatChem, 14(8). https://doi.org/10.1002/cctc.202101878","ama":"Weber S, Zimmermann RT, Bremer J, et al. Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3Reference Catalyst for CO2Methanation. ChemCatChem. 2022;14(8). doi:10.1002/cctc.202101878","chicago":"Weber, Sebastian, Ronny T. Zimmermann, Jens Bremer, Ken L. Abel, David Poppitz, Nils Prinz, Jan Ilsemann, et al. “Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3Reference Catalyst for CO2Methanation.” ChemCatChem 14, no. 8 (2022). https://doi.org/10.1002/cctc.202101878.","ieee":"S. Weber et al., “Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3Reference Catalyst for CO2Methanation,” ChemCatChem, vol. 14, no. 8, 2022, doi: 10.1002/cctc.202101878."},"date_updated":"2023-01-31T14:05:50Z","publisher":"Wiley","volume":14,"date_created":"2023-01-31T14:04:55Z","author":[{"first_name":"Sebastian","last_name":"Weber","full_name":"Weber, Sebastian"},{"first_name":"Ronny T.","last_name":"Zimmermann","full_name":"Zimmermann, Ronny T."},{"first_name":"Jens","last_name":"Bremer","full_name":"Bremer, Jens"},{"first_name":"Ken L.","full_name":"Abel, Ken L.","last_name":"Abel"},{"first_name":"David","last_name":"Poppitz","full_name":"Poppitz, David"},{"full_name":"Prinz, Nils","last_name":"Prinz","first_name":"Nils"},{"last_name":"Ilsemann","full_name":"Ilsemann, Jan","first_name":"Jan"},{"first_name":"Sven","id":"76968","full_name":"Strübbe, Sven","last_name":"Strübbe"},{"last_name":"Yang","full_name":"Yang, Qingxin","first_name":"Qingxin"},{"full_name":"Pashminehazar, Reihaneh","last_name":"Pashminehazar","first_name":"Reihaneh"},{"first_name":"Federico","full_name":"Monaco, Federico","last_name":"Monaco"},{"first_name":"Peter","last_name":"Cloetens","full_name":"Cloetens, Peter"},{"first_name":"Xiaohui","last_name":"Huang","full_name":"Huang, Xiaohui"},{"first_name":"Christian","full_name":"Kübel, Christian","last_name":"Kübel"},{"first_name":"Evgenii","full_name":"Kondratenko, Evgenii","last_name":"Kondratenko"},{"first_name":"Matthias","last_name":"Bauer","full_name":"Bauer, Matthias"},{"last_name":"Bäumer","full_name":"Bäumer, Marcus","first_name":"Marcus"},{"last_name":"Zobel","full_name":"Zobel, Mirijam","first_name":"Mirijam"},{"first_name":"Roger","last_name":"Gläser","full_name":"Gläser, Roger"},{"full_name":"Sundmacher, Kai","last_name":"Sundmacher","first_name":"Kai"},{"first_name":"Thomas L.","full_name":"Sheppard, Thomas L.","last_name":"Sheppard"}],"title":"Digitization in Catalysis Research: Towards a Holistic Description of a Ni/Al2O3Reference Catalyst for CO2Methanation","doi":"10.1002/cctc.202101878","publication":"ChemCatChem","type":"journal_article","status":"public","_id":"41208","user_id":"76968","keyword":["Inorganic Chemistry","Organic Chemistry","Physical and Theoretical Chemistry","Catalysis"],"language":[{"iso":"eng"}]},{"citation":{"ama":"Schlicher S, Prinz N, Bürger J, et al. Quality or Quantity? How Structural Parameters Affect Catalytic Activity of Iron Oxides for CO Oxidation. Catalysts. 2022;12(6). doi:10.3390/catal12060675","ieee":"S. Schlicher et al., “Quality or Quantity? How Structural Parameters Affect Catalytic Activity of Iron Oxides for CO Oxidation,” Catalysts, vol. 12, no. 6, Art. no. 675, 2022, doi: 10.3390/catal12060675.","chicago":"Schlicher, Steffen, Nils Prinz, Julius Bürger, Andreas Omlor, Christian Singer, Mirijam Zobel, Roland Schoch, et al. “Quality or Quantity? How Structural Parameters Affect Catalytic Activity of Iron Oxides for CO Oxidation.” Catalysts 12, no. 6 (2022). https://doi.org/10.3390/catal12060675.","apa":"Schlicher, S., Prinz, N., Bürger, J., Omlor, A., Singer, C., Zobel, M., Schoch, R., Lindner, J. K. N., Schünemann, V., Kureti, S., & Bauer, M. (2022). Quality or Quantity? How Structural Parameters Affect Catalytic Activity of Iron Oxides for CO Oxidation. Catalysts, 12(6), Article 675. https://doi.org/10.3390/catal12060675","bibtex":"@article{Schlicher_Prinz_Bürger_Omlor_Singer_Zobel_Schoch_Lindner_Schünemann_Kureti_et al._2022, title={Quality or Quantity? How Structural Parameters Affect Catalytic Activity of Iron Oxides for CO Oxidation}, volume={12}, DOI={10.3390/catal12060675}, number={6675}, journal={Catalysts}, publisher={MDPI AG}, author={Schlicher, Steffen and Prinz, Nils and Bürger, Julius and Omlor, Andreas and Singer, Christian and Zobel, Mirijam and Schoch, Roland and Lindner, Jörg K. N. and Schünemann, Volker and Kureti, Sven and et al.}, year={2022} }","short":"S. Schlicher, N. Prinz, J. Bürger, A. Omlor, C. Singer, M. Zobel, R. Schoch, J.K.N. Lindner, V. Schünemann, S. Kureti, M. Bauer, Catalysts 12 (2022).","mla":"Schlicher, Steffen, et al. “Quality or Quantity? How Structural Parameters Affect Catalytic Activity of Iron Oxides for CO Oxidation.” Catalysts, vol. 12, no. 6, 675, MDPI AG, 2022, doi:10.3390/catal12060675."},"intvolume":" 12","publication_status":"published","publication_identifier":{"issn":["2073-4344"]},"doi":"10.3390/catal12060675","author":[{"first_name":"Steffen","last_name":"Schlicher","full_name":"Schlicher, Steffen"},{"last_name":"Prinz","full_name":"Prinz, Nils","first_name":"Nils"},{"full_name":"Bürger, Julius","id":"46952","last_name":"Bürger","first_name":"Julius"},{"last_name":"Omlor","full_name":"Omlor, Andreas","first_name":"Andreas"},{"full_name":"Singer, Christian","last_name":"Singer","first_name":"Christian"},{"first_name":"Mirijam","full_name":"Zobel, Mirijam","last_name":"Zobel"},{"first_name":"Roland","full_name":"Schoch, Roland","id":"48467","last_name":"Schoch","orcid":"0000-0003-2061-7289"},{"full_name":"Lindner, Jörg K. N.","id":"20797","last_name":"Lindner","first_name":"Jörg K. N."},{"first_name":"Volker","full_name":"Schünemann, Volker","last_name":"Schünemann"},{"first_name":"Sven","last_name":"Kureti","full_name":"Kureti, Sven"},{"orcid":"0000-0002-9294-6076","last_name":"Bauer","id":"47241","full_name":"Bauer, Matthias","first_name":"Matthias"}],"volume":12,"date_updated":"2023-08-17T06:57:31Z","status":"public","type":"journal_article","article_number":"675","user_id":"14931","department":[{"_id":"35"},{"_id":"306"},{"_id":"15"}],"_id":"40987","year":"2022","issue":"6","title":"Quality or Quantity? How Structural Parameters Affect Catalytic Activity of Iron Oxides for CO Oxidation","date_created":"2023-01-30T16:24:41Z","publisher":"MDPI AG","abstract":[{"text":"et al., “Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids,” Angewandte Chemie International Edition, vol. 60, no. 28, pp. 15371–15375, 2021, doi: 10.1002/anie.202103215.","chicago":"Gurinov, Andrei, Benedikt Sieland, Andrey Kuzhelev, Hossam Elgabarty, Thomas Kühne, Thomas Prisner, Jan Paradies, Marc Baldus, Konstantin L. Ivanov, and Svetlana Pylaeva. “Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids.” Angewandte Chemie International Edition 60, no. 28 (2021): 15371–75. https://doi.org/10.1002/anie.202103215.","ama":"Gurinov A, Sieland B, Kuzhelev A, et al. Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids. Angewandte Chemie International Edition. 2021;60(28):15371-15375. doi:10.1002/anie.202103215","bibtex":"@article{Gurinov_Sieland_Kuzhelev_Elgabarty_Kühne_Prisner_Paradies_Baldus_Ivanov_Pylaeva_2021, title={Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids}, volume={60}, DOI={10.1002/anie.202103215}, number={28}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Gurinov, Andrei and Sieland, Benedikt and Kuzhelev, Andrey and Elgabarty, Hossam and Kühne, Thomas and Prisner, Thomas and Paradies, Jan and Baldus, Marc and Ivanov, Konstantin L. and Pylaeva, Svetlana}, year={2021}, pages={15371–15375} }","mla":"Gurinov, Andrei, et al. “Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids.” Angewandte Chemie International Edition, vol. 60, no. 28, Wiley, 2021, pp. 15371–75, doi:10.1002/anie.202103215.","short":"A. Gurinov, B. Sieland, A. Kuzhelev, H. Elgabarty, T. Kühne, T. Prisner, J. Paradies, M. Baldus, K.L. Ivanov, S. Pylaeva, Angewandte Chemie International Edition 60 (2021) 15371–15375.","apa":"Gurinov, A., Sieland, B., Kuzhelev, A., Elgabarty, H., Kühne, T., Prisner, T., Paradies, J., Baldus, M., Ivanov, K. L., & Pylaeva, S. (2021). Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids. Angewandte Chemie International Edition, 60(28), 15371–15375. https://doi.org/10.1002/anie.202103215"},"_id":"33653","department":[{"_id":"613"}],"user_id":"60250","keyword":["General Chemistry","Catalysis"],"language":[{"iso":"eng"}],"publication":"Angewandte Chemie International Edition","type":"journal_article","status":"public"},{"publication_identifier":{"issn":["0926-3373"]},"publication_status":"published","year":"2021","intvolume":" 304","citation":{"apa":"da Silva, M. A. R., Silva, I. F., Xue, Q., Lo, B. T. W., Tarakina, N. V., Nunes, B. N., Adler, P., Sahoo, S. K., Bahnemann, D. W., López-Salas, N., Savateev, A., Ribeiro, C., Kühne, T., Antonietti, M., & Teixeira, I. F. (2021). Sustainable oxidation catalysis supported by light: Fe-poly (heptazine imide) as a heterogeneous single-atom photocatalyst. Applied Catalysis B: Environmental, 304, Article 120965. https://doi.org/10.1016/j.apcatb.2021.120965","bibtex":"@article{da Silva_Silva_Xue_Lo_Tarakina_Nunes_Adler_Sahoo_Bahnemann_López-Salas_et al._2021, title={Sustainable oxidation catalysis supported by light: Fe-poly (heptazine imide) as a heterogeneous single-atom photocatalyst}, volume={304}, DOI={10.1016/j.apcatb.2021.120965}, number={120965}, journal={Applied Catalysis B: Environmental}, publisher={Elsevier BV}, author={da Silva, Marcos A.R. and Silva, Ingrid F. and Xue, Qi and Lo, Benedict T.W. and Tarakina, Nadezda V. and Nunes, Barbara N. and Adler, Peter and Sahoo, Sudhir K. and Bahnemann, Detlef W. and López-Salas, Nieves and et al.}, year={2021} }","mla":"da Silva, Marcos A. R., et al. “Sustainable Oxidation Catalysis Supported by Light: Fe-Poly (Heptazine Imide) as a Heterogeneous Single-Atom Photocatalyst.” Applied Catalysis B: Environmental, vol. 304, 120965, Elsevier BV, 2021, doi:10.1016/j.apcatb.2021.120965.","short":"M.A.R. da Silva, I.F. Silva, Q. Xue, B.T.W. Lo, N.V. Tarakina, B.N. Nunes, P. Adler, S.K. Sahoo, D.W. Bahnemann, N. López-Salas, A. Savateev, C. Ribeiro, T. Kühne, M. Antonietti, I.F. Teixeira, Applied Catalysis B: Environmental 304 (2021).","ama":"da Silva MAR, Silva IF, Xue Q, et al. Sustainable oxidation catalysis supported by light: Fe-poly (heptazine imide) as a heterogeneous single-atom photocatalyst. Applied Catalysis B: Environmental. 2021;304. doi:10.1016/j.apcatb.2021.120965","ieee":"M. A. R. da Silva et al., “Sustainable oxidation catalysis supported by light: Fe-poly (heptazine imide) as a heterogeneous single-atom photocatalyst,” Applied Catalysis B: Environmental, vol. 304, Art. no. 120965, 2021, doi: 10.1016/j.apcatb.2021.120965.","chicago":"Silva, Marcos A.R. da, Ingrid F. Silva, Qi Xue, Benedict T.W. Lo, Nadezda V. Tarakina, Barbara N. Nunes, Peter Adler, et al. “Sustainable Oxidation Catalysis Supported by Light: Fe-Poly (Heptazine Imide) as a Heterogeneous Single-Atom Photocatalyst.” Applied Catalysis B: Environmental 304 (2021). https://doi.org/10.1016/j.apcatb.2021.120965."},"date_updated":"2022-10-11T08:14:47Z","publisher":"Elsevier BV","volume":304,"author":[{"first_name":"Marcos A.R.","full_name":"da Silva, Marcos A.R.","last_name":"da Silva"},{"full_name":"Silva, Ingrid F.","last_name":"Silva","first_name":"Ingrid F."},{"first_name":"Qi","full_name":"Xue, Qi","last_name":"Xue"},{"full_name":"Lo, Benedict T.W.","last_name":"Lo","first_name":"Benedict T.W."},{"first_name":"Nadezda V.","last_name":"Tarakina","full_name":"Tarakina, Nadezda V."},{"last_name":"Nunes","full_name":"Nunes, Barbara N.","first_name":"Barbara N."},{"first_name":"Peter","full_name":"Adler, Peter","last_name":"Adler"},{"first_name":"Sudhir K.","full_name":"Sahoo, Sudhir K.","last_name":"Sahoo"},{"last_name":"Bahnemann","full_name":"Bahnemann, Detlef W.","first_name":"Detlef W."},{"first_name":"Nieves","full_name":"López-Salas, Nieves","last_name":"López-Salas"},{"last_name":"Savateev","full_name":"Savateev, Aleksandr","first_name":"Aleksandr"},{"first_name":"Caue","last_name":"Ribeiro","full_name":"Ribeiro, Caue"},{"first_name":"Thomas","id":"49079","full_name":"Kühne, Thomas","last_name":"Kühne"},{"full_name":"Antonietti, Markus","last_name":"Antonietti","first_name":"Markus"},{"full_name":"Teixeira, Ivo F.","last_name":"Teixeira","first_name":"Ivo F."}],"date_created":"2022-10-11T08:14:22Z","title":"Sustainable oxidation catalysis supported by light: Fe-poly (heptazine imide) as a heterogeneous single-atom photocatalyst","doi":"10.1016/j.apcatb.2021.120965","publication":"Applied Catalysis B: Environmental","type":"journal_article","status":"public","_id":"33681","department":[{"_id":"613"}],"user_id":"71051","keyword":["Process Chemistry and Technology","General Environmental Science","Catalysis"],"article_number":"120965","language":[{"iso":"eng"}]},{"publication_status":"published","publication_identifier":{"issn":["1433-7851","1521-3773"]},"citation":{"apa":"Jach, F., Wagner, F. R., Amber, Z. H., Rüsing, M., Hunger, J., Prots, Y., Kaiser, M., Bobnar, M., Jesche, A., Eng, L. M., Ruck, M., & Höhn, P. (2021). Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands. Angewandte Chemie International Edition, 60(29), 15879–15885. https://doi.org/10.1002/anie.202103268","mla":"Jach, Franziska, et al. “Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands.” Angewandte Chemie International Edition, vol. 60, no. 29, Wiley, 2021, pp. 15879–85, doi:10.1002/anie.202103268.","short":"F. Jach, F.R. Wagner, Z.H. Amber, M. Rüsing, J. Hunger, Y. Prots, M. Kaiser, M. Bobnar, A. Jesche, L.M. Eng, M. Ruck, P. Höhn, Angewandte Chemie International Edition 60 (2021) 15879–15885.","bibtex":"@article{Jach_Wagner_Amber_Rüsing_Hunger_Prots_Kaiser_Bobnar_Jesche_Eng_et al._2021, title={Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands}, volume={60}, DOI={10.1002/anie.202103268}, number={29}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Jach, Franziska and Wagner, Frank R. and Amber, Zeeshan H. and Rüsing, Michael and Hunger, Jens and Prots, Yurii and Kaiser, Martin and Bobnar, Matej and Jesche, Anton and Eng, Lukas M. and et al.}, year={2021}, pages={15879–15885} }","ieee":"F. Jach et al., “Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands,” Angewandte Chemie International Edition, vol. 60, no. 29, pp. 15879–15885, 2021, doi: 10.1002/anie.202103268.","chicago":"Jach, Franziska, Frank R. Wagner, Zeeshan H. Amber, Michael Rüsing, Jens Hunger, Yurii Prots, Martin Kaiser, et al. “Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands.” Angewandte Chemie International Edition 60, no. 29 (2021): 15879–85. https://doi.org/10.1002/anie.202103268.","ama":"Jach F, Wagner FR, Amber ZH, et al. Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands. Angewandte Chemie International Edition. 2021;60(29):15879-15885. doi:10.1002/anie.202103268"},"intvolume":" 60","page":"15879-15885","author":[{"first_name":"Franziska","last_name":"Jach","full_name":"Jach, Franziska"},{"first_name":"Frank R.","full_name":"Wagner, Frank R.","last_name":"Wagner"},{"first_name":"Zeeshan H.","full_name":"Amber, Zeeshan H.","last_name":"Amber"},{"first_name":"Michael","full_name":"Rüsing, Michael","id":"22501","orcid":"0000-0003-4682-4577","last_name":"Rüsing"},{"first_name":"Jens","full_name":"Hunger, Jens","last_name":"Hunger"},{"full_name":"Prots, Yurii","last_name":"Prots","first_name":"Yurii"},{"last_name":"Kaiser","full_name":"Kaiser, Martin","first_name":"Martin"},{"first_name":"Matej","full_name":"Bobnar, Matej","last_name":"Bobnar"},{"first_name":"Anton","last_name":"Jesche","full_name":"Jesche, Anton"},{"first_name":"Lukas M.","full_name":"Eng, Lukas M.","last_name":"Eng"},{"first_name":"Michael","full_name":"Ruck, Michael","last_name":"Ruck"},{"first_name":"Peter","full_name":"Höhn, Peter","last_name":"Höhn"}],"volume":60,"date_updated":"2023-10-11T08:24:32Z","doi":"10.1002/anie.202103268","type":"journal_article","status":"public","user_id":"22501","_id":"47965","extern":"1","article_type":"original","issue":"29","quality_controlled":"1","year":"2021","date_created":"2023-10-11T08:21:55Z","publisher":"Wiley","title":"Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands","publication":"Angewandte Chemie International Edition","abstract":[{"lang":"eng","text":"Exceptionally electron-rich, nearly trigonal-planar tricyanidometalate anions [Fe(CN)3]7− and [Ru(CN)3]7− were stabilized in LiSr3[Fe(CN)3] and AE3.5[M(CN)3] (AE=Sr, Ba; M=Fe, Ru). They are the first examples of group 8 elements with the oxidation state of −IV. Microcrystalline powders were obtained by a solid-state route, single crystals from alkali metal flux. While LiSr3[Fe(CN)3] crystallizes in P63/m, the polar space group P63 with three-fold cell volume for AE3.5[M(CN)3] is confirmed by second harmonic generation. X-ray diffraction, IR and Raman spectroscopy reveal longer C−N distances (124–128 pm) and much lower stretching frequencies (1484–1634 cm−1) than in classical cyanidometalates. Weak C−N bonds in combination with strong M−C π-bonding is a scheme also known for carbonylmetalates. Instead of the formal notation [Fe−IV(CN−)3]7−, quantum chemical calculations reveal non-innocent intermediate-valent CN1.67− ligands and a closed-shell d10 configuration for Fe, that is, Fe2−."}],"language":[{"iso":"eng"}],"keyword":["General Chemistry","Catalysis"]},{"publication_status":"published","publication_identifier":{"issn":["0947-6539","1521-3765"]},"citation":{"apa":"Albrecht, R., Hoelzel, M., Beccard, H., Rüsing, M., Eng, L., Doert, T., & Ruck, M. (2021). Potassium Ion Conductivity in the Cubic Labyrinth of a Piezoelectric, Antiferromagnetic Oxoferrate(III) Tellurate(VI). Chemistry – A European Journal, 27(57), 14299–14306. https://doi.org/10.1002/chem.202102464","ama":"Albrecht R, Hoelzel M, Beccard H, et al. Potassium Ion Conductivity in the Cubic Labyrinth of a Piezoelectric, Antiferromagnetic Oxoferrate(III) Tellurate(VI). Chemistry – A European Journal. 2021;27(57):14299-14306. doi:10.1002/chem.202102464","mla":"Albrecht, Ralf, et al. “Potassium Ion Conductivity in the Cubic Labyrinth of a Piezoelectric, Antiferromagnetic Oxoferrate(III) Tellurate(VI).” Chemistry – A European Journal, vol. 27, no. 57, Wiley, 2021, pp. 14299–306, doi:10.1002/chem.202102464.","short":"R. Albrecht, M. Hoelzel, H. Beccard, M. Rüsing, L. Eng, T. Doert, M. Ruck, Chemistry – A European Journal 27 (2021) 14299–14306.","bibtex":"@article{Albrecht_Hoelzel_Beccard_Rüsing_Eng_Doert_Ruck_2021, title={Potassium Ion Conductivity in the Cubic Labyrinth of a Piezoelectric, Antiferromagnetic Oxoferrate(III) Tellurate(VI)}, volume={27}, DOI={10.1002/chem.202102464}, number={57}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Albrecht, Ralf and Hoelzel, Markus and Beccard, Henrik and Rüsing, Michael and Eng, Lukas and Doert, Thomas and Ruck, Michael}, year={2021}, pages={14299–14306} }","ieee":"R. Albrecht et al., “Potassium Ion Conductivity in the Cubic Labyrinth of a Piezoelectric, Antiferromagnetic Oxoferrate(III) Tellurate(VI),” Chemistry – A European Journal, vol. 27, no. 57, pp. 14299–14306, 2021, doi: 10.1002/chem.202102464.","chicago":"Albrecht, Ralf, Markus Hoelzel, Henrik Beccard, Michael Rüsing, Lukas Eng, Thomas Doert, and Michael Ruck. “Potassium Ion Conductivity in the Cubic Labyrinth of a Piezoelectric, Antiferromagnetic Oxoferrate(III) Tellurate(VI).” Chemistry – A European Journal 27, no. 57 (2021): 14299–306. https://doi.org/10.1002/chem.202102464."},"page":"14299-14306","intvolume":" 27","date_updated":"2023-10-11T08:41:35Z","author":[{"first_name":"Ralf","full_name":"Albrecht, Ralf","last_name":"Albrecht"},{"first_name":"Markus","full_name":"Hoelzel, Markus","last_name":"Hoelzel"},{"first_name":"Henrik","full_name":"Beccard, Henrik","last_name":"Beccard"},{"id":"22501","full_name":"Rüsing, Michael","orcid":"0000-0003-4682-4577","last_name":"Rüsing","first_name":"Michael"},{"first_name":"Lukas","last_name":"Eng","full_name":"Eng, Lukas"},{"first_name":"Thomas","full_name":"Doert, Thomas","last_name":"Doert"},{"first_name":"Michael","full_name":"Ruck, Michael","last_name":"Ruck"}],"volume":27,"doi":"10.1002/chem.202102464","type":"journal_article","status":"public","_id":"47977","user_id":"22501","extern":"1","quality_controlled":"1","issue":"57","year":"2021","publisher":"Wiley","date_created":"2023-10-11T08:39:51Z","title":"Potassium Ion Conductivity in the Cubic Labyrinth of a Piezoelectric, Antiferromagnetic Oxoferrate(III) Tellurate(VI)","publication":"Chemistry – A European Journal","abstract":[{"text":"Orange-colored crystals of the oxoferrate tellurate K12+6xFe6Te4−xO27 [x=0.222(4)] were synthesized in a potassium hydroxide hydroflux with a molar water–base ratio n(H2O)/n(KOH) of 1.5 starting from Fe(NO3)3 ⋅ 9H2O, TeO2 and H2O2 at about 200 °C. By using (NH4)2TeO4 instead of TeO2, a fine powder consisting of microcrystalline spheres of K12+6xFe6Te4−xO27 was obtained. K12+6xFe6Te4−xO27 crystallizes in the acentric cubic space group Iurn:x-wiley:09476539:media:chem202102464:chem202102464-math-0001 3d. [FeIIIO5] pyramids share their apical atoms in [Fe2O9] groups and two of their edges with [TeVIO6] octahedra to form an open framework that consists of two loosely connected, but not interpenetrating, chiral networks. The flexibility of the hinged oxometalate network manifests in a piezoelectric response similar to that of LiNbO3.The potassium cations are mobile in channels that run along the <111> directions and cross in cavities acting as nodes. The ion conductivity of cold-pressed pellets of ball-milled K12+6xFe6Te4−xO27 is 2.3×10^(−4) S ⋅ cm^(−1) at room temperature. Magnetization measurements and neutron diffraction indicate antiferromagnetic coupling in the [Fe2O9] groups.","lang":"eng"}],"keyword":["General Chemistry","Catalysis","Organic Chemistry"],"language":[{"iso":"eng"}]},{"type":"journal_article","status":"public","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"_id":"41001","article_type":"original","publication_status":"published","publication_identifier":{"issn":["2155-5435","2155-5435"]},"citation":{"short":"F. Ziegler, H. Kraus, M.J. Benedikter, D. Wang, J.R. Bruckner, M. Nowakowski, K. Weißer, H. Solodenko, G. Schmitz, M. Bauer, N. Hansen, M.R. Buchmeiser, ACS Catalysis 11 (2021) 11570–11578.","mla":"Ziegler, Felix, et al. “Confinement Effects for Efficient Macrocyclization Reactions with Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes.” ACS Catalysis, vol. 11, no. 18, American Chemical Society (ACS), 2021, pp. 11570–78, doi:10.1021/acscatal.1c03057.","bibtex":"@article{Ziegler_Kraus_Benedikter_Wang_Bruckner_Nowakowski_Weißer_Solodenko_Schmitz_Bauer_et al._2021, title={Confinement Effects for Efficient Macrocyclization Reactions with Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes}, volume={11}, DOI={10.1021/acscatal.1c03057}, number={18}, journal={ACS Catalysis}, publisher={American Chemical Society (ACS)}, author={Ziegler, Felix and Kraus, Hamzeh and Benedikter, Mathis J. and Wang, Dongren and Bruckner, Johanna R. and Nowakowski, Michał and Weißer, Kilian and Solodenko, Helena and Schmitz, Guido and Bauer, Matthias and et al.}, year={2021}, pages={11570–11578} }","apa":"Ziegler, F., Kraus, H., Benedikter, M. J., Wang, D., Bruckner, J. R., Nowakowski, M., Weißer, K., Solodenko, H., Schmitz, G., Bauer, M., Hansen, N., & Buchmeiser, M. R. (2021). Confinement Effects for Efficient Macrocyclization Reactions with Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes. ACS Catalysis, 11(18), 11570–11578. https://doi.org/10.1021/acscatal.1c03057","ama":"Ziegler F, Kraus H, Benedikter MJ, et al. Confinement Effects for Efficient Macrocyclization Reactions with Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes. ACS Catalysis. 2021;11(18):11570-11578. doi:10.1021/acscatal.1c03057","chicago":"Ziegler, Felix, Hamzeh Kraus, Mathis J. Benedikter, Dongren Wang, Johanna R. Bruckner, Michał Nowakowski, Kilian Weißer, et al. “Confinement Effects for Efficient Macrocyclization Reactions with Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes.” ACS Catalysis 11, no. 18 (2021): 11570–78. https://doi.org/10.1021/acscatal.1c03057.","ieee":"F. Ziegler et al., “Confinement Effects for Efficient Macrocyclization Reactions with Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes,” ACS Catalysis, vol. 11, no. 18, pp. 11570–11578, 2021, doi: 10.1021/acscatal.1c03057."},"page":"11570-11578","intvolume":" 11","author":[{"full_name":"Ziegler, Felix","last_name":"Ziegler","first_name":"Felix"},{"first_name":"Hamzeh","last_name":"Kraus","full_name":"Kraus, Hamzeh"},{"first_name":"Mathis J.","last_name":"Benedikter","full_name":"Benedikter, Mathis J."},{"full_name":"Wang, Dongren","last_name":"Wang","first_name":"Dongren"},{"first_name":"Johanna R.","full_name":"Bruckner, Johanna R.","last_name":"Bruckner"},{"first_name":"Michał","full_name":"Nowakowski, Michał","id":"78878","last_name":"Nowakowski","orcid":"0000-0002-3734-7011"},{"full_name":"Weißer, Kilian","last_name":"Weißer","first_name":"Kilian"},{"full_name":"Solodenko, Helena","last_name":"Solodenko","first_name":"Helena"},{"first_name":"Guido","last_name":"Schmitz","full_name":"Schmitz, Guido"},{"last_name":"Bauer","orcid":"0000-0002-9294-6076","id":"47241","full_name":"Bauer, Matthias","first_name":"Matthias"},{"last_name":"Hansen","full_name":"Hansen, Niels","first_name":"Niels"},{"last_name":"Buchmeiser","full_name":"Buchmeiser, Michael R.","first_name":"Michael R."}],"volume":11,"date_updated":"2024-05-07T11:44:19Z","doi":"10.1021/acscatal.1c03057","publication":"ACS Catalysis","abstract":[{"lang":"eng","text":"For entropic reasons, the synthesis of macrocycles via olefin ring-closing metathesis (RCM) is impeded by competing acyclic diene metathesis (ADMET) oligomerization. With cationic molybdenum imido alkylidene N-heterocyclic carbene (NHC) complexes confined in tailored ordered mesoporous silica, RCM can be run with macrocyclization selectivities up to 98% and high substrate concentrations up to 0.1 M. Molecular dynamics simulations show that the high conversions are a direct result of the proximity between the surface-bound catalyst, proven by extended X-ray absorption spectroscopy, and the surface-located substrates. Back-diffusion of the macrocycles decreases with decreasing pore diameter of the silica and is responsible for the high macrocyclization efficiency. Also, Z-selectivity increases with decreasing pore diameter and increasing Tolman electronic parameter of the NHC. Running reactions at different concentrations allows for identifying the optimum substrate concentration for each material and substrate combination."}],"language":[{"iso":"eng"}],"keyword":["Catalysis","General Chemistry"],"issue":"18","year":"2021","date_created":"2023-01-30T16:49:07Z","publisher":"American Chemical Society (ACS)","title":"Confinement Effects for Efficient Macrocyclization Reactions with Supported Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes"}]