--- _id: '60216' abstract: - lang: eng text: Hydride donors such as DIBAL or CuH react with ZnO and ZrO2 via hydrogen spillover. This suggests that hydrogen spillover in catalysts based on these metal oxides may take place via initial hydride transfer and not via proton–electron transfer. author: - first_name: Michael full_name: Benz, Michael last_name: Benz - first_name: Osman full_name: Bunjaku, Osman last_name: Bunjaku - first_name: Michał full_name: Nowakowski, Michał id: '78878' last_name: Nowakowski orcid: 0000-0002-3734-7011 - first_name: Alexander full_name: Allgaier, Alexander last_name: Allgaier - first_name: Indro full_name: Biswas, Indro last_name: Biswas - first_name: Joris full_name: van Slageren, Joris last_name: van Slageren - first_name: Matthias full_name: Bauer, Matthias id: '47241' last_name: Bauer orcid: 0000-0002-9294-6076 - first_name: Deven P. full_name: Estes, Deven P. last_name: Estes citation: ama: 'Benz M, Bunjaku O, Nowakowski M, et al. Hydrogen spillover through hydride transfer: the reaction of ZnO and ZrO2 with strong hydride donors. Catalysis Science & Technology. 2024;14(20):5854-5863. doi:10.1039/d4cy00504j' apa: 'Benz, M., Bunjaku, O., Nowakowski, M., Allgaier, A., Biswas, I., van Slageren, J., Bauer, M., & Estes, D. P. (2024). Hydrogen spillover through hydride transfer: the reaction of ZnO and ZrO2 with strong hydride donors. Catalysis Science & Technology, 14(20), 5854–5863. https://doi.org/10.1039/d4cy00504j' bibtex: '@article{Benz_Bunjaku_Nowakowski_Allgaier_Biswas_van Slageren_Bauer_Estes_2024, title={Hydrogen spillover through hydride transfer: the reaction of ZnO and ZrO2 with strong hydride donors}, volume={14}, DOI={10.1039/d4cy00504j}, number={20}, journal={Catalysis Science & Technology}, publisher={Royal Society of Chemistry (RSC)}, author={Benz, Michael and Bunjaku, Osman and Nowakowski, Michał and Allgaier, Alexander and Biswas, Indro and van Slageren, Joris and Bauer, Matthias and Estes, Deven P.}, year={2024}, pages={5854–5863} }' chicago: 'Benz, Michael, Osman Bunjaku, Michał Nowakowski, Alexander Allgaier, Indro Biswas, Joris van Slageren, Matthias Bauer, and Deven P. Estes. “Hydrogen Spillover through Hydride Transfer: The Reaction of ZnO and ZrO2 with Strong Hydride Donors.” Catalysis Science & Technology 14, no. 20 (2024): 5854–63. https://doi.org/10.1039/d4cy00504j.' ieee: 'M. Benz et al., “Hydrogen spillover through hydride transfer: the reaction of ZnO and ZrO2 with strong hydride donors,” Catalysis Science & Technology, vol. 14, no. 20, pp. 5854–5863, 2024, doi: 10.1039/d4cy00504j.' mla: 'Benz, Michael, et al. “Hydrogen Spillover through Hydride Transfer: The Reaction of ZnO and ZrO2 with Strong Hydride Donors.” Catalysis Science & Technology, vol. 14, no. 20, Royal Society of Chemistry (RSC), 2024, pp. 5854–63, doi:10.1039/d4cy00504j.' short: M. Benz, O. Bunjaku, M. Nowakowski, A. Allgaier, I. Biswas, J. van Slageren, M. Bauer, D.P. Estes, Catalysis Science & Technology 14 (2024) 5854–5863. date_created: 2025-06-16T08:55:24Z date_updated: 2025-08-15T12:42:34Z department: - _id: '306' doi: 10.1039/d4cy00504j intvolume: ' 14' issue: '20' keyword: - Xray language: - iso: eng page: 5854-5863 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 - 2044-4761 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: 'Hydrogen spillover through hydride transfer: the reaction of ZnO and ZrO2 with strong hydride donors' type: journal_article user_id: '48467' volume: 14 year: '2024' ... --- _id: '54851' abstract: - lang: eng text: Composites of different graphene oxide types, TiO2 materials, and especially synthetic routes influence the photocatalytic activity of the resulting material. author: - first_name: Marta full_name: Rosenthal, Marta last_name: Rosenthal - first_name: Timur full_name: Biktagirov, Timur id: '65612' last_name: Biktagirov - first_name: Wolf Gero full_name: Schmidt, Wolf Gero id: '468' last_name: Schmidt orcid: 0000-0002-2717-5076 - first_name: René full_name: Wilhelm, René last_name: Wilhelm citation: ama: Rosenthal M, Biktagirov T, Schmidt WG, Wilhelm R. Synthesis of new graphene oxide/TiO2 and TiO2/SiO2 nanocomposites and their evaluation as photocatalysts. Catalysis Science & Technology. 2023;13(15):4367-4377. doi:10.1039/d3cy00461a apa: Rosenthal, M., Biktagirov, T., Schmidt, W. G., & Wilhelm, R. (2023). Synthesis of new graphene oxide/TiO2 and TiO2/SiO2 nanocomposites and their evaluation as photocatalysts. Catalysis Science & Technology, 13(15), 4367–4377. https://doi.org/10.1039/d3cy00461a bibtex: '@article{Rosenthal_Biktagirov_Schmidt_Wilhelm_2023, title={Synthesis of new graphene oxide/TiO2 and TiO2/SiO2 nanocomposites and their evaluation as photocatalysts}, volume={13}, DOI={10.1039/d3cy00461a}, number={15}, journal={Catalysis Science & Technology}, publisher={Royal Society of Chemistry (RSC)}, author={Rosenthal, Marta and Biktagirov, Timur and Schmidt, Wolf Gero and Wilhelm, René}, year={2023}, pages={4367–4377} }' chicago: 'Rosenthal, Marta, Timur Biktagirov, Wolf Gero Schmidt, and René Wilhelm. “Synthesis of New Graphene Oxide/TiO2 and TiO2/SiO2 Nanocomposites and Their Evaluation as Photocatalysts.” Catalysis Science & Technology 13, no. 15 (2023): 4367–77. https://doi.org/10.1039/d3cy00461a.' ieee: 'M. Rosenthal, T. Biktagirov, W. G. Schmidt, and R. Wilhelm, “Synthesis of new graphene oxide/TiO2 and TiO2/SiO2 nanocomposites and their evaluation as photocatalysts,” Catalysis Science & Technology, vol. 13, no. 15, pp. 4367–4377, 2023, doi: 10.1039/d3cy00461a.' mla: Rosenthal, Marta, et al. “Synthesis of New Graphene Oxide/TiO2 and TiO2/SiO2 Nanocomposites and Their Evaluation as Photocatalysts.” Catalysis Science & Technology, vol. 13, no. 15, Royal Society of Chemistry (RSC), 2023, pp. 4367–77, doi:10.1039/d3cy00461a. short: M. Rosenthal, T. Biktagirov, W.G. Schmidt, R. Wilhelm, Catalysis Science & Technology 13 (2023) 4367–4377. date_created: 2024-06-24T06:12:50Z date_updated: 2024-06-24T06:30:04Z department: - _id: '15' - _id: '170' - _id: '295' - _id: '27' - _id: '230' doi: 10.1039/d3cy00461a intvolume: ' 13' issue: '15' language: - iso: eng page: 4367-4377 project: - _id: '52' name: 'PC2: Computing Resources Provided by the Paderborn Center for Parallel Computing' publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 - 2044-4761 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: Synthesis of new graphene oxide/TiO2 and TiO2/SiO2 nanocomposites and their evaluation as photocatalysts type: journal_article user_id: '16199' volume: 13 year: '2023' ... --- _id: '52343' abstract: - lang: eng text: Improved enantioselectivity in the 1,2-addition was observed for chiral Rh norbornadiene catalysts immobilized on ordered mesoporous silica with small pores. Confinement effects were rationalized by experimental and computational studies. article_type: original author: - first_name: Manuel full_name: Kirchhof, Manuel last_name: Kirchhof - first_name: Katrin full_name: Gugeler, Katrin last_name: Gugeler - first_name: Ann-Katrin full_name: Beurer, Ann-Katrin last_name: Beurer - first_name: Felix Richard full_name: Fischer, Felix Richard last_name: Fischer - first_name: Derman full_name: Batman, Derman last_name: Batman - first_name: Soeren M. full_name: Bauch, Soeren M. last_name: Bauch - first_name: Sofia full_name: Kolin, Sofia last_name: Kolin - first_name: Elliot full_name: Nicholas, Elliot last_name: Nicholas - first_name: Roland full_name: Schoch, Roland id: '48467' last_name: Schoch orcid: 0000-0003-2061-7289 - first_name: Charlotte full_name: Vogler, Charlotte last_name: Vogler - first_name: Shravan R. full_name: Kousik, Shravan R. last_name: Kousik - first_name: Anna full_name: Zens, Anna last_name: Zens - first_name: Bernd full_name: Plietker, Bernd last_name: Plietker - first_name: Petia full_name: Atanasova, Petia last_name: Atanasova - first_name: Stefan full_name: Naumann, Stefan last_name: Naumann - first_name: Matthias full_name: Bauer, Matthias id: '47241' last_name: Bauer orcid: 0000-0002-9294-6076 - first_name: Johanna R. full_name: Bruckner, Johanna R. last_name: Bruckner - first_name: Yvonne full_name: Traa, Yvonne last_name: Traa - first_name: Johannes full_name: Kästner, Johannes last_name: Kästner - first_name: Sabine full_name: Laschat, Sabine last_name: Laschat citation: ama: 'Kirchhof M, Gugeler K, Beurer A-K, et al. Tethering chiral Rh diene complexes inside mesoporous solids: experimental and theoretical study of substituent, pore and linker effects on asymmetric catalysis. Catalysis Science Technology. 2023;13(12):3709-3724. doi:10.1039/d3cy00381g' apa: 'Kirchhof, M., Gugeler, K., Beurer, A.-K., Fischer, F. R., Batman, D., Bauch, S. M., Kolin, S., Nicholas, E., Schoch, R., Vogler, C., Kousik, S. R., Zens, A., Plietker, B., Atanasova, P., Naumann, S., Bauer, M., Bruckner, J. R., Traa, Y., Kästner, J., & Laschat, S. (2023). Tethering chiral Rh diene complexes inside mesoporous solids: experimental and theoretical study of substituent, pore and linker effects on asymmetric catalysis. Catalysis Science Technology, 13(12), 3709–3724. https://doi.org/10.1039/d3cy00381g' bibtex: '@article{Kirchhof_Gugeler_Beurer_Fischer_Batman_Bauch_Kolin_Nicholas_Schoch_Vogler_et al._2023, title={Tethering chiral Rh diene complexes inside mesoporous solids: experimental and theoretical study of substituent, pore and linker effects on asymmetric catalysis}, volume={13}, DOI={10.1039/d3cy00381g}, number={12}, journal={Catalysis Science Technology}, publisher={Royal Society of Chemistry (RSC)}, author={Kirchhof, Manuel and Gugeler, Katrin and Beurer, Ann-Katrin and Fischer, Felix Richard and Batman, Derman and Bauch, Soeren M. and Kolin, Sofia and Nicholas, Elliot and Schoch, Roland and Vogler, Charlotte and et al.}, year={2023}, pages={3709–3724} }' chicago: 'Kirchhof, Manuel, Katrin Gugeler, Ann-Katrin Beurer, Felix Richard Fischer, Derman Batman, Soeren M. Bauch, Sofia Kolin, et al. “Tethering Chiral Rh Diene Complexes inside Mesoporous Solids: Experimental and Theoretical Study of Substituent, Pore and Linker Effects on Asymmetric Catalysis.” Catalysis Science Technology 13, no. 12 (2023): 3709–24. https://doi.org/10.1039/d3cy00381g.' ieee: 'M. Kirchhof et al., “Tethering chiral Rh diene complexes inside mesoporous solids: experimental and theoretical study of substituent, pore and linker effects on asymmetric catalysis,” Catalysis Science Technology, vol. 13, no. 12, pp. 3709–3724, 2023, doi: 10.1039/d3cy00381g.' mla: 'Kirchhof, Manuel, et al. “Tethering Chiral Rh Diene Complexes inside Mesoporous Solids: Experimental and Theoretical Study of Substituent, Pore and Linker Effects on Asymmetric Catalysis.” Catalysis Science Technology, vol. 13, no. 12, Royal Society of Chemistry (RSC), 2023, pp. 3709–24, doi:10.1039/d3cy00381g.' short: M. Kirchhof, K. Gugeler, A.-K. Beurer, F.R. Fischer, D. Batman, S.M. Bauch, S. Kolin, E. Nicholas, R. Schoch, C. Vogler, S.R. Kousik, A. Zens, B. Plietker, P. Atanasova, S. Naumann, M. Bauer, J.R. Bruckner, Y. Traa, J. Kästner, S. Laschat, Catalysis Science Technology 13 (2023) 3709–3724. date_created: 2024-03-07T09:12:06Z date_updated: 2025-06-16T09:00:17Z department: - _id: '306' doi: 10.1039/d3cy00381g intvolume: ' 13' issue: '12' keyword: - Catalysis language: - iso: eng page: 3709-3724 publication: Catalysis Science Technology publication_identifier: issn: - 2044-4753 - 2044-4761 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: 'Tethering chiral Rh diene complexes inside mesoporous solids: experimental and theoretical study of substituent, pore and linker effects on asymmetric catalysis' type: journal_article user_id: '48467' volume: 13 year: '2023' ... --- _id: '64032' abstract: - lang: eng text: Ruthenium nanoparticles (Ru NPs) stabilized by bis-diphenylphosphinobutane (dppb) and surface-saturated with hydrogen have been exposed to gaseous 15NH3 and studied using solid-state 15N CP MAS NMR. Three signals have been observed at 24.5, −12 and −42 ppm (reference external liquid ammonia) which are assigned to chemisorbed ammonia species RuNHx. Sample exposure to vacuum or aging leads to conversion of the 24.5 ppm species into the other ones, a process which is reversed by re-exposure to hydrogen gas. Exposure to a mixture of 15NH3 and 13CO leads to the formation of surface bound urea as demonstrated by 15N and 13C CP MAS NMR. To understand the surface reactions of ammonia and the 15N NMR results, quantum chemical calculations of the structures, energies and 15N chemical shifts of ammonia species on Ru6 and Ru55 model clusters have been performed. The calculations indicate that under the experimental conditions applied, the fractions of RuNH3 and RuNH2 species are similar, independent of the H2 pressure. No RuN and RuNH species are formed which are calculated to resonate at a lower field than the signals observed experimentally. However, the 15N chemical shifts of RuNH2 depend on the number of neighboring surface hydrogens and hence on the H2 pressure. Thus, the signal at 24.5 ppm is assigned to RuNH2 in a neighborhood rich in surface hydrogens. RuNH2 depleted in neighboring surface hydrogens and RuNH3 resonated both in a similar chemical shift range to which the signals at −12 and −42 belong. A change of the hydrogen pressure then leads to interconversion of hydrogen-rich and hydrogen-poor neighborhoods of RuNH2 but does not alter the fractions of RuNH3 and RuNH2 according to the calculated stability diagram. Nevertheless, dissociation of RuNH3 into RuNH2 and surface hydrogen is expected to take place during the initial ammonia adsorption process and at low H2 pressures and high temperatures. Finally, some preliminary quantum chemical calculations suggest stepwise binding of two NH2 groups to adsorbed CO leading to surface bound urea where the oxygen is coordinated to Ru. author: - first_name: Niels full_name: Rothermel, Niels last_name: Rothermel - first_name: Hans-Heinrich full_name: Limbach, Hans-Heinrich last_name: Limbach - first_name: Iker full_name: Del Rosal, Iker last_name: Del Rosal - first_name: Romuald full_name: Poteau, Romuald last_name: Poteau - first_name: Gabriel full_name: Mencia, Gabriel last_name: Mencia - first_name: Bruno full_name: Chaudret, Bruno last_name: Chaudret - first_name: Gerd full_name: Buntkowsky, Gerd last_name: Buntkowsky - first_name: Torsten full_name: Gutmann, Torsten id: '118165' last_name: Gutmann citation: ama: Rothermel N, Limbach H-H, Del Rosal I, et al. Surface reactions of ammonia on ruthenium nanoparticles revealed by 15N and 13C solid-state NMR. Catalysis Science & Technology. 2021;11(13):4509–4520. doi:10.1039/D0CY02476G apa: Rothermel, N., Limbach, H.-H., Del Rosal, I., Poteau, R., Mencia, G., Chaudret, B., Buntkowsky, G., & Gutmann, T. (2021). Surface reactions of ammonia on ruthenium nanoparticles revealed by 15N and 13C solid-state NMR. Catalysis Science & Technology, 11(13), 4509–4520. https://doi.org/10.1039/D0CY02476G bibtex: '@article{Rothermel_Limbach_Del Rosal_Poteau_Mencia_Chaudret_Buntkowsky_Gutmann_2021, title={Surface reactions of ammonia on ruthenium nanoparticles revealed by 15N and 13C solid-state NMR}, volume={11}, DOI={10.1039/D0CY02476G}, number={13}, journal={Catalysis Science & Technology}, publisher={The Royal Society of Chemistry}, author={Rothermel, Niels and Limbach, Hans-Heinrich and Del Rosal, Iker and Poteau, Romuald and Mencia, Gabriel and Chaudret, Bruno and Buntkowsky, Gerd and Gutmann, Torsten}, year={2021}, pages={4509–4520} }' chicago: 'Rothermel, Niels, Hans-Heinrich Limbach, Iker Del Rosal, Romuald Poteau, Gabriel Mencia, Bruno Chaudret, Gerd Buntkowsky, and Torsten Gutmann. “Surface Reactions of Ammonia on Ruthenium Nanoparticles Revealed by 15N and 13C Solid-State NMR.” Catalysis Science & Technology 11, no. 13 (2021): 4509–4520. https://doi.org/10.1039/D0CY02476G.' ieee: 'N. Rothermel et al., “Surface reactions of ammonia on ruthenium nanoparticles revealed by 15N and 13C solid-state NMR,” Catalysis Science & Technology, vol. 11, no. 13, pp. 4509–4520, 2021, doi: 10.1039/D0CY02476G.' mla: Rothermel, Niels, et al. “Surface Reactions of Ammonia on Ruthenium Nanoparticles Revealed by 15N and 13C Solid-State NMR.” Catalysis Science & Technology, vol. 11, no. 13, The Royal Society of Chemistry, 2021, pp. 4509–4520, doi:10.1039/D0CY02476G. short: N. Rothermel, H.-H. Limbach, I. Del Rosal, R. Poteau, G. Mencia, B. Chaudret, G. Buntkowsky, T. Gutmann, Catalysis Science & Technology 11 (2021) 4509–4520. date_created: 2026-02-07T16:06:48Z date_updated: 2026-02-17T16:13:50Z doi: 10.1039/D0CY02476G extern: '1' intvolume: ' 11' issue: '13' language: - iso: eng page: 4509–4520 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 publisher: The Royal Society of Chemistry status: public title: Surface reactions of ammonia on ruthenium nanoparticles revealed by 15N and 13C solid-state NMR type: journal_article user_id: '100715' volume: 11 year: '2021' ... --- _id: '64006' abstract: - lang: eng text: Three chiral dirhodium coordination polymers Rh2–Ln (n = 1–3) have been synthesized via ligand exchange between dirhodium trifluoroacetate Rh2(TFA)4 and differently sized chiral dicarboxylic acids derived from l-tert-leucine. SEM images indicate that the Rh2–Ln (n = 1–3) polymers have a lamellar structure. XPS data demonstrate that the oxidation state of rhodium in the dirhodium nodes is maintained during the synthesis of the polymers. The coordination polymers have been further characterized by FTIR, 1H → 13C CP MAS NMR and 19F MAS NMR spectroscopy to prove the formation of polymers via ligand exchange. Although the quantitative 19F MAS NMR spectra reveal incomplete ligand substitution in the coordination polymers, these catalysts show excellent activity and selectivity in the asymmetric cyclopropanation reaction between styrene and diazooxindole. In particular, the enantioselectivity has been significantly improved compared with previously designed dirhodium coordination polymers, which were synthesized from aromatic dicarboxylic acids derived from l-phenylalanine. Meanwhile, the dirhodium polymers can be easily recycled five times without significant reduction in their catalytic efficiency. author: - first_name: Zhenzhong full_name: Li, Zhenzhong last_name: Li - first_name: Lorenz full_name: Rösler, Lorenz last_name: Rösler - first_name: Till full_name: Wissel, Till last_name: Wissel - first_name: Hergen full_name: Breitzke, Hergen last_name: Breitzke - first_name: Kathrin full_name: Hofmann, Kathrin last_name: Hofmann - first_name: Hans-Heinrich full_name: Limbach, Hans-Heinrich last_name: Limbach - first_name: Torsten full_name: Gutmann, Torsten id: '118165' last_name: Gutmann - first_name: Gerd full_name: Buntkowsky, Gerd last_name: Buntkowsky citation: ama: Li Z, Rösler L, Wissel T, et al. Design and characterization of novel dirhodium coordination polymers – the impact of ligand size on selectivity in asymmetric cyclopropanation. Catalysis Science & Technology. 2021;11(10):3481–3492. doi:10.1039/D1CY00109D apa: Li, Z., Rösler, L., Wissel, T., Breitzke, H., Hofmann, K., Limbach, H.-H., Gutmann, T., & Buntkowsky, G. (2021). Design and characterization of novel dirhodium coordination polymers – the impact of ligand size on selectivity in asymmetric cyclopropanation. Catalysis Science & Technology, 11(10), 3481–3492. https://doi.org/10.1039/D1CY00109D bibtex: '@article{Li_Rösler_Wissel_Breitzke_Hofmann_Limbach_Gutmann_Buntkowsky_2021, title={Design and characterization of novel dirhodium coordination polymers – the impact of ligand size on selectivity in asymmetric cyclopropanation}, volume={11}, DOI={10.1039/D1CY00109D}, number={10}, journal={Catalysis Science & Technology}, publisher={The Royal Society of Chemistry}, author={Li, Zhenzhong and Rösler, Lorenz and Wissel, Till and Breitzke, Hergen and Hofmann, Kathrin and Limbach, Hans-Heinrich and Gutmann, Torsten and Buntkowsky, Gerd}, year={2021}, pages={3481–3492} }' chicago: 'Li, Zhenzhong, Lorenz Rösler, Till Wissel, Hergen Breitzke, Kathrin Hofmann, Hans-Heinrich Limbach, Torsten Gutmann, and Gerd Buntkowsky. “Design and Characterization of Novel Dirhodium Coordination Polymers – the Impact of Ligand Size on Selectivity in Asymmetric Cyclopropanation.” Catalysis Science & Technology 11, no. 10 (2021): 3481–3492. https://doi.org/10.1039/D1CY00109D.' ieee: 'Z. Li et al., “Design and characterization of novel dirhodium coordination polymers – the impact of ligand size on selectivity in asymmetric cyclopropanation,” Catalysis Science & Technology, vol. 11, no. 10, pp. 3481–3492, 2021, doi: 10.1039/D1CY00109D.' mla: Li, Zhenzhong, et al. “Design and Characterization of Novel Dirhodium Coordination Polymers – the Impact of Ligand Size on Selectivity in Asymmetric Cyclopropanation.” Catalysis Science & Technology, vol. 11, no. 10, The Royal Society of Chemistry, 2021, pp. 3481–3492, doi:10.1039/D1CY00109D. short: Z. Li, L. Rösler, T. Wissel, H. Breitzke, K. Hofmann, H.-H. Limbach, T. Gutmann, G. Buntkowsky, Catalysis Science & Technology 11 (2021) 3481–3492. date_created: 2026-02-07T15:55:39Z date_updated: 2026-02-17T16:15:33Z doi: 10.1039/D1CY00109D extern: '1' intvolume: ' 11' issue: '10' language: - iso: eng page: 3481–3492 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 publisher: The Royal Society of Chemistry status: public title: Design and characterization of novel dirhodium coordination polymers – the impact of ligand size on selectivity in asymmetric cyclopropanation type: journal_article user_id: '100715' volume: 11 year: '2021' ... --- _id: '64023' abstract: - lang: eng text: The structure of vanadium oxide (VOx) species in vanadium containing MCM-41 catalysts prepared by co-condensation or grafting, respectively, was investigated by a combination of Raman scattering, UV-vis diffuse reflectance, ATR-IR, and magic angle spinning (MAS) 51V as well as 29Si NMR spectroscopy techniques. Simulations of the 51V MAS NMR spectra allowed the determination of chemical shift and quadrupole tensor parameters, which give valuable information about the nature of the VOx units. Structural transformations of the supported vanadium oxide species for the catalyst in the dehydrated state and hydrated state were investigated to examine the effect of water molecules on the VOx structures. The results reveal the presence of different VOx structures for the hydrated samples, including dimeric species, oligomeric chains and isolated trigonal pyramid units. Upon dehydration, the predominance of oligomeric and/or dimeric units for the sample prepared by grafting was observed, while a considerable amount of isolated units was additionally detected for the sample prepared by co-condensation. author: - first_name: Marcos full_name: Oliveira, Marcos last_name: Oliveira - first_name: Dominik full_name: Seeburg, Dominik last_name: Seeburg - first_name: Jana full_name: Weiß, Jana last_name: Weiß - first_name: Sebastian full_name: Wohlrab, Sebastian last_name: Wohlrab - first_name: Gerd full_name: Buntkowsky, Gerd last_name: Buntkowsky - first_name: Ursula full_name: Bentrup, Ursula last_name: Bentrup - first_name: Torsten full_name: Gutmann, Torsten id: '118165' last_name: Gutmann citation: ama: Oliveira M, Seeburg D, Weiß J, et al. Structural characterization of vanadium environments in MCM-41 molecular sieve catalysts by solid state 51V NMR. Catalysis Science & Technology. 2019;9(21):6180–6190. doi:10.1039/C9CY01410A apa: Oliveira, M., Seeburg, D., Weiß, J., Wohlrab, S., Buntkowsky, G., Bentrup, U., & Gutmann, T. (2019). Structural characterization of vanadium environments in MCM-41 molecular sieve catalysts by solid state 51V NMR. Catalysis Science & Technology, 9(21), 6180–6190. https://doi.org/10.1039/C9CY01410A bibtex: '@article{Oliveira_Seeburg_Weiß_Wohlrab_Buntkowsky_Bentrup_Gutmann_2019, title={Structural characterization of vanadium environments in MCM-41 molecular sieve catalysts by solid state 51V NMR}, volume={9}, DOI={10.1039/C9CY01410A}, number={21}, journal={Catalysis Science & Technology}, publisher={The Royal Society of Chemistry}, author={Oliveira, Marcos and Seeburg, Dominik and Weiß, Jana and Wohlrab, Sebastian and Buntkowsky, Gerd and Bentrup, Ursula and Gutmann, Torsten}, year={2019}, pages={6180–6190} }' chicago: 'Oliveira, Marcos, Dominik Seeburg, Jana Weiß, Sebastian Wohlrab, Gerd Buntkowsky, Ursula Bentrup, and Torsten Gutmann. “Structural Characterization of Vanadium Environments in MCM-41 Molecular Sieve Catalysts by Solid State 51V NMR.” Catalysis Science & Technology 9, no. 21 (2019): 6180–6190. https://doi.org/10.1039/C9CY01410A.' ieee: 'M. Oliveira et al., “Structural characterization of vanadium environments in MCM-41 molecular sieve catalysts by solid state 51V NMR,” Catalysis Science & Technology, vol. 9, no. 21, pp. 6180–6190, 2019, doi: 10.1039/C9CY01410A.' mla: Oliveira, Marcos, et al. “Structural Characterization of Vanadium Environments in MCM-41 Molecular Sieve Catalysts by Solid State 51V NMR.” Catalysis Science & Technology, vol. 9, no. 21, The Royal Society of Chemistry, 2019, pp. 6180–6190, doi:10.1039/C9CY01410A. short: M. Oliveira, D. Seeburg, J. Weiß, S. Wohlrab, G. Buntkowsky, U. Bentrup, T. Gutmann, Catalysis Science & Technology 9 (2019) 6180–6190. date_created: 2026-02-07T16:04:18Z date_updated: 2026-02-17T16:14:18Z doi: 10.1039/C9CY01410A extern: '1' intvolume: ' 9' issue: '21' language: - iso: eng page: 6180–6190 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 publisher: The Royal Society of Chemistry status: public title: Structural characterization of vanadium environments in MCM-41 molecular sieve catalysts by solid state 51V NMR type: journal_article user_id: '100715' volume: 9 year: '2019' ... --- _id: '63991' abstract: - lang: eng text: A series of 1 and 2 nm sized platinum nanoparticles (Pt-NPs) deposited on different support materials, namely, gamma-alumina (gamma-Al2O3), titanium dioxide (TiO2), silicon dioxide (SiO2) and fumed silica are investigated by solid-state NMR and dynamic nuclear polarization enhanced NMR spectroscopy (DNP). DNP signal enhancement factors up to 170 enable gaining deeper insight into the surface chemistry of Pt-NPs. Carbon monoxide is used as a probe molecule to analyze the adsorption process and the surface chemistry on the supported Pt-NPs. The studied systems show significant catalytic activity in carbon monoxide oxidation on their surface at room temperature. The underlying catalytic mechanism is the water-gas shift reaction. In the case of alumina as the support the produced CO2 reacts with the surface to form carbonate, which is revealed by solid-state NMR. A similar carbonate formation is also observed when physical mixtures of neat alumina with silica, fumed silica and titania supported Pt-NPs are studied. author: - first_name: V. full_name: Klimavicius, V. last_name: Klimavicius - first_name: S. full_name: Neumann, S. last_name: Neumann - first_name: S. full_name: Kunz, S. last_name: Kunz - first_name: Torsten full_name: Gutmann, Torsten id: '118165' last_name: Gutmann - first_name: G. full_name: Buntkowsky, G. last_name: Buntkowsky citation: ama: Klimavicius V, Neumann S, Kunz S, Gutmann T, Buntkowsky G. Room temperature CO oxidation catalysed by supported Pt nanoparticles revealed by solid-state NMR and DNP spectroscopy. Catalysis Science & Technology. 2019;9(14):3743–3752. doi:10.1039/c9cy00684b apa: Klimavicius, V., Neumann, S., Kunz, S., Gutmann, T., & Buntkowsky, G. (2019). Room temperature CO oxidation catalysed by supported Pt nanoparticles revealed by solid-state NMR and DNP spectroscopy. Catalysis Science & Technology, 9(14), 3743–3752. https://doi.org/10.1039/c9cy00684b bibtex: '@article{Klimavicius_Neumann_Kunz_Gutmann_Buntkowsky_2019, title={Room temperature CO oxidation catalysed by supported Pt nanoparticles revealed by solid-state NMR and DNP spectroscopy}, volume={9}, DOI={10.1039/c9cy00684b}, number={14}, journal={Catalysis Science & Technology}, author={Klimavicius, V. and Neumann, S. and Kunz, S. and Gutmann, Torsten and Buntkowsky, G.}, year={2019}, pages={3743–3752} }' chicago: 'Klimavicius, V., S. Neumann, S. Kunz, Torsten Gutmann, and G. Buntkowsky. “Room Temperature CO Oxidation Catalysed by Supported Pt Nanoparticles Revealed by Solid-State NMR and DNP Spectroscopy.” Catalysis Science & Technology 9, no. 14 (2019): 3743–3752. https://doi.org/10.1039/c9cy00684b.' ieee: 'V. Klimavicius, S. Neumann, S. Kunz, T. Gutmann, and G. Buntkowsky, “Room temperature CO oxidation catalysed by supported Pt nanoparticles revealed by solid-state NMR and DNP spectroscopy,” Catalysis Science & Technology, vol. 9, no. 14, pp. 3743–3752, 2019, doi: 10.1039/c9cy00684b.' mla: Klimavicius, V., et al. “Room Temperature CO Oxidation Catalysed by Supported Pt Nanoparticles Revealed by Solid-State NMR and DNP Spectroscopy.” Catalysis Science & Technology, vol. 9, no. 14, 2019, pp. 3743–3752, doi:10.1039/c9cy00684b. short: V. Klimavicius, S. Neumann, S. Kunz, T. Gutmann, G. Buntkowsky, Catalysis Science & Technology 9 (2019) 3743–3752. date_created: 2026-02-07T15:47:21Z date_updated: 2026-02-17T16:16:33Z doi: 10.1039/c9cy00684b extern: '1' intvolume: ' 9' issue: '14' keyword: - Chemistry - gamma-alumina - hydrogenation - silica - c-13 - interactions - metal-catalysts - particle-size - platinum nanoparticles - sites - surface - water-gas shift language: - iso: eng page: 3743–3752 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 status: public title: Room temperature CO oxidation catalysed by supported Pt nanoparticles revealed by solid-state NMR and DNP spectroscopy type: journal_article user_id: '100715' volume: 9 year: '2019' ... --- _id: '41040' abstract: - lang: eng text:

Intermediate species formed during CO2 methanation over Rh/Al2O3 and Rh/SiO2 catalysts.

author: - first_name: Natalia M. full_name: Martin, Natalia M. last_name: Martin - first_name: Felix full_name: Hemmingsson, Felix last_name: Hemmingsson - first_name: Xueting full_name: Wang, Xueting last_name: Wang - first_name: Lindsay R. full_name: Merte, Lindsay R. last_name: Merte - first_name: Uta full_name: Hejral, Uta last_name: Hejral - first_name: Johan full_name: Gustafson, Johan last_name: Gustafson - first_name: Magnus full_name: Skoglundh, Magnus last_name: Skoglundh - first_name: Debora Motta full_name: Meira, Debora Motta last_name: Meira - first_name: Ann-Christin full_name: Dippel, Ann-Christin last_name: Dippel - first_name: Olof full_name: Gutowski, Olof last_name: Gutowski - first_name: Matthias full_name: Bauer, Matthias id: '47241' last_name: Bauer orcid: 0000-0002-9294-6076 - first_name: Per-Anders full_name: Carlsson, Per-Anders last_name: Carlsson citation: ama: Martin NM, Hemmingsson F, Wang X, et al. Structure–function relationship during CO2 methanation over Rh/Al2O3 and Rh/SiO2 catalysts under atmospheric pressure conditions. Catalysis Science & Technology. 2018;8(10):2686-2696. doi:10.1039/c8cy00516h apa: Martin, N. M., Hemmingsson, F., Wang, X., Merte, L. R., Hejral, U., Gustafson, J., Skoglundh, M., Meira, D. M., Dippel, A.-C., Gutowski, O., Bauer, M., & Carlsson, P.-A. (2018). Structure–function relationship during CO2 methanation over Rh/Al2O3 and Rh/SiO2 catalysts under atmospheric pressure conditions. Catalysis Science & Technology, 8(10), 2686–2696. https://doi.org/10.1039/c8cy00516h bibtex: '@article{Martin_Hemmingsson_Wang_Merte_Hejral_Gustafson_Skoglundh_Meira_Dippel_Gutowski_et al._2018, title={Structure–function relationship during CO2 methanation over Rh/Al2O3 and Rh/SiO2 catalysts under atmospheric pressure conditions}, volume={8}, DOI={10.1039/c8cy00516h}, number={10}, journal={Catalysis Science & Technology}, publisher={Royal Society of Chemistry (RSC)}, author={Martin, Natalia M. and Hemmingsson, Felix and Wang, Xueting and Merte, Lindsay R. and Hejral, Uta and Gustafson, Johan and Skoglundh, Magnus and Meira, Debora Motta and Dippel, Ann-Christin and Gutowski, Olof and et al.}, year={2018}, pages={2686–2696} }' chicago: 'Martin, Natalia M., Felix Hemmingsson, Xueting Wang, Lindsay R. Merte, Uta Hejral, Johan Gustafson, Magnus Skoglundh, et al. “Structure–Function Relationship during CO2 Methanation over Rh/Al2O3 and Rh/SiO2 Catalysts under Atmospheric Pressure Conditions.” Catalysis Science & Technology 8, no. 10 (2018): 2686–96. https://doi.org/10.1039/c8cy00516h.' ieee: 'N. M. Martin et al., “Structure–function relationship during CO2 methanation over Rh/Al2O3 and Rh/SiO2 catalysts under atmospheric pressure conditions,” Catalysis Science & Technology, vol. 8, no. 10, pp. 2686–2696, 2018, doi: 10.1039/c8cy00516h.' mla: Martin, Natalia M., et al. “Structure–Function Relationship during CO2 Methanation over Rh/Al2O3 and Rh/SiO2 Catalysts under Atmospheric Pressure Conditions.” Catalysis Science & Technology, vol. 8, no. 10, Royal Society of Chemistry (RSC), 2018, pp. 2686–96, doi:10.1039/c8cy00516h. short: N.M. Martin, F. Hemmingsson, X. Wang, L.R. Merte, U. Hejral, J. Gustafson, M. Skoglundh, D.M. Meira, A.-C. Dippel, O. Gutowski, M. Bauer, P.-A. Carlsson, Catalysis Science & Technology 8 (2018) 2686–2696. date_created: 2023-01-30T18:42:40Z date_updated: 2023-01-31T08:28:05Z department: - _id: '35' - _id: '306' doi: 10.1039/c8cy00516h intvolume: ' 8' issue: '10' keyword: - Catalysis language: - iso: eng page: 2686-2696 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 - 2044-4761 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: Structure–function relationship during CO2 methanation over Rh/Al2O3 and Rh/SiO2 catalysts under atmospheric pressure conditions type: journal_article user_id: '27611' volume: 8 year: '2018' ... --- _id: '64010' abstract: - lang: eng text: Seven novel dirhodium coordination polymers (Rh-2-Ln) (n = 1-7) are prepared by employing bitopic ligands to connect dirhodium nodes. The formation of the framework is confirmed by attenuated total reflectance Fourier transform infrared (ATR-FTIR) and H-1 C-13 cross polarization magic angle spinning nuclear magnetic resonance (CP MAS NMR) spectroscopy. Defect sites resulting from incomplete ligand substitution are revealed by F-19 MAS NMR. The random stacking behavior of the frameworks in the obtained solid is analyzed by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The Rh-2/O interaction in neighboring layers is investigated by diffuse reflectance ultra-violet visible light (DR-UV-vis) spectroscopy and X-ray photoelectron spectroscopy (XPS). This interaction is relevant to understand the catalytic behavior of various Rh-2-Ln catalysts in the cyclopropanation of styrene with ethyl diazoacetate (EDA). In this context, the structure-reactivity relationship is discussed by taking into consideration both interlayer Rh-2/O interactions and steric effects of side chains. author: - first_name: J. Q. full_name: Liu, J. Q. last_name: Liu - first_name: Y. P. full_name: Xu, Y. P. last_name: Xu - first_name: P. B. full_name: Groszewicz, P. B. last_name: Groszewicz - first_name: M. full_name: Brodrecht, M. last_name: Brodrecht - first_name: C. full_name: Fasel, C. last_name: Fasel - first_name: K. full_name: Hofmann, K. last_name: Hofmann - first_name: X. J. full_name: Tan, X. J. last_name: Tan - first_name: Torsten full_name: Gutmann, Torsten id: '118165' last_name: Gutmann - first_name: G. full_name: Buntkowsky, G. last_name: Buntkowsky citation: ama: 'Liu JQ, Xu YP, Groszewicz PB, et al. Novel dirhodium coordination polymers: the impact of side chains on cyclopropanation. Catalysis Science & Technology. 2018;8(20):5190–5200. doi:10.1039/c8cy01493k' apa: 'Liu, J. Q., Xu, Y. P., Groszewicz, P. B., Brodrecht, M., Fasel, C., Hofmann, K., Tan, X. J., Gutmann, T., & Buntkowsky, G. (2018). Novel dirhodium coordination polymers: the impact of side chains on cyclopropanation. Catalysis Science & Technology, 8(20), 5190–5200. https://doi.org/10.1039/c8cy01493k' bibtex: '@article{Liu_Xu_Groszewicz_Brodrecht_Fasel_Hofmann_Tan_Gutmann_Buntkowsky_2018, title={Novel dirhodium coordination polymers: the impact of side chains on cyclopropanation}, volume={8}, DOI={10.1039/c8cy01493k}, number={20}, journal={Catalysis Science & Technology}, author={Liu, J. Q. and Xu, Y. P. and Groszewicz, P. B. and Brodrecht, M. and Fasel, C. and Hofmann, K. and Tan, X. J. and Gutmann, Torsten and Buntkowsky, G.}, year={2018}, pages={5190–5200} }' chicago: 'Liu, J. Q., Y. P. Xu, P. B. Groszewicz, M. Brodrecht, C. Fasel, K. Hofmann, X. J. Tan, Torsten Gutmann, and G. Buntkowsky. “Novel Dirhodium Coordination Polymers: The Impact of Side Chains on Cyclopropanation.” Catalysis Science & Technology 8, no. 20 (2018): 5190–5200. https://doi.org/10.1039/c8cy01493k.' ieee: 'J. Q. Liu et al., “Novel dirhodium coordination polymers: the impact of side chains on cyclopropanation,” Catalysis Science & Technology, vol. 8, no. 20, pp. 5190–5200, 2018, doi: 10.1039/c8cy01493k.' mla: 'Liu, J. Q., et al. “Novel Dirhodium Coordination Polymers: The Impact of Side Chains on Cyclopropanation.” Catalysis Science & Technology, vol. 8, no. 20, 2018, pp. 5190–5200, doi:10.1039/c8cy01493k.' short: J.Q. Liu, Y.P. Xu, P.B. Groszewicz, M. Brodrecht, C. Fasel, K. Hofmann, X.J. Tan, T. Gutmann, G. Buntkowsky, Catalysis Science & Technology 8 (2018) 5190–5200. date_created: 2026-02-07T15:57:34Z date_updated: 2026-02-17T16:15:22Z doi: 10.1039/c8cy01493k extern: '1' intvolume: ' 8' issue: '20' keyword: - Chemistry - asymmetric cyclopropanation - c-h insertion - carbene transformations - carboxylates - catalysts - functionalization - immobilization - metal-organic frameworks - nmr - solid support language: - iso: eng page: 5190–5200 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 status: public title: 'Novel dirhodium coordination polymers: the impact of side chains on cyclopropanation' type: journal_article user_id: '100715' volume: 8 year: '2018' ... --- _id: '41045' abstract: - lang: eng text:

CO2 methanation over Rh/Al2O3, Rh/CeO2 and Ni/CeO2 at 350 °C highlighting the different surface speciation during reaction.

author: - first_name: Natalia M. full_name: Martin, Natalia M. last_name: Martin - first_name: Peter full_name: Velin, Peter last_name: Velin - first_name: Magnus full_name: Skoglundh, Magnus last_name: Skoglundh - first_name: Matthias full_name: Bauer, Matthias id: '47241' last_name: Bauer orcid: 0000-0002-9294-6076 - first_name: Per-Anders full_name: Carlsson, Per-Anders last_name: Carlsson citation: ama: Martin NM, Velin P, Skoglundh M, Bauer M, Carlsson P-A. Catalytic hydrogenation of CO2 to methane over supported Pd, Rh and Ni catalysts. Catalysis Science & Technology. 2017;7(5):1086-1094. doi:10.1039/c6cy02536f apa: Martin, N. M., Velin, P., Skoglundh, M., Bauer, M., & Carlsson, P.-A. (2017). Catalytic hydrogenation of CO2 to methane over supported Pd, Rh and Ni catalysts. Catalysis Science & Technology, 7(5), 1086–1094. https://doi.org/10.1039/c6cy02536f bibtex: '@article{Martin_Velin_Skoglundh_Bauer_Carlsson_2017, title={Catalytic hydrogenation of CO2 to methane over supported Pd, Rh and Ni catalysts}, volume={7}, DOI={10.1039/c6cy02536f}, number={5}, journal={Catalysis Science & Technology}, publisher={Royal Society of Chemistry (RSC)}, author={Martin, Natalia M. and Velin, Peter and Skoglundh, Magnus and Bauer, Matthias and Carlsson, Per-Anders}, year={2017}, pages={1086–1094} }' chicago: 'Martin, Natalia M., Peter Velin, Magnus Skoglundh, Matthias Bauer, and Per-Anders Carlsson. “Catalytic Hydrogenation of CO2 to Methane over Supported Pd, Rh and Ni Catalysts.” Catalysis Science & Technology 7, no. 5 (2017): 1086–94. https://doi.org/10.1039/c6cy02536f.' ieee: 'N. M. Martin, P. Velin, M. Skoglundh, M. Bauer, and P.-A. Carlsson, “Catalytic hydrogenation of CO2 to methane over supported Pd, Rh and Ni catalysts,” Catalysis Science & Technology, vol. 7, no. 5, pp. 1086–1094, 2017, doi: 10.1039/c6cy02536f.' mla: Martin, Natalia M., et al. “Catalytic Hydrogenation of CO2 to Methane over Supported Pd, Rh and Ni Catalysts.” Catalysis Science & Technology, vol. 7, no. 5, Royal Society of Chemistry (RSC), 2017, pp. 1086–94, doi:10.1039/c6cy02536f. short: N.M. Martin, P. Velin, M. Skoglundh, M. Bauer, P.-A. Carlsson, Catalysis Science & Technology 7 (2017) 1086–1094. date_created: 2023-01-30T18:50:10Z date_updated: 2023-01-31T08:28:17Z department: - _id: '35' - _id: '306' doi: 10.1039/c6cy02536f intvolume: ' 7' issue: '5' keyword: - Catalysis language: - iso: eng page: 1086-1094 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 - 2044-4761 publication_status: published publisher: Royal Society of Chemistry (RSC) status: public title: Catalytic hydrogenation of CO2 to methane over supported Pd, Rh and Ni catalysts type: journal_article user_id: '27611' volume: 7 year: '2017' ... --- _id: '64011' abstract: - lang: eng text: Catalytically active dirhodium sheet-like coordination polymers are synthesized from their precursors via ligand exchange. The individual lamellae of the dirhodium-bdc frameworks are stacked as parallel sheets, which are randomly oriented or slightly ordered. As inorganic building blocks Rh2(TFA)4 and Rh2(OAc)4, and as organic linker benzene 1,4-dicarboxylate (bdc) are employed. The successful synthesis of the Rh2-bdc(Tf) and Rh2-bdc(Ac) catalysts is proven by ATR-IR, XPS and 13C CP MAS NMR. Residual trifluoroacetate species are investigated by quantitative 19F MAS NMR which further reflects the configuration of trifluoroacetate in the obtained Rh2-bdc(Tf), and defects in the structure. DR-UV-vis and XPS demonstrate that the oxidation state and the Rh-Rh single bond in the dirhodium node are maintained during the ligand substitution process. The stability and reusability of the catalysts are verified by TG-DTA measurements and leaching tests. The catalysts show similar catalytic efficiency as the homogeneous catalyst in the model cyclopropanation between ethyl diazoacetate (EDA) and styrene. author: - first_name: Jiquan full_name: Liu, Jiquan last_name: Liu - first_name: Claudia full_name: Fasel, Claudia last_name: Fasel - first_name: Pedro full_name: Braga-Groszewicz, Pedro last_name: Braga-Groszewicz - first_name: Niels full_name: Rothermel, Niels last_name: Rothermel - first_name: Aany Sofia full_name: Lilly Thankamony, Aany Sofia last_name: Lilly Thankamony - first_name: Grit full_name: Sauer, Grit last_name: Sauer - first_name: Yeping full_name: Xu, Yeping last_name: Xu - first_name: Torsten full_name: Gutmann, Torsten id: '118165' last_name: Gutmann - first_name: Gerd full_name: Buntkowsky, Gerd last_name: Buntkowsky citation: ama: Liu J, Fasel C, Braga-Groszewicz P, et al. Heterogeneous self-supported dirhodium(ii) catalysts with high catalytic efficiency in cyclopropanation - a structural study. Catalysis Science & Technology. 2016;6(21):7830–7840. doi:10.1039/C6CY00915H apa: Liu, J., Fasel, C., Braga-Groszewicz, P., Rothermel, N., Lilly Thankamony, A. S., Sauer, G., Xu, Y., Gutmann, T., & Buntkowsky, G. (2016). Heterogeneous self-supported dirhodium(ii) catalysts with high catalytic efficiency in cyclopropanation - a structural study. Catalysis Science & Technology, 6(21), 7830–7840. https://doi.org/10.1039/C6CY00915H bibtex: '@article{Liu_Fasel_Braga-Groszewicz_Rothermel_Lilly Thankamony_Sauer_Xu_Gutmann_Buntkowsky_2016, title={Heterogeneous self-supported dirhodium(ii) catalysts with high catalytic efficiency in cyclopropanation - a structural study}, volume={6}, DOI={10.1039/C6CY00915H}, number={21}, journal={Catalysis Science & Technology}, publisher={The Royal Society of Chemistry}, author={Liu, Jiquan and Fasel, Claudia and Braga-Groszewicz, Pedro and Rothermel, Niels and Lilly Thankamony, Aany Sofia and Sauer, Grit and Xu, Yeping and Gutmann, Torsten and Buntkowsky, Gerd}, year={2016}, pages={7830–7840} }' chicago: 'Liu, Jiquan, Claudia Fasel, Pedro Braga-Groszewicz, Niels Rothermel, Aany Sofia Lilly Thankamony, Grit Sauer, Yeping Xu, Torsten Gutmann, and Gerd Buntkowsky. “Heterogeneous Self-Supported Dirhodium(Ii) Catalysts with High Catalytic Efficiency in Cyclopropanation - a Structural Study.” Catalysis Science & Technology 6, no. 21 (2016): 7830–7840. https://doi.org/10.1039/C6CY00915H.' ieee: 'J. Liu et al., “Heterogeneous self-supported dirhodium(ii) catalysts with high catalytic efficiency in cyclopropanation - a structural study,” Catalysis Science & Technology, vol. 6, no. 21, pp. 7830–7840, 2016, doi: 10.1039/C6CY00915H.' mla: Liu, Jiquan, et al. “Heterogeneous Self-Supported Dirhodium(Ii) Catalysts with High Catalytic Efficiency in Cyclopropanation - a Structural Study.” Catalysis Science & Technology, vol. 6, no. 21, The Royal Society of Chemistry, 2016, pp. 7830–7840, doi:10.1039/C6CY00915H. short: J. Liu, C. Fasel, P. Braga-Groszewicz, N. Rothermel, A.S. Lilly Thankamony, G. Sauer, Y. Xu, T. Gutmann, G. Buntkowsky, Catalysis Science & Technology 6 (2016) 7830–7840. date_created: 2026-02-07T15:58:38Z date_updated: 2026-02-17T16:15:20Z doi: 10.1039/C6CY00915H extern: '1' intvolume: ' 6' issue: '21' language: - iso: eng page: 7830–7840 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 publisher: The Royal Society of Chemistry status: public title: Heterogeneous self-supported dirhodium(ii) catalysts with high catalytic efficiency in cyclopropanation - a structural study type: journal_article user_id: '100715' volume: 6 year: '2016' ... --- _id: '64026' author: - first_name: Eoin full_name: Rafter, Eoin last_name: Rafter - first_name: Torsten full_name: Gutmann, Torsten id: '118165' last_name: Gutmann - first_name: Florian full_name: Loew, Florian last_name: Loew - first_name: Gerd full_name: Buntkowsky, Gerd last_name: Buntkowsky - first_name: Karine full_name: Philippot, Karine last_name: Philippot - first_name: Bruno full_name: Chaudret, Bruno last_name: Chaudret - first_name: Piet W. N. M. full_name: van Leeuwen, Piet W. N. M. last_name: van Leeuwen citation: ama: Rafter E, Gutmann T, Loew F, et al. Secondary phosphine oxides as pre-ligands for nanoparticle stabilization. Catalysis Science & Technology. 2013;3(3):595–599. doi:10.1039/c2cy20683h apa: Rafter, E., Gutmann, T., Loew, F., Buntkowsky, G., Philippot, K., Chaudret, B., & van Leeuwen, P. W. N. M. (2013). Secondary phosphine oxides as pre-ligands for nanoparticle stabilization. Catalysis Science & Technology, 3(3), 595–599. https://doi.org/10.1039/c2cy20683h bibtex: '@article{Rafter_Gutmann_Loew_Buntkowsky_Philippot_Chaudret_van Leeuwen_2013, title={Secondary phosphine oxides as pre-ligands for nanoparticle stabilization}, volume={3}, DOI={10.1039/c2cy20683h}, number={3}, journal={Catalysis Science & Technology}, author={Rafter, Eoin and Gutmann, Torsten and Loew, Florian and Buntkowsky, Gerd and Philippot, Karine and Chaudret, Bruno and van Leeuwen, Piet W. N. M.}, year={2013}, pages={595–599} }' chicago: 'Rafter, Eoin, Torsten Gutmann, Florian Loew, Gerd Buntkowsky, Karine Philippot, Bruno Chaudret, and Piet W. N. M. van Leeuwen. “Secondary Phosphine Oxides as Pre-Ligands for Nanoparticle Stabilization.” Catalysis Science & Technology 3, no. 3 (2013): 595–599. https://doi.org/10.1039/c2cy20683h.' ieee: 'E. Rafter et al., “Secondary phosphine oxides as pre-ligands for nanoparticle stabilization,” Catalysis Science & Technology, vol. 3, no. 3, pp. 595–599, 2013, doi: 10.1039/c2cy20683h.' mla: Rafter, Eoin, et al. “Secondary Phosphine Oxides as Pre-Ligands for Nanoparticle Stabilization.” Catalysis Science & Technology, vol. 3, no. 3, 2013, pp. 595–599, doi:10.1039/c2cy20683h. short: E. Rafter, T. Gutmann, F. Loew, G. Buntkowsky, K. Philippot, B. Chaudret, P.W.N.M. van Leeuwen, Catalysis Science & Technology 3 (2013) 595–599. date_created: 2026-02-07T16:05:06Z date_updated: 2026-02-17T16:14:11Z doi: 10.1039/c2cy20683h extern: '1' intvolume: ' 3' issue: '3' language: - iso: eng page: 595–599 publication: Catalysis Science & Technology publication_identifier: issn: - 2044-4753 status: public title: Secondary phosphine oxides as pre-ligands for nanoparticle stabilization type: journal_article user_id: '100715' volume: 3 year: '2013' ...