---
_id: '59510'
abstract:
- lang: eng
  text: <jats:p>The use of organo-catalysis in continuous-flow reactor systems is
    gaining attention in medicinal chemistry due to its cost-effectiveness and reduced
    chemical waste. In this study, bioactive curcumin (CUM) derivatives were synthesized
    in a continuously operated microfluidic reactor (MFR), using piperidine-based
    polymeric networks as catalysts. Piperidine methacrylate and piperidine acrylate
    were synthesized and subsequently copolymerized with complementary monomers (MMA
    or DMAA) and crosslinkers (EGDMA or MBAM) via photopolymerization, yielding different
    polymeric networks. Initially, batch reactions were optimized for the organo-catalytic
    Knoevenagel condensation between CUM and 4-nitrobenzaldehyde, under various conditions,
    in the presence of polymer networks. Conversion was assessed using offline 1H
    NMR spectroscopy, revealing an increase in conversion with enhanced swelling properties
    of the polymer networks, which facilitated greater accessibility of catalytic
    sites. In continuous-flow MFR experiments, optimized polymer gel dots exhibited
    superior catalytic performance, achieving a conversion of up to 72%, compared
    to other compositions. This improvement was attributed to the enhanced swelling
    in the reaction mixture (DMSO/methanol, 7:3 v/v) at 40 °C over 72 h. Furthermore,
    the MFR system enabled the efficient synthesis of a series of CUM derivatives,
    demonstrating significantly higher conversion rates than traditional batch reactions.
    Notably, while batch reactions required 90% catalyst loading in the gel, the MFR
    system achieved a comparable or superior performance with only 50% catalyst, resulting
    in a higher turnover number. These findings underscore the advantages of continuous-flow
    organo-catalysis in enhancing catalytic efficiency and sustainability in organic
    synthesis.</jats:p>
article_number: '278'
author:
- first_name: Naresh
  full_name: Killi, Naresh
  last_name: Killi
- first_name: Katja
  full_name: Rumpke, Katja
  last_name: Rumpke
- first_name: Dirk
  full_name: Kuckling, Dirk
  id: '287'
  last_name: Kuckling
citation:
  ama: Killi N, Rumpke K, Kuckling D. Synthesis of Curcumin Derivatives via Knoevenagel
    Reaction Within a Continuously Driven Microfluidic Reactor Using Polymeric Networks
    Containing Piperidine as a Catalyst. <i>Gels</i>. 2025;11(4). doi:<a href="https://doi.org/10.3390/gels11040278">10.3390/gels11040278</a>
  apa: Killi, N., Rumpke, K., &#38; Kuckling, D. (2025). Synthesis of Curcumin Derivatives
    via Knoevenagel Reaction Within a Continuously Driven Microfluidic Reactor Using
    Polymeric Networks Containing Piperidine as a Catalyst. <i>Gels</i>, <i>11</i>(4),
    Article 278. <a href="https://doi.org/10.3390/gels11040278">https://doi.org/10.3390/gels11040278</a>
  bibtex: '@article{Killi_Rumpke_Kuckling_2025, title={Synthesis of Curcumin Derivatives
    via Knoevenagel Reaction Within a Continuously Driven Microfluidic Reactor Using
    Polymeric Networks Containing Piperidine as a Catalyst}, volume={11}, DOI={<a
    href="https://doi.org/10.3390/gels11040278">10.3390/gels11040278</a>}, number={4278},
    journal={Gels}, publisher={MDPI AG}, author={Killi, Naresh and Rumpke, Katja and
    Kuckling, Dirk}, year={2025} }'
  chicago: Killi, Naresh, Katja Rumpke, and Dirk Kuckling. “Synthesis of Curcumin
    Derivatives via Knoevenagel Reaction Within a Continuously Driven Microfluidic
    Reactor Using Polymeric Networks Containing Piperidine as a Catalyst.” <i>Gels</i>
    11, no. 4 (2025). <a href="https://doi.org/10.3390/gels11040278">https://doi.org/10.3390/gels11040278</a>.
  ieee: 'N. Killi, K. Rumpke, and D. Kuckling, “Synthesis of Curcumin Derivatives
    via Knoevenagel Reaction Within a Continuously Driven Microfluidic Reactor Using
    Polymeric Networks Containing Piperidine as a Catalyst,” <i>Gels</i>, vol. 11,
    no. 4, Art. no. 278, 2025, doi: <a href="https://doi.org/10.3390/gels11040278">10.3390/gels11040278</a>.'
  mla: Killi, Naresh, et al. “Synthesis of Curcumin Derivatives via Knoevenagel Reaction
    Within a Continuously Driven Microfluidic Reactor Using Polymeric Networks Containing
    Piperidine as a Catalyst.” <i>Gels</i>, vol. 11, no. 4, 278, MDPI AG, 2025, doi:<a
    href="https://doi.org/10.3390/gels11040278">10.3390/gels11040278</a>.
  short: N. Killi, K. Rumpke, D. Kuckling, Gels 11 (2025).
date_created: 2025-04-11T07:12:02Z
date_updated: 2025-04-11T07:13:26Z
department:
- _id: '163'
doi: 10.3390/gels11040278
intvolume: '        11'
issue: '4'
keyword:
- flow chemistry
- heterogeneous catalysis
- sustainable synthesis
- organo-catalysis
- polymeric gel dots
language:
- iso: eng
main_file_link:
- url: https://www.mdpi.com/2310-2861/11/4/278
publication: Gels
publication_identifier:
  issn:
  - 2310-2861
publication_status: published
publisher: MDPI AG
status: public
title: Synthesis of Curcumin Derivatives via Knoevenagel Reaction Within a Continuously
  Driven Microfluidic Reactor Using Polymeric Networks Containing Piperidine as a
  Catalyst
type: journal_article
user_id: '94'
volume: 11
year: '2025'
...
---
_id: '63970'
abstract:
- lang: eng
  text: Abstract Recent advances in solid-state nuclear magnetic resonance (NMR) spectroscopy,
    combined with dynamic nuclear polarization (DNP), quantum chemical DFT calculations,
    and gas-phase NMR spectroscopy investigating the structure and reactivity of heterogeneous
    catalysts are reviewed. The investigated catalysts range from classical mononuclear
    catalysts, like immobilized derivates of Wilkinson’s catalysts over binuclear
    catalysts such as the dirhodium paddlewheel catalyst to catalytic nanoparticles,
    employing various support materials, such as mesoporous silica gels, coordination
    polymers, and biomaterials such as cellulose.
author:
- first_name: Nadia
  full_name: Haro Mares, Nadia
  last_name: Haro Mares
- first_name: Millena
  full_name: Logrado, Millena
  last_name: Logrado
- first_name: Jan
  full_name: Kergassner, Jan
  last_name: Kergassner
- first_name: Bingyu
  full_name: Zhang, Bingyu
  last_name: Zhang
- first_name: Torsten
  full_name: Gutmann, Torsten
  id: '118165'
  last_name: Gutmann
- first_name: Gerd
  full_name: Buntkowsky, Gerd
  last_name: Buntkowsky
citation:
  ama: Haro Mares N, Logrado M, Kergassner J, Zhang B, Gutmann T, Buntkowsky G. Solid-State
    NMR of Heterogeneous Catalysts. <i>ChemCatChem</i>. Published online 2024:e202401159.
    doi:<a href="https://doi.org/10.1002/cctc.202401159">10.1002/cctc.202401159</a>
  apa: Haro Mares, N., Logrado, M., Kergassner, J., Zhang, B., Gutmann, T., &#38;
    Buntkowsky, G. (2024). Solid-State NMR of Heterogeneous Catalysts. <i>ChemCatChem</i>,
    e202401159. <a href="https://doi.org/10.1002/cctc.202401159">https://doi.org/10.1002/cctc.202401159</a>
  bibtex: '@article{Haro Mares_Logrado_Kergassner_Zhang_Gutmann_Buntkowsky_2024, title={Solid-State
    NMR of Heterogeneous Catalysts}, DOI={<a href="https://doi.org/10.1002/cctc.202401159">10.1002/cctc.202401159</a>},
    journal={ChemCatChem}, publisher={John Wiley &#38; Sons, Ltd}, author={Haro Mares,
    Nadia and Logrado, Millena and Kergassner, Jan and Zhang, Bingyu and Gutmann,
    Torsten and Buntkowsky, Gerd}, year={2024}, pages={e202401159} }'
  chicago: Haro Mares, Nadia, Millena Logrado, Jan Kergassner, Bingyu Zhang, Torsten
    Gutmann, and Gerd Buntkowsky. “Solid-State NMR of Heterogeneous Catalysts.” <i>ChemCatChem</i>,
    2024, e202401159. <a href="https://doi.org/10.1002/cctc.202401159">https://doi.org/10.1002/cctc.202401159</a>.
  ieee: 'N. Haro Mares, M. Logrado, J. Kergassner, B. Zhang, T. Gutmann, and G. Buntkowsky,
    “Solid-State NMR of Heterogeneous Catalysts,” <i>ChemCatChem</i>, p. e202401159,
    2024, doi: <a href="https://doi.org/10.1002/cctc.202401159">10.1002/cctc.202401159</a>.'
  mla: Haro Mares, Nadia, et al. “Solid-State NMR of Heterogeneous Catalysts.” <i>ChemCatChem</i>,
    John Wiley &#38; Sons, Ltd, 2024, p. e202401159, doi:<a href="https://doi.org/10.1002/cctc.202401159">10.1002/cctc.202401159</a>.
  short: N. Haro Mares, M. Logrado, J. Kergassner, B. Zhang, T. Gutmann, G. Buntkowsky,
    ChemCatChem (2024) e202401159.
date_created: 2026-02-07T15:40:38Z
date_updated: 2026-02-17T16:17:30Z
doi: 10.1002/cctc.202401159
extern: '1'
keyword:
- solid-state nmr
- heterogeneous catalysis
- dynamic nuclear polarization
- Nanocatalysis
- Surface-reactions
language:
- iso: eng
page: e202401159
publication: ChemCatChem
publication_identifier:
  issn:
  - 1867-3880
publisher: John Wiley & Sons, Ltd
status: public
title: Solid-State NMR of Heterogeneous Catalysts
type: journal_article
user_id: '100715'
year: '2024'
...
---
_id: '35645'
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.
article_type: original
author:
- first_name: Amit
  full_name: Kumar, Amit
  last_name: Kumar
- first_name: Dirk
  full_name: Kuckling, Dirk
  id: '287'
  last_name: Kuckling
- first_name: Leena
  full_name: Nebhani, Leena
  last_name: Nebhani
citation:
  ama: Kumar A, Kuckling D, Nebhani L. Quinuclidine-Immobilized Porous Polymeric Microparticles
    as a Compelling Catalyst for the Baylis–Hillman Reaction. <i>ACS Applied Polymer
    Materials</i>. 2022;4(12):8996-9005. doi:<a href="https://doi.org/10.1021/acsapm.2c01330">10.1021/acsapm.2c01330</a>
  apa: Kumar, A., Kuckling, D., &#38; Nebhani, L. (2022). Quinuclidine-Immobilized
    Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman
    Reaction. <i>ACS Applied Polymer Materials</i>, <i>4</i>(12), 8996–9005. <a href="https://doi.org/10.1021/acsapm.2c01330">https://doi.org/10.1021/acsapm.2c01330</a>
  bibtex: '@article{Kumar_Kuckling_Nebhani_2022, title={Quinuclidine-Immobilized Porous
    Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction},
    volume={4}, DOI={<a href="https://doi.org/10.1021/acsapm.2c01330">10.1021/acsapm.2c01330</a>},
    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} }'
  chicago: 'Kumar, Amit, Dirk Kuckling, and Leena Nebhani. “Quinuclidine-Immobilized
    Porous Polymeric Microparticles as a Compelling Catalyst for the Baylis–Hillman
    Reaction.” <i>ACS Applied Polymer Materials</i> 4, no. 12 (2022): 8996–9005. <a
    href="https://doi.org/10.1021/acsapm.2c01330">https://doi.org/10.1021/acsapm.2c01330</a>.'
  ieee: 'A. Kumar, D. Kuckling, and L. Nebhani, “Quinuclidine-Immobilized Porous Polymeric
    Microparticles as a Compelling Catalyst for the Baylis–Hillman Reaction,” <i>ACS
    Applied Polymer Materials</i>, vol. 4, no. 12, pp. 8996–9005, 2022, doi: <a href="https://doi.org/10.1021/acsapm.2c01330">10.1021/acsapm.2c01330</a>.'
  mla: Kumar, Amit, et al. “Quinuclidine-Immobilized Porous Polymeric Microparticles
    as a Compelling Catalyst for the Baylis–Hillman Reaction.” <i>ACS Applied Polymer
    Materials</i>, vol. 4, no. 12, American Chemical Society (ACS), 2022, pp. 8996–9005,
    doi:<a href="https://doi.org/10.1021/acsapm.2c01330">10.1021/acsapm.2c01330</a>.
  short: A. Kumar, D. Kuckling, L. Nebhani, ACS Applied Polymer Materials 4 (2022)
    8996–9005.
date_created: 2023-01-10T08:07:12Z
date_updated: 2023-01-10T08:12:15Z
department:
- _id: '163'
doi: 10.1021/acsapm.2c01330
intvolume: '         4'
issue: '12'
keyword:
- distillation−precipitation polymerization
- porous microparticles
- heterogeneous catalysis Baylis−Hillman reaction
- reusable catalyst
language:
- iso: eng
main_file_link:
- url: https://pubs.acs.org/doi/10.1021/acsapm.2c01330
page: 8996-9005
publication: ACS Applied Polymer Materials
publication_identifier:
  issn:
  - 2637-6105
  - 2637-6105
publication_status: published
publisher: American Chemical Society (ACS)
status: public
title: Quinuclidine-Immobilized Porous Polymeric Microparticles as a Compelling Catalyst
  for the Baylis–Hillman Reaction
type: journal_article
user_id: '94'
volume: 4
year: '2022'
...
---
_id: '63960'
abstract:
- lang: eng
  text: Recent advances in solid-state nuclear magnetic resonance (NMR) spectroscopy
    and dynamic nuclear polarization (DNP) of nanostructured materials are reviewed.
    A first group of materials is based on crystalline nanocellulose (CNC) or microcrystalline
    cellulose (MCC), which are used as carrier materials for dye molecules, catalysts
    or in combination with heterocyclic molecules as ion conducting membranes. These
    materials have widespread applications in sensorics, optics, catalysis or fuel
    cell research. A second group are metal oxides such as V-Mo-W oxides, which are
    of enormous importance in the manufacturing process of basic chemicals. The third
    group are catalytically active nanocrystalline metal nanoparticles, coated with
    protectants or embedded in polymers. The last group includes of lead-free perovskite
    materials, which are employed as environmentally benign substitution materials
    for conventional lead-based electronics materials. These materials are discussed
    in terms of their application and physico-chemical characterization by solid-state
    NMR techniques, combined with gas-phase NMR and quantum-chemical modelling on
    the density functional theory (DFT) level. The application of multinuclear 1H,
    2H, 13C, 15N and 23Na solid state NMR techniques under static or MAS conditions
    for the characterization of these materials, their surfaces and processes on their
    surfaces is discussed. Moreover, the analytic power of the combination of these
    techniques with DNP for the identification of low-concentrated carbon and nitrogen
    containing surface species in natural abundance is reviewed. Finally, approaches
    for sensitivity enhancement by DNP of quadrupolar nuclei such as 17O and 51V are
    presented that enable the identification of catalytic sites in metal oxide catalysts.
author:
- first_name: Torsten
  full_name: Gutmann, Torsten
  id: '118165'
  last_name: Gutmann
- first_name: Pedro B.
  full_name: Groszewicz, Pedro B.
  last_name: Groszewicz
- first_name: Gerd
  full_name: Buntkowsky, Gerd
  last_name: Buntkowsky
citation:
  ama: Gutmann T, Groszewicz PB, Buntkowsky G. Solid-state NMR of nanocrystals. <i>Annual
    Reports on NMR Spectroscopy</i>. 2019;97:1–82. doi:<a href="https://doi.org/10.1016/bs.arnmr.2018.12.001">10.1016/bs.arnmr.2018.12.001</a>
  apa: Gutmann, T., Groszewicz, P. B., &#38; Buntkowsky, G. (2019). Solid-state NMR
    of nanocrystals. <i>Annual Reports on NMR Spectroscopy</i>, <i>97</i>, 1–82. <a
    href="https://doi.org/10.1016/bs.arnmr.2018.12.001">https://doi.org/10.1016/bs.arnmr.2018.12.001</a>
  bibtex: '@article{Gutmann_Groszewicz_Buntkowsky_2019, title={Solid-state NMR of
    nanocrystals}, volume={97}, DOI={<a href="https://doi.org/10.1016/bs.arnmr.2018.12.001">10.1016/bs.arnmr.2018.12.001</a>},
    journal={Annual Reports on NMR Spectroscopy}, author={Gutmann, Torsten and Groszewicz,
    Pedro B. and Buntkowsky, Gerd}, year={2019}, pages={1–82} }'
  chicago: 'Gutmann, Torsten, Pedro B. Groszewicz, and Gerd Buntkowsky. “Solid-State
    NMR of Nanocrystals.” <i>Annual Reports on NMR Spectroscopy</i> 97 (2019): 1–82.
    <a href="https://doi.org/10.1016/bs.arnmr.2018.12.001">https://doi.org/10.1016/bs.arnmr.2018.12.001</a>.'
  ieee: 'T. Gutmann, P. B. Groszewicz, and G. Buntkowsky, “Solid-state NMR of nanocrystals,”
    <i>Annual Reports on NMR Spectroscopy</i>, vol. 97, pp. 1–82, 2019, doi: <a href="https://doi.org/10.1016/bs.arnmr.2018.12.001">10.1016/bs.arnmr.2018.12.001</a>.'
  mla: Gutmann, Torsten, et al. “Solid-State NMR of Nanocrystals.” <i>Annual Reports
    on NMR Spectroscopy</i>, vol. 97, 2019, pp. 1–82, doi:<a href="https://doi.org/10.1016/bs.arnmr.2018.12.001">10.1016/bs.arnmr.2018.12.001</a>.
  short: T. Gutmann, P.B. Groszewicz, G. Buntkowsky, Annual Reports on NMR Spectroscopy
    97 (2019) 1–82.
date_created: 2026-02-07T15:37:03Z
date_updated: 2026-02-17T16:17:56Z
doi: 10.1016/bs.arnmr.2018.12.001
extern: '1'
intvolume: '        97'
keyword:
- solid-state nmr
- heterogeneous catalysis
- dynamic nuclear polarization
- Ferroelectrics
- Nanocatalysis
- Surface reactions
language:
- iso: eng
page: 1–82
publication: Annual Reports on NMR Spectroscopy
status: public
title: Solid-state NMR of nanocrystals
type: journal_article
user_id: '100715'
volume: 97
year: '2019'
...
---
_id: '63956'
abstract:
- lang: eng
  text: The synthesis of novel robust and stable iridium-based immobilized catalysts
    on silica-polymer hybrid materials (Si-PB-Ir) is described. These catalysts are
    characterized by a combination of 1D P-31 CP-MAS and 2D P-31-H-1 HETCOR and J-resolved
    multinuclear solid state NMR experiments. Different binding situations such as
    singly and multiply coordinated phosphines are identified. Density functional
    theory (DFT) calculations are performed to corroborate the interpretation of the
    experimental NMR data, in order to propose a structural model of the heterogenized
    catalysts. Finally, the catalytic activity of the Si-PB-Ir catalysts is investigated
    for the hydrogenation of styrene employing para-enriched hydrogen gas.
author:
- first_name: Torsten
  full_name: Gutmann, Torsten
  id: '118165'
  last_name: Gutmann
- first_name: S.
  full_name: Alkhagani, S.
  last_name: Alkhagani
- first_name: N.
  full_name: Rothermel, N.
  last_name: Rothermel
- first_name: H. H.
  full_name: Limbach, H. H.
  last_name: Limbach
- first_name: H.
  full_name: Breitzke, H.
  last_name: Breitzke
- first_name: G.
  full_name: Buntkowsky, G.
  last_name: Buntkowsky
citation:
  ama: Gutmann T, Alkhagani S, Rothermel N, Limbach HH, Breitzke H, Buntkowsky G.
    P-31-Solid-State NMR Characterization and Catalytic Hydrogenation Tests of Novel
    heterogenized Iridium-Catalysts. <i>Zeitschrift Fur Physikalische Chemie-International
    Journal of Research in Physical Chemistry &#38; Chemical Physics</i>. 2017;231(3):653–669.
    doi:<a href="https://doi.org/10.1515/zpch-2016-0837">10.1515/zpch-2016-0837</a>
  apa: Gutmann, T., Alkhagani, S., Rothermel, N., Limbach, H. H., Breitzke, H., &#38;
    Buntkowsky, G. (2017). P-31-Solid-State NMR Characterization and Catalytic Hydrogenation
    Tests of Novel heterogenized Iridium-Catalysts. <i>Zeitschrift Fur Physikalische
    Chemie-International Journal of Research in Physical Chemistry &#38; Chemical
    Physics</i>, <i>231</i>(3), 653–669. <a href="https://doi.org/10.1515/zpch-2016-0837">https://doi.org/10.1515/zpch-2016-0837</a>
  bibtex: '@article{Gutmann_Alkhagani_Rothermel_Limbach_Breitzke_Buntkowsky_2017,
    title={P-31-Solid-State NMR Characterization and Catalytic Hydrogenation Tests
    of Novel heterogenized Iridium-Catalysts}, volume={231}, DOI={<a href="https://doi.org/10.1515/zpch-2016-0837">10.1515/zpch-2016-0837</a>},
    number={3}, journal={Zeitschrift Fur Physikalische Chemie-International Journal
    of Research in Physical Chemistry &#38; Chemical Physics}, author={Gutmann, Torsten
    and Alkhagani, S. and Rothermel, N. and Limbach, H. H. and Breitzke, H. and Buntkowsky,
    G.}, year={2017}, pages={653–669} }'
  chicago: 'Gutmann, Torsten, S. Alkhagani, N. Rothermel, H. H. Limbach, H. Breitzke,
    and G. Buntkowsky. “P-31-Solid-State NMR Characterization and Catalytic Hydrogenation
    Tests of Novel Heterogenized Iridium-Catalysts.” <i>Zeitschrift Fur Physikalische
    Chemie-International Journal of Research in Physical Chemistry &#38; Chemical
    Physics</i> 231, no. 3 (2017): 653–669. <a href="https://doi.org/10.1515/zpch-2016-0837">https://doi.org/10.1515/zpch-2016-0837</a>.'
  ieee: 'T. Gutmann, S. Alkhagani, N. Rothermel, H. H. Limbach, H. Breitzke, and G.
    Buntkowsky, “P-31-Solid-State NMR Characterization and Catalytic Hydrogenation
    Tests of Novel heterogenized Iridium-Catalysts,” <i>Zeitschrift Fur Physikalische
    Chemie-International Journal of Research in Physical Chemistry &#38; Chemical
    Physics</i>, vol. 231, no. 3, pp. 653–669, 2017, doi: <a href="https://doi.org/10.1515/zpch-2016-0837">10.1515/zpch-2016-0837</a>.'
  mla: Gutmann, Torsten, et al. “P-31-Solid-State NMR Characterization and Catalytic
    Hydrogenation Tests of Novel Heterogenized Iridium-Catalysts.” <i>Zeitschrift
    Fur Physikalische Chemie-International Journal of Research in Physical Chemistry
    &#38; Chemical Physics</i>, vol. 231, no. 3, 2017, pp. 653–669, doi:<a href="https://doi.org/10.1515/zpch-2016-0837">10.1515/zpch-2016-0837</a>.
  short: T. Gutmann, S. Alkhagani, N. Rothermel, H.H. Limbach, H. Breitzke, G. Buntkowsky,
    Zeitschrift Fur Physikalische Chemie-International Journal of Research in Physical
    Chemistry &#38; Chemical Physics 231 (2017) 653–669.
date_created: 2026-02-07T15:35:41Z
date_updated: 2026-02-17T16:18:04Z
doi: 10.1515/zpch-2016-0837
extern: '1'
intvolume: '       231'
issue: '3'
keyword:
- Chemistry
- dynamic nuclear-polarization
- solid-state nmr
- DFT
- heterogeneous catalysis
- hydrido complexes
- hydrogenation
- immobilized catalyst
- inorganic hybrid
- iridium
- materials
- mesoporous
- molecular-orbital methods
- PHIP
- phosphine complexes
- reusable catalysts
- silica
- solid-state-NMR
- wilkinsons catalyst
language:
- iso: eng
page: 653–669
publication: Zeitschrift Fur Physikalische Chemie-International Journal of Research
  in Physical Chemistry & Chemical Physics
publication_identifier:
  issn:
  - 0942-9352
status: public
title: P-31-Solid-State NMR Characterization and Catalytic Hydrogenation Tests of
  Novel heterogenized Iridium-Catalysts
type: journal_article
user_id: '100715'
volume: 231
year: '2017'
...
---
_id: '64047'
abstract:
- lang: eng
  text: A novel strategy for the immobilization of Wilkinson’s catalyst on silica
    nanoparticles is presented, employing pyridyl linkers as anchoring groups. The
    coordination binding of the catalyst to the pyridyl linker via ligand exchange
    of the trans-phosphine group is verified by 1 D and 2 D solid-state NMR spectroscopy.
    Catalytic activities are monitored by GC employing the hydrogenation of styrene
    as model reaction, and the leaching properties as well as the robustness of the
    catalyst are investigated. The resulting immobilized catalyst shows high catalytic
    activity, which is within a factor of three comparable to the homogeneous catalyst,
    and excellent stability in leaching tests. Finally, it is efficient to produce
    hyperpolarization in solution by employing parahydrogen-enriched hydrogen gas
    for hydrogenation.
author:
- first_name: Mohamad
  full_name: Srour, Mohamad
  last_name: Srour
- first_name: Sara
  full_name: Hadjiali, Sara
  last_name: Hadjiali
- first_name: Grit
  full_name: Sauer, Grit
  last_name: Sauer
- first_name: Kai
  full_name: Brunnengräber, Kai
  last_name: Brunnengräber
- first_name: Hergen
  full_name: Breitzke, Hergen
  last_name: Breitzke
- first_name: Yeping
  full_name: Xu, Yeping
  last_name: Xu
- first_name: Heiko
  full_name: Weidler, Heiko
  last_name: Weidler
- 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: Srour M, Hadjiali S, Sauer G, et al. Synthesis and Solid-State NMR Characterization
    of a Robust, Pyridyl-Based Immobilized Wilkinson’s Type Catalyst with High Catalytic
    Performance. <i>ChemCatChem</i>. 2016;8(21):3409–3416. doi:<a href="https://doi.org/10.1002/cctc.201600882">10.1002/cctc.201600882</a>
  apa: Srour, M., Hadjiali, S., Sauer, G., Brunnengräber, K., Breitzke, H., Xu, Y.,
    Weidler, H., Limbach, H.-H., Gutmann, T., &#38; Buntkowsky, G. (2016). Synthesis
    and Solid-State NMR Characterization of a Robust, Pyridyl-Based Immobilized Wilkinson’s
    Type Catalyst with High Catalytic Performance. <i>ChemCatChem</i>, <i>8</i>(21),
    3409–3416. <a href="https://doi.org/10.1002/cctc.201600882">https://doi.org/10.1002/cctc.201600882</a>
  bibtex: '@article{Srour_Hadjiali_Sauer_Brunnengräber_Breitzke_Xu_Weidler_Limbach_Gutmann_Buntkowsky_2016,
    title={Synthesis and Solid-State NMR Characterization of a Robust, Pyridyl-Based
    Immobilized Wilkinson’s Type Catalyst with High Catalytic Performance}, volume={8},
    DOI={<a href="https://doi.org/10.1002/cctc.201600882">10.1002/cctc.201600882</a>},
    number={21}, journal={ChemCatChem}, author={Srour, Mohamad and Hadjiali, Sara
    and Sauer, Grit and Brunnengräber, Kai and Breitzke, Hergen and Xu, Yeping and
    Weidler, Heiko and Limbach, Hans-Heinrich and Gutmann, Torsten and Buntkowsky,
    Gerd}, year={2016}, pages={3409–3416} }'
  chicago: 'Srour, Mohamad, Sara Hadjiali, Grit Sauer, Kai Brunnengräber, Hergen Breitzke,
    Yeping Xu, Heiko Weidler, Hans-Heinrich Limbach, Torsten Gutmann, and Gerd Buntkowsky.
    “Synthesis and Solid-State NMR Characterization of a Robust, Pyridyl-Based Immobilized
    Wilkinson’s Type Catalyst with High Catalytic Performance.” <i>ChemCatChem</i>
    8, no. 21 (2016): 3409–3416. <a href="https://doi.org/10.1002/cctc.201600882">https://doi.org/10.1002/cctc.201600882</a>.'
  ieee: 'M. Srour <i>et al.</i>, “Synthesis and Solid-State NMR Characterization of
    a Robust, Pyridyl-Based Immobilized Wilkinson’s Type Catalyst with High Catalytic
    Performance,” <i>ChemCatChem</i>, vol. 8, no. 21, pp. 3409–3416, 2016, doi: <a
    href="https://doi.org/10.1002/cctc.201600882">10.1002/cctc.201600882</a>.'
  mla: Srour, Mohamad, et al. “Synthesis and Solid-State NMR Characterization of a
    Robust, Pyridyl-Based Immobilized Wilkinson’s Type Catalyst with High Catalytic
    Performance.” <i>ChemCatChem</i>, vol. 8, no. 21, 2016, pp. 3409–3416, doi:<a
    href="https://doi.org/10.1002/cctc.201600882">10.1002/cctc.201600882</a>.
  short: M. Srour, S. Hadjiali, G. Sauer, K. Brunnengräber, H. Breitzke, Y. Xu, H.
    Weidler, H.-H. Limbach, T. Gutmann, G. Buntkowsky, ChemCatChem 8 (2016) 3409–3416.
date_created: 2026-02-07T16:12:46Z
date_updated: 2026-02-17T16:13:06Z
doi: 10.1002/cctc.201600882
extern: '1'
intvolume: '         8'
issue: '21'
keyword:
- heterogeneous catalysis
- hydrogenation
- immobilization
- phosphane ligands
- rhodium
language:
- iso: eng
page: 3409–3416
publication: ChemCatChem
status: public
title: Synthesis and Solid-State NMR Characterization of a Robust, Pyridyl-Based Immobilized
  Wilkinson’s Type Catalyst with High Catalytic Performance
type: journal_article
user_id: '100715'
volume: 8
year: '2016'
...
---
_id: '63963'
abstract:
- lang: eng
  text: A novel heterogeneous dirhodium catalyst has been synthesized. This stable
    catalyst is constructed from dirhodium acetate dimer (Rh2(OAc)4) units, which
    are covalently linked to amine- and carboxyl-bifunctionalized mesoporous silica
    (SBA-15NH2COOH). It shows good efficiency in catalyzing the cyclopropanation
    reaction of styrene and ethyl diazoacetate (EDA) forming cis- and trans-1-ethoxycarbonyl-2-phenylcyclopropane.
    To characterize the structure of this catalyst and to confirm the successful immobilization,
    heteronuclear solid-state NMR experiments have been performed. The high application
    potential of dynamic nuclear polarization (DNP) NMR for the analysis of binding
    sites in this novel catalyst is demonstrated. Signal-enhanced 13C CP MAS and 15N
    CP MAS techniques have been employed to detect different carboxyl and amine binding
    sites in natural abundance on a fast time scale. The interpretation of the experimental
    chemical shift values for different binding sites has been corroborated by quantum
    chemical calculations on dirhodium model complexes.
author:
- first_name: Torsten
  full_name: Gutmann, Torsten
  id: '118165'
  last_name: Gutmann
- first_name: Jiquan
  full_name: Liu, Jiquan
  last_name: Liu
- first_name: Niels
  full_name: Rothermel, Niels
  last_name: Rothermel
- first_name: Yeping
  full_name: Xu, Yeping
  last_name: Xu
- first_name: Eva
  full_name: Jaumann, Eva
  last_name: Jaumann
- first_name: Mayke
  full_name: Werner, Mayke
  last_name: Werner
- first_name: Hergen
  full_name: Breitzke, Hergen
  last_name: Breitzke
- first_name: Snorri T.
  full_name: Sigurdsson, Snorri T.
  last_name: Sigurdsson
- first_name: Gerd
  full_name: Buntkowsky, Gerd
  last_name: Buntkowsky
citation:
  ama: 'Gutmann T, Liu J, Rothermel N, et al. Natural Abundance 15N NMR by Dynamic
    Nuclear Polarization: Fast Analysis of Binding Sites of a Novel Amine-Carboxyl-Linked
    Immobilized Dirhodium Catalyst. <i>Chemistry A European Journal</i>. 2015;21(9):3798–3805.
    doi:<a href="https://doi.org/10.1002/chem.201405043">10.1002/chem.201405043</a>'
  apa: 'Gutmann, T., Liu, J., Rothermel, N., Xu, Y., Jaumann, E., Werner, M., Breitzke,
    H., Sigurdsson, S. T., &#38; Buntkowsky, G. (2015). Natural Abundance 15N NMR
    by Dynamic Nuclear Polarization: Fast Analysis of Binding Sites of a Novel Amine-Carboxyl-Linked
    Immobilized Dirhodium Catalyst. <i>Chemistry A European Journal</i>, <i>21</i>(9),
    3798–3805. <a href="https://doi.org/10.1002/chem.201405043">https://doi.org/10.1002/chem.201405043</a>'
  bibtex: '@article{Gutmann_Liu_Rothermel_Xu_Jaumann_Werner_Breitzke_Sigurdsson_Buntkowsky_2015,
    title={Natural Abundance 15N NMR by Dynamic Nuclear Polarization: Fast Analysis
    of Binding Sites of a Novel Amine-Carboxyl-Linked Immobilized Dirhodium Catalyst},
    volume={21}, DOI={<a href="https://doi.org/10.1002/chem.201405043">10.1002/chem.201405043</a>},
    number={9}, journal={Chemistry A European Journal}, publisher={WILEY-VCH Verlag},
    author={Gutmann, Torsten and Liu, Jiquan and Rothermel, Niels and Xu, Yeping and
    Jaumann, Eva and Werner, Mayke and Breitzke, Hergen and Sigurdsson, Snorri T.
    and Buntkowsky, Gerd}, year={2015}, pages={3798–3805} }'
  chicago: 'Gutmann, Torsten, Jiquan Liu, Niels Rothermel, Yeping Xu, Eva Jaumann,
    Mayke Werner, Hergen Breitzke, Snorri T. Sigurdsson, and Gerd Buntkowsky. “Natural
    Abundance 15N NMR by Dynamic Nuclear Polarization: Fast Analysis of Binding Sites
    of a Novel Amine-Carboxyl-Linked Immobilized Dirhodium Catalyst.” <i>Chemistry
    A European Journal</i> 21, no. 9 (2015): 3798–3805. <a href="https://doi.org/10.1002/chem.201405043">https://doi.org/10.1002/chem.201405043</a>.'
  ieee: 'T. Gutmann <i>et al.</i>, “Natural Abundance 15N NMR by Dynamic Nuclear Polarization:
    Fast Analysis of Binding Sites of a Novel Amine-Carboxyl-Linked Immobilized Dirhodium
    Catalyst,” <i>Chemistry A European Journal</i>, vol. 21, no. 9, pp. 3798–3805,
    2015, doi: <a href="https://doi.org/10.1002/chem.201405043">10.1002/chem.201405043</a>.'
  mla: 'Gutmann, Torsten, et al. “Natural Abundance 15N NMR by Dynamic Nuclear Polarization:
    Fast Analysis of Binding Sites of a Novel Amine-Carboxyl-Linked Immobilized Dirhodium
    Catalyst.” <i>Chemistry A European Journal</i>, vol. 21, no. 9, WILEY-VCH Verlag,
    2015, pp. 3798–3805, doi:<a href="https://doi.org/10.1002/chem.201405043">10.1002/chem.201405043</a>.'
  short: T. Gutmann, J. Liu, N. Rothermel, Y. Xu, E. Jaumann, M. Werner, H. Breitzke,
    S.T. Sigurdsson, G. Buntkowsky, Chemistry A European Journal 21 (2015) 3798–3805.
date_created: 2026-02-07T15:38:07Z
date_updated: 2026-02-17T16:17:50Z
doi: 10.1002/chem.201405043
extern: '1'
intvolume: '        21'
issue: '9'
keyword:
- heterogeneous catalysis
- immobilized catalyst
- dynamic nuclear polarization
- hyperpolarization
- NMR spectroscopy
language:
- iso: eng
page: 3798–3805
publication: Chemistry A European Journal
publisher: WILEY-VCH Verlag
status: public
title: 'Natural Abundance 15N NMR by Dynamic Nuclear Polarization: Fast Analysis of
  Binding Sites of a Novel Amine-Carboxyl-Linked Immobilized Dirhodium Catalyst'
type: journal_article
user_id: '100715'
volume: 21
year: '2015'
...
