---
_id: '51045'
author:
- first_name: Jil
full_name: Muller, Jil
id: '91668'
last_name: Muller
orcid: 0000-0002-4394-7531
citation:
ama: Muller J. Women and early modern Philosophy and Science. Rivista di storia
della filosofia. 2018;73(4):673-676. doi:10.3280/SF2018-004006
apa: Muller, J. (2018). Women and early modern Philosophy and Science. In Rivista
di storia della filosofia (Vol. 73, Issue 4, pp. 673–676). Franco Angeli.
https://doi.org/10.3280/SF2018-004006
bibtex: '@article{Muller_2018, place={Milan}, title={Women and early modern Philosophy
and Science}, volume={73}, DOI={10.3280/SF2018-004006},
number={4}, journal={Rivista di storia della filosofia}, publisher={ Franco Angeli},
author={Muller, Jil}, year={2018}, pages={673–676} }'
chicago: 'Muller, Jil. “Women and Early Modern Philosophy and Science.” Rivista
Di Storia Della Filosofia. Milan: Franco Angeli, 2018. https://doi.org/10.3280/SF2018-004006.'
ieee: 'J. Muller, “Women and early modern Philosophy and Science,” Rivista di
storia della filosofia, vol. 73, no. 4. Franco Angeli, Milan, pp. 673–676,
2018, doi: 10.3280/SF2018-004006.'
mla: Muller, Jil. “Women and Early Modern Philosophy and Science.” Rivista Di
Storia Della Filosofia, vol. 73, no. 4, Franco Angeli, 2018, pp. 673–76,
doi:10.3280/SF2018-004006.
short: J. Muller, Rivista Di Storia Della Filosofia 73 (2018) 673–676.
date_created: 2024-01-30T14:02:52Z
date_updated: 2026-02-16T12:50:46Z
doi: 10.3280/SF2018-004006
intvolume: ' 73'
issue: '4'
language:
- iso: eng
page: 673-676
place: Milan
publication: Rivista di storia della filosofia
publication_identifier:
issn:
- 0393-2516
publication_status: published
publisher: ' Franco Angeli'
status: public
title: Women and early modern Philosophy and Science
type: review
user_id: '91668'
volume: 73
year: '2018'
...
---
_id: '64054'
abstract:
- lang: eng
text: In this work, the preparation of porous hybrid particle-based films by core-shell
particle design and convenient film preparation is reported. Monodisperse core
particles consisting of poly(methyl methacrylate‑co‑allyl methacrylate) (P(MMA‑co‑ALMA))
were synthesized by starved-feed emulsion polymerization followed by the introduction
of an initiator-containing monomer (inimer) for subsequent atom transfer radical
polymerization (ATRP). The inimer shell allowed for the introduction of allylhydrido
polycarbosilane (SMP-10) under ATRP conditions by grafting to the core particles.
The functionalization of the prepared core-shell particles was investigated by
IR spectroscopy (FTIR), scanning transmission electron microscopy (STEM) and solid-state
NMR combined with dynamic nuclear polarization (DNP). The obtained hard core/soft
preceramic shell particles were subjected to the melt-shear organization technique,
enabling a convenient alignment into a colloidal crystal structure in one single
step without the presence of a dispersion medium or solvent for the designed particles.
Moreover, the hybrid particle-based films were converted into a porous ceramic
structure upon thermal treatment. As a result, freestanding ceramic porous films
have been obtained after degradation of the organic template core particles. Noteworthy,
the conversion of the matrix material consisting of SMP-10 into the ceramic occurred
with preservation of the pristine colloidal crystal template structure. Herein,
the first example of core-shell particle preparation by combining different polymerization
methodologies and application of the convenient melt-shear organization technique
is shown, paving a new way to ceramic materials with tailored morphology and porosity.
author:
- first_name: Steffen
full_name: Vowinkel, Steffen
last_name: Vowinkel
- first_name: Anna
full_name: Boehm, Anna
last_name: Boehm
- first_name: Timmy
full_name: Schäfer, Timmy
last_name: Schäfer
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: Emanuel
full_name: Ionescu, Emanuel
last_name: Ionescu
- first_name: Markus
full_name: Gallei, Markus
last_name: Gallei
citation:
ama: Vowinkel S, Boehm A, Schäfer T, Gutmann T, Ionescu E, Gallei M. Preceramic
core-shell particles for the preparation of hybrid colloidal crystal films by
melt-shear organization and conversion into porous ceramics. Materials &
Design. 2018;160:926–935. doi:10.1016/j.matdes.2018.10.032
apa: Vowinkel, S., Boehm, A., Schäfer, T., Gutmann, T., Ionescu, E., & Gallei,
M. (2018). Preceramic core-shell particles for the preparation of hybrid colloidal
crystal films by melt-shear organization and conversion into porous ceramics.
Materials & Design, 160, 926–935. https://doi.org/10.1016/j.matdes.2018.10.032
bibtex: '@article{Vowinkel_Boehm_Schäfer_Gutmann_Ionescu_Gallei_2018, title={Preceramic
core-shell particles for the preparation of hybrid colloidal crystal films by
melt-shear organization and conversion into porous ceramics}, volume={160}, DOI={10.1016/j.matdes.2018.10.032},
journal={Materials & Design}, author={Vowinkel, Steffen and Boehm, Anna and
Schäfer, Timmy and Gutmann, Torsten and Ionescu, Emanuel and Gallei, Markus},
year={2018}, pages={926–935} }'
chicago: 'Vowinkel, Steffen, Anna Boehm, Timmy Schäfer, Torsten Gutmann, Emanuel
Ionescu, and Markus Gallei. “Preceramic Core-Shell Particles for the Preparation
of Hybrid Colloidal Crystal Films by Melt-Shear Organization and Conversion into
Porous Ceramics.” Materials & Design 160 (2018): 926–935. https://doi.org/10.1016/j.matdes.2018.10.032.'
ieee: 'S. Vowinkel, A. Boehm, T. Schäfer, T. Gutmann, E. Ionescu, and M. Gallei,
“Preceramic core-shell particles for the preparation of hybrid colloidal crystal
films by melt-shear organization and conversion into porous ceramics,” Materials
& Design, vol. 160, pp. 926–935, 2018, doi: 10.1016/j.matdes.2018.10.032.'
mla: Vowinkel, Steffen, et al. “Preceramic Core-Shell Particles for the Preparation
of Hybrid Colloidal Crystal Films by Melt-Shear Organization and Conversion into
Porous Ceramics.” Materials & Design, vol. 160, 2018, pp. 926–935,
doi:10.1016/j.matdes.2018.10.032.
short: S. Vowinkel, A. Boehm, T. Schäfer, T. Gutmann, E. Ionescu, M. Gallei, Materials
& Design 160 (2018) 926–935.
date_created: 2026-02-07T16:15:42Z
date_updated: 2026-02-17T16:12:52Z
doi: 10.1016/j.matdes.2018.10.032
extern: '1'
intvolume: ' 160'
keyword:
- emulsion polymerization
- self-assembly
- ATRP
- Colloidal crystal
- Hybrid film
- Particle processing
language:
- iso: eng
page: 926–935
publication: Materials & Design
status: public
title: Preceramic core-shell particles for the preparation of hybrid colloidal crystal
films by melt-shear organization and conversion into porous ceramics
type: journal_article
user_id: '100715'
volume: 160
year: '2018'
...
---
_id: '64031'
abstract:
- lang: eng
text: The activation of C-H bonds of alkanes remains a major challenge for chemistry.
In a series of deuteration experiments with D-2 in contact with bis-(diphenylphosphino)
butane (dppb) stabilized ruthenium nanoparticles (liquid substrates, 60 degrees
C, 6 bar D-2) we have observed a surprisingly large reactivity of cyclopentane
as compared to cyclohexane and other alkanes. DFT calculations using a ligand-free
Ru13H17 model cluster as catalyst indicate oxidative C-H cleavage of the bound
substrates as rate limiting reaction step. They also indicate similar binding
and activation enthalpies of reactions of cyclopentane and cyclohexane.
author:
- first_name: N.
full_name: Rothermel, N.
last_name: Rothermel
- first_name: D.
full_name: Bouzouita, D.
last_name: Bouzouita
- first_name: T.
full_name: Rother, T.
last_name: Rother
- first_name: I.
full_name: Rosal, I.
last_name: Rosal
- first_name: S.
full_name: Tricard, S.
last_name: Tricard
- first_name: R.
full_name: Poteau, R.
last_name: Poteau
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: B.
full_name: Chaudret, B.
last_name: Chaudret
- first_name: H. H.
full_name: Limbach, H. H.
last_name: Limbach
- first_name: G.
full_name: Buntkowsky, G.
last_name: Buntkowsky
citation:
ama: 'Rothermel N, Bouzouita D, Rother T, et al. Surprising Differences of Alkane
C-H Activation Catalyzed by Ruthenium Nanoparticles: Complex Surface-Substrate
Recognition? ChemCatChem. 2018;10(19):4243–4247. doi:10.1002/cctc.201801022'
apa: 'Rothermel, N., Bouzouita, D., Rother, T., Rosal, I., Tricard, S., Poteau,
R., Gutmann, T., Chaudret, B., Limbach, H. H., & Buntkowsky, G. (2018). Surprising
Differences of Alkane C-H Activation Catalyzed by Ruthenium Nanoparticles: Complex
Surface-Substrate Recognition? ChemCatChem, 10(19), 4243–4247. https://doi.org/10.1002/cctc.201801022'
bibtex: '@article{Rothermel_Bouzouita_Rother_Rosal_Tricard_Poteau_Gutmann_Chaudret_Limbach_Buntkowsky_2018,
title={Surprising Differences of Alkane C-H Activation Catalyzed by Ruthenium
Nanoparticles: Complex Surface-Substrate Recognition?}, volume={10}, DOI={10.1002/cctc.201801022},
number={19}, journal={ChemCatChem}, author={Rothermel, N. and Bouzouita, D. and
Rother, T. and Rosal, I. and Tricard, S. and Poteau, R. and Gutmann, Torsten and
Chaudret, B. and Limbach, H. H. and Buntkowsky, G.}, year={2018}, pages={4243–4247}
}'
chicago: 'Rothermel, N., D. Bouzouita, T. Rother, I. Rosal, S. Tricard, R. Poteau,
Torsten Gutmann, B. Chaudret, H. H. Limbach, and G. Buntkowsky. “Surprising Differences
of Alkane C-H Activation Catalyzed by Ruthenium Nanoparticles: Complex Surface-Substrate
Recognition?” ChemCatChem 10, no. 19 (2018): 4243–4247. https://doi.org/10.1002/cctc.201801022.'
ieee: 'N. Rothermel et al., “Surprising Differences of Alkane C-H Activation
Catalyzed by Ruthenium Nanoparticles: Complex Surface-Substrate Recognition?,”
ChemCatChem, vol. 10, no. 19, pp. 4243–4247, 2018, doi: 10.1002/cctc.201801022.'
mla: 'Rothermel, N., et al. “Surprising Differences of Alkane C-H Activation Catalyzed
by Ruthenium Nanoparticles: Complex Surface-Substrate Recognition?” ChemCatChem,
vol. 10, no. 19, 2018, pp. 4243–4247, doi:10.1002/cctc.201801022.'
short: N. Rothermel, D. Bouzouita, T. Rother, I. Rosal, S. Tricard, R. Poteau, T.
Gutmann, B. Chaudret, H.H. Limbach, G. Buntkowsky, ChemCatChem 10 (2018) 4243–4247.
date_created: 2026-02-07T16:06:27Z
date_updated: 2026-02-17T16:13:52Z
doi: 10.1002/cctc.201801022
extern: '1'
intvolume: ' 10'
issue: '19'
language:
- iso: eng
page: 4243–4247
publication: ChemCatChem
status: public
title: 'Surprising Differences of Alkane C-H Activation Catalyzed by Ruthenium Nanoparticles:
Complex Surface-Substrate Recognition?'
type: journal_article
user_id: '100715'
volume: 10
year: '2018'
...
---
_id: '64007'
abstract:
- lang: eng
text: The equilibration of H2, HD and D2 between the gas phase and surface hydrides
of solid organic-ligand-stabilized Ru metal nanoparticles has been studied by
gas phase 1H NMR spectroscopy using closed NMR tubes as batch reactors at room
temperature and 800 mbar. When two different nanoparticle systems, Ru/PVP (PVP
[identical with] polyvinylpyrrolidone) and Ru/HDA (HDA [identical with] hexadecylamine)
were exposed to D2 gas, only the release of HD from the hydride containing surface
could be detected in the initial stages of the reaction, but no H2. In the case
of Ru/HDA also the reverse experiment was performed where surface deuterated nanoparticles
were exposed to H2. In that case, the conversion of H2 into gaseous HD was detected.
In order to analyze the experimental kinetic and spectroscopic data, we explored
two different mechanisms taking into account potential kinetic and equilibrium
H/D isotope effects. Firstly, we explored the dissociative exchange mechanism
consisting of dissociative adsorption of dihydrogen, fast hydride surface diffusion
and associative desorption of dihydrogen. It is shown that if D2 is the reaction
partner, only H2 will be released in the beginning of the reaction, and HD only
in later reaction stages. The second mechanism, dubbed here associative exchange
consists of the binding of dihydrogen to Ru surface atoms, followed by a H-transfer
to or by H-exchange with an adjacent hydride site, and finally of the associative
desorption of dihydrogen. In that case, in the exchange with D2, only HD will
be released in the beginning of the reaction. Our experimental results are not
compatible with the dissociative exchange but can be explained in terms of the
associative exchange. Whereas the former will dominate at low temperatures and
pressures, the latter will prevail around room temperature and normal pressures
where transition metal nanoparticles are generally used as reaction catalysts.
author:
- first_name: Hans-Heinrich
full_name: Limbach, Hans-Heinrich
last_name: Limbach
- first_name: Tal
full_name: Pery, Tal
last_name: Pery
- first_name: Niels
full_name: Rothermel, Niels
last_name: Rothermel
- first_name: Bruno
full_name: Chaudret, Bruno
last_name: Chaudret
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: Gerd
full_name: Buntkowsky, Gerd
last_name: Buntkowsky
citation:
ama: 'Limbach H-H, Pery T, Rothermel N, Chaudret B, Gutmann T, Buntkowsky G. Gas
phase 1H NMR studies and kinetic modeling of dihydrogen isotope equilibration
catalyzed by Ru-nanoparticles under normal conditions: dissociative vs. associative
exchange. Physical Chemistry Chemical Physics. 2018;20(16):10697–10712.
doi:10.1039/C7CP07770J'
apa: 'Limbach, H.-H., Pery, T., Rothermel, N., Chaudret, B., Gutmann, T., &
Buntkowsky, G. (2018). Gas phase 1H NMR studies and kinetic modeling of dihydrogen
isotope equilibration catalyzed by Ru-nanoparticles under normal conditions: dissociative
vs. associative exchange. Physical Chemistry Chemical Physics, 20(16),
10697–10712. https://doi.org/10.1039/C7CP07770J'
bibtex: '@article{Limbach_Pery_Rothermel_Chaudret_Gutmann_Buntkowsky_2018, title={Gas
phase 1H NMR studies and kinetic modeling of dihydrogen isotope equilibration
catalyzed by Ru-nanoparticles under normal conditions: dissociative vs. associative
exchange}, volume={20}, DOI={10.1039/C7CP07770J},
number={16}, journal={Physical Chemistry Chemical Physics}, publisher={The Royal
Society of Chemistry}, author={Limbach, Hans-Heinrich and Pery, Tal and Rothermel,
Niels and Chaudret, Bruno and Gutmann, Torsten and Buntkowsky, Gerd}, year={2018},
pages={10697–10712} }'
chicago: 'Limbach, Hans-Heinrich, Tal Pery, Niels Rothermel, Bruno Chaudret, Torsten
Gutmann, and Gerd Buntkowsky. “Gas Phase 1H NMR Studies and Kinetic Modeling of
Dihydrogen Isotope Equilibration Catalyzed by Ru-Nanoparticles under Normal Conditions:
Dissociative vs. Associative Exchange.” Physical Chemistry Chemical Physics
20, no. 16 (2018): 10697–10712. https://doi.org/10.1039/C7CP07770J.'
ieee: 'H.-H. Limbach, T. Pery, N. Rothermel, B. Chaudret, T. Gutmann, and G. Buntkowsky,
“Gas phase 1H NMR studies and kinetic modeling of dihydrogen isotope equilibration
catalyzed by Ru-nanoparticles under normal conditions: dissociative vs. associative
exchange,” Physical Chemistry Chemical Physics, vol. 20, no. 16, pp. 10697–10712,
2018, doi: 10.1039/C7CP07770J.'
mla: 'Limbach, Hans-Heinrich, et al. “Gas Phase 1H NMR Studies and Kinetic Modeling
of Dihydrogen Isotope Equilibration Catalyzed by Ru-Nanoparticles under Normal
Conditions: Dissociative vs. Associative Exchange.” Physical Chemistry Chemical
Physics, vol. 20, no. 16, The Royal Society of Chemistry, 2018, pp. 10697–10712,
doi:10.1039/C7CP07770J.'
short: H.-H. Limbach, T. Pery, N. Rothermel, B. Chaudret, T. Gutmann, G. Buntkowsky,
Physical Chemistry Chemical Physics 20 (2018) 10697–10712.
date_created: 2026-02-07T15:56:08Z
date_updated: 2026-02-17T16:15:31Z
doi: 10.1039/C7CP07770J
extern: '1'
intvolume: ' 20'
issue: '16'
language:
- iso: eng
page: 10697–10712
publication: Physical Chemistry Chemical Physics
publisher: The Royal Society of Chemistry
status: public
title: 'Gas phase 1H NMR studies and kinetic modeling of dihydrogen isotope equilibration
catalyzed by Ru-nanoparticles under normal conditions: dissociative vs. associative
exchange'
type: journal_article
user_id: '100715'
volume: 20
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: '64014'
abstract:
- lang: eng
text: Many efforts have been made to isolate native nanocrystals from raw materials
in the last two decades, such as cellulose nanocrystals (CNCs), but existing methods
still suffer from low yields, complicated synthesis processes, and nonuniform
sizes of obtained CNCs. This study concerns a facile, self-terminating, and efficient
method for the formation of uniform CNCs in high yields during the periodate oxidation
process within Pickering emulsions. A biphasic system containing hexane with dissolved
hexylamine and an aqueous solution of sodium periodate (NaIO4) was used as the
reaction medium. Regulated by hexylamine, owing to its limited solubility in water,
the pH value of the aqueous phase was enhanced to around 9.8, leading to the precipitation
of sodium orthoperiodate (Na2H3IO6) nanoplates and thus the formation of the initial
Pickering emulsions. During the gradual formation of cellulose nanofibers and
then CNCs, CNCs were attracted to stabilize the interface of the Pickering emulsions,
which prevented further decomposition of CNCs by the oxidizing agent in aqueous
suspensions. Thus, this isolation strategy secured the efficient separation of
CNCs based on their own particular amphiphilic properties and achieved a high
yield of up to 56 wt%.
author:
- first_name: P. W.
full_name: Liu, P. W.
last_name: Liu
- first_name: B.
full_name: Pang, B.
last_name: Pang
- first_name: L.
full_name: Tian, L.
last_name: Tian
- first_name: T.
full_name: Schafer, T.
last_name: Schafer
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: H.
full_name: Liu, H.
last_name: Liu
- first_name: C. A.
full_name: Volkert, C. A.
last_name: Volkert
- first_name: G.
full_name: Buntkowsky, G.
last_name: Buntkowsky
- first_name: K.
full_name: Zhang, K.
last_name: Zhang
citation:
ama: Liu PW, Pang B, Tian L, et al. Efficient, Self-Terminating Isolation of Cellulose
Nanocrystals through Periodate Oxidation in Pickering Emulsions. ChemSusChem.
2018;11(20):3581–3585. doi:10.1002/cssc.201801678
apa: Liu, P. W., Pang, B., Tian, L., Schafer, T., Gutmann, T., Liu, H., Volkert,
C. A., Buntkowsky, G., & Zhang, K. (2018). Efficient, Self-Terminating Isolation
of Cellulose Nanocrystals through Periodate Oxidation in Pickering Emulsions.
ChemSusChem, 11(20), 3581–3585. https://doi.org/10.1002/cssc.201801678
bibtex: '@article{Liu_Pang_Tian_Schafer_Gutmann_Liu_Volkert_Buntkowsky_Zhang_2018,
title={Efficient, Self-Terminating Isolation of Cellulose Nanocrystals through
Periodate Oxidation in Pickering Emulsions}, volume={11}, DOI={10.1002/cssc.201801678},
number={20}, journal={ChemSusChem}, author={Liu, P. W. and Pang, B. and Tian,
L. and Schafer, T. and Gutmann, Torsten and Liu, H. and Volkert, C. A. and Buntkowsky,
G. and Zhang, K.}, year={2018}, pages={3581–3585} }'
chicago: 'Liu, P. W., B. Pang, L. Tian, T. Schafer, Torsten Gutmann, H. Liu, C.
A. Volkert, G. Buntkowsky, and K. Zhang. “Efficient, Self-Terminating Isolation
of Cellulose Nanocrystals through Periodate Oxidation in Pickering Emulsions.”
ChemSusChem 11, no. 20 (2018): 3581–3585. https://doi.org/10.1002/cssc.201801678.'
ieee: 'P. W. Liu et al., “Efficient, Self-Terminating Isolation of Cellulose
Nanocrystals through Periodate Oxidation in Pickering Emulsions,” ChemSusChem,
vol. 11, no. 20, pp. 3581–3585, 2018, doi: 10.1002/cssc.201801678.'
mla: Liu, P. W., et al. “Efficient, Self-Terminating Isolation of Cellulose Nanocrystals
through Periodate Oxidation in Pickering Emulsions.” ChemSusChem, vol.
11, no. 20, 2018, pp. 3581–3585, doi:10.1002/cssc.201801678.
short: P.W. Liu, B. Pang, L. Tian, T. Schafer, T. Gutmann, H. Liu, C.A. Volkert,
G. Buntkowsky, K. Zhang, ChemSusChem 11 (2018) 3581–3585.
date_created: 2026-02-07T16:00:36Z
date_updated: 2026-02-17T16:15:14Z
doi: 10.1002/cssc.201801678
extern: '1'
intvolume: ' 11'
issue: '20'
language:
- iso: eng
page: 3581–3585
publication: ChemSusChem
status: public
title: Efficient, Self-Terminating Isolation of Cellulose Nanocrystals through Periodate
Oxidation in Pickering Emulsions
type: journal_article
user_id: '100715'
volume: 11
year: '2018'
...
---
_id: '64000'
abstract:
- lang: eng
text: Surface enhanced solid-state NMR by dynamic nuclear polarization (DNP SENS)
enables the characterization of the inner-pore surface functionalization of porous
etched ion-track membranes exhibiting low specific surface areas compared to typical
SBA- or MCM-type mesoporous silica materials. The membranes were conformally coated
with a 5 nm thin SiO2 layer by atomic layer deposition. This layer was subsequently
modified by aminopropyl silane linkers that allow further functionalization via
the terminal amine group. The results evidence that in principle DNP SENS is a
capable tool to analyze more complex porous systems, e.g. bioinspired functional
etched ion-track membranes down to the molecular level. These results are relevant
also for single nanopore systems, for which a direct analysis of the channel surface
functionalization is not feasible by classical characterization methods. The applicability
of DNP SENS to complex porous systems requires the optimization of the sample
preparation and measurement parameters.
author:
- first_name: B.
full_name: Kumari, B.
last_name: Kumari
- first_name: D.
full_name: John, D.
last_name: John
- first_name: P.
full_name: Hoffmann, P.
last_name: Hoffmann
- first_name: A.
full_name: Spende, A.
last_name: Spende
- first_name: M. E.
full_name: Toimil-Molares, M. E.
last_name: Toimil-Molares
- first_name: C.
full_name: Trautmann, C.
last_name: Trautmann
- first_name: C.
full_name: Hess, C.
last_name: Hess
- first_name: P.
full_name: Ruff, P.
last_name: Ruff
- first_name: M.
full_name: Schulze, M.
last_name: Schulze
- first_name: R.
full_name: Stark, R.
last_name: Stark
- first_name: G.
full_name: Buntkowsky, G.
last_name: Buntkowsky
- first_name: A.
full_name: Andrieu-Brunsen, A.
last_name: Andrieu-Brunsen
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
citation:
ama: Kumari B, John D, Hoffmann P, et al. Surface Enhanced DNP Assisted Solid-State
NMR of Functionatized SiO2 Coated Potycarbonate Membranes. Zeitschrift Fur
Physikalische Chemie-International Journal of Research in Physical Chemistry &
Chemical Physics. 2018;232(7-8):1173–1186. doi:10.1515/zpch-2017-1032
apa: Kumari, B., John, D., Hoffmann, P., Spende, A., Toimil-Molares, M. E., Trautmann,
C., Hess, C., Ruff, P., Schulze, M., Stark, R., Buntkowsky, G., Andrieu-Brunsen,
A., & Gutmann, T. (2018). Surface Enhanced DNP Assisted Solid-State NMR of
Functionatized SiO2 Coated Potycarbonate Membranes. Zeitschrift Fur Physikalische
Chemie-International Journal of Research in Physical Chemistry & Chemical
Physics, 232(7–8), 1173–1186. https://doi.org/10.1515/zpch-2017-1032
bibtex: '@article{Kumari_John_Hoffmann_Spende_Toimil-Molares_Trautmann_Hess_Ruff_Schulze_Stark_et
al._2018, title={Surface Enhanced DNP Assisted Solid-State NMR of Functionatized
SiO2 Coated Potycarbonate Membranes}, volume={232}, DOI={10.1515/zpch-2017-1032},
number={7–8}, journal={Zeitschrift Fur Physikalische Chemie-International Journal
of Research in Physical Chemistry & Chemical Physics}, author={Kumari, B.
and John, D. and Hoffmann, P. and Spende, A. and Toimil-Molares, M. E. and Trautmann,
C. and Hess, C. and Ruff, P. and Schulze, M. and Stark, R. and et al.}, year={2018},
pages={1173–1186} }'
chicago: 'Kumari, B., D. John, P. Hoffmann, A. Spende, M. E. Toimil-Molares, C.
Trautmann, C. Hess, et al. “Surface Enhanced DNP Assisted Solid-State NMR of Functionatized
SiO2 Coated Potycarbonate Membranes.” Zeitschrift Fur Physikalische Chemie-International
Journal of Research in Physical Chemistry & Chemical Physics 232, no.
7–8 (2018): 1173–1186. https://doi.org/10.1515/zpch-2017-1032.'
ieee: 'B. Kumari et al., “Surface Enhanced DNP Assisted Solid-State NMR of
Functionatized SiO2 Coated Potycarbonate Membranes,” Zeitschrift Fur Physikalische
Chemie-International Journal of Research in Physical Chemistry & Chemical
Physics, vol. 232, no. 7–8, pp. 1173–1186, 2018, doi: 10.1515/zpch-2017-1032.'
mla: Kumari, B., et al. “Surface Enhanced DNP Assisted Solid-State NMR of Functionatized
SiO2 Coated Potycarbonate Membranes.” Zeitschrift Fur Physikalische Chemie-International
Journal of Research in Physical Chemistry & Chemical Physics, vol. 232,
no. 7–8, 2018, pp. 1173–1186, doi:10.1515/zpch-2017-1032.
short: B. Kumari, D. John, P. Hoffmann, A. Spende, M.E. Toimil-Molares, C. Trautmann,
C. Hess, P. Ruff, M. Schulze, R. Stark, G. Buntkowsky, A. Andrieu-Brunsen, T.
Gutmann, Zeitschrift Fur Physikalische Chemie-International Journal of Research
in Physical Chemistry & Chemical Physics 232 (2018) 1173–1186.
date_created: 2026-02-07T15:52:47Z
date_updated: 2026-02-17T16:15:45Z
doi: 10.1515/zpch-2017-1032
extern: '1'
intvolume: ' 232'
issue: 7-8
language:
- iso: eng
page: 1173–1186
publication: Zeitschrift Fur Physikalische Chemie-International Journal of Research
in Physical Chemistry & Chemical Physics
publication_identifier:
issn:
- 0942-9352
status: public
title: Surface Enhanced DNP Assisted Solid-State NMR of Functionatized SiO2 Coated
Potycarbonate Membranes
type: journal_article
user_id: '100715'
volume: 232
year: '2018'
...
---
_id: '63999'
abstract:
- lang: eng
text: The behavior of mixtures of 1-octanol with water with different molar ratios
confined inside the mesoporous silica SBA-15 was investigated by a combination
of solid-state NMR spectroscopy and molecular dynamics (MD) simulations. Two-dimensional
H-1-Si-29 FSLG-HET-COR NMR spectra revealed the orientation of 1-octanol relative
to the pore walls. These arrangements are in good agreement with the preferred
structures found by MD. In addition, MD simulations also shed light on molecular
orientations and interactions in the pore center region, which are not resolvable
by solid-state NMR.
author:
- first_name: B.
full_name: Kumari, B.
last_name: Kumari
- first_name: M.
full_name: Brodrecht, M.
last_name: Brodrecht
- first_name: H.
full_name: Breitzke, H.
last_name: Breitzke
- first_name: M.
full_name: Werner, M.
last_name: Werner
- first_name: B.
full_name: Grunberg, B.
last_name: Grunberg
- first_name: H. H.
full_name: Limbach, H. H.
last_name: Limbach
- first_name: S.
full_name: Forg, S.
last_name: Forg
- first_name: E. P.
full_name: Sanjon, E. P.
last_name: Sanjon
- first_name: B.
full_name: Drossel, B.
last_name: Drossel
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: G.
full_name: Buntkowsky, G.
last_name: Buntkowsky
citation:
ama: 'Kumari B, Brodrecht M, Breitzke H, et al. Mixtures of Alcohols and Water confined
in Mesoporous Silica: A Combined Solid-State NMR and Molecular Dynamics Simulation
Study. Journal of Physical Chemistry C. 2018;122(34):19540–19550. doi:10.1021/acs.jpcc.8b04745'
apa: 'Kumari, B., Brodrecht, M., Breitzke, H., Werner, M., Grunberg, B., Limbach,
H. H., Forg, S., Sanjon, E. P., Drossel, B., Gutmann, T., & Buntkowsky, G.
(2018). Mixtures of Alcohols and Water confined in Mesoporous Silica: A Combined
Solid-State NMR and Molecular Dynamics Simulation Study. Journal of Physical
Chemistry C, 122(34), 19540–19550. https://doi.org/10.1021/acs.jpcc.8b04745'
bibtex: '@article{Kumari_Brodrecht_Breitzke_Werner_Grunberg_Limbach_Forg_Sanjon_Drossel_Gutmann_et
al._2018, title={Mixtures of Alcohols and Water confined in Mesoporous Silica:
A Combined Solid-State NMR and Molecular Dynamics Simulation Study}, volume={122},
DOI={10.1021/acs.jpcc.8b04745},
number={34}, journal={Journal of Physical Chemistry C}, author={Kumari, B. and
Brodrecht, M. and Breitzke, H. and Werner, M. and Grunberg, B. and Limbach, H.
H. and Forg, S. and Sanjon, E. P. and Drossel, B. and Gutmann, Torsten and et
al.}, year={2018}, pages={19540–19550} }'
chicago: 'Kumari, B., M. Brodrecht, H. Breitzke, M. Werner, B. Grunberg, H. H. Limbach,
S. Forg, et al. “Mixtures of Alcohols and Water Confined in Mesoporous Silica:
A Combined Solid-State NMR and Molecular Dynamics Simulation Study.” Journal
of Physical Chemistry C 122, no. 34 (2018): 19540–19550. https://doi.org/10.1021/acs.jpcc.8b04745.'
ieee: 'B. Kumari et al., “Mixtures of Alcohols and Water confined in Mesoporous
Silica: A Combined Solid-State NMR and Molecular Dynamics Simulation Study,” Journal
of Physical Chemistry C, vol. 122, no. 34, pp. 19540–19550, 2018, doi: 10.1021/acs.jpcc.8b04745.'
mla: 'Kumari, B., et al. “Mixtures of Alcohols and Water Confined in Mesoporous
Silica: A Combined Solid-State NMR and Molecular Dynamics Simulation Study.” Journal
of Physical Chemistry C, vol. 122, no. 34, 2018, pp. 19540–19550, doi:10.1021/acs.jpcc.8b04745.'
short: B. Kumari, M. Brodrecht, H. Breitzke, M. Werner, B. Grunberg, H.H. Limbach,
S. Forg, E.P. Sanjon, B. Drossel, T. Gutmann, G. Buntkowsky, Journal of Physical
Chemistry C 122 (2018) 19540–19550.
date_created: 2026-02-07T15:51:48Z
date_updated: 2026-02-17T16:15:56Z
doi: 10.1021/acs.jpcc.8b04745
extern: '1'
intvolume: ' 122'
issue: '34'
language:
- iso: eng
page: 19540–19550
publication: Journal of Physical Chemistry C
publication_identifier:
issn:
- 1932-7447
status: public
title: 'Mixtures of Alcohols and Water confined in Mesoporous Silica: A Combined Solid-State
NMR and Molecular Dynamics Simulation Study'
type: journal_article
user_id: '100715'
volume: 122
year: '2018'
...
---
_id: '63978'
abstract:
- lang: eng
text: The colligative property freezing point depression is evaluated as a means
for estimating the extent of aggregation for solutions of poly(ethylene oxide)
alcohol (C10E6) nonionic surfactant in cyclohexane. Combined with additional measurements
of self-diffusion coefficients, it is shown that both unaggregated C10E6 as well
as reverse micelles are significantly present for the entire range of measured
C10E6 concentration (0.048−2.35 mol kg−1). A change in speciation near 0.2 mol
kg−1 is indicated by the results from both freezing point depression and selfdiffusion
coefficient measurements. It is shown that average reverse micelle radii and aggregation
numbers obtained from the ratio of solvent and C10E6 self-diffusion coefficients
are consistent with prior reported results. However, unreasonably small radii
for the reverse micelles as well as for the cyclohexane were obtained from analysis
of the results by the Stokes−Einstein equation using additional measured solution
viscosities. The concentration of reverse micelles and unaggregated C10E6 was
calculated from the freezing point depression results using the aggregation numbers
obtained from ratio of self-diffusion coefficients. These concentrations indicate
that the reverse micelles become smaller in average size and increase in number
with increasing temperature without an increase in unaggregated C10E6.
author:
- first_name: Markus M.
full_name: Hoffmann, Markus M.
last_name: Hoffmann
- first_name: Sarah
full_name: Bothe, Sarah
last_name: Bothe
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: Gerd
full_name: Buntkowsky, Gerd
last_name: Buntkowsky
citation:
ama: Hoffmann MM, Bothe S, Gutmann T, Buntkowsky G. Combining Freezing Point Depression
and Self-Diffusion Data for Characterizing Aggregation. Journal of Physical
Chemistry B. 2018;122(18):4913–4921. doi:10.1021/acs.jpcb.8b03456
apa: Hoffmann, M. M., Bothe, S., Gutmann, T., & Buntkowsky, G. (2018). Combining
Freezing Point Depression and Self-Diffusion Data for Characterizing Aggregation.
Journal of Physical Chemistry B, 122(18), 4913–4921. https://doi.org/10.1021/acs.jpcb.8b03456
bibtex: '@article{Hoffmann_Bothe_Gutmann_Buntkowsky_2018, title={Combining Freezing
Point Depression and Self-Diffusion Data for Characterizing Aggregation}, volume={122},
DOI={10.1021/acs.jpcb.8b03456},
number={18}, journal={Journal of Physical Chemistry B}, publisher={American Chemical
Society}, author={Hoffmann, Markus M. and Bothe, Sarah and Gutmann, Torsten and
Buntkowsky, Gerd}, year={2018}, pages={4913–4921} }'
chicago: 'Hoffmann, Markus M., Sarah Bothe, Torsten Gutmann, and Gerd Buntkowsky.
“Combining Freezing Point Depression and Self-Diffusion Data for Characterizing
Aggregation.” Journal of Physical Chemistry B 122, no. 18 (2018): 4913–4921.
https://doi.org/10.1021/acs.jpcb.8b03456.'
ieee: 'M. M. Hoffmann, S. Bothe, T. Gutmann, and G. Buntkowsky, “Combining Freezing
Point Depression and Self-Diffusion Data for Characterizing Aggregation,” Journal
of Physical Chemistry B, vol. 122, no. 18, pp. 4913–4921, 2018, doi: 10.1021/acs.jpcb.8b03456.'
mla: Hoffmann, Markus M., et al. “Combining Freezing Point Depression and Self-Diffusion
Data for Characterizing Aggregation.” Journal of Physical Chemistry B,
vol. 122, no. 18, American Chemical Society, 2018, pp. 4913–4921, doi:10.1021/acs.jpcb.8b03456.
short: M.M. Hoffmann, S. Bothe, T. Gutmann, G. Buntkowsky, Journal of Physical Chemistry
B 122 (2018) 4913–4921.
date_created: 2026-02-07T15:43:11Z
date_updated: 2026-02-17T16:17:10Z
doi: 10.1021/acs.jpcb.8b03456
extern: '1'
intvolume: ' 122'
issue: '18'
language:
- iso: eng
page: 4913–4921
publication: Journal of Physical Chemistry B
publisher: American Chemical Society
status: public
title: Combining Freezing Point Depression and Self-Diffusion Data for Characterizing
Aggregation
type: journal_article
user_id: '100715'
volume: 122
year: '2018'
...
---
_id: '63938'
author:
- first_name: Yuan
full_name: Cao, Yuan
last_name: Cao
- first_name: Li
full_name: Zhao, Li
last_name: Zhao
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: Yeping
full_name: Xu, Yeping
last_name: Xu
- first_name: Lin
full_name: Dong, Lin
last_name: Dong
- first_name: Gerd
full_name: Buntkowsky, Gerd
last_name: Buntkowsky
- first_name: Fei
full_name: Gao, Fei
last_name: Gao
citation:
ama: Cao Y, Zhao L, Gutmann T, et al. Getting Insights into the Influence of Crystal
Plane Effect of Shaped Ceria on Its Catalytic Performances. Journal of Physical
Chemistry C. 2018;122(35):20402–20409. doi:10.1021/acs.jpcc.8b06138
apa: Cao, Y., Zhao, L., Gutmann, T., Xu, Y., Dong, L., Buntkowsky, G., & Gao,
F. (2018). Getting Insights into the Influence of Crystal Plane Effect of Shaped
Ceria on Its Catalytic Performances. Journal of Physical Chemistry C, 122(35),
20402–20409. https://doi.org/10.1021/acs.jpcc.8b06138
bibtex: '@article{Cao_Zhao_Gutmann_Xu_Dong_Buntkowsky_Gao_2018, title={Getting Insights
into the Influence of Crystal Plane Effect of Shaped Ceria on Its Catalytic Performances},
volume={122}, DOI={10.1021/acs.jpcc.8b06138},
number={35}, journal={Journal of Physical Chemistry C}, publisher={American Chemical
Society}, author={Cao, Yuan and Zhao, Li and Gutmann, Torsten and Xu, Yeping and
Dong, Lin and Buntkowsky, Gerd and Gao, Fei}, year={2018}, pages={20402–20409}
}'
chicago: 'Cao, Yuan, Li Zhao, Torsten Gutmann, Yeping Xu, Lin Dong, Gerd Buntkowsky,
and Fei Gao. “Getting Insights into the Influence of Crystal Plane Effect of Shaped
Ceria on Its Catalytic Performances.” Journal of Physical Chemistry C 122,
no. 35 (2018): 20402–20409. https://doi.org/10.1021/acs.jpcc.8b06138.'
ieee: 'Y. Cao et al., “Getting Insights into the Influence of Crystal Plane
Effect of Shaped Ceria on Its Catalytic Performances,” Journal of Physical
Chemistry C, vol. 122, no. 35, pp. 20402–20409, 2018, doi: 10.1021/acs.jpcc.8b06138.'
mla: Cao, Yuan, et al. “Getting Insights into the Influence of Crystal Plane Effect
of Shaped Ceria on Its Catalytic Performances.” Journal of Physical Chemistry
C, vol. 122, no. 35, American Chemical Society, 2018, pp. 20402–20409, doi:10.1021/acs.jpcc.8b06138.
short: Y. Cao, L. Zhao, T. Gutmann, Y. Xu, L. Dong, G. Buntkowsky, F. Gao, Journal
of Physical Chemistry C 122 (2018) 20402–20409.
date_created: 2026-02-07T09:08:25Z
date_updated: 2026-02-17T16:18:45Z
doi: 10.1021/acs.jpcc.8b06138
extern: '1'
intvolume: ' 122'
issue: '35'
language:
- iso: eng
page: 20402–20409
publication: Journal of Physical Chemistry C
publication_identifier:
issn:
- 1932-7447
publisher: American Chemical Society
status: public
title: Getting Insights into the Influence of Crystal Plane Effect of Shaped Ceria
on Its Catalytic Performances
type: journal_article
user_id: '100715'
volume: 122
year: '2018'
...
---
_id: '63940'
author:
- first_name: Laurynas
full_name: Dagys, Laurynas
last_name: Dagys
- first_name: Vytautas
full_name: Klimavicius, Vytautas
last_name: Klimavicius
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: Gerd
full_name: Buntkowsky, Gerd
last_name: Buntkowsky
- first_name: Vytautas
full_name: Balevicius, Vytautas
last_name: Balevicius
citation:
ama: 'Dagys L, Klimavicius V, Gutmann T, Buntkowsky G, Balevicius V. Quasi-Equilibria
and Polarization Transfer Between Adjacent and Remote Spins: 1H–13C CP MAS Kinetics
in Glycine. Journal of Physical Chemistry A. 2018;122(45):8938–8947. doi:10.1021/acs.jpca.8b09036'
apa: 'Dagys, L., Klimavicius, V., Gutmann, T., Buntkowsky, G., & Balevicius,
V. (2018). Quasi-Equilibria and Polarization Transfer Between Adjacent and Remote
Spins: 1H–13C CP MAS Kinetics in Glycine. Journal of Physical Chemistry A,
122(45), 8938–8947. https://doi.org/10.1021/acs.jpca.8b09036'
bibtex: '@article{Dagys_Klimavicius_Gutmann_Buntkowsky_Balevicius_2018, title={Quasi-Equilibria
and Polarization Transfer Between Adjacent and Remote Spins: 1H–13C CP MAS Kinetics
in Glycine}, volume={122}, DOI={10.1021/acs.jpca.8b09036},
number={45}, journal={Journal of Physical Chemistry A}, publisher={American Chemical
Society}, author={Dagys, Laurynas and Klimavicius, Vytautas and Gutmann, Torsten
and Buntkowsky, Gerd and Balevicius, Vytautas}, year={2018}, pages={8938–8947}
}'
chicago: 'Dagys, Laurynas, Vytautas Klimavicius, Torsten Gutmann, Gerd Buntkowsky,
and Vytautas Balevicius. “Quasi-Equilibria and Polarization Transfer Between Adjacent
and Remote Spins: 1H–13C CP MAS Kinetics in Glycine.” Journal of Physical Chemistry
A 122, no. 45 (2018): 8938–8947. https://doi.org/10.1021/acs.jpca.8b09036.'
ieee: 'L. Dagys, V. Klimavicius, T. Gutmann, G. Buntkowsky, and V. Balevicius, “Quasi-Equilibria
and Polarization Transfer Between Adjacent and Remote Spins: 1H–13C CP MAS Kinetics
in Glycine,” Journal of Physical Chemistry A, vol. 122, no. 45, pp. 8938–8947,
2018, doi: 10.1021/acs.jpca.8b09036.'
mla: 'Dagys, Laurynas, et al. “Quasi-Equilibria and Polarization Transfer Between
Adjacent and Remote Spins: 1H–13C CP MAS Kinetics in Glycine.” Journal of Physical
Chemistry A, vol. 122, no. 45, American Chemical Society, 2018, pp. 8938–8947,
doi:10.1021/acs.jpca.8b09036.'
short: L. Dagys, V. Klimavicius, T. Gutmann, G. Buntkowsky, V. Balevicius, Journal
of Physical Chemistry A 122 (2018) 8938–8947.
date_created: 2026-02-07T09:09:32Z
date_updated: 2026-02-17T16:18:41Z
doi: 10.1021/acs.jpca.8b09036
extern: '1'
intvolume: ' 122'
issue: '45'
language:
- iso: eng
page: 8938–8947
publication: Journal of Physical Chemistry A
publisher: American Chemical Society
status: public
title: 'Quasi-Equilibria and Polarization Transfer Between Adjacent and Remote Spins:
1H–13C CP MAS Kinetics in Glycine'
type: journal_article
user_id: '100715'
volume: 122
year: '2018'
...
---
_id: '63926'
abstract:
- lang: eng
text: Synthesis of novel trityl-nitroxyl biradicals and their performance as polarization
agents in DNP-enhanced solid-state MAS NMR spectroscopy is presented. Signal enhancements
in H-1, H-1 -{\textgreater} C-13 CP MAS, and C-13 MAS experiments obtained with
these radicals dissolved in 1,1,2,2-tetrachloroethane (TCE) solution are compared
with the enhancements obtained from TCE solutions of binitroxyl radicals. The
signal enhancements are correlated with the distance between the radical centers
of the biradicals, as determined by theoretical structure calculations. Some of
the biradical TCE solutions display direct-channel resonances in C-13 MAS experiments
as well as indirect channel resonances induced via the proton spin reservoir.
Differential scanning calorimetry reveals that only these solutions do not form
any solid crystalline phases upon rapid cooling, suggesting that molecular motions
needed for polarization transfer from radicals to C-13 via the proton spin reservoir
remain active at the experimental low temperatures of nominal 120 K. DNP magnetic
field sweep enhancement profiles for selected new biradicals are presented as
well. These indicate that the DNP transfer is dominated by the cross-effect mechanism.
author:
- first_name: S.
full_name: Bothe, S.
last_name: Bothe
- first_name: J.
full_name: Nowag, J.
last_name: Nowag
- first_name: V.
full_name: Klimavicius, V.
last_name: Klimavicius
- first_name: M.
full_name: Hoffmann, M.
last_name: Hoffmann
- first_name: T. I.
full_name: Troitskaya, T. I.
last_name: Troitskaya
- first_name: E. V.
full_name: Amosov, E. V.
last_name: Amosov
- first_name: V. M.
full_name: Tormyshev, V. M.
last_name: Tormyshev
- first_name: I.
full_name: Kirilyuk, I.
last_name: Kirilyuk
- first_name: A.
full_name: Taratayko, A.
last_name: Taratayko
- first_name: A.
full_name: Kuzhelev, A.
last_name: Kuzhelev
- first_name: D.
full_name: Parkhomenko, D.
last_name: Parkhomenko
- first_name: E.
full_name: Bagryanskaya, E.
last_name: Bagryanskaya
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: G.
full_name: Buntkowsky, G.
last_name: Buntkowsky
citation:
ama: Bothe S, Nowag J, Klimavicius V, et al. Novel Biradicals for Direct Excitation
Highfield Dynamic Nuclear Polarization. Journal of Physical Chemistry C.
2018;122(21):11422–11432. doi:10.1021/acs.jpcc.8b02570
apa: Bothe, S., Nowag, J., Klimavicius, V., Hoffmann, M., Troitskaya, T. I., Amosov,
E. V., Tormyshev, V. M., Kirilyuk, I., Taratayko, A., Kuzhelev, A., Parkhomenko,
D., Bagryanskaya, E., Gutmann, T., & Buntkowsky, G. (2018). Novel Biradicals
for Direct Excitation Highfield Dynamic Nuclear Polarization. Journal of Physical
Chemistry C, 122(21), 11422–11432. https://doi.org/10.1021/acs.jpcc.8b02570
bibtex: '@article{Bothe_Nowag_Klimavicius_Hoffmann_Troitskaya_Amosov_Tormyshev_Kirilyuk_Taratayko_Kuzhelev_et
al._2018, title={Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear
Polarization}, volume={122}, DOI={10.1021/acs.jpcc.8b02570},
number={21}, journal={Journal of Physical Chemistry C}, author={Bothe, S. and
Nowag, J. and Klimavicius, V. and Hoffmann, M. and Troitskaya, T. I. and Amosov,
E. V. and Tormyshev, V. M. and Kirilyuk, I. and Taratayko, A. and Kuzhelev, A.
and et al.}, year={2018}, pages={11422–11432} }'
chicago: 'Bothe, S., J. Nowag, V. Klimavicius, M. Hoffmann, T. I. Troitskaya, E.
V. Amosov, V. M. Tormyshev, et al. “Novel Biradicals for Direct Excitation Highfield
Dynamic Nuclear Polarization.” Journal of Physical Chemistry C 122, no.
21 (2018): 11422–11432. https://doi.org/10.1021/acs.jpcc.8b02570.'
ieee: 'S. Bothe et al., “Novel Biradicals for Direct Excitation Highfield
Dynamic Nuclear Polarization,” Journal of Physical Chemistry C, vol. 122,
no. 21, pp. 11422–11432, 2018, doi: 10.1021/acs.jpcc.8b02570.'
mla: Bothe, S., et al. “Novel Biradicals for Direct Excitation Highfield Dynamic
Nuclear Polarization.” Journal of Physical Chemistry C, vol. 122, no. 21,
2018, pp. 11422–11432, doi:10.1021/acs.jpcc.8b02570.
short: S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov,
V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A. Kuzhelev, D. Parkhomenko, E. Bagryanskaya,
T. Gutmann, G. Buntkowsky, Journal of Physical Chemistry C 122 (2018) 11422–11432.
date_created: 2026-02-07T08:59:17Z
date_updated: 2026-02-17T16:19:13Z
doi: 10.1021/acs.jpcc.8b02570
extern: '1'
intvolume: ' 122'
issue: '21'
language:
- iso: eng
page: 11422–11432
publication: Journal of Physical Chemistry C
publication_identifier:
issn:
- 1932-7447
status: public
title: Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
type: journal_article
user_id: '100715'
volume: 122
year: '2018'
...
---
_id: '63928'
abstract:
- lang: eng
text: A series of novel functionalized mesoporous silica-based materials with well-defined
pore diameters, surface functionalization and surface morphology is synthesized
by co-condensation or grafting techniques and characterized by solid-state NMR
spectroscopy, DNP enhanced solid state-NMR and thermodynamic techniques. These
materials are employed as host-systems for small-guest molecules like water, small
alcohols, carbonic acids, small aromatic molecules, binary mixtures and others.
The phase-behavior of these confined guests is studied by combinations of one
dimensional solid-state NMR techniques (H-1 MAS, H-2-line shape analysis, C-13
CPMAS) and two-dimensional correlation experiments like H-1-Si-29- solid-state
HETCOR.
author:
- first_name: M.
full_name: Brodrecht, M.
last_name: Brodrecht
- first_name: B.
full_name: Kumari, B.
last_name: Kumari
- first_name: H.
full_name: Breitzke, H.
last_name: Breitzke
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: G.
full_name: Buntkowsky, G.
last_name: Buntkowsky
citation:
ama: Brodrecht M, Kumari B, Breitzke H, Gutmann T, Buntkowsky G. Chemically Modified
Silica Materials as Model Systems for the Characterization of Water-Surface Interactions.
Zeitschrift Fur Physikalische Chemie-International Journal of Research in Physical
Chemistry & Chemical Physics. 2018;232(7-8):1127–1146. doi:10.1515/zpch-2017-1059
apa: Brodrecht, M., Kumari, B., Breitzke, H., Gutmann, T., & Buntkowsky, G.
(2018). Chemically Modified Silica Materials as Model Systems for the Characterization
of Water-Surface Interactions. Zeitschrift Fur Physikalische Chemie-International
Journal of Research in Physical Chemistry & Chemical Physics, 232(7–8),
1127–1146. https://doi.org/10.1515/zpch-2017-1059
bibtex: '@article{Brodrecht_Kumari_Breitzke_Gutmann_Buntkowsky_2018, title={Chemically
Modified Silica Materials as Model Systems for the Characterization of Water-Surface
Interactions}, volume={232}, DOI={10.1515/zpch-2017-1059},
number={7–8}, journal={Zeitschrift Fur Physikalische Chemie-International Journal
of Research in Physical Chemistry & Chemical Physics}, author={Brodrecht,
M. and Kumari, B. and Breitzke, H. and Gutmann, Torsten and Buntkowsky, G.}, year={2018},
pages={1127–1146} }'
chicago: 'Brodrecht, M., B. Kumari, H. Breitzke, Torsten Gutmann, and G. Buntkowsky.
“Chemically Modified Silica Materials as Model Systems for the Characterization
of Water-Surface Interactions.” Zeitschrift Fur Physikalische Chemie-International
Journal of Research in Physical Chemistry & Chemical Physics 232, no.
7–8 (2018): 1127–1146. https://doi.org/10.1515/zpch-2017-1059.'
ieee: 'M. Brodrecht, B. Kumari, H. Breitzke, T. Gutmann, and G. Buntkowsky, “Chemically
Modified Silica Materials as Model Systems for the Characterization of Water-Surface
Interactions,” Zeitschrift Fur Physikalische Chemie-International Journal of
Research in Physical Chemistry & Chemical Physics, vol. 232, no. 7–8,
pp. 1127–1146, 2018, doi: 10.1515/zpch-2017-1059.'
mla: Brodrecht, M., et al. “Chemically Modified Silica Materials as Model Systems
for the Characterization of Water-Surface Interactions.” Zeitschrift Fur Physikalische
Chemie-International Journal of Research in Physical Chemistry & Chemical
Physics, vol. 232, no. 7–8, 2018, pp. 1127–1146, doi:10.1515/zpch-2017-1059.
short: M. Brodrecht, B. Kumari, H. Breitzke, T. Gutmann, G. Buntkowsky, Zeitschrift
Fur Physikalische Chemie-International Journal of Research in Physical Chemistry
& Chemical Physics 232 (2018) 1127–1146.
date_created: 2026-02-07T09:00:34Z
date_updated: 2026-02-17T16:19:09Z
doi: 10.1515/zpch-2017-1059
extern: '1'
intvolume: ' 232'
issue: 7-8
language:
- iso: eng
page: 1127–1146
publication: Zeitschrift Fur Physikalische Chemie-International Journal of Research
in Physical Chemistry & Chemical Physics
publication_identifier:
issn:
- 0942-9352
status: public
title: Chemically Modified Silica Materials as Model Systems for the Characterization
of Water-Surface Interactions
type: journal_article
user_id: '100715'
volume: 232
year: '2018'
...
---
_id: '63929'
author:
- first_name: Martin
full_name: Brodrecht, Martin
last_name: Brodrecht
- first_name: Hergen
full_name: Breitzke, Hergen
last_name: Breitzke
- first_name: Torsten
full_name: Gutmann, Torsten
id: '118165'
last_name: Gutmann
- first_name: Gerd
full_name: Buntkowsky, Gerd
last_name: Buntkowsky
citation:
ama: Brodrecht M, Breitzke H, Gutmann T, Buntkowsky G. Biofunctionalization of Nano
Channels by Direct In-Pore Solid-Phase Peptide Synthesis. Chemistry A European
Journal. 2018;24(67):17814–17822. doi:10.1002/chem.201804065
apa: Brodrecht, M., Breitzke, H., Gutmann, T., & Buntkowsky, G. (2018). Biofunctionalization
of Nano Channels by Direct In-Pore Solid-Phase Peptide Synthesis. Chemistry
A European Journal, 24(67), 17814–17822. https://doi.org/10.1002/chem.201804065
bibtex: '@article{Brodrecht_Breitzke_Gutmann_Buntkowsky_2018, title={Biofunctionalization
of Nano Channels by Direct In-Pore Solid-Phase Peptide Synthesis}, volume={24},
DOI={10.1002/chem.201804065},
number={67}, journal={Chemistry A European Journal}, author={Brodrecht, Martin
and Breitzke, Hergen and Gutmann, Torsten and Buntkowsky, Gerd}, year={2018},
pages={17814–17822} }'
chicago: 'Brodrecht, Martin, Hergen Breitzke, Torsten Gutmann, and Gerd Buntkowsky.
“Biofunctionalization of Nano Channels by Direct In-Pore Solid-Phase Peptide Synthesis.”
Chemistry A European Journal 24, no. 67 (2018): 17814–17822. https://doi.org/10.1002/chem.201804065.'
ieee: 'M. Brodrecht, H. Breitzke, T. Gutmann, and G. Buntkowsky, “Biofunctionalization
of Nano Channels by Direct In-Pore Solid-Phase Peptide Synthesis,” Chemistry
A European Journal, vol. 24, no. 67, pp. 17814–17822, 2018, doi: 10.1002/chem.201804065.'
mla: Brodrecht, Martin, et al. “Biofunctionalization of Nano Channels by Direct
In-Pore Solid-Phase Peptide Synthesis.” Chemistry A European Journal, vol.
24, no. 67, 2018, pp. 17814–17822, doi:10.1002/chem.201804065.
short: M. Brodrecht, H. Breitzke, T. Gutmann, G. Buntkowsky, Chemistry A European
Journal 24 (2018) 17814–17822.
date_created: 2026-02-07T09:00:57Z
date_updated: 2026-02-17T16:19:07Z
doi: 10.1002/chem.201804065
extern: '1'
intvolume: ' 24'
issue: '67'
language:
- iso: eng
page: 17814–17822
publication: Chemistry A European Journal
status: public
title: Biofunctionalization of Nano Channels by Direct In-Pore Solid-Phase Peptide
Synthesis
type: journal_article
user_id: '100715'
volume: 24
year: '2018'
...
---
_id: '63924'
abstract:
- lang: eng
text: In a systematic study on the synthesis of aluminophosphates (AlPOs) under
ionothermal conditions, initially using 1-butyl-3-methylimidazolium bromide ([C4mim]Br)
as ionic liquid solvent and structure-directing agent, the effect of the reaction
conditions (i.e. molar P/Al, F/Al and ionic liquid/Al ratios, alternative fluoride
sources, influence of the ionic liquid’s cation or anion, temperature, reaction
time) on the framework type was studied in detail. In [C4mim]Br, the formation
of the more thermodynamically stable AEL framework type proceeds via AFI. The
framework type can be changed by choosing another anion or cation of the ionic
liquid. Hence, the successful ionothermal synthesis of the AFI framework AlPO
is reported by using either N-ethylpyridinium bromide ([C2py]Br) or 1-butyl-3-methylimidazolium
chloride ([C4mim]Cl). The mineraliser [Me4N]F, rather than HF, has been used for
the first time as an alternative fluoride source in ionothermal synthesis, which
can also affect the framework type. Hence, a very efficient synthesis of the LTA
framework type is reported in [C4mim]Br using [Me4N]F. Ab initio molecular dynamics
(AIMD) studies showed that the anion bridges between the aluminium atoms of the
framework and the cation. The interaction is more favoured in the presence of
the bromide than the chloride, which may be a clue to the question why the AEL
framework is not formed in the chloride-based ionic liquid. This study opens several
routes to pursue in the future as numerous ionic liquids are available which can
be used in ionothermal synthesis.
author:
- first_name: Muhammad Mohsin
full_name: Azim, Muhammad Mohsin
last_name: Azim
- first_name: Alfonso
full_name: Pensado, Alfonso
last_name: Pensado
- first_name: Barbara
full_name: Kirchner, Barbara
last_name: Kirchner
- 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
- first_name: Annegret
full_name: Stark, Annegret
last_name: Stark
citation:
ama: 'Azim MM, Pensado A, Kirchner B, et al. Ionothermal synthesis of crystalline
microporous aluminophosphates: Systematic study on the conditions affecting the
framework type. Microporous and Mesoporous Materials. 2018;266:204–213.
doi:10.1016/j.micromeso.2018.02.053'
apa: 'Azim, M. M., Pensado, A., Kirchner, B., Gutmann, T., Groszewicz, P. B., Buntkowsky,
G., & Stark, A. (2018). Ionothermal synthesis of crystalline microporous aluminophosphates:
Systematic study on the conditions affecting the framework type. Microporous
and Mesoporous Materials, 266, 204–213. https://doi.org/10.1016/j.micromeso.2018.02.053'
bibtex: '@article{Azim_Pensado_Kirchner_Gutmann_Groszewicz_Buntkowsky_Stark_2018,
title={Ionothermal synthesis of crystalline microporous aluminophosphates: Systematic
study on the conditions affecting the framework type}, volume={266}, DOI={10.1016/j.micromeso.2018.02.053},
journal={Microporous and Mesoporous Materials}, author={Azim, Muhammad Mohsin
and Pensado, Alfonso and Kirchner, Barbara and Gutmann, Torsten and Groszewicz,
Pedro B. and Buntkowsky, Gerd and Stark, Annegret}, year={2018}, pages={204–213}
}'
chicago: 'Azim, Muhammad Mohsin, Alfonso Pensado, Barbara Kirchner, Torsten Gutmann,
Pedro B. Groszewicz, Gerd Buntkowsky, and Annegret Stark. “Ionothermal Synthesis
of Crystalline Microporous Aluminophosphates: Systematic Study on the Conditions
Affecting the Framework Type.” Microporous and Mesoporous Materials 266
(2018): 204–213. https://doi.org/10.1016/j.micromeso.2018.02.053.'
ieee: 'M. M. Azim et al., “Ionothermal synthesis of crystalline microporous
aluminophosphates: Systematic study on the conditions affecting the framework
type,” Microporous and Mesoporous Materials, vol. 266, pp. 204–213, 2018,
doi: 10.1016/j.micromeso.2018.02.053.'
mla: 'Azim, Muhammad Mohsin, et al. “Ionothermal Synthesis of Crystalline Microporous
Aluminophosphates: Systematic Study on the Conditions Affecting the Framework
Type.” Microporous and Mesoporous Materials, vol. 266, 2018, pp. 204–213,
doi:10.1016/j.micromeso.2018.02.053.'
short: M.M. Azim, A. Pensado, B. Kirchner, T. Gutmann, P.B. Groszewicz, G. Buntkowsky,
A. Stark, Microporous and Mesoporous Materials 266 (2018) 204–213.
date_created: 2026-02-07T08:58:23Z
date_updated: 2026-02-17T16:19:17Z
doi: 10.1016/j.micromeso.2018.02.053
extern: '1'
intvolume: ' 266'
keyword:
- Aluminophosphates
- Ionic liquids
- Ionothermal synthesis
- Microporous materials
- Zeolite analogous
language:
- iso: eng
page: 204–213
publication: Microporous and Mesoporous Materials
status: public
title: 'Ionothermal synthesis of crystalline microporous aluminophosphates: Systematic
study on the conditions affecting the framework type'
type: journal_article
user_id: '100715'
volume: 266
year: '2018'
...
---
_id: '64277'
abstract:
- lang: eng
text: "Abstract\r\n Let \r\n \r\n
\ \r\n
\ \r\n G\r\n
\ /\r\n H\r\n
\ \r\n \r\n
\ \r\n {G/H}\r\n
\ \r\n
be a reductive symmetric space of split rank one and let K
be a maximal compact subgroup of G. In a previous article
the first two authors introduced a notion of cusp forms for \r\n \r\n
\ \r\n
\ \r\n G\r\n
\ /\r\n H\r\n
\ \r\n \r\n
\ \r\n {G/H}\r\n
\ \r\n .
We show that the space of cusp forms coincides with the closure of the space of
K-finite generalized matrix coefficients of discrete
series representations if and only if there exist no K-spherical
discrete series representations. Moreover, we prove that every K-spherical
discrete series representation occurs with multiplicity one in the Plancherel
decomposition of \r\n
\ \r\n \r\n
\ \r\n G\r\n
\ /\r\n H\r\n
\ \r\n \r\n
\ \r\n {G/H}\r\n
\ \r\n ."
author:
- first_name: Erik P.
full_name: van den Ban, Erik P.
last_name: van den Ban
- first_name: Job J.
full_name: Kuit, Job J.
last_name: Kuit
- first_name: Henrik
full_name: Schlichtkrull, Henrik
last_name: Schlichtkrull
citation:
ama: van den Ban EP, Kuit JJ, Schlichtkrull H. K-invariant cusp forms for reductive
symmetric spaces of split rank one. Forum Mathematicum. 2018;31(2):341-349.
doi:10.1515/forum-2018-0150
apa: van den Ban, E. P., Kuit, J. J., & Schlichtkrull, H. (2018). K-invariant
cusp forms for reductive symmetric spaces of split rank one. Forum Mathematicum,
31(2), 341–349. https://doi.org/10.1515/forum-2018-0150
bibtex: '@article{van den Ban_Kuit_Schlichtkrull_2018, title={K-invariant cusp forms
for reductive symmetric spaces of split rank one}, volume={31}, DOI={10.1515/forum-2018-0150},
number={2}, journal={Forum Mathematicum}, publisher={Walter de Gruyter GmbH},
author={van den Ban, Erik P. and Kuit, Job J. and Schlichtkrull, Henrik}, year={2018},
pages={341–349} }'
chicago: 'Ban, Erik P. van den, Job J. Kuit, and Henrik Schlichtkrull. “K-Invariant
Cusp Forms for Reductive Symmetric Spaces of Split Rank One.” Forum Mathematicum
31, no. 2 (2018): 341–49. https://doi.org/10.1515/forum-2018-0150.'
ieee: 'E. P. van den Ban, J. J. Kuit, and H. Schlichtkrull, “K-invariant cusp forms
for reductive symmetric spaces of split rank one,” Forum Mathematicum,
vol. 31, no. 2, pp. 341–349, 2018, doi: 10.1515/forum-2018-0150.'
mla: van den Ban, Erik P., et al. “K-Invariant Cusp Forms for Reductive Symmetric
Spaces of Split Rank One.” Forum Mathematicum, vol. 31, no. 2, Walter de
Gruyter GmbH, 2018, pp. 341–49, doi:10.1515/forum-2018-0150.
short: E.P. van den Ban, J.J. Kuit, H. Schlichtkrull, Forum Mathematicum 31 (2018)
341–349.
date_created: 2026-02-19T13:28:57Z
date_updated: 2026-02-19T13:29:20Z
doi: 10.1515/forum-2018-0150
intvolume: ' 31'
issue: '2'
language:
- iso: eng
page: 341-349
publication: Forum Mathematicum
publication_identifier:
issn:
- 1435-5337
- 0933-7741
publication_status: published
publisher: Walter de Gruyter GmbH
status: public
title: K-invariant cusp forms for reductive symmetric spaces of split rank one
type: journal_article
user_id: '52730'
volume: 31
year: '2018'
...
---
_id: '64278'
author:
- first_name: Mogens
full_name: Flensted-Jensen, Mogens
last_name: Flensted-Jensen
- first_name: Job J.
full_name: Kuit, Job J.
last_name: Kuit
citation:
ama: Flensted-Jensen M, Kuit JJ. Cuspidal integrals for SL(3)/Ke. Indagationes
Mathematicae. 2018;29(5):1235-1258. doi:10.1016/j.indag.2018.05.005
apa: Flensted-Jensen, M., & Kuit, J. J. (2018). Cuspidal integrals for SL(3)/Ke.
Indagationes Mathematicae, 29(5), 1235–1258. https://doi.org/10.1016/j.indag.2018.05.005
bibtex: '@article{Flensted-Jensen_Kuit_2018, title={Cuspidal integrals for SL(3)/Ke},
volume={29}, DOI={10.1016/j.indag.2018.05.005},
number={5}, journal={Indagationes Mathematicae}, publisher={Elsevier BV}, author={Flensted-Jensen,
Mogens and Kuit, Job J.}, year={2018}, pages={1235–1258} }'
chicago: 'Flensted-Jensen, Mogens, and Job J. Kuit. “Cuspidal Integrals for SL(3)/Ke.”
Indagationes Mathematicae 29, no. 5 (2018): 1235–58. https://doi.org/10.1016/j.indag.2018.05.005.'
ieee: 'M. Flensted-Jensen and J. J. Kuit, “Cuspidal integrals for SL(3)/Ke,” Indagationes
Mathematicae, vol. 29, no. 5, pp. 1235–1258, 2018, doi: 10.1016/j.indag.2018.05.005.'
mla: Flensted-Jensen, Mogens, and Job J. Kuit. “Cuspidal Integrals for SL(3)/Ke.”
Indagationes Mathematicae, vol. 29, no. 5, Elsevier BV, 2018, pp. 1235–58,
doi:10.1016/j.indag.2018.05.005.
short: M. Flensted-Jensen, J.J. Kuit, Indagationes Mathematicae 29 (2018) 1235–1258.
date_created: 2026-02-19T13:29:55Z
date_updated: 2026-02-19T13:30:32Z
doi: 10.1016/j.indag.2018.05.005
intvolume: ' 29'
issue: '5'
language:
- iso: eng
page: 1235-1258
publication: Indagationes Mathematicae
publication_identifier:
issn:
- 0019-3577
publication_status: published
publisher: Elsevier BV
status: public
title: Cuspidal integrals for SL(3)/Ke
type: journal_article
user_id: '52730'
volume: 29
year: '2018'
...
---
_id: '51085'
author:
- first_name: Heinrich
full_name: Klingmann, Heinrich
id: '55566'
last_name: Klingmann
citation:
ama: 'Klingmann H. Lateinamerikanische Perkussionsinstrumente im Unterricht. In:
Kraemer R-D, Rüdiger W, eds. Ensemblespiel und Klassenmusizieren in Schule
und Musikschule. Ein Handbuch für die Praxis. Vol 41. 4th ed. Forum Musikpädagogik.
Wißner-Verlag; 2018:413-450.'
apa: Klingmann, H. (2018). Lateinamerikanische Perkussionsinstrumente im Unterricht.
In R.-D. Kraemer & W. Rüdiger (Eds.), Ensemblespiel und Klassenmusizieren
in Schule und Musikschule. Ein Handbuch für die Praxis. (4th ed., Vol. 41,
pp. 413–450). Wißner-Verlag.
bibtex: '@inbook{Klingmann_2018, place={Augsburg}, edition={4}, series={Forum Musikpädagogik},
title={Lateinamerikanische Perkussionsinstrumente im Unterricht.}, volume={41},
booktitle={Ensemblespiel und Klassenmusizieren in Schule und Musikschule. Ein
Handbuch für die Praxis.}, publisher={Wißner-Verlag}, author={Klingmann, Heinrich},
editor={Kraemer, Rudolf-Dieter and Rüdiger, Wolfgang}, year={2018}, pages={413–450},
collection={Forum Musikpädagogik} }'
chicago: 'Klingmann, Heinrich. “Lateinamerikanische Perkussionsinstrumente im Unterricht.”
In Ensemblespiel und Klassenmusizieren in Schule und Musikschule. Ein Handbuch
für die Praxis., edited by Rudolf-Dieter Kraemer and Wolfgang Rüdiger, 4th
ed., 41:413–50. Forum Musikpädagogik. Augsburg: Wißner-Verlag, 2018.'
ieee: 'H. Klingmann, “Lateinamerikanische Perkussionsinstrumente im Unterricht.,”
in Ensemblespiel und Klassenmusizieren in Schule und Musikschule. Ein Handbuch
für die Praxis., 4th ed., vol. 41, R.-D. Kraemer and W. Rüdiger, Eds. Augsburg:
Wißner-Verlag, 2018, pp. 413–450.'
mla: Klingmann, Heinrich. “Lateinamerikanische Perkussionsinstrumente im Unterricht.”
Ensemblespiel und Klassenmusizieren in Schule und Musikschule. Ein Handbuch
für die Praxis., edited by Rudolf-Dieter Kraemer and Wolfgang Rüdiger, 4th
ed., vol. 41, Wißner-Verlag, 2018, pp. 413–50.
short: 'H. Klingmann, in: R.-D. Kraemer, W. Rüdiger (Eds.), Ensemblespiel und Klassenmusizieren
in Schule und Musikschule. Ein Handbuch für die Praxis., 4th ed., Wißner-Verlag,
Augsburg, 2018, pp. 413–450.'
date_created: 2024-01-31T08:47:55Z
date_updated: 2026-02-23T15:01:18Z
department:
- _id: '753'
edition: '4'
editor:
- first_name: Rudolf-Dieter
full_name: Kraemer, Rudolf-Dieter
last_name: Kraemer
- first_name: Wolfgang
full_name: Rüdiger, Wolfgang
last_name: Rüdiger
intvolume: ' 41'
language:
- iso: ger
page: 413-450
place: Augsburg
publication: Ensemblespiel und Klassenmusizieren in Schule und Musikschule. Ein Handbuch
für die Praxis.
publication_identifier:
isbn:
- 978-3-95786-186-3
publisher: Wißner-Verlag
series_title: Forum Musikpädagogik
status: public
title: Lateinamerikanische Perkussionsinstrumente im Unterricht.
type: book_chapter
user_id: '14972'
volume: 41
year: '2018'
...
---
_id: '64371'
author:
- first_name: Martin R.
full_name: Hofmann, Martin R.
last_name: Hofmann
- first_name: Marcel
full_name: Lenz, Marcel
last_name: Lenz
- first_name: Robin
full_name: Krug, Robin
last_name: Krug
- first_name: Nils Christopher
full_name: Gerhardt, Nils Christopher
id: '115298'
last_name: Gerhardt
orcid: 0009-0002-5538-231X
- first_name: Kirsten
full_name: Schmieder, Kirsten
last_name: Schmieder
- first_name: Christopher
full_name: Dillmann, Christopher
last_name: Dillmann
- first_name: Hubert
full_name: Welp, Hubert
last_name: Welp
citation:
ama: 'Hofmann MR, Lenz M, Krug R, et al. Brain tissue analysis using texture features
based on optical coherence tomography images. In: Optical Coherence Tomography
and Coherence Domain Optical Methods in Biomedicine XXII. ; 2018. doi:10.1117/12.2292032'
apa: Hofmann, M. R., Lenz, M., Krug, R., Gerhardt, N. C., Schmieder, K., Dillmann,
C., & Welp, H. (2018). Brain tissue analysis using texture features based
on optical coherence tomography images. Optical Coherence Tomography and Coherence
Domain Optical Methods in Biomedicine XXII. https://doi.org/10.1117/12.2292032
bibtex: '@inproceedings{Hofmann_Lenz_Krug_Gerhardt_Schmieder_Dillmann_Welp_2018,
title={Brain tissue analysis using texture features based on optical coherence
tomography images}, DOI={10.1117/12.2292032},
booktitle={Optical Coherence Tomography and Coherence Domain Optical Methods in
Biomedicine XXII}, author={Hofmann, Martin R. and Lenz, Marcel and Krug, Robin
and Gerhardt, Nils Christopher and Schmieder, Kirsten and Dillmann, Christopher
and Welp, Hubert}, year={2018} }'
chicago: Hofmann, Martin R., Marcel Lenz, Robin Krug, Nils Christopher Gerhardt,
Kirsten Schmieder, Christopher Dillmann, and Hubert Welp. “Brain Tissue Analysis
Using Texture Features Based on Optical Coherence Tomography Images.” In Optical
Coherence Tomography and Coherence Domain Optical Methods in Biomedicine XXII,
2018. https://doi.org/10.1117/12.2292032.
ieee: 'M. R. Hofmann et al., “Brain tissue analysis using texture features
based on optical coherence tomography images,” 2018, doi: 10.1117/12.2292032.'
mla: Hofmann, Martin R., et al. “Brain Tissue Analysis Using Texture Features Based
on Optical Coherence Tomography Images.” Optical Coherence Tomography and Coherence
Domain Optical Methods in Biomedicine XXII, 2018, doi:10.1117/12.2292032.
short: 'M.R. Hofmann, M. Lenz, R. Krug, N.C. Gerhardt, K. Schmieder, C. Dillmann,
H. Welp, in: Optical Coherence Tomography and Coherence Domain Optical Methods
in Biomedicine XXII, 2018.'
date_created: 2026-02-20T10:04:04Z
date_updated: 2026-02-25T13:45:03Z
department:
- _id: '977'
doi: 10.1117/12.2292032
language:
- iso: eng
publication: Optical Coherence Tomography and Coherence Domain Optical Methods in
Biomedicine XXII
status: public
title: Brain tissue analysis using texture features based on optical coherence tomography
images
type: conference
user_id: '15911'
year: '2018'
...
---
_id: '64372'
author:
- first_name: Marcel
full_name: Lenz, Marcel
last_name: Lenz
- first_name: Robin
full_name: Krug, Robin
last_name: Krug
- first_name: Nils Christopher
full_name: Gerhardt, Nils Christopher
id: '115298'
last_name: Gerhardt
orcid: 0009-0002-5538-231X
- first_name: Kirsten
full_name: Schmieder, Kirsten
last_name: Schmieder
- first_name: Martin R.
full_name: Hofmann, Martin R.
last_name: Hofmann
- first_name: Christopher
full_name: Dillmann, Christopher
last_name: Dillmann
- first_name: Hubert
full_name: Welp, Hubert
last_name: Welp
citation:
ama: 'Lenz M, Krug R, Gerhardt NC, et al. Classification of brain tissue with optical
coherence tomography by employing texture analysis. In: Optics, Photonics,
and Digital Technologies for Imaging Applications V. ; 2018. doi:10.1117/12.2307701'
apa: Lenz, M., Krug, R., Gerhardt, N. C., Schmieder, K., Hofmann, M. R., Dillmann,
C., & Welp, H. (2018). Classification of brain tissue with optical coherence
tomography by employing texture analysis. Optics, Photonics, and Digital Technologies
for Imaging Applications V. https://doi.org/10.1117/12.2307701
bibtex: '@inproceedings{Lenz_Krug_Gerhardt_Schmieder_Hofmann_Dillmann_Welp_2018,
title={Classification of brain tissue with optical coherence tomography by employing
texture analysis}, DOI={10.1117/12.2307701},
booktitle={Optics, Photonics, and Digital Technologies for Imaging Applications
V}, author={Lenz, Marcel and Krug, Robin and Gerhardt, Nils Christopher and Schmieder,
Kirsten and Hofmann, Martin R. and Dillmann, Christopher and Welp, Hubert}, year={2018}
}'
chicago: Lenz, Marcel, Robin Krug, Nils Christopher Gerhardt, Kirsten Schmieder,
Martin R. Hofmann, Christopher Dillmann, and Hubert Welp. “Classification of Brain
Tissue with Optical Coherence Tomography by Employing Texture Analysis.” In Optics,
Photonics, and Digital Technologies for Imaging Applications V, 2018. https://doi.org/10.1117/12.2307701.
ieee: 'M. Lenz et al., “Classification of brain tissue with optical coherence
tomography by employing texture analysis,” 2018, doi: 10.1117/12.2307701.'
mla: Lenz, Marcel, et al. “Classification of Brain Tissue with Optical Coherence
Tomography by Employing Texture Analysis.” Optics, Photonics, and Digital Technologies
for Imaging Applications V, 2018, doi:10.1117/12.2307701.
short: 'M. Lenz, R. Krug, N.C. Gerhardt, K. Schmieder, M.R. Hofmann, C. Dillmann,
H. Welp, in: Optics, Photonics, and Digital Technologies for Imaging Applications
V, 2018.'
date_created: 2026-02-20T10:04:04Z
date_updated: 2026-02-25T13:45:18Z
department:
- _id: '977'
doi: 10.1117/12.2307701
language:
- iso: eng
publication: Optics, Photonics, and Digital Technologies for Imaging Applications
V
status: public
title: Classification of brain tissue with optical coherence tomography by employing
texture analysis
type: conference
user_id: '15911'
year: '2018'
...