---
_id: '14687'
abstract:
- lang: eng
text: The short history of research on Li-O2 batteries has seen a remarkable number
of mechanistic U-turns over the years. From the initial use of carbonate electrolytes,
that were then found to be entirely unsuitable, to the belief that (su)peroxide
was solely responsible for degradation, before the more reactive singlet oxygen
was found to form, to the hypothesis that capacity depends on a competing surface/solution
mechanism before a practically exclusive solution mechanism was identified. Herein,
we argue for an ever-fresh look at the reported data without bias towards supposedly
established explanations. We explain how the latest findings on rate and capacity
limits, as well as the origin of side reactions, are connected via the disproportionation
(DISP) step in the (dis)charge mechanism. Therefrom, directions emerge for the
design of electrolytes and mediators on how to suppress side reactions and to
enable high rate and high reversible capacity.
article_number: e202316476
article_processing_charge: Yes (via OA deal)
article_type: review
author:
- first_name: Rajesh B
full_name: Jethwa, Rajesh B
id: 4cc538d5-803f-11ed-ab7e-8139573aad8f
last_name: Jethwa
orcid: 0000-0002-0404-4356
- first_name: Soumyadip
full_name: Mondal, Soumyadip
id: d25d21ef-dc8d-11ea-abe3-ec4576307f48
last_name: Mondal
- first_name: Bhargavi
full_name: Pant, Bhargavi
id: 50c64d4d-eb97-11eb-a6c2-d33e5e14f112
last_name: Pant
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
citation:
ama: Jethwa RB, Mondal S, Pant B, Freunberger SA. To DISP or not? The far‐reaching
reaction mechanisms underpinning Lithium‐air batteries. Angewandte Chemie International
Edition. 2023. doi:10.1002/anie.202316476
apa: Jethwa, R. B., Mondal, S., Pant, B., & Freunberger, S. A. (2023). To DISP
or not? The far‐reaching reaction mechanisms underpinning Lithium‐air batteries.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202316476
chicago: Jethwa, Rajesh B, Soumyadip Mondal, Bhargavi Pant, and Stefan Alexander
Freunberger. “To DISP or Not? The Far‐reaching Reaction Mechanisms Underpinning
Lithium‐air Batteries.” Angewandte Chemie International Edition. Wiley,
2023. https://doi.org/10.1002/anie.202316476.
ieee: R. B. Jethwa, S. Mondal, B. Pant, and S. A. Freunberger, “To DISP or not?
The far‐reaching reaction mechanisms underpinning Lithium‐air batteries,” Angewandte
Chemie International Edition. Wiley, 2023.
ista: Jethwa RB, Mondal S, Pant B, Freunberger SA. 2023. To DISP or not? The far‐reaching
reaction mechanisms underpinning Lithium‐air batteries. Angewandte Chemie International
Edition., e202316476.
mla: Jethwa, Rajesh B., et al. “To DISP or Not? The Far‐reaching Reaction Mechanisms
Underpinning Lithium‐air Batteries.” Angewandte Chemie International Edition,
e202316476, Wiley, 2023, doi:10.1002/anie.202316476.
short: R.B. Jethwa, S. Mondal, B. Pant, S.A. Freunberger, Angewandte Chemie International
Edition (2023).
date_created: 2023-12-15T16:10:13Z
date_published: 2023-12-14T00:00:00Z
date_updated: 2024-02-15T14:43:05Z
day: '14'
department:
- _id: StFr
- _id: GradSch
doi: 10.1002/anie.202316476
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: ' https://doi.org/10.1002/anie.202316476'
month: '12'
oa: 1
oa_version: Published Version
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: epub_ahead
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: To DISP or not? The far‐reaching reaction mechanisms underpinning Lithium‐air
batteries
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '14861'
abstract:
- lang: eng
text: Cover Page
article_number: ' e202304138'
article_processing_charge: No
author:
- first_name: Lea Marie
full_name: Becker, Lea Marie
id: 36336939-eb97-11eb-a6c2-c83f1214ca79
last_name: Becker
orcid: 0000-0002-6401-5151
- first_name: Mélanie
full_name: Berbon, Mélanie
last_name: Berbon
- first_name: Alicia
full_name: Vallet, Alicia
last_name: Vallet
- first_name: Axelle
full_name: Grelard, Axelle
last_name: Grelard
- first_name: Estelle
full_name: Morvan, Estelle
last_name: Morvan
- first_name: Benjamin
full_name: Bardiaux, Benjamin
last_name: Bardiaux
- first_name: Roman
full_name: Lichtenecker, Roman
last_name: Lichtenecker
- first_name: Matthias
full_name: Ernst, Matthias
last_name: Ernst
- first_name: Antoine
full_name: Loquet, Antoine
last_name: Loquet
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
citation:
ama: 'Becker LM, Berbon M, Vallet A, et al. Cover Picture: The Rigid Core and
Flexible Surface of Amyloid Fibrils Probed by Magic‐Angle‐Spinning NMR Spectroscopy
of Aromatic Residues. Vol 62. Wiley; 2023. doi:10.1002/anie.202304138'
apa: 'Becker, L. M., Berbon, M., Vallet, A., Grelard, A., Morvan, E., Bardiaux,
B., … Schanda, P. (2023). Cover Picture: The rigid core and flexible surface
of amyloid fibrils probed by Magic‐Angle‐Spinning NMR spectroscopy of aromatic
residues. Angewandte Chemie International Edition (Vol. 62). Wiley.
https://doi.org/10.1002/anie.202304138'
chicago: 'Becker, Lea Marie, Mélanie Berbon, Alicia Vallet, Axelle Grelard, Estelle
Morvan, Benjamin Bardiaux, Roman Lichtenecker, Matthias Ernst, Antoine Loquet,
and Paul Schanda. Cover Picture: The Rigid Core and Flexible Surface of Amyloid
Fibrils Probed by Magic‐Angle‐Spinning NMR Spectroscopy of Aromatic Residues.
Angewandte Chemie International Edition. Vol. 62. Wiley, 2023. https://doi.org/10.1002/anie.202304138.'
ieee: 'L. M. Becker et al., Cover Picture: The rigid core and flexible
surface of amyloid fibrils probed by Magic‐Angle‐Spinning NMR spectroscopy of
aromatic residues, vol. 62, no. 19. Wiley, 2023.'
ista: 'Becker LM, Berbon M, Vallet A, Grelard A, Morvan E, Bardiaux B, Lichtenecker
R, Ernst M, Loquet A, Schanda P. 2023. Cover Picture: The rigid core and flexible
surface of amyloid fibrils probed by Magic‐Angle‐Spinning NMR spectroscopy of
aromatic residues, Wiley,p.'
mla: 'Becker, Lea Marie, et al. “Cover Picture: The Rigid Core and Flexible Surface
of Amyloid Fibrils Probed by Magic‐Angle‐Spinning NMR Spectroscopy of Aromatic
Residues.” Angewandte Chemie International Edition, vol. 62, no. 19, e202304138,
Wiley, 2023, doi:10.1002/anie.202304138.'
short: 'L.M. Becker, M. Berbon, A. Vallet, A. Grelard, E. Morvan, B. Bardiaux, R.
Lichtenecker, M. Ernst, A. Loquet, P. Schanda, Cover Picture: The Rigid Core and
Flexible Surface of Amyloid Fibrils Probed by Magic‐Angle‐Spinning NMR Spectroscopy
of Aromatic Residues, Wiley, 2023.'
date_created: 2024-01-22T11:54:34Z
date_published: 2023-05-02T00:00:00Z
date_updated: 2024-01-23T08:48:14Z
day: '02'
department:
- _id: PaSc
doi: 10.1002/anie.202304138
intvolume: ' 62'
issue: '19'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.202304138
month: '05'
oa: 1
oa_version: Published Version
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
related_material:
link:
- relation: translation
url: https://doi.org/10.1002/ange.202304138
record:
- id: '12675'
relation: other
status: public
status: public
title: 'Cover Picture: The rigid core and flexible surface of amyloid fibrils probed
by Magic‐Angle‐Spinning NMR spectroscopy of aromatic residues'
type: other_academic_publication
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 62
year: '2023'
...
---
_id: '12675'
abstract:
- lang: eng
text: Aromatic side chains are important reporters of the plasticity of proteins,
and often form important contacts in protein--protein interactions. By studying
a pair of structurally homologous cross-β amyloid fibrils, HET-s and HELLF, with
a specific isotope-labeling approach and magic-angle-spinning (MAS) NMR, we have
characterized the dynamic behavior of Phe and Tyr aromatic rings to show that
the hydrophobic amyloid core is rigid, without any sign of "breathing motions"
over hundreds of milliseconds at least. Aromatic residues exposed at the fibril
surface have a rigid ring axis but undergo ring flips, on a variety of time scales
from ns to µs. Our approach provides direct insight into hydrophobic-core motions,
enabling a better evaluation of the conformational heterogeneity generated from
a NMR structural ensemble of such amyloid cross-β architecture.
acknowledgement: We thank AlbertA. Smith (Leipzig)for insightful discussions. This
work was supported by funding from the European Research Council (StG-2012-311318
to P.S.) and used the platforms of the Grenoble Instruct-ERIC center (ISBG;UMS 3518
CNRS-CEA-UJF-EMBL) within the Grenoble Partnership for Structural Biology(PSB) and
facilities and expertiseof the Biophysical and Structural Chemistry platform (BPCS)
at IECB,CNRSUAR3033,INSERMUS001 and Bordeaux University.
article_number: e202219314
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Lea Marie
full_name: Becker, Lea Marie
id: 36336939-eb97-11eb-a6c2-c83f1214ca79
last_name: Becker
orcid: 0000-0002-6401-5151
- first_name: Mélanie
full_name: Berbon, Mélanie
last_name: Berbon
- first_name: Alicia
full_name: Vallet, Alicia
last_name: Vallet
- first_name: Axelle
full_name: Grelard, Axelle
last_name: Grelard
- first_name: Estelle
full_name: Morvan, Estelle
last_name: Morvan
- first_name: Benjamin
full_name: Bardiaux, Benjamin
last_name: Bardiaux
- first_name: Roman
full_name: Lichtenecker, Roman
last_name: Lichtenecker
- first_name: Matthias
full_name: Ernst, Matthias
last_name: Ernst
- first_name: Antoine
full_name: Loquet, Antoine
last_name: Loquet
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
citation:
ama: Becker LM, Berbon M, Vallet A, et al. The rigid core and flexible surface of
amyloid fibrils probed by Magic‐Angle Spinning NMR of aromatic residues. Angewandte
Chemie International Edition. 2023;62(19). doi:10.1002/anie.202219314
apa: Becker, L. M., Berbon, M., Vallet, A., Grelard, A., Morvan, E., Bardiaux, B.,
… Schanda, P. (2023). The rigid core and flexible surface of amyloid fibrils probed
by Magic‐Angle Spinning NMR of aromatic residues. Angewandte Chemie International
Edition. Wiley. https://doi.org/10.1002/anie.202219314
chicago: Becker, Lea Marie, Mélanie Berbon, Alicia Vallet, Axelle Grelard, Estelle
Morvan, Benjamin Bardiaux, Roman Lichtenecker, Matthias Ernst, Antoine Loquet,
and Paul Schanda. “The Rigid Core and Flexible Surface of Amyloid Fibrils Probed
by Magic‐Angle Spinning NMR of Aromatic Residues.” Angewandte Chemie International
Edition. Wiley, 2023. https://doi.org/10.1002/anie.202219314.
ieee: L. M. Becker et al., “The rigid core and flexible surface of amyloid
fibrils probed by Magic‐Angle Spinning NMR of aromatic residues,” Angewandte
Chemie International Edition, vol. 62, no. 19. Wiley, 2023.
ista: Becker LM, Berbon M, Vallet A, Grelard A, Morvan E, Bardiaux B, Lichtenecker
R, Ernst M, Loquet A, Schanda P. 2023. The rigid core and flexible surface of
amyloid fibrils probed by Magic‐Angle Spinning NMR of aromatic residues. Angewandte
Chemie International Edition. 62(19), e202219314.
mla: Becker, Lea Marie, et al. “The Rigid Core and Flexible Surface of Amyloid Fibrils
Probed by Magic‐Angle Spinning NMR of Aromatic Residues.” Angewandte Chemie
International Edition, vol. 62, no. 19, e202219314, Wiley, 2023, doi:10.1002/anie.202219314.
short: L.M. Becker, M. Berbon, A. Vallet, A. Grelard, E. Morvan, B. Bardiaux, R.
Lichtenecker, M. Ernst, A. Loquet, P. Schanda, Angewandte Chemie International
Edition 62 (2023).
date_created: 2023-02-24T10:45:01Z
date_published: 2023-05-01T00:00:00Z
date_updated: 2024-02-21T12:14:06Z
day: '01'
ddc:
- '540'
department:
- _id: GradSch
- _id: PaSc
doi: 10.1002/anie.202219314
external_id:
isi:
- '000956919900001'
pmid:
- '36738230'
file:
- access_level: open_access
checksum: 7dd083ed8850faa55c34e411ed390de9
content_type: application/pdf
creator: dernst
date_created: 2023-08-16T12:33:31Z
date_updated: 2023-08-16T12:33:31Z
file_id: '14072'
file_name: 2023_AngewChemInt_Becker.pdf
file_size: 1422445
relation: main_file
success: 1
file_date_updated: 2023-08-16T12:33:31Z
has_accepted_license: '1'
intvolume: ' 62'
isi: 1
issue: '19'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
pmid: 1
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
link:
- description: News on ISTA website
relation: press_release
url: https://ista.ac.at/en/news/dancing-styles-of-atoms/
record:
- id: '14861'
relation: other
status: public
- id: '12497'
relation: research_data
status: public
status: public
title: The rigid core and flexible surface of amyloid fibrils probed by Magic‐Angle
Spinning NMR of aromatic residues
tmp:
image: /images/cc_by_nc.png
legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
short: CC BY-NC (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 62
year: '2023'
...
---
_id: '12922'
abstract:
- lang: eng
text: The influence of structural modifications on the catalytic activity of carbon
materials is poorly understood. A collection of carbonaceous materials with different
pore networks and high nitrogen content was characterized and used to catalyze
four reactions to deduce structure–activity relationships. The CO2 cycloaddition
and Knoevenagel reaction depend on Lewis basic sites (electron-rich nitrogen species).
The absence of large conjugated carbon domains resulting from the introduction
of large amounts of nitrogen in the carbon network is responsible for poor redox
activity, as observed through the catalytic reduction of nitrobenzene with hydrazine
and the catalytic oxidation of 3,3′,5,5′-tetramethylbenzidine using hydroperoxide.
The material with the highest activity towards Lewis acid catalysis (in the hydrolysis
of (dimethoxymethyl)benzene to benzaldehyde) is the most effective for small molecule
activation and presents the highest concentration of electron-poor nitrogen species.
article_number: e202211663
article_processing_charge: No
article_type: original
author:
- first_name: Enrico
full_name: Lepre, Enrico
last_name: Lepre
- first_name: Sylvain
full_name: Rat, Sylvain
last_name: Rat
- first_name: Cristian
full_name: Cavedon, Cristian
last_name: Cavedon
- first_name: Peter H.
full_name: Seeberger, Peter H.
last_name: Seeberger
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Markus
full_name: Antonietti, Markus
last_name: Antonietti
- first_name: Nieves
full_name: López‐Salas, Nieves
last_name: López‐Salas
citation:
ama: Lepre E, Rat S, Cavedon C, et al. Catalytic properties of high nitrogen content
carbonaceous materials. Angewandte Chemie International Edition. 2023;62(2).
doi:10.1002/anie.202211663
apa: Lepre, E., Rat, S., Cavedon, C., Seeberger, P. H., Pieber, B., Antonietti,
M., & López‐Salas, N. (2023). Catalytic properties of high nitrogen content
carbonaceous materials. Angewandte Chemie International Edition. Wiley.
https://doi.org/10.1002/anie.202211663
chicago: Lepre, Enrico, Sylvain Rat, Cristian Cavedon, Peter H. Seeberger, Bartholomäus
Pieber, Markus Antonietti, and Nieves López‐Salas. “Catalytic Properties of High
Nitrogen Content Carbonaceous Materials.” Angewandte Chemie International Edition.
Wiley, 2023. https://doi.org/10.1002/anie.202211663.
ieee: E. Lepre et al., “Catalytic properties of high nitrogen content carbonaceous
materials,” Angewandte Chemie International Edition, vol. 62, no. 2. Wiley,
2023.
ista: Lepre E, Rat S, Cavedon C, Seeberger PH, Pieber B, Antonietti M, López‐Salas
N. 2023. Catalytic properties of high nitrogen content carbonaceous materials.
Angewandte Chemie International Edition. 62(2), e202211663.
mla: Lepre, Enrico, et al. “Catalytic Properties of High Nitrogen Content Carbonaceous
Materials.” Angewandte Chemie International Edition, vol. 62, no. 2, e202211663,
Wiley, 2023, doi:10.1002/anie.202211663.
short: E. Lepre, S. Rat, C. Cavedon, P.H. Seeberger, B. Pieber, M. Antonietti, N.
López‐Salas, Angewandte Chemie International Edition 62 (2023).
date_created: 2023-05-08T08:28:14Z
date_published: 2023-01-09T00:00:00Z
date_updated: 2023-08-21T09:18:12Z
day: '09'
doi: 10.1002/anie.202211663
extern: '1'
intvolume: ' 62'
issue: '2'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.202211663
month: '01'
oa: 1
oa_version: Published Version
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Catalytic properties of high nitrogen content carbonaceous materials
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 62
year: '2023'
...
---
_id: '11451'
abstract:
- lang: eng
text: The precursor conversion chemistry and surface chemistry of Cu3N and Cu3PdN
nanocrystals are unknown or contested. Here, we first obtain phase-pure, colloidally
stable nanocubes. Second, we elucidate the pathway by which copper(II) nitrate
and oleylamine form Cu3N. We find that oleylamine is both a reductant and a nitrogen
source. Oleylamine is oxidized by nitrate to a primary aldimine, which reacts
further with excess oleylamine to a secondary aldimine, eliminating ammonia. Ammonia
reacts with CuI to form Cu3N. Third, we investigated the surface chemistry and
find a mixed ligand shell of aliphatic amines and carboxylates (formed in situ).
While the carboxylates appear tightly bound, the amines are easily desorbed from
the surface. Finally, we show that doping with palladium decreases the band gap
and the material becomes semi-metallic. These results bring insight into the chemistry
of metal nitrides and might help the development of other metal nitride nanocrystals.
acknowledgement: 'J.D.R. and M.P. acknowledge the SNF Eccellenza funding scheme (project
number: 194172). We acknowledge DESY (Hamburg, Germany), a member of the Helmholtz
Association HGF, for the provision of experimental facilities. Parts of this research
were carried out at beamline P21.1, PETRA III. We thank Dr. Soham Banerjee for acquiring
the PDF data and helpful advice. A.R. acknowledges the support from the Analytical
Chemistry Trust Fund for her CAMS-UK Fellowship. C.K. acknowledges the support from
the Department of Chemistry, UCL. The authors acknowledge Dr Stephan Lany from NREL
for providing the Cu3N DFT calculations. The authors thank Prof. Raymond Schaak
and Dr. Robert William Lord for helpful advice and suggestions regarding the purification
procedure. Open access funding provided by Universitat Basel.'
article_number: e202207013
article_processing_charge: No
article_type: original
author:
- first_name: Mahsa
full_name: Parvizian, Mahsa
last_name: Parvizian
- first_name: Alejandra
full_name: Duràn Balsa, Alejandra
last_name: Duràn Balsa
- first_name: Rohan
full_name: Pokratath, Rohan
last_name: Pokratath
- first_name: Curran
full_name: Kalha, Curran
last_name: Kalha
- first_name: Seungho
full_name: Lee, Seungho
id: BB243B88-D767-11E9-B658-BC13E6697425
last_name: Lee
orcid: 0000-0002-6962-8598
- first_name: Dietger
full_name: Van Den Eynden, Dietger
last_name: Van Den Eynden
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Anna
full_name: Regoutz, Anna
last_name: Regoutz
- first_name: Jonathan
full_name: De Roo, Jonathan
last_name: De Roo
citation:
ama: Parvizian M, Duràn Balsa A, Pokratath R, et al. The chemistry of Cu₃N and Cu₃PdN
nanocrystals. Angewandte Chemie - International Edition. 2022;61(31). doi:10.1002/anie.202207013
apa: Parvizian, M., Duràn Balsa, A., Pokratath, R., Kalha, C., Lee, S., Van Den
Eynden, D., … De Roo, J. (2022). The chemistry of Cu₃N and Cu₃PdN nanocrystals.
Angewandte Chemie - International Edition. Wiley. https://doi.org/10.1002/anie.202207013
chicago: Parvizian, Mahsa, Alejandra Duràn Balsa, Rohan Pokratath, Curran Kalha,
Seungho Lee, Dietger Van Den Eynden, Maria Ibáñez, Anna Regoutz, and Jonathan
De Roo. “The Chemistry of Cu₃N and Cu₃PdN Nanocrystals.” Angewandte Chemie
- International Edition. Wiley, 2022. https://doi.org/10.1002/anie.202207013.
ieee: M. Parvizian et al., “The chemistry of Cu₃N and Cu₃PdN nanocrystals,”
Angewandte Chemie - International Edition, vol. 61, no. 31. Wiley, 2022.
ista: Parvizian M, Duràn Balsa A, Pokratath R, Kalha C, Lee S, Van Den Eynden D,
Ibáñez M, Regoutz A, De Roo J. 2022. The chemistry of Cu₃N and Cu₃PdN nanocrystals.
Angewandte Chemie - International Edition. 61(31), e202207013.
mla: Parvizian, Mahsa, et al. “The Chemistry of Cu₃N and Cu₃PdN Nanocrystals.” Angewandte
Chemie - International Edition, vol. 61, no. 31, e202207013, Wiley, 2022,
doi:10.1002/anie.202207013.
short: M. Parvizian, A. Duràn Balsa, R. Pokratath, C. Kalha, S. Lee, D. Van Den
Eynden, M. Ibáñez, A. Regoutz, J. De Roo, Angewandte Chemie - International Edition
61 (2022).
date_created: 2022-06-19T22:01:58Z
date_published: 2022-08-01T00:00:00Z
date_updated: 2023-08-03T07:19:12Z
day: '01'
ddc:
- '540'
department:
- _id: MaIb
doi: 10.1002/anie.202207013
external_id:
isi:
- '000811084000001'
pmid:
- '35612297'
file:
- access_level: open_access
checksum: 2a3ee0bb59e044b808ebe85cd94ac899
content_type: application/pdf
creator: dernst
date_created: 2022-07-29T09:29:20Z
date_updated: 2022-07-29T09:29:20Z
file_id: '11696'
file_name: 2022_AngewandteChemieInternat_Parvizian.pdf
file_size: 1303202
relation: main_file
success: 1
file_date_updated: 2022-07-29T09:29:20Z
has_accepted_license: '1'
intvolume: ' 61'
isi: 1
issue: '31'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: Angewandte Chemie - International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
record:
- id: '11695'
relation: research_data
status: public
scopus_import: '1'
status: public
title: The chemistry of Cu₃N and Cu₃PdN nanocrystals
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 61
year: '2022'
...
---
_id: '11705'
abstract:
- lang: eng
text: 'The broad implementation of thermoelectricity requires high-performance and
low-cost materials. One possibility is employing surfactant-free solution synthesis
to produce nanopowders. We propose the strategy of functionalizing “naked” particles’
surface by inorganic molecules to control the nanostructure and, consequently,
thermoelectric performance. In particular, we use bismuth thiolates to functionalize
surfactant-free SnTe particles’ surfaces. Upon thermal processing, bismuth thiolates
decomposition renders SnTe-Bi2S3 nanocomposites with synergistic functions: 1)
carrier concentration optimization by Bi doping; 2) Seebeck coefficient enhancement
and bipolar effect suppression by energy filtering; and 3) lattice thermal conductivity
reduction by small grain domains, grain boundaries and nanostructuration. Overall,
the SnTe-Bi2S3 nanocomposites exhibit peak z T up to 1.3 at 873 K and an average
z T of ≈0.6 at 300–873 K, which is among the highest reported for solution-processed
SnTe.'
acknowledged_ssus:
- _id: EM-Fac
- _id: NanoFab
acknowledgement: This research was supported by the Scientific Service Units (SSU)
of IST Austria through resources provided by Electron Microscopy Facility (EMF)
and the Nanofabrication Facility (NNF). This work was financially supported by IST
Austria and the Werner Siemens Foundation. C.C. acknowledges funding from the FWF
“Lise Meitner Fellowship” grant agreement M 2889-N. Lise Meitner Project (M2889-N).
Y.L. acknowledges funding from the European Union's Horizon 2020 research and innovation
program under the Marie Sklodowska-Curie grant agreement No. 754411. R.L.B. thanks
the National Science Foundation for support under DMR-1904719. MCS acknowledge MINECO
Juan de la Cierva Incorporation fellowship (JdlCI 2019) and Severo Ochoa. M.C.S.
and J.A. acknowledge funding from Generalitat de Catalunya 2017 SGR 327. ICN2 is
supported by the Severo Ochoa program from Spanish MINECO (Grant no. SEV-2017-0706)
and is funded by the CERCA Programme/Generalitat de Catalunya. This study was supported
by MCIN with funding from European Union NextGenerationEU (PRTR-C17.I1) and Generalitat
de Catalunya.
article_number: e202207002
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Cheng
full_name: Chang, Cheng
id: 9E331C2E-9F27-11E9-AE48-5033E6697425
last_name: Chang
orcid: 0000-0002-9515-4277
- first_name: Yu
full_name: Liu, Yu
id: 2A70014E-F248-11E8-B48F-1D18A9856A87
last_name: Liu
orcid: 0000-0001-7313-6740
- first_name: Seungho
full_name: Lee, Seungho
id: BB243B88-D767-11E9-B658-BC13E6697425
last_name: Lee
orcid: 0000-0002-6962-8598
- first_name: Maria
full_name: Spadaro, Maria
last_name: Spadaro
- first_name: Kristopher M.
full_name: Koskela, Kristopher M.
last_name: Koskela
- first_name: Tobias
full_name: Kleinhanns, Tobias
id: 8BD9DE16-AB3C-11E9-9C8C-2A03E6697425
last_name: Kleinhanns
- first_name: Tommaso
full_name: Costanzo, Tommaso
id: D93824F4-D9BA-11E9-BB12-F207E6697425
last_name: Costanzo
orcid: 0000-0001-9732-3815
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Richard L.
full_name: Brutchey, Richard L.
last_name: Brutchey
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
citation:
ama: 'Chang C, Liu Y, Lee S, et al. Surface functionalization of surfactant-free
particles: A strategy to tailor the properties of nanocomposites for enhanced
thermoelectric performance. Angewandte Chemie - International Edition.
2022;61(35). doi:10.1002/anie.202207002'
apa: 'Chang, C., Liu, Y., Lee, S., Spadaro, M., Koskela, K. M., Kleinhanns, T.,
… Ibáñez, M. (2022). Surface functionalization of surfactant-free particles: A
strategy to tailor the properties of nanocomposites for enhanced thermoelectric
performance. Angewandte Chemie - International Edition. Wiley. https://doi.org/10.1002/anie.202207002'
chicago: 'Chang, Cheng, Yu Liu, Seungho Lee, Maria Spadaro, Kristopher M. Koskela,
Tobias Kleinhanns, Tommaso Costanzo, Jordi Arbiol, Richard L. Brutchey, and Maria
Ibáñez. “Surface Functionalization of Surfactant-Free Particles: A Strategy to
Tailor the Properties of Nanocomposites for Enhanced Thermoelectric Performance.”
Angewandte Chemie - International Edition. Wiley, 2022. https://doi.org/10.1002/anie.202207002.'
ieee: 'C. Chang et al., “Surface functionalization of surfactant-free particles:
A strategy to tailor the properties of nanocomposites for enhanced thermoelectric
performance,” Angewandte Chemie - International Edition, vol. 61, no. 35.
Wiley, 2022.'
ista: 'Chang C, Liu Y, Lee S, Spadaro M, Koskela KM, Kleinhanns T, Costanzo T, Arbiol
J, Brutchey RL, Ibáñez M. 2022. Surface functionalization of surfactant-free particles:
A strategy to tailor the properties of nanocomposites for enhanced thermoelectric
performance. Angewandte Chemie - International Edition. 61(35), e202207002.'
mla: 'Chang, Cheng, et al. “Surface Functionalization of Surfactant-Free Particles:
A Strategy to Tailor the Properties of Nanocomposites for Enhanced Thermoelectric
Performance.” Angewandte Chemie - International Edition, vol. 61, no. 35,
e202207002, Wiley, 2022, doi:10.1002/anie.202207002.'
short: C. Chang, Y. Liu, S. Lee, M. Spadaro, K.M. Koskela, T. Kleinhanns, T. Costanzo,
J. Arbiol, R.L. Brutchey, M. Ibáñez, Angewandte Chemie - International Edition
61 (2022).
date_created: 2022-07-31T22:01:48Z
date_published: 2022-08-26T00:00:00Z
date_updated: 2023-08-03T12:23:52Z
day: '26'
ddc:
- '540'
department:
- _id: MaIb
- _id: EM-Fac
doi: 10.1002/anie.202207002
ec_funded: 1
external_id:
isi:
- '000828274200001'
file:
- access_level: open_access
checksum: ad601f2b9e26e46ab4785162be58b5ed
content_type: application/pdf
creator: dernst
date_created: 2023-02-02T08:01:00Z
date_updated: 2023-02-02T08:01:00Z
file_id: '12476'
file_name: 2022_AngewandteChemieInternat_Chang.pdf
file_size: 4072650
relation: main_file
success: 1
file_date_updated: 2023-02-02T08:01:00Z
has_accepted_license: '1'
intvolume: ' 61'
isi: 1
issue: '35'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
project:
- _id: 9B8804FC-BA93-11EA-9121-9846C619BF3A
grant_number: M02889
name: Bottom-up Engineering for Thermoelectric Applications
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
publication: Angewandte Chemie - International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Surface functionalization of surfactant-free particles: A strategy to tailor
the properties of nanocomposites for enhanced thermoelectric performance'
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 61
year: '2022'
...
---
_id: '11955'
abstract:
- lang: eng
text: Covalent organic frameworks (COFs) are structurally tuneable, porous and crystalline
polymers constructed through the covalent attachment of small organic building
blocks as elementary units. Using the myriad of such building blocks, a broad
spectrum of functionalities has been applied for COF syntheses for broad applications,
including heterogeneous catalysis. Herein, we report the synthesis of a new family
of porous and crystalline COFs using a novel acridine linker and benzene-1,3,5-tricarbaldehyde
derivatives bearing a variable number of hydroxy groups. With the broad absorption
in the visible light region, the COFs were applied as photocatalysts in metallaphotocatalytic
C−N cross-coupling. The fully β-ketoenamine linked COF showed the highest activity,
due to the increased charge separation upon irradiation. The COF showed good to
excellent yields for several aryl bromides, good recyclability and even catalyzed
the organic transformation in presence of green light as energy source.
article_number: e202117738
article_processing_charge: No
article_type: original
author:
- first_name: Michael
full_name: Traxler, Michael
last_name: Traxler
- first_name: Sebastian
full_name: Gisbertz, Sebastian
last_name: Gisbertz
- first_name: Pradip
full_name: Pachfule, Pradip
last_name: Pachfule
- first_name: Johannes
full_name: Schmidt, Johannes
last_name: Schmidt
- first_name: Jérôme
full_name: Roeser, Jérôme
last_name: Roeser
- first_name: Susanne
full_name: Reischauer, Susanne
last_name: Reischauer
- first_name: Jabor
full_name: Rabeah, Jabor
last_name: Rabeah
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Arne
full_name: Thomas, Arne
last_name: Thomas
citation:
ama: Traxler M, Gisbertz S, Pachfule P, et al. Acridine‐functionalized covalent
organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C−N cross‐coupling.
Angewandte Chemie International Edition. 2022;61(21). doi:10.1002/anie.202117738
apa: Traxler, M., Gisbertz, S., Pachfule, P., Schmidt, J., Roeser, J., Reischauer,
S., … Thomas, A. (2022). Acridine‐functionalized covalent organic frameworks (COFs)
as photocatalysts for metallaphotocatalytic C−N cross‐coupling. Angewandte
Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202117738
chicago: Traxler, Michael, Sebastian Gisbertz, Pradip Pachfule, Johannes Schmidt,
Jérôme Roeser, Susanne Reischauer, Jabor Rabeah, Bartholomäus Pieber, and Arne
Thomas. “Acridine‐functionalized Covalent Organic Frameworks (COFs) as Photocatalysts
for Metallaphotocatalytic C−N Cross‐coupling.” Angewandte Chemie International
Edition. Wiley, 2022. https://doi.org/10.1002/anie.202117738.
ieee: M. Traxler et al., “Acridine‐functionalized covalent organic frameworks
(COFs) as photocatalysts for metallaphotocatalytic C−N cross‐coupling,” Angewandte
Chemie International Edition, vol. 61, no. 21. Wiley, 2022.
ista: Traxler M, Gisbertz S, Pachfule P, Schmidt J, Roeser J, Reischauer S, Rabeah
J, Pieber B, Thomas A. 2022. Acridine‐functionalized covalent organic frameworks
(COFs) as photocatalysts for metallaphotocatalytic C−N cross‐coupling. Angewandte
Chemie International Edition. 61(21), e202117738.
mla: Traxler, Michael, et al. “Acridine‐functionalized Covalent Organic Frameworks
(COFs) as Photocatalysts for Metallaphotocatalytic C−N Cross‐coupling.” Angewandte
Chemie International Edition, vol. 61, no. 21, e202117738, Wiley, 2022, doi:10.1002/anie.202117738.
short: M. Traxler, S. Gisbertz, P. Pachfule, J. Schmidt, J. Roeser, S. Reischauer,
J. Rabeah, B. Pieber, A. Thomas, Angewandte Chemie International Edition 61 (2022).
date_created: 2022-08-24T10:41:25Z
date_published: 2022-05-16T00:00:00Z
date_updated: 2023-02-21T10:09:11Z
day: '16'
doi: 10.1002/anie.202117738
extern: '1'
external_id:
pmid:
- '35188714'
intvolume: ' 61'
issue: '21'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.202117738
month: '05'
oa: 1
oa_version: Published Version
pmid: 1
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Acridine‐functionalized covalent organic frameworks (COFs) as photocatalysts
for metallaphotocatalytic C−N cross‐coupling
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2022'
...
---
_id: '12228'
abstract:
- lang: eng
text: The question of how RNA, as the principal carrier of genetic information evolved
is fundamentally important for our understanding of the origin of life. The RNA
molecule is far too complex to have formed in one evolutionary step, suggesting
that ancestral proto-RNAs (first ancestor of RNA) may have existed, which evolved
over time into the RNA of today. Here we show that isoxazole nucleosides, which
are quickly formed from hydroxylamine, cyanoacetylene, urea and ribose, are plausible
precursors for RNA. The isoxazole nucleoside can rearrange within an RNA-strand
to give cytidine, which leads to an increase of pairing stability. If the proto-RNA
contains a canonical seed-nucleoside with defined stereochemistry, the seed-nucleoside
can control the configuration of the anomeric center that forms during the in-RNA
transformation. The results demonstrate that RNA could have emerged from evolutionarily
primitive precursor isoxazole ribosides after strand formation.
acknowledgement: We thank Stefan Wiedemann for the synthesis of reference compounds
and Pia Heinrichs for assistance in the NMR measurements of the oligonucleotides.
We also thank Dr. Luis Escobar and Jonas Feldmann for valued discussions. This work
was supported by the German Research Foundation (DFG) for financial support via
CRC1309 (Project ID 325871075, A04), CRC1361 (Project ID 893547839, P02) and CRC1032
(Project ID 201269156, A5). This project has received funding from the European
Research Council (ERC) under the European Union's Horizon 2020 research and innovation
program under grant agreement No 741912 (EpiR). We are grateful for additional funding
from the Volkswagen Foundation (EvoRib). Open Access funding enabled and organized
by Projekt DEAL.
article_number: e202211945
article_processing_charge: No
article_type: original
author:
- first_name: Felix
full_name: Xu, Felix
last_name: Xu
- first_name: Antony
full_name: Crisp, Antony
last_name: Crisp
- first_name: Thea
full_name: Schinkel, Thea
last_name: Schinkel
- first_name: Romeo C. A.
full_name: Dubini, Romeo C. A.
last_name: Dubini
- first_name: Sarah
full_name: Hübner, Sarah
last_name: Hübner
- first_name: Sidney
full_name: Becker, Sidney
last_name: Becker
- first_name: Florian
full_name: Schelter, Florian
last_name: Schelter
- first_name: Petra
full_name: Rovo, Petra
id: c316e53f-b965-11eb-b128-bb26acc59c00
last_name: Rovo
orcid: 0000-0001-8729-7326
- first_name: Thomas
full_name: Carell, Thomas
last_name: Carell
citation:
ama: Xu F, Crisp A, Schinkel T, et al. Isoxazole nucleosides as building blocks
for a plausible proto‐RNA. Angewandte Chemie International Edition. 2022;61(45).
doi:10.1002/anie.202211945
apa: Xu, F., Crisp, A., Schinkel, T., Dubini, R. C. A., Hübner, S., Becker, S.,
… Carell, T. (2022). Isoxazole nucleosides as building blocks for a plausible
proto‐RNA. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202211945
chicago: Xu, Felix, Antony Crisp, Thea Schinkel, Romeo C. A. Dubini, Sarah Hübner,
Sidney Becker, Florian Schelter, Petra Rovo, and Thomas Carell. “Isoxazole Nucleosides
as Building Blocks for a Plausible Proto‐RNA.” Angewandte Chemie International
Edition. Wiley, 2022. https://doi.org/10.1002/anie.202211945.
ieee: F. Xu et al., “Isoxazole nucleosides as building blocks for a plausible
proto‐RNA,” Angewandte Chemie International Edition, vol. 61, no. 45. Wiley,
2022.
ista: Xu F, Crisp A, Schinkel T, Dubini RCA, Hübner S, Becker S, Schelter F, Rovo
P, Carell T. 2022. Isoxazole nucleosides as building blocks for a plausible proto‐RNA.
Angewandte Chemie International Edition. 61(45), e202211945.
mla: Xu, Felix, et al. “Isoxazole Nucleosides as Building Blocks for a Plausible
Proto‐RNA.” Angewandte Chemie International Edition, vol. 61, no. 45, e202211945,
Wiley, 2022, doi:10.1002/anie.202211945.
short: F. Xu, A. Crisp, T. Schinkel, R.C.A. Dubini, S. Hübner, S. Becker, F. Schelter,
P. Rovo, T. Carell, Angewandte Chemie International Edition 61 (2022).
date_created: 2023-01-16T09:49:05Z
date_published: 2022-11-07T00:00:00Z
date_updated: 2023-08-04T09:32:42Z
day: '07'
ddc:
- '540'
department:
- _id: NMR
doi: 10.1002/anie.202211945
external_id:
isi:
- '000866428500001'
file:
- access_level: open_access
checksum: 4e8152454d12025d13f6e6e9ca06b5d0
content_type: application/pdf
creator: dernst
date_created: 2023-01-27T10:28:45Z
date_updated: 2023-01-27T10:28:45Z
file_id: '12422'
file_name: 2022_AngewandteChemieInternat_Xu.pdf
file_size: 1076715
relation: main_file
success: 1
file_date_updated: 2023-01-27T10:28:45Z
has_accepted_license: '1'
intvolume: ' 61'
isi: 1
issue: '45'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Isoxazole nucleosides as building blocks for a plausible proto‐RNA
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 61
year: '2022'
...
---
_id: '12924'
abstract:
- lang: eng
text: We demonstrate that several visible-light-mediated carbon−heteroatom cross-coupling
reactions can be carried out using a photoactive NiII precatalyst that forms in
situ from a nickel salt and a bipyridine ligand decorated with two carbazole groups
(Ni(Czbpy)Cl2). The activation of this precatalyst towards cross-coupling reactions
follows a hitherto undisclosed mechanism that is different from previously reported
light-responsive nickel complexes that undergo metal-to-ligand charge transfer.
Theoretical and spectroscopic investigations revealed that irradiation of Ni(Czbpy)Cl2
with visible light causes an initial intraligand charge transfer event that triggers
productive catalysis. Ligand polymerization affords a porous, recyclable organic
polymer for heterogeneous nickel catalysis of cross-coupling reactions. The heterogeneous
catalyst shows stable performance in a packed-bed flow reactor during a week of
continuous operation.
article_number: e202211433
article_processing_charge: No
article_type: original
author:
- first_name: Cristian
full_name: Cavedon, Cristian
last_name: Cavedon
- first_name: Sebastian
full_name: Gisbertz, Sebastian
last_name: Gisbertz
- first_name: Susanne
full_name: Reischauer, Susanne
last_name: Reischauer
- first_name: Sarah
full_name: Vogl, Sarah
last_name: Vogl
- first_name: Eric
full_name: Sperlich, Eric
last_name: Sperlich
- first_name: John H.
full_name: Burke, John H.
last_name: Burke
- first_name: Rachel F.
full_name: Wallick, Rachel F.
last_name: Wallick
- first_name: Stefanie
full_name: Schrottke, Stefanie
last_name: Schrottke
- first_name: Wei‐Hsin
full_name: Hsu, Wei‐Hsin
last_name: Hsu
- first_name: Lucia
full_name: Anghileri, Lucia
last_name: Anghileri
- first_name: Yannik
full_name: Pfeifer, Yannik
last_name: Pfeifer
- first_name: Noah
full_name: Richter, Noah
last_name: Richter
- first_name: Christian
full_name: Teutloff, Christian
last_name: Teutloff
- first_name: Henrike
full_name: Müller‐Werkmeister, Henrike
last_name: Müller‐Werkmeister
- first_name: Dario
full_name: Cambié, Dario
last_name: Cambié
- first_name: Peter H.
full_name: Seeberger, Peter H.
last_name: Seeberger
- first_name: Josh
full_name: Vura‐Weis, Josh
last_name: Vura‐Weis
- first_name: Renske M.
full_name: van der Veen, Renske M.
last_name: van der Veen
- first_name: Arne
full_name: Thomas, Arne
last_name: Thomas
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
citation:
ama: Cavedon C, Gisbertz S, Reischauer S, et al. Intraligand charge transfer enables
visible‐light‐mediated Nickel‐catalyzed cross-coupling reactions. Angewandte
Chemie International Edition. 2022;61(46). doi:10.1002/anie.202211433
apa: Cavedon, C., Gisbertz, S., Reischauer, S., Vogl, S., Sperlich, E., Burke, J.
H., … Pieber, B. (2022). Intraligand charge transfer enables visible‐light‐mediated
Nickel‐catalyzed cross-coupling reactions. Angewandte Chemie International
Edition. Wiley. https://doi.org/10.1002/anie.202211433
chicago: Cavedon, Cristian, Sebastian Gisbertz, Susanne Reischauer, Sarah Vogl,
Eric Sperlich, John H. Burke, Rachel F. Wallick, et al. “Intraligand Charge Transfer
Enables Visible‐light‐mediated Nickel‐catalyzed Cross-Coupling Reactions.” Angewandte
Chemie International Edition. Wiley, 2022. https://doi.org/10.1002/anie.202211433.
ieee: C. Cavedon et al., “Intraligand charge transfer enables visible‐light‐mediated
Nickel‐catalyzed cross-coupling reactions,” Angewandte Chemie International
Edition, vol. 61, no. 46. Wiley, 2022.
ista: Cavedon C, Gisbertz S, Reischauer S, Vogl S, Sperlich E, Burke JH, Wallick
RF, Schrottke S, Hsu W, Anghileri L, Pfeifer Y, Richter N, Teutloff C, Müller‐Werkmeister
H, Cambié D, Seeberger PH, Vura‐Weis J, van der Veen RM, Thomas A, Pieber B. 2022.
Intraligand charge transfer enables visible‐light‐mediated Nickel‐catalyzed cross-coupling
reactions. Angewandte Chemie International Edition. 61(46), e202211433.
mla: Cavedon, Cristian, et al. “Intraligand Charge Transfer Enables Visible‐light‐mediated
Nickel‐catalyzed Cross-Coupling Reactions.” Angewandte Chemie International
Edition, vol. 61, no. 46, e202211433, Wiley, 2022, doi:10.1002/anie.202211433.
short: C. Cavedon, S. Gisbertz, S. Reischauer, S. Vogl, E. Sperlich, J.H. Burke,
R.F. Wallick, S. Schrottke, W. Hsu, L. Anghileri, Y. Pfeifer, N. Richter, C. Teutloff,
H. Müller‐Werkmeister, D. Cambié, P.H. Seeberger, J. Vura‐Weis, R.M. van der Veen,
A. Thomas, B. Pieber, Angewandte Chemie International Edition 61 (2022).
date_created: 2023-05-08T08:30:11Z
date_published: 2022-11-14T00:00:00Z
date_updated: 2023-05-15T08:27:25Z
day: '14'
doi: 10.1002/anie.202211433
extern: '1'
intvolume: ' 61'
issue: '46'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.202211433
month: '11'
oa: 1
oa_version: Published Version
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Intraligand charge transfer enables visible‐light‐mediated Nickel‐catalyzed
cross-coupling reactions
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2022'
...
---
_id: '13358'
abstract:
- lang: eng
text: DNA nanotechnology offers a versatile toolbox for precise spatial and temporal
manipulation of matter on the nanoscale. However, rendering DNA-based systems
responsive to light has remained challenging. Herein, we describe the remote manipulation
of native (non-photoresponsive) chiral plasmonic molecules (CPMs) using light.
Our strategy is based on the use of a photoresponsive medium comprising a merocyanine-based
photoacid. Upon exposure to visible light, the medium decreases its pH, inducing
the formation of DNA triplex links, leading to a spatial reconfiguration of the
CPMs. The process can be reversed simply by turning the light off and it can be
repeated for multiple cycles. The degree of the overall chirality change in an
ensemble of CPMs depends on the CPM fraction undergoing reconfiguration, which,
remarkably, depends on and can be tuned by the intensity of incident light. Such
a dynamic, remotely controlled system could aid in further advancing DNA-based
devices and nanomaterials.
article_processing_charge: No
article_type: original
author:
- first_name: Joonas
full_name: Ryssy, Joonas
last_name: Ryssy
- first_name: Ashwin K.
full_name: Natarajan, Ashwin K.
last_name: Natarajan
- first_name: Jinhua
full_name: Wang, Jinhua
last_name: Wang
- first_name: Arttu J.
full_name: Lehtonen, Arttu J.
last_name: Lehtonen
- first_name: Minh‐Kha
full_name: Nguyen, Minh‐Kha
last_name: Nguyen
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Anton
full_name: Kuzyk, Anton
last_name: Kuzyk
citation:
ama: Ryssy J, Natarajan AK, Wang J, et al. Light‐responsive dynamic DNA‐origami‐based
plasmonic assemblies. Angewandte Chemie International Edition. 2021;60(11):5859-5863.
doi:10.1002/anie.202014963
apa: Ryssy, J., Natarajan, A. K., Wang, J., Lehtonen, A. J., Nguyen, M., Klajn,
R., & Kuzyk, A. (2021). Light‐responsive dynamic DNA‐origami‐based plasmonic
assemblies. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.202014963
chicago: Ryssy, Joonas, Ashwin K. Natarajan, Jinhua Wang, Arttu J. Lehtonen, Minh‐Kha
Nguyen, Rafal Klajn, and Anton Kuzyk. “Light‐responsive Dynamic DNA‐origami‐based
Plasmonic Assemblies.” Angewandte Chemie International Edition. Wiley,
2021. https://doi.org/10.1002/anie.202014963.
ieee: J. Ryssy et al., “Light‐responsive dynamic DNA‐origami‐based plasmonic
assemblies,” Angewandte Chemie International Edition, vol. 60, no. 11.
Wiley, pp. 5859–5863, 2021.
ista: Ryssy J, Natarajan AK, Wang J, Lehtonen AJ, Nguyen M, Klajn R, Kuzyk A. 2021.
Light‐responsive dynamic DNA‐origami‐based plasmonic assemblies. Angewandte Chemie
International Edition. 60(11), 5859–5863.
mla: Ryssy, Joonas, et al. “Light‐responsive Dynamic DNA‐origami‐based Plasmonic
Assemblies.” Angewandte Chemie International Edition, vol. 60, no. 11,
Wiley, 2021, pp. 5859–63, doi:10.1002/anie.202014963.
short: J. Ryssy, A.K. Natarajan, J. Wang, A.J. Lehtonen, M. Nguyen, R. Klajn, A.
Kuzyk, Angewandte Chemie International Edition 60 (2021) 5859–5863.
date_created: 2023-08-01T09:35:06Z
date_published: 2021-03-08T00:00:00Z
date_updated: 2023-08-02T07:22:23Z
day: '08'
doi: 10.1002/anie.202014963
extern: '1'
intvolume: ' 60'
issue: '11'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.202014963
month: '03'
oa: 1
oa_version: Published Version
page: 5859-5863
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
link:
- relation: erratum
url: https://doi.org/10.1002/anie.202210394
scopus_import: '1'
status: public
title: Light‐responsive dynamic DNA‐origami‐based plasmonic assemblies
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 60
year: '2021'
...
---
_id: '11956'
abstract:
- lang: eng
text: Controlling the selectivity of a chemical reaction with external stimuli is
common in thermal processes, but rare in visible-light photocatalysis. Here we
show that the redox potential of a carbon nitride photocatalyst (CN-OA-m) can
be tuned by changing the irradiation wavelength to generate electron holes with
different oxidation potentials. This tuning was the key to realizing photo-chemo-enzymatic
cascades that give either the (S)- or the (R)-enantiomer of phenylethanol. In
combination with an unspecific peroxygenase from Agrocybe aegerita, green light
irradiation of CN-OA-m led to the enantioselective hydroxylation of ethylbenzene
to (R)-1-phenylethanol (99 % ee). In contrast, blue light irradiation triggered
the photocatalytic oxidation of ethylbenzene to acetophenone, which in turn was
enantioselectively reduced with an alcohol dehydrogenase from Rhodococcus ruber
to form (S)-1-phenylethanol (93 % ee).
article_processing_charge: No
article_type: original
author:
- first_name: Luca
full_name: Schmermund, Luca
last_name: Schmermund
- first_name: Susanne
full_name: Reischauer, Susanne
last_name: Reischauer
- first_name: Sarah
full_name: Bierbaumer, Sarah
last_name: Bierbaumer
- first_name: Christoph K.
full_name: Winkler, Christoph K.
last_name: Winkler
- first_name: Alba
full_name: Diaz‐Rodriguez, Alba
last_name: Diaz‐Rodriguez
- first_name: Lee J.
full_name: Edwards, Lee J.
last_name: Edwards
- first_name: Selin
full_name: Kara, Selin
last_name: Kara
- first_name: Tamara
full_name: Mielke, Tamara
last_name: Mielke
- first_name: Jared
full_name: Cartwright, Jared
last_name: Cartwright
- first_name: Gideon
full_name: Grogan, Gideon
last_name: Grogan
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Wolfgang
full_name: Kroutil, Wolfgang
last_name: Kroutil
citation:
ama: Schmermund L, Reischauer S, Bierbaumer S, et al. Chromoselective photocatalysis
enables stereocomplementary biocatalytic pathways. Angewandte Chemie International
Edition. 2021;60(13):6965-6969. doi:10.1002/anie.202100164
apa: Schmermund, L., Reischauer, S., Bierbaumer, S., Winkler, C. K., Diaz‐Rodriguez,
A., Edwards, L. J., … Kroutil, W. (2021). Chromoselective photocatalysis enables
stereocomplementary biocatalytic pathways. Angewandte Chemie International
Edition. Wiley. https://doi.org/10.1002/anie.202100164
chicago: Schmermund, Luca, Susanne Reischauer, Sarah Bierbaumer, Christoph K. Winkler,
Alba Diaz‐Rodriguez, Lee J. Edwards, Selin Kara, et al. “Chromoselective Photocatalysis
Enables Stereocomplementary Biocatalytic Pathways.” Angewandte Chemie International
Edition. Wiley, 2021. https://doi.org/10.1002/anie.202100164.
ieee: L. Schmermund et al., “Chromoselective photocatalysis enables stereocomplementary
biocatalytic pathways,” Angewandte Chemie International Edition, vol. 60,
no. 13. Wiley, pp. 6965–6969, 2021.
ista: Schmermund L, Reischauer S, Bierbaumer S, Winkler CK, Diaz‐Rodriguez A, Edwards
LJ, Kara S, Mielke T, Cartwright J, Grogan G, Pieber B, Kroutil W. 2021. Chromoselective
photocatalysis enables stereocomplementary biocatalytic pathways. Angewandte Chemie
International Edition. 60(13), 6965–6969.
mla: Schmermund, Luca, et al. “Chromoselective Photocatalysis Enables Stereocomplementary
Biocatalytic Pathways.” Angewandte Chemie International Edition, vol. 60,
no. 13, Wiley, 2021, pp. 6965–69, doi:10.1002/anie.202100164.
short: L. Schmermund, S. Reischauer, S. Bierbaumer, C.K. Winkler, A. Diaz‐Rodriguez,
L.J. Edwards, S. Kara, T. Mielke, J. Cartwright, G. Grogan, B. Pieber, W. Kroutil,
Angewandte Chemie International Edition 60 (2021) 6965–6969.
date_created: 2022-08-24T10:47:16Z
date_published: 2021-03-22T00:00:00Z
date_updated: 2023-02-21T10:09:14Z
day: '22'
doi: 10.1002/anie.202100164
extern: '1'
intvolume: ' 60'
issue: '13'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.202100164
month: '03'
oa: 1
oa_version: Published Version
page: 6965-6969
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Chromoselective photocatalysis enables stereocomplementary biocatalytic pathways
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 60
year: '2021'
...
---
_id: '7847'
abstract:
- lang: eng
text: 'Water-in-salt electrolytes based on highly concentrated bis(trifluoromethyl)sulfonimide
(TFSI) promise aqueous electrolytes with stabilities nearing 3 V. However, especially
with an electrode approaching the cathodic (reductive) stability, cycling stability
is insufficient. While stability critically relies on a solid electrolyte interphase
(SEI), the mechanism behind the cathodic stability limit remains unclear. Here,
we reveal two distinct reduction potentials for the chemical environments of ''free''
and ''bound'' water and that both contribute to SEI formation. Free-water is reduced
~1V above bound water in a hydrogen evolution reaction (HER) and responsible for
SEI formation via reactive intermediates of the HER; concurrent LiTFSI precipitation/dissolution
establishes a dynamic interface. The free-water population emerges, therefore,
as the handle to extend the cathodic limit of aqueous electrolytes and the battery
cycling stability. '
article_processing_charge: No
article_type: original
author:
- first_name: Roza
full_name: Bouchal, Roza
last_name: Bouchal
- first_name: Zhujie
full_name: Li, Zhujie
last_name: Li
- first_name: Chandra
full_name: Bongu, Chandra
last_name: Bongu
- first_name: Steven
full_name: Le Vot, Steven
last_name: Le Vot
- first_name: Romain
full_name: Berthelot, Romain
last_name: Berthelot
- first_name: Benjamin
full_name: Rotenberg, Benjamin
last_name: Rotenberg
- first_name: Fréderic
full_name: Favier, Fréderic
last_name: Favier
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
- first_name: Mathieu
full_name: Salanne, Mathieu
last_name: Salanne
- first_name: Olivier
full_name: Fontaine, Olivier
last_name: Fontaine
citation:
ama: Bouchal R, Li Z, Bongu C, et al. Competitive salt precipitation/dissolution
during free‐water reduction in water‐in‐salt electrolyte. Angewandte Chemie
International Edition. 2020;59(37):15913-1591. doi:10.1002/anie.202005378
apa: Bouchal, R., Li, Z., Bongu, C., Le Vot, S., Berthelot, R., Rotenberg, B., …
Fontaine, O. (2020). Competitive salt precipitation/dissolution during free‐water
reduction in water‐in‐salt electrolyte. Angewandte Chemie International Edition.
Wiley. https://doi.org/10.1002/anie.202005378
chicago: Bouchal, Roza, Zhujie Li, Chandra Bongu, Steven Le Vot, Romain Berthelot,
Benjamin Rotenberg, Fréderic Favier, Stefan Alexander Freunberger, Mathieu Salanne,
and Olivier Fontaine. “Competitive Salt Precipitation/Dissolution during Free‐water
Reduction in Water‐in‐salt Electrolyte.” Angewandte Chemie International Edition.
Wiley, 2020. https://doi.org/10.1002/anie.202005378.
ieee: R. Bouchal et al., “Competitive salt precipitation/dissolution during
free‐water reduction in water‐in‐salt electrolyte,” Angewandte Chemie International
Edition, vol. 59, no. 37. Wiley, pp. 15913–1591, 2020.
ista: Bouchal R, Li Z, Bongu C, Le Vot S, Berthelot R, Rotenberg B, Favier F, Freunberger
SA, Salanne M, Fontaine O. 2020. Competitive salt precipitation/dissolution during
free‐water reduction in water‐in‐salt electrolyte. Angewandte Chemie International
Edition. 59(37), 15913–1591.
mla: Bouchal, Roza, et al. “Competitive Salt Precipitation/Dissolution during Free‐water
Reduction in Water‐in‐salt Electrolyte.” Angewandte Chemie International Edition,
vol. 59, no. 37, Wiley, 2020, pp. 15913–1591, doi:10.1002/anie.202005378.
short: R. Bouchal, Z. Li, C. Bongu, S. Le Vot, R. Berthelot, B. Rotenberg, F. Favier,
S.A. Freunberger, M. Salanne, O. Fontaine, Angewandte Chemie International Edition
59 (2020) 15913–1591.
date_created: 2020-05-14T21:00:30Z
date_published: 2020-09-07T00:00:00Z
date_updated: 2023-09-05T16:02:53Z
day: '07'
ddc:
- '540'
- '546'
department:
- _id: StFr
doi: 10.1002/anie.202005378
external_id:
isi:
- '000541488700001'
pmid:
- '32390281'
file:
- access_level: open_access
checksum: 7b6c2fc20e9b0ff4353352f7a7004e2d
content_type: application/pdf
creator: dernst
date_created: 2020-09-17T08:57:16Z
date_updated: 2020-09-17T08:57:16Z
file_id: '8400'
file_name: 2020_AngChemieINT_Buchal.pdf
file_size: 1966184
relation: main_file
success: 1
file_date_updated: 2020-09-17T08:57:16Z
has_accepted_license: '1'
intvolume: ' 59'
isi: 1
issue: '37'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 15913-1591
pmid: 1
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Competitive salt precipitation/dissolution during free‐water reduction in water‐in‐salt
electrolyte
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 59
year: '2020'
...
---
_id: '8329'
abstract:
- lang: eng
text: We show the synthesis of a redox‐active quinone, 2‐methoxy‐1,4‐hydroquinone
(MHQ), from a bio‐based feedstock and its suitability as electrolyte in aqueous
redox flow batteries. We identified semiquinone intermediates at insufficiently
low pH and quinoid radicals as responsible for decomposition of MHQ under electrochemical
conditions. Both can be avoided and/or stabilized, respectively, using H 3 PO
4 electrolyte, allowing for reversible cycling in a redox flow battery for hundreds
of cycles.
acknowledgement: The Austrian Research Promotion Agency (FFG) is gratefully acknowledged
for financial support of the project LignoBatt (860429).
article_processing_charge: No
article_type: original
author:
- first_name: Werner
full_name: Schlemmer, Werner
last_name: Schlemmer
- first_name: Philipp
full_name: Nothdurft, Philipp
last_name: Nothdurft
- first_name: Alina
full_name: Petzold, Alina
last_name: Petzold
- first_name: Philipp
full_name: Frühwirt, Philipp
last_name: Frühwirt
- first_name: Max
full_name: Schmallegger, Max
last_name: Schmallegger
- first_name: Georg
full_name: Gescheidt-Demner, Georg
last_name: Gescheidt-Demner
- first_name: Roland
full_name: Fischer, Roland
last_name: Fischer
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
- first_name: Wolfgang
full_name: Kern, Wolfgang
last_name: Kern
- first_name: Stefan
full_name: Spirk, Stefan
last_name: Spirk
citation:
ama: Schlemmer W, Nothdurft P, Petzold A, et al. 2‐methoxyhydroquinone from vanillin
for aqueous redox‐flow batteries. Angewandte Chemie International Edition.
2020;59(51):22943-22946. doi:10.1002/anie.202008253
apa: Schlemmer, W., Nothdurft, P., Petzold, A., Frühwirt, P., Schmallegger, M.,
Gescheidt-Demner, G., … Spirk, S. (2020). 2‐methoxyhydroquinone from vanillin
for aqueous redox‐flow batteries. Angewandte Chemie International Edition.
Wiley. https://doi.org/10.1002/anie.202008253
chicago: Schlemmer, Werner, Philipp Nothdurft, Alina Petzold, Philipp Frühwirt,
Max Schmallegger, Georg Gescheidt-Demner, Roland Fischer, Stefan Alexander Freunberger,
Wolfgang Kern, and Stefan Spirk. “2‐methoxyhydroquinone from Vanillin for Aqueous
Redox‐flow Batteries.” Angewandte Chemie International Edition. Wiley,
2020. https://doi.org/10.1002/anie.202008253.
ieee: W. Schlemmer et al., “2‐methoxyhydroquinone from vanillin for aqueous
redox‐flow batteries,” Angewandte Chemie International Edition, vol. 59,
no. 51. Wiley, pp. 22943–22946, 2020.
ista: Schlemmer W, Nothdurft P, Petzold A, Frühwirt P, Schmallegger M, Gescheidt-Demner
G, Fischer R, Freunberger SA, Kern W, Spirk S. 2020. 2‐methoxyhydroquinone from
vanillin for aqueous redox‐flow batteries. Angewandte Chemie International Edition.
59(51), 22943–22946.
mla: Schlemmer, Werner, et al. “2‐methoxyhydroquinone from Vanillin for Aqueous
Redox‐flow Batteries.” Angewandte Chemie International Edition, vol. 59,
no. 51, Wiley, 2020, pp. 22943–46, doi:10.1002/anie.202008253.
short: W. Schlemmer, P. Nothdurft, A. Petzold, P. Frühwirt, M. Schmallegger, G.
Gescheidt-Demner, R. Fischer, S.A. Freunberger, W. Kern, S. Spirk, Angewandte
Chemie International Edition 59 (2020) 22943–22946.
date_created: 2020-09-03T16:10:56Z
date_published: 2020-12-14T00:00:00Z
date_updated: 2023-09-05T16:03:47Z
day: '14'
department:
- _id: StFr
doi: 10.1002/anie.202008253
external_id:
isi:
- '000576148700001'
intvolume: ' 59'
isi: 1
issue: '51'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.202008253
month: '12'
oa: 1
oa_version: Published Version
page: 22943-22946
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
record:
- id: '9780'
relation: research_data
status: public
scopus_import: '1'
status: public
title: 2‐methoxyhydroquinone from vanillin for aqueous redox‐flow batteries
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 59
year: '2020'
...
---
_id: '7276'
abstract:
- lang: eng
text: Singlet oxygen (1O2) causes a major fraction of the parasitic chemistry during
the cycling of non‐aqueous alkali metal‐O2 batteries and also contributes to interfacial
reactivity of transition‐metal oxide intercalation compounds. We introduce DABCOnium,
the mono alkylated form of 1,4‐diazabicyclo[2.2.2]octane (DABCO), as an efficient
1O2 quencher with an unusually high oxidative stability of ca. 4.2 V vs. Li/Li+.
Previous quenchers are strongly Lewis basic amines with too low oxidative stability.
DABCOnium is an ionic liquid, non‐volatile, highly soluble in the electrolyte,
stable against superoxide and peroxide, and compatible with lithium metal. The
electrochemical stability covers the required range for metal–O2 batteries and
greatly reduces 1O2 related parasitic chemistry as demonstrated for the Li–O2
cell.
article_processing_charge: No
article_type: original
author:
- first_name: Yann K.
full_name: Petit, Yann K.
last_name: Petit
- first_name: Christian
full_name: Leypold, Christian
last_name: Leypold
- first_name: Nika
full_name: Mahne, Nika
last_name: Mahne
- first_name: Eléonore
full_name: Mourad, Eléonore
last_name: Mourad
- first_name: Lukas
full_name: Schafzahl, Lukas
last_name: Schafzahl
- first_name: Christian
full_name: Slugovc, Christian
last_name: Slugovc
- first_name: Sergey M.
full_name: Borisov, Sergey M.
last_name: Borisov
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
citation:
ama: 'Petit YK, Leypold C, Mahne N, et al. DABCOnium: An efficient and high-voltage
stable singlet oxygen quencher for metal-O2 cells. Angewandte Chemie International
Edition. 2019;58(20):6535-6539. doi:10.1002/anie.201901869'
apa: 'Petit, Y. K., Leypold, C., Mahne, N., Mourad, E., Schafzahl, L., Slugovc,
C., … Freunberger, S. A. (2019). DABCOnium: An efficient and high-voltage stable
singlet oxygen quencher for metal-O2 cells. Angewandte Chemie International
Edition. Wiley. https://doi.org/10.1002/anie.201901869'
chicago: 'Petit, Yann K., Christian Leypold, Nika Mahne, Eléonore Mourad, Lukas
Schafzahl, Christian Slugovc, Sergey M. Borisov, and Stefan Alexander Freunberger.
“DABCOnium: An Efficient and High-Voltage Stable Singlet Oxygen Quencher for Metal-O2
Cells.” Angewandte Chemie International Edition. Wiley, 2019. https://doi.org/10.1002/anie.201901869.'
ieee: 'Y. K. Petit et al., “DABCOnium: An efficient and high-voltage stable
singlet oxygen quencher for metal-O2 cells,” Angewandte Chemie International
Edition, vol. 58, no. 20. Wiley, pp. 6535–6539, 2019.'
ista: 'Petit YK, Leypold C, Mahne N, Mourad E, Schafzahl L, Slugovc C, Borisov SM,
Freunberger SA. 2019. DABCOnium: An efficient and high-voltage stable singlet
oxygen quencher for metal-O2 cells. Angewandte Chemie International Edition. 58(20),
6535–6539.'
mla: 'Petit, Yann K., et al. “DABCOnium: An Efficient and High-Voltage Stable Singlet
Oxygen Quencher for Metal-O2 Cells.” Angewandte Chemie International Edition,
vol. 58, no. 20, Wiley, 2019, pp. 6535–39, doi:10.1002/anie.201901869.'
short: Y.K. Petit, C. Leypold, N. Mahne, E. Mourad, L. Schafzahl, C. Slugovc, S.M.
Borisov, S.A. Freunberger, Angewandte Chemie International Edition 58 (2019) 6535–6539.
date_created: 2020-01-15T07:19:27Z
date_published: 2019-05-13T00:00:00Z
date_updated: 2021-01-12T08:12:42Z
day: '13'
ddc:
- '540'
doi: 10.1002/anie.201901869
extern: '1'
file:
- access_level: open_access
checksum: 9620b6a511a910d7abe1f26c42dc7f83
content_type: application/pdf
creator: dernst
date_created: 2020-01-22T16:16:54Z
date_updated: 2020-07-14T12:47:55Z
file_id: '7356'
file_name: 2019_AngewChemie_Petit.pdf
file_size: 952737
relation: main_file
file_date_updated: 2020-07-14T12:47:55Z
has_accepted_license: '1'
intvolume: ' 58'
issue: '20'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: 6535-6539
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: 'DABCOnium: An efficient and high-voltage stable singlet oxygen quencher for
metal-O2 cells'
tmp:
image: /images/cc_by_nc_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
(CC BY-NC-ND 4.0)
short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 58
year: '2019'
...
---
_id: '11957'
abstract:
- lang: eng
text: Cross-coupling reactions mediated by dual nickel/photocatalysis are synthetically
attractive but rely mainly on expensive, non-recyclable noble-metal complexes
as photocatalysts. Heterogeneous semiconductors, which are commonly used for artificial
photosynthesis and wastewater treatment, are a sustainable alternative. Graphitic
carbon nitrides, a class of metal-free polymers that can be easily prepared from
bulk chemicals, are heterogeneous semiconductors with high potential for photocatalytic
organic transformations. Here, we demonstrate that graphitic carbon nitrides in
combination with nickel catalysis can induce selective C−O cross-couplings of
carboxylic acids with aryl halides, yielding the respective aryl esters in excellent
yield and selectivity. The heterogeneous organic photocatalyst exhibits a broad
substrate scope, is able to harvest green light, and can be recycled multiple
times. In situ FTIR was used to track the reaction progress to study this transformation
at different irradiation wavelengths and reaction scales.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Jamal A.
full_name: Malik, Jamal A.
last_name: Malik
- first_name: Cristian
full_name: Cavedon, Cristian
last_name: Cavedon
- first_name: Sebastian
full_name: Gisbertz, Sebastian
last_name: Gisbertz
- first_name: Aleksandr
full_name: Savateev, Aleksandr
last_name: Savateev
- first_name: Daniel
full_name: Cruz, Daniel
last_name: Cruz
- first_name: Tobias
full_name: Heil, Tobias
last_name: Heil
- first_name: Guigang
full_name: Zhang, Guigang
last_name: Zhang
- first_name: Peter H.
full_name: Seeberger, Peter H.
last_name: Seeberger
citation:
ama: 'Pieber B, Malik JA, Cavedon C, et al. Semi‐heterogeneous dual nickel/photocatalysis
using carbon nitrides: Esterification of carboxylic acids with aryl halides. Angewandte
Chemie International Edition. 2019;58(28):9575-9580. doi:10.1002/anie.201902785'
apa: 'Pieber, B., Malik, J. A., Cavedon, C., Gisbertz, S., Savateev, A., Cruz, D.,
… Seeberger, P. H. (2019). Semi‐heterogeneous dual nickel/photocatalysis using
carbon nitrides: Esterification of carboxylic acids with aryl halides. Angewandte
Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201902785'
chicago: 'Pieber, Bartholomäus, Jamal A. Malik, Cristian Cavedon, Sebastian Gisbertz,
Aleksandr Savateev, Daniel Cruz, Tobias Heil, Guigang Zhang, and Peter H. Seeberger.
“Semi‐heterogeneous Dual Nickel/Photocatalysis Using Carbon Nitrides: Esterification
of Carboxylic Acids with Aryl Halides.” Angewandte Chemie International Edition.
Wiley, 2019. https://doi.org/10.1002/anie.201902785.'
ieee: 'B. Pieber et al., “Semi‐heterogeneous dual nickel/photocatalysis using
carbon nitrides: Esterification of carboxylic acids with aryl halides,” Angewandte
Chemie International Edition, vol. 58, no. 28. Wiley, pp. 9575–9580, 2019.'
ista: 'Pieber B, Malik JA, Cavedon C, Gisbertz S, Savateev A, Cruz D, Heil T, Zhang
G, Seeberger PH. 2019. Semi‐heterogeneous dual nickel/photocatalysis using carbon
nitrides: Esterification of carboxylic acids with aryl halides. Angewandte Chemie
International Edition. 58(28), 9575–9580.'
mla: 'Pieber, Bartholomäus, et al. “Semi‐heterogeneous Dual Nickel/Photocatalysis
Using Carbon Nitrides: Esterification of Carboxylic Acids with Aryl Halides.”
Angewandte Chemie International Edition, vol. 58, no. 28, Wiley, 2019,
pp. 9575–80, doi:10.1002/anie.201902785.'
short: B. Pieber, J.A. Malik, C. Cavedon, S. Gisbertz, A. Savateev, D. Cruz, T.
Heil, G. Zhang, P.H. Seeberger, Angewandte Chemie International Edition 58 (2019)
9575–9580.
date_created: 2022-08-24T10:50:19Z
date_published: 2019-07-08T00:00:00Z
date_updated: 2023-02-21T10:09:16Z
day: '08'
doi: 10.1002/anie.201902785
extern: '1'
external_id:
pmid:
- '31050132'
intvolume: ' 58'
issue: '28'
language:
- iso: eng
month: '07'
oa_version: None
page: 9575-9580
pmid: 1
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Semi‐heterogeneous dual nickel/photocatalysis using carbon nitrides: Esterification
of carboxylic acids with aryl halides'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 58
year: '2019'
...
---
_id: '7277'
abstract:
- lang: eng
text: 'Solid alkali metal carbonates are universal passivation layer components
of intercalation battery materials and common side products in metal‐O2 batteries,
and are believed to form and decompose reversibly in metal‐O2/CO2 cells. In these
cathodes, Li2CO3 decomposes to CO2 when exposed to potentials above 3.8 V vs.
Li/Li+. However, O2 evolution, as would be expected according to the decomposition
reaction 2 Li2CO3→4 Li++4 e−+2 CO2+O2, is not detected. O atoms are thus unaccounted
for, which was previously ascribed to unidentified parasitic reactions. Here,
we show that highly reactive singlet oxygen (1O2) forms upon oxidizing Li2CO3
in an aprotic electrolyte and therefore does not evolve as O2. These results have
substantial implications for the long‐term cyclability of batteries: they underpin
the importance of avoiding 1O2 in metal‐O2 batteries, question the possibility
of a reversible metal‐O2/CO2 battery based on a carbonate discharge product, and
help explain the interfacial reactivity of transition‐metal cathodes with residual
Li2CO3.'
article_processing_charge: No
article_type: original
author:
- first_name: Nika
full_name: Mahne, Nika
last_name: Mahne
- first_name: Sara E.
full_name: Renfrew, Sara E.
last_name: Renfrew
- first_name: Bryan D.
full_name: McCloskey, Bryan D.
last_name: McCloskey
- first_name: Stefan Alexander
full_name: Freunberger, Stefan Alexander
id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
last_name: Freunberger
orcid: 0000-0003-2902-5319
citation:
ama: Mahne N, Renfrew SE, McCloskey BD, Freunberger SA. Electrochemical oxidation
of Lithium Carbonate generates singlet oxygen. Angewandte Chemie International
Edition. 2018;57(19):5529-5533. doi:10.1002/anie.201802277
apa: Mahne, N., Renfrew, S. E., McCloskey, B. D., & Freunberger, S. A. (2018).
Electrochemical oxidation of Lithium Carbonate generates singlet oxygen. Angewandte
Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201802277
chicago: Mahne, Nika, Sara E. Renfrew, Bryan D. McCloskey, and Stefan Alexander
Freunberger. “Electrochemical Oxidation of Lithium Carbonate Generates Singlet
Oxygen.” Angewandte Chemie International Edition. Wiley, 2018. https://doi.org/10.1002/anie.201802277.
ieee: N. Mahne, S. E. Renfrew, B. D. McCloskey, and S. A. Freunberger, “Electrochemical
oxidation of Lithium Carbonate generates singlet oxygen,” Angewandte Chemie
International Edition, vol. 57, no. 19. Wiley, pp. 5529–5533, 2018.
ista: Mahne N, Renfrew SE, McCloskey BD, Freunberger SA. 2018. Electrochemical oxidation
of Lithium Carbonate generates singlet oxygen. Angewandte Chemie International
Edition. 57(19), 5529–5533.
mla: Mahne, Nika, et al. “Electrochemical Oxidation of Lithium Carbonate Generates
Singlet Oxygen.” Angewandte Chemie International Edition, vol. 57, no.
19, Wiley, 2018, pp. 5529–33, doi:10.1002/anie.201802277.
short: N. Mahne, S.E. Renfrew, B.D. McCloskey, S.A. Freunberger, Angewandte Chemie
International Edition 57 (2018) 5529–5533.
date_created: 2020-01-15T07:20:09Z
date_published: 2018-03-15T00:00:00Z
date_updated: 2021-01-12T08:12:42Z
day: '15'
ddc:
- '540'
doi: 10.1002/anie.201802277
extern: '1'
file:
- access_level: open_access
checksum: 45868d0adc2d13a506bb9a59eb4f409c
content_type: application/pdf
creator: dernst
date_created: 2020-01-22T16:28:31Z
date_updated: 2020-07-14T12:47:55Z
file_id: '7357'
file_name: 2018_AngewChemie_Mahne.pdf
file_size: 657963
relation: main_file
file_date_updated: 2020-07-14T12:47:55Z
has_accepted_license: '1'
intvolume: ' 57'
issue: '19'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 5529-5533
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Electrochemical oxidation of Lithium Carbonate generates singlet oxygen
tmp:
image: /images/cc_by_nc_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
(CC BY-NC-ND 4.0)
short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 57
year: '2018'
...
---
_id: '5982'
abstract:
- lang: eng
text: In the present work, we detail a fast and simple solution-based method to
synthesize hexagonal SnSe2 nanoplates (NPLs) and their use to produce crystallographically
textured SnSe2 nanomaterials. We also demonstrate that the same strategy can be
used to produce orthorhombic SnSe nanostructures and nanomaterials. NPLs are grown
through a screw dislocation-driven mechanism. This mechanism typically results
in pyramidal structures, but we demonstrate here that the growth from multiple
dislocations results in flower-like structures. Crystallographically textured
SnSe2 bulk nanomaterials obtained from the hot pressing of these SnSe2 structures
display highly anisotropic charge and heat transport properties and thermoelectric
(TE) figures of merit limited by relatively low electrical conductivities. To
improve this parameter, SnSe2 NPLs are blended here with metal nanoparticles.
The electrical conductivities of the blends are significantly improved with respect
to bare SnSe2 NPLs, what translates into a three-fold increase of the TE Figure
of merit, reaching unprecedented ZT values up to 0.65.
article_processing_charge: No
article_type: original
author:
- first_name: Yu
full_name: Zhang, Yu
last_name: Zhang
- first_name: Yu
full_name: Liu, Yu
last_name: Liu
- first_name: Khak Ho
full_name: Lim, Khak Ho
last_name: Lim
- first_name: Congcong
full_name: Xing, Congcong
last_name: Xing
- first_name: Mengyao
full_name: Li, Mengyao
last_name: Li
- first_name: Ting
full_name: Zhang, Ting
last_name: Zhang
- first_name: Pengyi
full_name: Tang, Pengyi
last_name: Tang
- first_name: Jordi
full_name: Arbiol, Jordi
last_name: Arbiol
- first_name: Jordi
full_name: Llorca, Jordi
last_name: Llorca
- first_name: Ka Ming
full_name: Ng, Ka Ming
last_name: Ng
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Pablo
full_name: Guardia, Pablo
last_name: Guardia
- first_name: Mirko
full_name: Prato, Mirko
last_name: Prato
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Zhang Y, Liu Y, Lim KH, et al. Tin diselenide molecular precursor for solution-processable
thermoelectric materials. Angewandte Chemie International Edition. 2018;57(52):17063-17068.
doi:10.1002/anie.201809847
apa: Zhang, Y., Liu, Y., Lim, K. H., Xing, C., Li, M., Zhang, T., … Cabot, A. (2018).
Tin diselenide molecular precursor for solution-processable thermoelectric materials.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201809847
chicago: Zhang, Yu, Yu Liu, Khak Ho Lim, Congcong Xing, Mengyao Li, Ting Zhang,
Pengyi Tang, et al. “Tin Diselenide Molecular Precursor for Solution-Processable
Thermoelectric Materials.” Angewandte Chemie International Edition. Wiley,
2018. https://doi.org/10.1002/anie.201809847.
ieee: Y. Zhang et al., “Tin diselenide molecular precursor for solution-processable
thermoelectric materials,” Angewandte Chemie International Edition, vol.
57, no. 52. Wiley, pp. 17063–17068, 2018.
ista: Zhang Y, Liu Y, Lim KH, Xing C, Li M, Zhang T, Tang P, Arbiol J, Llorca J,
Ng KM, Ibáñez M, Guardia P, Prato M, Cadavid D, Cabot A. 2018. Tin diselenide
molecular precursor for solution-processable thermoelectric materials. Angewandte
Chemie International Edition. 57(52), 17063–17068.
mla: Zhang, Yu, et al. “Tin Diselenide Molecular Precursor for Solution-Processable
Thermoelectric Materials.” Angewandte Chemie International Edition, vol.
57, no. 52, Wiley, 2018, pp. 17063–68, doi:10.1002/anie.201809847.
short: Y. Zhang, Y. Liu, K.H. Lim, C. Xing, M. Li, T. Zhang, P. Tang, J. Arbiol,
J. Llorca, K.M. Ng, M. Ibáñez, P. Guardia, M. Prato, D. Cadavid, A. Cabot, Angewandte
Chemie International Edition 57 (2018) 17063–17068.
date_created: 2019-02-14T10:23:27Z
date_published: 2018-12-21T00:00:00Z
date_updated: 2023-09-19T14:28:31Z
day: '21'
department:
- _id: MaIb
doi: 10.1002/anie.201809847
external_id:
isi:
- '000454575500020'
intvolume: ' 57'
isi: 1
issue: '52'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://upcommons.upc.edu/bitstream/2117/130444/1/Zhang%20preprint.pdf
month: '12'
oa: 1
oa_version: Submitted Version
page: 17063-17068
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Tin diselenide molecular precursor for solution-processable thermoelectric
materials
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 57
year: '2018'
...
---
_id: '13377'
abstract:
- lang: eng
text: Confining organic molecules to the surfaces of inorganic nanoparticles can
induce intermolecular interactions between them, which can affect the composition
of the mixed self-assembled monolayers obtained by co-adsorption from solution
of two different molecules. Two thiolated ligands (a dialkylviologen and a zwitterionic
sulfobetaine) that can interact with each other electrostatically were coadsorbed
onto gold nanoparticles. The nanoparticles favor a narrow range of ratios of these
two molecules that is largely independent of the molar ratio in solution. Changing
the solution molar ratio of the two ligands by a factor of 5 000 affects the on-nanoparticle
ratio of these ligands by only threefold. This behavior is reminiscent of the
formation of insoluble inorganic salts (such as AgCl), which similarly compensate
positive and negative charges upon crystallizing. Our results pave the way towards
developing well-defined hybrid organic–inorganic nanostructures.
article_processing_charge: No
article_type: original
author:
- first_name: Zonglin
full_name: Chu, Zonglin
last_name: Chu
- first_name: Yanxiao
full_name: Han, Yanxiao
last_name: Han
- first_name: Petr
full_name: Král, Petr
last_name: Král
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
citation:
ama: 'Chu Z, Han Y, Král P, Klajn R. “Precipitation on nanoparticles”: Attractive
intermolecular interactions stabilize specific ligand ratios on the surfaces of
nanoparticles. Angewandte Chemie International Edition. 2018;57(24):7023-7027.
doi:10.1002/anie.201800673'
apa: 'Chu, Z., Han, Y., Král, P., & Klajn, R. (2018). “Precipitation on nanoparticles”:
Attractive intermolecular interactions stabilize specific ligand ratios on the
surfaces of nanoparticles. Angewandte Chemie International Edition. Wiley.
https://doi.org/10.1002/anie.201800673'
chicago: 'Chu, Zonglin, Yanxiao Han, Petr Král, and Rafal Klajn. “‘Precipitation
on Nanoparticles’: Attractive Intermolecular Interactions Stabilize Specific Ligand
Ratios on the Surfaces of Nanoparticles.” Angewandte Chemie International Edition.
Wiley, 2018. https://doi.org/10.1002/anie.201800673.'
ieee: 'Z. Chu, Y. Han, P. Král, and R. Klajn, “‘Precipitation on nanoparticles’:
Attractive intermolecular interactions stabilize specific ligand ratios on the
surfaces of nanoparticles,” Angewandte Chemie International Edition, vol.
57, no. 24. Wiley, pp. 7023–7027, 2018.'
ista: 'Chu Z, Han Y, Král P, Klajn R. 2018. “Precipitation on nanoparticles”: Attractive
intermolecular interactions stabilize specific ligand ratios on the surfaces of
nanoparticles. Angewandte Chemie International Edition. 57(24), 7023–7027.'
mla: 'Chu, Zonglin, et al. “‘Precipitation on Nanoparticles’: Attractive Intermolecular
Interactions Stabilize Specific Ligand Ratios on the Surfaces of Nanoparticles.”
Angewandte Chemie International Edition, vol. 57, no. 24, Wiley, 2018,
pp. 7023–27, doi:10.1002/anie.201800673.'
short: Z. Chu, Y. Han, P. Král, R. Klajn, Angewandte Chemie International Edition
57 (2018) 7023–7027.
date_created: 2023-08-01T09:40:16Z
date_published: 2018-06-11T00:00:00Z
date_updated: 2023-08-07T11:14:28Z
day: '11'
doi: 10.1002/anie.201800673
extern: '1'
external_id:
pmid:
- '29673022'
intvolume: ' 57'
issue: '24'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.201800673
month: '06'
oa: 1
oa_version: Published Version
page: 7023-7027
pmid: 1
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: '“Precipitation on nanoparticles”: Attractive intermolecular interactions stabilize
specific ligand ratios on the surfaces of nanoparticles'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 57
year: '2018'
...
---
_id: '11958'
abstract:
- lang: eng
text: Solid reagents, leaching catalysts, and heterogeneous photocatalysts are commonly
employed in batch processes but are ill-suited for continuous-flow chemistry.
Heterogeneous catalysts for thermal reactions are typically used in packed-bed
reactors, which cannot be penetrated by light and thus are not suitable for photocatalytic
reactions involving solids. We demonstrate that serial micro-batch reactors (SMBRs)
allow for the continuous utilization of solid materials together with liquids
and gases in flow. This technology was utilized to develop selective and efficient
fluorination reactions using a modified graphitic carbon nitride heterogeneous
catalyst instead of costly homogeneous metal polypyridyl complexes. The merger
of this inexpensive, recyclable catalyst and the SMBR approach enables sustainable
and scalable photocatalysis.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Menny
full_name: Shalom, Menny
last_name: Shalom
- first_name: Markus
full_name: Antonietti, Markus
last_name: Antonietti
- first_name: Peter H.
full_name: Seeberger, Peter H.
last_name: Seeberger
- first_name: Kerry
full_name: Gilmore, Kerry
last_name: Gilmore
citation:
ama: Pieber B, Shalom M, Antonietti M, Seeberger PH, Gilmore K. Continuous heterogeneous
photocatalysis in serial micro-batch reactors. Angewandte Chemie International
Edition. 2018;57(31):9976-9979. doi:10.1002/anie.201712568
apa: Pieber, B., Shalom, M., Antonietti, M., Seeberger, P. H., & Gilmore, K.
(2018). Continuous heterogeneous photocatalysis in serial micro-batch reactors.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201712568
chicago: Pieber, Bartholomäus, Menny Shalom, Markus Antonietti, Peter H. Seeberger,
and Kerry Gilmore. “Continuous Heterogeneous Photocatalysis in Serial Micro-Batch
Reactors.” Angewandte Chemie International Edition. Wiley, 2018. https://doi.org/10.1002/anie.201712568.
ieee: B. Pieber, M. Shalom, M. Antonietti, P. H. Seeberger, and K. Gilmore, “Continuous
heterogeneous photocatalysis in serial micro-batch reactors,” Angewandte Chemie
International Edition, vol. 57, no. 31. Wiley, pp. 9976–9979, 2018.
ista: Pieber B, Shalom M, Antonietti M, Seeberger PH, Gilmore K. 2018. Continuous
heterogeneous photocatalysis in serial micro-batch reactors. Angewandte Chemie
International Edition. 57(31), 9976–9979.
mla: Pieber, Bartholomäus, et al. “Continuous Heterogeneous Photocatalysis in Serial
Micro-Batch Reactors.” Angewandte Chemie International Edition, vol. 57,
no. 31, Wiley, 2018, pp. 9976–79, doi:10.1002/anie.201712568.
short: B. Pieber, M. Shalom, M. Antonietti, P.H. Seeberger, K. Gilmore, Angewandte
Chemie International Edition 57 (2018) 9976–9979.
date_created: 2022-08-24T10:57:25Z
date_published: 2018-07-26T00:00:00Z
date_updated: 2023-02-21T10:09:18Z
day: '26'
doi: 10.1002/anie.201712568
extern: '1'
external_id:
pmid:
- '29377383'
intvolume: ' 57'
issue: '31'
language:
- iso: eng
month: '07'
oa_version: None
page: 9976-9979
pmid: 1
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- ' 1521-3773'
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Continuous heterogeneous photocatalysis in serial micro-batch reactors
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 57
year: '2018'
...
---
_id: '8451'
abstract:
- lang: eng
text: The structure, dynamics, and function of membrane proteins are intimately
linked to the properties of the membrane environment in which the proteins are
embedded. For structural and biophysical characterization, membrane proteins generally
need to be extracted from the membrane and reconstituted in a suitable membrane‐mimicking
environment. Ensuring functional and structural integrity in these environments
is often a major concern. The styrene/maleic acid co‐polymer has recently been
shown to be able to extract lipid/membrane protein patches directly from native
membranes to form nanosize discoidal proteolipid particles, also referred to as
native nanodiscs. In this work, we show that high‐resolution solid‐state NMR spectra
can be obtained from an integral membrane protein in native nanodiscs, as exemplified
by the 2×34 kDa bacterial cation diffusion facilitator CzcD.
article_processing_charge: No
article_type: original
author:
- first_name: Beate
full_name: Bersch, Beate
last_name: Bersch
- first_name: Jonas M.
full_name: Dörr, Jonas M.
last_name: Dörr
- first_name: Audrey
full_name: Hessel, Audrey
last_name: Hessel
- first_name: J. Antoinette
full_name: Killian, J. Antoinette
last_name: Killian
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
citation:
ama: Bersch B, Dörr JM, Hessel A, Killian JA, Schanda P. Proton-detected solid-state
NMR spectroscopy of a Zinc diffusion facilitator protein in native nanodiscs.
Angewandte Chemie International Edition. 2017;56(9):2508-2512. doi:10.1002/anie.201610441
apa: Bersch, B., Dörr, J. M., Hessel, A., Killian, J. A., & Schanda, P. (2017).
Proton-detected solid-state NMR spectroscopy of a Zinc diffusion facilitator protein
in native nanodiscs. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201610441
chicago: Bersch, Beate, Jonas M. Dörr, Audrey Hessel, J. Antoinette Killian, and
Paul Schanda. “Proton-Detected Solid-State NMR Spectroscopy of a Zinc Diffusion
Facilitator Protein in Native Nanodiscs.” Angewandte Chemie International Edition.
Wiley, 2017. https://doi.org/10.1002/anie.201610441.
ieee: B. Bersch, J. M. Dörr, A. Hessel, J. A. Killian, and P. Schanda, “Proton-detected
solid-state NMR spectroscopy of a Zinc diffusion facilitator protein in native
nanodiscs,” Angewandte Chemie International Edition, vol. 56, no. 9. Wiley,
pp. 2508–2512, 2017.
ista: Bersch B, Dörr JM, Hessel A, Killian JA, Schanda P. 2017. Proton-detected
solid-state NMR spectroscopy of a Zinc diffusion facilitator protein in native
nanodiscs. Angewandte Chemie International Edition. 56(9), 2508–2512.
mla: Bersch, Beate, et al. “Proton-Detected Solid-State NMR Spectroscopy of a Zinc
Diffusion Facilitator Protein in Native Nanodiscs.” Angewandte Chemie International
Edition, vol. 56, no. 9, Wiley, 2017, pp. 2508–12, doi:10.1002/anie.201610441.
short: B. Bersch, J.M. Dörr, A. Hessel, J.A. Killian, P. Schanda, Angewandte Chemie
International Edition 56 (2017) 2508–2512.
date_created: 2020-09-18T10:06:50Z
date_published: 2017-01-27T00:00:00Z
date_updated: 2021-01-12T08:19:22Z
day: '27'
doi: 10.1002/anie.201610441
extern: '1'
intvolume: ' 56'
issue: '9'
language:
- iso: eng
month: '01'
oa_version: None
page: 2508-2512
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Proton-detected solid-state NMR spectroscopy of a Zinc diffusion facilitator
protein in native nanodiscs
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 56
year: '2017'
...