---
_id: '7289'
abstract:
- lang: eng
text: Aprotic sodium–O2 batteries require the reversible formation/dissolution of
sodium superoxide (NaO2) on cycling. Poor cycle life has been associated with
parasitic chemistry caused by the reactivity of electrolyte and electrode with
NaO2, a strong nucleophile and base. Its reactivity can, however, not consistently
explain the side reactions and irreversibility. Herein we show that singlet oxygen
(1O2) forms at all stages of cycling and that it is a main driver for parasitic
chemistry. It was detected in‐ and ex‐situ via a 1O2 trap that selectively and
rapidly forms a stable adduct with 1O2. The 1O2 formation mechanism involves proton‐mediated
superoxide disproportionation on discharge, rest, and charge below ca. 3.3 V,
and direct electrochemical 1O2 evolution above ca. 3.3 V. Trace water, which is
needed for high capacities also drives parasitic chemistry. Controlling the highly
reactive singlet oxygen is thus crucial for achieving highly reversible cell operation.
article_processing_charge: No
article_type: original
author:
- first_name: Lukas
full_name: Schafzahl, Lukas
last_name: Schafzahl
- first_name: Nika
full_name: Mahne, Nika
last_name: Mahne
- first_name: Bettina
full_name: Schafzahl, Bettina
last_name: Schafzahl
- first_name: Martin
full_name: Wilkening, Martin
last_name: Wilkening
- 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: Schafzahl L, Mahne N, Schafzahl B, et al. Singlet oxygen during cycling of
the aprotic sodium-O2 battery. Angewandte Chemie International Edition.
2017;56(49):15728-15732. doi:10.1002/anie.201709351
apa: Schafzahl, L., Mahne, N., Schafzahl, B., Wilkening, M., Slugovc, C., Borisov,
S. M., & Freunberger, S. A. (2017). Singlet oxygen during cycling of the aprotic
sodium-O2 battery. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201709351
chicago: Schafzahl, Lukas, Nika Mahne, Bettina Schafzahl, Martin Wilkening, Christian
Slugovc, Sergey M. Borisov, and Stefan Alexander Freunberger. “Singlet Oxygen
during Cycling of the Aprotic Sodium-O2 Battery.” Angewandte Chemie International
Edition. Wiley, 2017. https://doi.org/10.1002/anie.201709351.
ieee: L. Schafzahl et al., “Singlet oxygen during cycling of the aprotic
sodium-O2 battery,” Angewandte Chemie International Edition, vol. 56, no.
49. Wiley, pp. 15728–15732, 2017.
ista: Schafzahl L, Mahne N, Schafzahl B, Wilkening M, Slugovc C, Borisov SM, Freunberger
SA. 2017. Singlet oxygen during cycling of the aprotic sodium-O2 battery. Angewandte
Chemie International Edition. 56(49), 15728–15732.
mla: Schafzahl, Lukas, et al. “Singlet Oxygen during Cycling of the Aprotic Sodium-O2
Battery.” Angewandte Chemie International Edition, vol. 56, no. 49, Wiley,
2017, pp. 15728–32, doi:10.1002/anie.201709351.
short: L. Schafzahl, N. Mahne, B. Schafzahl, M. Wilkening, C. Slugovc, S.M. Borisov,
S.A. Freunberger, Angewandte Chemie International Edition 56 (2017) 15728–15732.
date_created: 2020-01-15T12:15:05Z
date_published: 2017-12-04T00:00:00Z
date_updated: 2021-01-12T08:12:47Z
day: '04'
ddc:
- '540'
doi: 10.1002/anie.201709351
extern: '1'
file:
- access_level: open_access
checksum: 3c5b1e51954554dffb13c7d58f69836c
content_type: application/pdf
creator: dernst
date_created: 2020-01-26T14:58:07Z
date_updated: 2020-07-14T12:47:55Z
file_id: '7362'
file_name: 2017_AngChemieInternat_Schafzahl.pdf
file_size: 1013492
relation: main_file
file_date_updated: 2020-07-14T12:47:55Z
has_accepted_license: '1'
intvolume: ' 56'
issue: '49'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 15728-15732
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Singlet oxygen during cycling of the aprotic sodium-O2 battery
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: 56
year: '2017'
...
---
_id: '13393'
abstract:
- lang: eng
text: Precise control of the self-assembly of selected components within complex
mixtures is a challenging goal whose realization is important for fabricating
novel nanomaterials. Herein we show that by decorating the surfaces of metallic
nanoparticles with differently substituted azobenzenes, it is possible to modulate
the wavelength of light at which the self-assembly of these nanoparticles is induced.
Exposing a mixture of two types of nanoparticles, each functionalized with a different
azobenzene, to UV or blue light induces the selective self-assembly of only one
type of nanoparticles. Irradiation with the other wavelength triggers the disassembly
of the aggregates, and the simultaneous self-assembly of nanoparticles of the
other type. By placing both types of azobenzenes on the same nanoparticles, we
created unique materials (“frustrated” nanoparticles) whose self-assembly is induced
irrespective of the wavelength of the incident light.
article_processing_charge: No
article_type: original
author:
- first_name: Debasish
full_name: Manna, Debasish
last_name: Manna
- first_name: Thumu
full_name: Udayabhaskararao, Thumu
last_name: Udayabhaskararao
- first_name: Hui
full_name: Zhao, Hui
last_name: Zhao
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
citation:
ama: Manna D, Udayabhaskararao T, Zhao H, Klajn R. Orthogonal light-induced self-assembly
of nanoparticles using differently substituted azobenzenes. Angewandte Chemie
International Edition. 2015;54(42):12394-12397. doi:10.1002/anie.201502419
apa: Manna, D., Udayabhaskararao, T., Zhao, H., & Klajn, R. (2015). Orthogonal
light-induced self-assembly of nanoparticles using differently substituted azobenzenes.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201502419
chicago: Manna, Debasish, Thumu Udayabhaskararao, Hui Zhao, and Rafal Klajn. “Orthogonal
Light-Induced Self-Assembly of Nanoparticles Using Differently Substituted Azobenzenes.”
Angewandte Chemie International Edition. Wiley, 2015. https://doi.org/10.1002/anie.201502419.
ieee: D. Manna, T. Udayabhaskararao, H. Zhao, and R. Klajn, “Orthogonal light-induced
self-assembly of nanoparticles using differently substituted azobenzenes,” Angewandte
Chemie International Edition, vol. 54, no. 42. Wiley, pp. 12394–12397, 2015.
ista: Manna D, Udayabhaskararao T, Zhao H, Klajn R. 2015. Orthogonal light-induced
self-assembly of nanoparticles using differently substituted azobenzenes. Angewandte
Chemie International Edition. 54(42), 12394–12397.
mla: Manna, Debasish, et al. “Orthogonal Light-Induced Self-Assembly of Nanoparticles
Using Differently Substituted Azobenzenes.” Angewandte Chemie International
Edition, vol. 54, no. 42, Wiley, 2015, pp. 12394–97, doi:10.1002/anie.201502419.
short: D. Manna, T. Udayabhaskararao, H. Zhao, R. Klajn, Angewandte Chemie International
Edition 54 (2015) 12394–12397.
date_created: 2023-08-01T09:44:19Z
date_published: 2015-10-01T00:00:00Z
date_updated: 2023-08-07T12:58:29Z
day: '01'
doi: 10.1002/anie.201502419
extern: '1'
external_id:
pmid:
- '25959725'
intvolume: ' 54'
issue: '42'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '10'
oa_version: None
page: 12394-12397
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: Orthogonal light-induced self-assembly of nanoparticles using differently substituted
azobenzenes
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 54
year: '2015'
...
---
_id: '8460'
abstract:
- lang: eng
text: The function of proteins depends on their ability to sample a variety of states
differing in structure and free energy. Deciphering how the various thermally
accessible conformations are connected, and understanding their structures and
relative energies is crucial in rationalizing protein function. Many biomolecular
reactions take place within microseconds to milliseconds, and this timescale is
therefore of central functional importance. Here we show that R1ρ relaxation dispersion
experiments in magic‐angle‐spinning solid‐state NMR spectroscopy make it possible
to investigate the thermodynamics and kinetics of such exchange process, and gain
insight into structural features of short‐lived states.
article_processing_charge: No
article_type: original
author:
- first_name: Peixiang
full_name: Ma, Peixiang
last_name: Ma
- first_name: Jens D.
full_name: Haller, Jens D.
last_name: Haller
- first_name: Jérémy
full_name: Zajakala, Jérémy
last_name: Zajakala
- first_name: Pavel
full_name: Macek, Pavel
last_name: Macek
- first_name: Astrid C.
full_name: Sivertsen, Astrid C.
last_name: Sivertsen
- first_name: Dieter
full_name: Willbold, Dieter
last_name: Willbold
- first_name: Jérôme
full_name: Boisbouvier, Jérôme
last_name: Boisbouvier
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
citation:
ama: Ma P, Haller JD, Zajakala J, et al. Probing transient conformational states
of proteins by solid-state R1ρ relaxation-dispersion NMR spectroscopy. Angewandte
Chemie International Edition. 2014;53(17):4312-4317. doi:10.1002/anie.201311275
apa: Ma, P., Haller, J. D., Zajakala, J., Macek, P., Sivertsen, A. C., Willbold,
D., … Schanda, P. (2014). Probing transient conformational states of proteins
by solid-state R1ρ relaxation-dispersion NMR spectroscopy. Angewandte Chemie
International Edition. Wiley. https://doi.org/10.1002/anie.201311275
chicago: Ma, Peixiang, Jens D. Haller, Jérémy Zajakala, Pavel Macek, Astrid C. Sivertsen,
Dieter Willbold, Jérôme Boisbouvier, and Paul Schanda. “Probing Transient Conformational
States of Proteins by Solid-State R1ρ Relaxation-Dispersion NMR Spectroscopy.”
Angewandte Chemie International Edition. Wiley, 2014. https://doi.org/10.1002/anie.201311275.
ieee: P. Ma et al., “Probing transient conformational states of proteins
by solid-state R1ρ relaxation-dispersion NMR spectroscopy,” Angewandte Chemie
International Edition, vol. 53, no. 17. Wiley, pp. 4312–4317, 2014.
ista: Ma P, Haller JD, Zajakala J, Macek P, Sivertsen AC, Willbold D, Boisbouvier
J, Schanda P. 2014. Probing transient conformational states of proteins by solid-state
R1ρ relaxation-dispersion NMR spectroscopy. Angewandte Chemie International Edition.
53(17), 4312–4317.
mla: Ma, Peixiang, et al. “Probing Transient Conformational States of Proteins by
Solid-State R1ρ Relaxation-Dispersion NMR Spectroscopy.” Angewandte Chemie
International Edition, vol. 53, no. 17, Wiley, 2014, pp. 4312–17, doi:10.1002/anie.201311275.
short: P. Ma, J.D. Haller, J. Zajakala, P. Macek, A.C. Sivertsen, D. Willbold, J.
Boisbouvier, P. Schanda, Angewandte Chemie International Edition 53 (2014) 4312–4317.
date_created: 2020-09-18T10:08:53Z
date_published: 2014-03-18T00:00:00Z
date_updated: 2021-01-12T08:19:25Z
day: '18'
doi: 10.1002/anie.201311275
extern: '1'
intvolume: ' 53'
issue: '17'
language:
- iso: eng
month: '03'
oa_version: None
page: 4312-4317
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Probing transient conformational states of proteins by solid-state R1ρ relaxation-dispersion
NMR spectroscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 53
year: '2014'
...
---
_id: '14301'
abstract:
- lang: eng
text: DNA has become a prime material for assembling complex three-dimensional objects
that promise utility in various areas of application. However, achieving user-defined
goals with DNA objects has been hampered by the difficulty to prepare them at
arbitrary concentrations and in user-defined solution conditions. Here, we describe
a method that solves this problem. The method is based on poly(ethylene glycol)-induced
depletion of species with high molecular weight. We demonstrate that our method
is applicable to a wide spectrum of DNA shapes and that it achieves excellent
recovery yields of target objects up to 97 %, while providing efficient separation
from non-integrated DNA strands. DNA objects may be prepared at concentrations
up to the limit of solubility, including the possibility for bringing DNA objects
into a solid phase. Due to the fidelity and simplicity of our method we anticipate
that it will help to catalyze the development of new types of applications that
use self-assembled DNA objects.
article_processing_charge: No
article_type: original
author:
- first_name: Evi
full_name: Stahl, Evi
last_name: Stahl
- first_name: Thomas
full_name: Martin, Thomas
last_name: Martin
- first_name: Florian M
full_name: Praetorius, Florian M
id: dfec9381-4341-11ee-8fd8-faa02bba7d62
last_name: Praetorius
- first_name: Hendrik
full_name: Dietz, Hendrik
last_name: Dietz
citation:
ama: Stahl E, Martin T, Praetorius FM, Dietz H. Facile and scalable preparation
of pure and dense DNA origami solutions. Angewandte Chemie International Edition.
2014;126(47):12949-12954. doi:10.1002/ange.201405991
apa: Stahl, E., Martin, T., Praetorius, F. M., & Dietz, H. (2014). Facile and
scalable preparation of pure and dense DNA origami solutions. Angewandte Chemie
International Edition. Wiley. https://doi.org/10.1002/ange.201405991
chicago: Stahl, Evi, Thomas Martin, Florian M Praetorius, and Hendrik Dietz. “Facile
and Scalable Preparation of Pure and Dense DNA Origami Solutions.” Angewandte
Chemie International Edition. Wiley, 2014. https://doi.org/10.1002/ange.201405991.
ieee: E. Stahl, T. Martin, F. M. Praetorius, and H. Dietz, “Facile and scalable
preparation of pure and dense DNA origami solutions,” Angewandte Chemie International
Edition, vol. 126, no. 47. Wiley, pp. 12949–12954, 2014.
ista: Stahl E, Martin T, Praetorius FM, Dietz H. 2014. Facile and scalable preparation
of pure and dense DNA origami solutions. Angewandte Chemie International Edition.
126(47), 12949–12954.
mla: Stahl, Evi, et al. “Facile and Scalable Preparation of Pure and Dense DNA Origami
Solutions.” Angewandte Chemie International Edition, vol. 126, no. 47,
Wiley, 2014, pp. 12949–54, doi:10.1002/ange.201405991.
short: E. Stahl, T. Martin, F.M. Praetorius, H. Dietz, Angewandte Chemie International
Edition 126 (2014) 12949–12954.
date_created: 2023-09-06T12:51:14Z
date_published: 2014-11-17T00:00:00Z
date_updated: 2023-11-07T12:14:30Z
day: '17'
doi: 10.1002/ange.201405991
extern: '1'
external_id:
pmid:
- '25346175'
intvolume: ' 126'
issue: '47'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/ange.201405991
month: '11'
oa: 1
oa_version: Published Version
page: 12949-12954
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: Facile and scalable preparation of pure and dense DNA origami solutions
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 126
year: '2014'
...
---
_id: '11959'
abstract:
- lang: eng
text: No catalyst required! A highly efficient, catalyst-free process to generate
diimide in situ from hydrazine monohydrate and molecular oxygen for the selective
reduction of alkenes has been developed. The use of a gas–liquid segmented flow
system allowed safe operating conditions and dramatically enhanced this atom-economical
reaction, resulting in short processing times.
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: Sabrina Teixeira
full_name: Martinez, Sabrina Teixeira
last_name: Martinez
- first_name: David
full_name: Cantillo, David
last_name: Cantillo
- first_name: C. Oliver
full_name: Kappe, C. Oliver
last_name: Kappe
citation:
ama: 'Pieber B, Martinez ST, Cantillo D, Kappe CO. In situ generation of diimide
from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins.
Angewandte Chemie International Edition. 2013;52(39):10241-10244. doi:10.1002/anie.201303528'
apa: 'Pieber, B., Martinez, S. T., Cantillo, D., & Kappe, C. O. (2013). In situ
generation of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation
of olefins. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201303528'
chicago: 'Pieber, Bartholomäus, Sabrina Teixeira Martinez, David Cantillo, and C.
Oliver Kappe. “In Situ Generation of Diimide from Hydrazine and Oxygen: Continuous-Flow
Transfer Hydrogenation of Olefins.” Angewandte Chemie International Edition.
Wiley, 2013. https://doi.org/10.1002/anie.201303528.'
ieee: 'B. Pieber, S. T. Martinez, D. Cantillo, and C. O. Kappe, “In situ generation
of diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of
olefins,” Angewandte Chemie International Edition, vol. 52, no. 39. Wiley,
pp. 10241–10244, 2013.'
ista: 'Pieber B, Martinez ST, Cantillo D, Kappe CO. 2013. In situ generation of
diimide from hydrazine and oxygen: Continuous-flow transfer hydrogenation of olefins.
Angewandte Chemie International Edition. 52(39), 10241–10244.'
mla: 'Pieber, Bartholomäus, et al. “In Situ Generation of Diimide from Hydrazine
and Oxygen: Continuous-Flow Transfer Hydrogenation of Olefins.” Angewandte
Chemie International Edition, vol. 52, no. 39, Wiley, 2013, pp. 10241–44,
doi:10.1002/anie.201303528.'
short: B. Pieber, S.T. Martinez, D. Cantillo, C.O. Kappe, Angewandte Chemie International
Edition 52 (2013) 10241–10244.
date_created: 2022-08-24T11:01:47Z
date_published: 2013-09-23T00:00:00Z
date_updated: 2023-02-21T10:09:21Z
day: '23'
doi: 10.1002/anie.201303528
extern: '1'
intvolume: ' 52'
issue: '39'
language:
- iso: eng
month: '09'
oa_version: None
page: 10241-10244
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: 'In situ generation of diimide from hydrazine and oxygen: Continuous-flow transfer
hydrogenation of olefins'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 52
year: '2013'
...
---
_id: '11960'
abstract:
- lang: eng
text: It's not magic! The effects observed in microwave-irradiated chemical transformations
can in most cases be rationalized by purely bulk thermal phenomena associated
with rapid heating to elevated temperatures. As discussed in this Essay, the existence
of so-called nonthermal or specific microwave effects is highly doubtful.
article_processing_charge: No
article_type: letter_note
author:
- first_name: C. Oliver
full_name: Kappe, C. Oliver
last_name: Kappe
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Doris
full_name: Dallinger, Doris
last_name: Dallinger
citation:
ama: 'Kappe CO, Pieber B, Dallinger D. Microwave effects in organic synthesis: Myth
or reality? Angewandte Chemie International Edition. 2013;52(4):1088-1094.
doi:10.1002/anie.201204103'
apa: 'Kappe, C. O., Pieber, B., & Dallinger, D. (2013). Microwave effects in
organic synthesis: Myth or reality? Angewandte Chemie International Edition.
Wiley. https://doi.org/10.1002/anie.201204103'
chicago: 'Kappe, C. Oliver, Bartholomäus Pieber, and Doris Dallinger. “Microwave
Effects in Organic Synthesis: Myth or Reality?” Angewandte Chemie International
Edition. Wiley, 2013. https://doi.org/10.1002/anie.201204103.'
ieee: 'C. O. Kappe, B. Pieber, and D. Dallinger, “Microwave effects in organic synthesis:
Myth or reality?,” Angewandte Chemie International Edition, vol. 52, no.
4. Wiley, pp. 1088–1094, 2013.'
ista: 'Kappe CO, Pieber B, Dallinger D. 2013. Microwave effects in organic synthesis:
Myth or reality? Angewandte Chemie International Edition. 52(4), 1088–1094.'
mla: 'Kappe, C. Oliver, et al. “Microwave Effects in Organic Synthesis: Myth or
Reality?” Angewandte Chemie International Edition, vol. 52, no. 4, Wiley,
2013, pp. 1088–94, doi:10.1002/anie.201204103.'
short: C.O. Kappe, B. Pieber, D. Dallinger, Angewandte Chemie International Edition
52 (2013) 1088–1094.
date_created: 2022-08-24T11:05:04Z
date_published: 2013-01-21T00:00:00Z
date_updated: 2023-02-21T10:09:26Z
day: '21'
doi: 10.1002/anie.201204103
extern: '1'
intvolume: ' 52'
issue: '4'
language:
- iso: eng
month: '01'
oa_version: None
page: 1088-1094
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: 'Microwave effects in organic synthesis: Myth or reality?'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 52
year: '2013'
...
---
_id: '7309'
abstract:
- lang: eng
text: Energy‐storage technologies, including electrical double‐layer capacitors
and rechargeable batteries, have attracted significant attention for applications
in portable electronic devices, electric vehicles, bulk electricity storage at
power stations, and “load leveling” of renewable sources, such as solar energy
and wind power. Transforming lithium batteries and electric double‐layer capacitors
requires a step change in the science underpinning these devices, including the
discovery of new materials, new electrochemistry, and an increased understanding
of the processes on which the devices depend. The Review will consider some of
the current scientific issues underpinning lithium batteries and electric double‐layer
capacitors.
article_processing_charge: No
article_type: original
author:
- first_name: Nam-Soon
full_name: Choi, Nam-Soon
last_name: Choi
- first_name: Zonghai
full_name: Chen, Zonghai
last_name: Chen
- 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: Xiulei
full_name: Ji, Xiulei
last_name: Ji
- first_name: Yang-Kook
full_name: Sun, Yang-Kook
last_name: Sun
- first_name: Khalil
full_name: Amine, Khalil
last_name: Amine
- first_name: Gleb
full_name: Yushin, Gleb
last_name: Yushin
- first_name: Linda F.
full_name: Nazar, Linda F.
last_name: Nazar
- first_name: Jaephil
full_name: Cho, Jaephil
last_name: Cho
- first_name: Peter G.
full_name: Bruce, Peter G.
last_name: Bruce
citation:
ama: Choi N-S, Chen Z, Freunberger SA, et al. Challenges facing Lithium batteries
and electrical double-layer capacitors. Angewandte Chemie International Edition.
2012;51(40):9994-10024. doi:10.1002/anie.201201429
apa: Choi, N.-S., Chen, Z., Freunberger, S. A., Ji, X., Sun, Y.-K., Amine, K., …
Bruce, P. G. (2012). Challenges facing Lithium batteries and electrical double-layer
capacitors. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201201429
chicago: Choi, Nam-Soon, Zonghai Chen, Stefan Alexander Freunberger, Xiulei Ji,
Yang-Kook Sun, Khalil Amine, Gleb Yushin, Linda F. Nazar, Jaephil Cho, and Peter
G. Bruce. “Challenges Facing Lithium Batteries and Electrical Double-Layer Capacitors.”
Angewandte Chemie International Edition. Wiley, 2012. https://doi.org/10.1002/anie.201201429.
ieee: N.-S. Choi et al., “Challenges facing Lithium batteries and electrical
double-layer capacitors,” Angewandte Chemie International Edition, vol.
51, no. 40. Wiley, pp. 9994–10024, 2012.
ista: Choi N-S, Chen Z, Freunberger SA, Ji X, Sun Y-K, Amine K, Yushin G, Nazar
LF, Cho J, Bruce PG. 2012. Challenges facing Lithium batteries and electrical
double-layer capacitors. Angewandte Chemie International Edition. 51(40), 9994–10024.
mla: Choi, Nam-Soon, et al. “Challenges Facing Lithium Batteries and Electrical
Double-Layer Capacitors.” Angewandte Chemie International Edition, vol.
51, no. 40, Wiley, 2012, pp. 9994–10024, doi:10.1002/anie.201201429.
short: N.-S. Choi, Z. Chen, S.A. Freunberger, X. Ji, Y.-K. Sun, K. Amine, G. Yushin,
L.F. Nazar, J. Cho, P.G. Bruce, Angewandte Chemie International Edition 51 (2012)
9994–10024.
date_created: 2020-01-15T12:19:11Z
date_published: 2012-10-01T00:00:00Z
date_updated: 2021-01-12T08:12:56Z
day: '01'
doi: 10.1002/anie.201201429
extern: '1'
intvolume: ' 51'
issue: '40'
language:
- iso: eng
month: '10'
oa_version: None
page: 9994-10024
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Challenges facing Lithium batteries and electrical double-layer capacitors
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 51
year: '2012'
...
---
_id: '8464'
abstract:
- lang: eng
text: 'Nonsymmetric motion: Solid‐state NMR measurements of dipolar coupling tensors
provide insight into protein dynamics. The hitherto ignored asymmetry of the dipolar
coupling tensor contains valuable information about motional asymmetry, which
was used in the first direct site‐resolved measurement of such tensors. Important
motions such as rotamer jumps can now be directly detected in the solid state.'
article_processing_charge: No
article_type: original
author:
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
- first_name: Matthias
full_name: Huber, Matthias
last_name: Huber
- first_name: Jérôme
full_name: Boisbouvier, Jérôme
last_name: Boisbouvier
- first_name: Beat H.
full_name: Meier, Beat H.
last_name: Meier
- first_name: Matthias
full_name: Ernst, Matthias
last_name: Ernst
citation:
ama: Schanda P, Huber M, Boisbouvier J, Meier BH, Ernst M. Solid-state NMR measurements
of asymmetric dipolar couplings provide insight into protein side-chain motion.
Angewandte Chemie International Edition. 2011;50(46):11005-11009. doi:10.1002/anie.201103944
apa: Schanda, P., Huber, M., Boisbouvier, J., Meier, B. H., & Ernst, M. (2011).
Solid-state NMR measurements of asymmetric dipolar couplings provide insight into
protein side-chain motion. Angewandte Chemie International Edition. Wiley.
https://doi.org/10.1002/anie.201103944
chicago: Schanda, Paul, Matthias Huber, Jérôme Boisbouvier, Beat H. Meier, and Matthias
Ernst. “Solid-State NMR Measurements of Asymmetric Dipolar Couplings Provide Insight
into Protein Side-Chain Motion.” Angewandte Chemie International Edition.
Wiley, 2011. https://doi.org/10.1002/anie.201103944.
ieee: P. Schanda, M. Huber, J. Boisbouvier, B. H. Meier, and M. Ernst, “Solid-state
NMR measurements of asymmetric dipolar couplings provide insight into protein
side-chain motion,” Angewandte Chemie International Edition, vol. 50, no.
46. Wiley, pp. 11005–11009, 2011.
ista: Schanda P, Huber M, Boisbouvier J, Meier BH, Ernst M. 2011. Solid-state NMR
measurements of asymmetric dipolar couplings provide insight into protein side-chain
motion. Angewandte Chemie International Edition. 50(46), 11005–11009.
mla: Schanda, Paul, et al. “Solid-State NMR Measurements of Asymmetric Dipolar Couplings
Provide Insight into Protein Side-Chain Motion.” Angewandte Chemie International
Edition, vol. 50, no. 46, Wiley, 2011, pp. 11005–09, doi:10.1002/anie.201103944.
short: P. Schanda, M. Huber, J. Boisbouvier, B.H. Meier, M. Ernst, Angewandte Chemie
International Edition 50 (2011) 11005–11009.
date_created: 2020-09-18T10:09:40Z
date_published: 2011-09-14T00:00:00Z
date_updated: 2021-01-12T08:19:27Z
day: '14'
doi: 10.1002/anie.201103944
extern: '1'
intvolume: ' 50'
issue: '46'
language:
- iso: eng
month: '09'
oa_version: None
page: 11005-11009
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
link:
- relation: erratum
url: https://doi.org/10.1002/anie.201206663
status: public
title: Solid-state NMR measurements of asymmetric dipolar couplings provide insight
into protein side-chain motion
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 50
year: '2011'
...
---
_id: '7314'
abstract:
- lang: eng
text: 'The electrolyte is one of the greatest challenges facing the development
of the non‐aqueous Li–O2 battery. Although ether‐based electrolytes do from Li2O2
on the first discharge, it is shown by various techniques that they also decompose
and that decomposition increases while Li2O2 decreases on cycling (see picture).
Thus, these electrolytes are not suitable. '
article_processing_charge: No
article_type: original
author:
- 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: Yuhui
full_name: Chen, Yuhui
last_name: Chen
- first_name: Nicholas E.
full_name: Drewett, Nicholas E.
last_name: Drewett
- first_name: Laurence J.
full_name: Hardwick, Laurence J.
last_name: Hardwick
- first_name: Fanny
full_name: Bardé, Fanny
last_name: Bardé
- first_name: Peter G.
full_name: Bruce, Peter G.
last_name: Bruce
citation:
ama: Freunberger SA, Chen Y, Drewett NE, Hardwick LJ, Bardé F, Bruce PG. The Lithium-Oxygen
battery with ether-based electrolytes. Angewandte Chemie International Edition.
2011;50(37):8609-8613. doi:10.1002/anie.201102357
apa: Freunberger, S. A., Chen, Y., Drewett, N. E., Hardwick, L. J., Bardé, F., &
Bruce, P. G. (2011). The Lithium-Oxygen battery with ether-based electrolytes.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201102357
chicago: Freunberger, Stefan Alexander, Yuhui Chen, Nicholas E. Drewett, Laurence
J. Hardwick, Fanny Bardé, and Peter G. Bruce. “The Lithium-Oxygen Battery with
Ether-Based Electrolytes.” Angewandte Chemie International Edition. Wiley,
2011. https://doi.org/10.1002/anie.201102357.
ieee: S. A. Freunberger, Y. Chen, N. E. Drewett, L. J. Hardwick, F. Bardé, and P.
G. Bruce, “The Lithium-Oxygen battery with ether-based electrolytes,” Angewandte
Chemie International Edition, vol. 50, no. 37. Wiley, pp. 8609–8613, 2011.
ista: Freunberger SA, Chen Y, Drewett NE, Hardwick LJ, Bardé F, Bruce PG. 2011.
The Lithium-Oxygen battery with ether-based electrolytes. Angewandte Chemie International
Edition. 50(37), 8609–8613.
mla: Freunberger, Stefan Alexander, et al. “The Lithium-Oxygen Battery with Ether-Based
Electrolytes.” Angewandte Chemie International Edition, vol. 50, no. 37,
Wiley, 2011, pp. 8609–13, doi:10.1002/anie.201102357.
short: S.A. Freunberger, Y. Chen, N.E. Drewett, L.J. Hardwick, F. Bardé, P.G. Bruce,
Angewandte Chemie International Edition 50 (2011) 8609–8613.
date_created: 2020-01-15T12:20:19Z
date_published: 2011-09-05T00:00:00Z
date_updated: 2021-01-12T08:12:59Z
day: '05'
doi: 10.1002/anie.201102357
extern: '1'
intvolume: ' 50'
issue: '37'
language:
- iso: eng
month: '09'
oa_version: None
page: 8609-8613
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: The Lithium-Oxygen battery with ether-based electrolytes
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 50
year: '2011'
...
---
_id: '7315'
abstract:
- lang: eng
text: 'Spectroscopic data (see picture) provide direct evidence that in non‐aqueous
Li+ electrolyte, O2 is reduced to O2−, which then forms LiO2 on the electrode
surface which disproportionates to Li2O2. On charging, Li2O2 decomposes directly,
in a one‐step reaction to evolve O2 and does not pass through LiO2 as an intermediate. '
article_processing_charge: No
article_type: original
author:
- first_name: Zhangquan
full_name: Peng, Zhangquan
last_name: Peng
- 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: Laurence J.
full_name: Hardwick, Laurence J.
last_name: Hardwick
- first_name: Yuhui
full_name: Chen, Yuhui
last_name: Chen
- first_name: Vincent
full_name: Giordani, Vincent
last_name: Giordani
- first_name: Fanny
full_name: Bardé, Fanny
last_name: Bardé
- first_name: Petr
full_name: Novák, Petr
last_name: Novák
- first_name: Duncan
full_name: Graham, Duncan
last_name: Graham
- first_name: Jean-Marie
full_name: Tarascon, Jean-Marie
last_name: Tarascon
- first_name: Peter G.
full_name: Bruce, Peter G.
last_name: Bruce
citation:
ama: Peng Z, Freunberger SA, Hardwick LJ, et al. Oxygen reactions in a non-aqueous
Li+ electrolyte. Angewandte Chemie International Edition. 2011;50(28):6351-6355.
doi:10.1002/anie.201100879
apa: Peng, Z., Freunberger, S. A., Hardwick, L. J., Chen, Y., Giordani, V., Bardé,
F., … Bruce, P. G. (2011). Oxygen reactions in a non-aqueous Li+ electrolyte.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201100879
chicago: Peng, Zhangquan, Stefan Alexander Freunberger, Laurence J. Hardwick, Yuhui
Chen, Vincent Giordani, Fanny Bardé, Petr Novák, Duncan Graham, Jean-Marie Tarascon,
and Peter G. Bruce. “Oxygen Reactions in a Non-Aqueous Li+ Electrolyte.” Angewandte
Chemie International Edition. Wiley, 2011. https://doi.org/10.1002/anie.201100879.
ieee: Z. Peng et al., “Oxygen reactions in a non-aqueous Li+ electrolyte,”
Angewandte Chemie International Edition, vol. 50, no. 28. Wiley, pp. 6351–6355,
2011.
ista: Peng Z, Freunberger SA, Hardwick LJ, Chen Y, Giordani V, Bardé F, Novák P,
Graham D, Tarascon J-M, Bruce PG. 2011. Oxygen reactions in a non-aqueous Li+
electrolyte. Angewandte Chemie International Edition. 50(28), 6351–6355.
mla: Peng, Zhangquan, et al. “Oxygen Reactions in a Non-Aqueous Li+ Electrolyte.”
Angewandte Chemie International Edition, vol. 50, no. 28, Wiley, 2011,
pp. 6351–55, doi:10.1002/anie.201100879.
short: Z. Peng, S.A. Freunberger, L.J. Hardwick, Y. Chen, V. Giordani, F. Bardé,
P. Novák, D. Graham, J.-M. Tarascon, P.G. Bruce, Angewandte Chemie International
Edition 50 (2011) 6351–6355.
date_created: 2020-01-15T12:20:31Z
date_published: 2011-07-04T00:00:00Z
date_updated: 2021-01-12T08:12:59Z
day: '04'
doi: 10.1002/anie.201100879
extern: '1'
intvolume: ' 50'
issue: '28'
language:
- iso: eng
month: '07'
oa_version: None
page: 6351-6355
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
publication_status: published
publisher: Wiley
status: public
title: Oxygen reactions in a non-aqueous Li+ electrolyte
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 50
year: '2011'
...
---
_id: '8474'
abstract:
- lang: eng
text: Hydrogen bonds are ubiquitous interactions in proteins, and are important
for their folding and functionality. Scalar coupling constants across hydrogen
bonds in the protein backbone, some as small as 0.5 Hz, can be directly measured
in the solid state by NMR spectroscopy (see figure). The nuclei on both sides
of the hydrogen bond can be identified and the size of the coupling constant can
be measured accurately.
article_processing_charge: No
article_type: original
author:
- first_name: Paul
full_name: Schanda, Paul
id: 7B541462-FAF6-11E9-A490-E8DFE5697425
last_name: Schanda
orcid: 0000-0002-9350-7606
- first_name: Matthias
full_name: Huber, Matthias
last_name: Huber
- first_name: René
full_name: Verel, René
last_name: Verel
- first_name: Matthias
full_name: Ernst, Matthias
last_name: Ernst
- first_name: "Beatâ\x80\NH."
full_name: "Meier, Beatâ\x80\NH."
last_name: Meier
citation:
ama: Schanda P, Huber M, Verel R, Ernst M, Meier B. Direct detection of 3hJN’ hydrogen-bond
scalar couplings in proteins by solid-state NMR spectroscopy. Angewandte Chemie
International Edition. 2009;48(49):9322-9325. doi:10.1002/anie.200904411
apa: Schanda, P., Huber, M., Verel, R., Ernst, M., & Meier, B. (2009). Direct
detection of 3hJN’ hydrogen-bond scalar couplings in proteins by solid-state NMR
spectroscopy. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.200904411
chicago: "Schanda, Paul, Matthias Huber, René Verel, Matthias Ernst, and Beatâ\x80\NH.
Meier. “Direct Detection of 3hJN’ Hydrogen-Bond Scalar Couplings in Proteins by
Solid-State NMR Spectroscopy.” Angewandte Chemie International Edition.
Wiley, 2009. https://doi.org/10.1002/anie.200904411."
ieee: P. Schanda, M. Huber, R. Verel, M. Ernst, and B. Meier, “Direct detection
of 3hJN’ hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy,”
Angewandte Chemie International Edition, vol. 48, no. 49. Wiley, pp. 9322–9325,
2009.
ista: Schanda P, Huber M, Verel R, Ernst M, Meier B. 2009. Direct detection of 3hJN’
hydrogen-bond scalar couplings in proteins by solid-state NMR spectroscopy. Angewandte
Chemie International Edition. 48(49), 9322–9325.
mla: Schanda, Paul, et al. “Direct Detection of 3hJN’ Hydrogen-Bond Scalar Couplings
in Proteins by Solid-State NMR Spectroscopy.” Angewandte Chemie International
Edition, vol. 48, no. 49, Wiley, 2009, pp. 9322–25, doi:10.1002/anie.200904411.
short: P. Schanda, M. Huber, R. Verel, M. Ernst, B. Meier, Angewandte Chemie International
Edition 48 (2009) 9322–9325.
date_created: 2020-09-18T10:11:33Z
date_published: 2009-11-17T00:00:00Z
date_updated: 2021-01-12T08:19:31Z
day: '17'
doi: 10.1002/anie.200904411
extern: '1'
intvolume: ' 48'
issue: '49'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '11'
oa_version: None
page: 9322-9325
publication: Angewandte Chemie International Edition
publication_identifier:
issn:
- 1433-7851
- 1521-3773
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Direct detection of 3hJN' hydrogen-bond scalar couplings in proteins by solid-state
NMR spectroscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 48
year: '2009'
...
---
_id: '13417'
abstract:
- lang: eng
text: 'Mission Impossible: Metal nanoparticles (NPs) coated with photoresponsive
ligands are used as “inks” for self-erasing “paper” whereby light-induced self-assembly
of the NPs is transduced into local color changes (see picture). Depending on
the degree of self-assembly, multicolor images can be written using only one type
of NP ink. Duration of image erasure is regulated by the surface concentration
of photoactive groups and can range from seconds to days.'
article_processing_charge: No
article_type: original
author:
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Paul J.
full_name: Wesson, Paul J.
last_name: Wesson
- first_name: Kyle J. M.
full_name: Bishop, Kyle J. M.
last_name: Bishop
- first_name: Bartosz A.
full_name: Grzybowski, Bartosz A.
last_name: Grzybowski
citation:
ama: Klajn R, Wesson PJ, Bishop KJM, Grzybowski BA. Writing self-erasing images
using metastable nanoparticle “inks.” Angewandte Chemie International Edition.
2009;48(38):7035-7039. doi:10.1002/anie.200901119
apa: Klajn, R., Wesson, P. J., Bishop, K. J. M., & Grzybowski, B. A. (2009).
Writing self-erasing images using metastable nanoparticle “inks.” Angewandte
Chemie International Edition. Wiley. https://doi.org/10.1002/anie.200901119
chicago: Klajn, Rafal, Paul J. Wesson, Kyle J. M. Bishop, and Bartosz A. Grzybowski.
“Writing Self-Erasing Images Using Metastable Nanoparticle ‘Inks.’” Angewandte
Chemie International Edition. Wiley, 2009. https://doi.org/10.1002/anie.200901119.
ieee: R. Klajn, P. J. Wesson, K. J. M. Bishop, and B. A. Grzybowski, “Writing self-erasing
images using metastable nanoparticle ‘inks,’” Angewandte Chemie International
Edition, vol. 48, no. 38. Wiley, pp. 7035–7039, 2009.
ista: Klajn R, Wesson PJ, Bishop KJM, Grzybowski BA. 2009. Writing self-erasing
images using metastable nanoparticle “inks”. Angewandte Chemie International Edition.
48(38), 7035–7039.
mla: Klajn, Rafal, et al. “Writing Self-Erasing Images Using Metastable Nanoparticle
‘Inks.’” Angewandte Chemie International Edition, vol. 48, no. 38, Wiley,
2009, pp. 7035–39, doi:10.1002/anie.200901119.
short: R. Klajn, P.J. Wesson, K.J.M. Bishop, B.A. Grzybowski, Angewandte Chemie
International Edition 48 (2009) 7035–7039.
date_created: 2023-08-01T10:29:38Z
date_published: 2009-09-01T00:00:00Z
date_updated: 2023-08-08T08:59:15Z
day: '01'
doi: 10.1002/anie.200901119
extern: '1'
external_id:
pmid:
- '19533698'
intvolume: ' 48'
issue: '38'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '09'
oa_version: None
page: 7035-7039
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: Writing self-erasing images using metastable nanoparticle “inks”
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 48
year: '2009'
...
---
_id: '13421'
abstract:
- lang: eng
text: Side-chain poly[2]catenanes at the click of a switch! A bistable side-chain
poly[2]catenane has been synthesized and found to form hierarchical self-assembled
hollow superstructures of nanoscale dimensions in solution. Molecular electromechanical
switching (see picture) of the material is demonstrated, and the ground-state
equilibrium thermodynamics and switching kinetics are examined as the initial
steps towards processible molecular-based electronic devices and nanoelectromechanical
systems.
article_processing_charge: No
article_type: original
author:
- first_name: Mark A.
full_name: Olson, Mark A.
last_name: Olson
- first_name: Adam B.
full_name: Braunschweig, Adam B.
last_name: Braunschweig
- first_name: Lei
full_name: Fang, Lei
last_name: Fang
- first_name: Taichi
full_name: Ikeda, Taichi
last_name: Ikeda
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Ali
full_name: Trabolsi, Ali
last_name: Trabolsi
- first_name: Paul J.
full_name: Wesson, Paul J.
last_name: Wesson
- first_name: Diego
full_name: Benítez, Diego
last_name: Benítez
- first_name: Chad A.
full_name: Mirkin, Chad A.
last_name: Mirkin
- first_name: Bartosz A.
full_name: Grzybowski, Bartosz A.
last_name: Grzybowski
- first_name: J. Fraser
full_name: Stoddart, J. Fraser
last_name: Stoddart
citation:
ama: Olson MA, Braunschweig AB, Fang L, et al. A bistable poly[2]catenane forms
nanosuperstructures. Angewandte Chemie International Edition. 2009;48(10):1792-1797.
doi:10.1002/anie.200804558
apa: Olson, M. A., Braunschweig, A. B., Fang, L., Ikeda, T., Klajn, R., Trabolsi,
A., … Stoddart, J. F. (2009). A bistable poly[2]catenane forms nanosuperstructures.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.200804558
chicago: Olson, Mark A., Adam B. Braunschweig, Lei Fang, Taichi Ikeda, Rafal Klajn,
Ali Trabolsi, Paul J. Wesson, et al. “A Bistable Poly[2]Catenane Forms Nanosuperstructures.”
Angewandte Chemie International Edition. Wiley, 2009. https://doi.org/10.1002/anie.200804558.
ieee: M. A. Olson et al., “A bistable poly[2]catenane forms nanosuperstructures,”
Angewandte Chemie International Edition, vol. 48, no. 10. Wiley, pp. 1792–1797,
2009.
ista: Olson MA, Braunschweig AB, Fang L, Ikeda T, Klajn R, Trabolsi A, Wesson PJ,
Benítez D, Mirkin CA, Grzybowski BA, Stoddart JF. 2009. A bistable poly[2]catenane
forms nanosuperstructures. Angewandte Chemie International Edition. 48(10), 1792–1797.
mla: Olson, Mark A., et al. “A Bistable Poly[2]Catenane Forms Nanosuperstructures.”
Angewandte Chemie International Edition, vol. 48, no. 10, Wiley, 2009,
pp. 1792–97, doi:10.1002/anie.200804558.
short: M.A. Olson, A.B. Braunschweig, L. Fang, T. Ikeda, R. Klajn, A. Trabolsi,
P.J. Wesson, D. Benítez, C.A. Mirkin, B.A. Grzybowski, J.F. Stoddart, Angewandte
Chemie International Edition 48 (2009) 1792–1797.
date_created: 2023-08-01T10:30:30Z
date_published: 2009-02-23T00:00:00Z
date_updated: 2023-08-08T11:12:29Z
day: '23'
doi: 10.1002/anie.200804558
extern: '1'
external_id:
pmid:
- '19180620'
intvolume: ' 48'
issue: '10'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '02'
oa_version: None
page: 1792-1797
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: A bistable poly[2]catenane forms nanosuperstructures
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 48
year: '2009'
...
---
_id: '13424'
abstract:
- lang: eng
text: 'Changing shapes: Metastable spherical aggregates of gold nanoparticles undergo
a one-to-one, thermally induced transformation into heterodimers comprising connected
plate and spherical domains. By controlling the reaction time, it is possible
to isolate a variety of structures differing in the relative sizes of the domains
and in the overall optical properties (see picture).'
article_processing_charge: No
article_type: original
author:
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Anatoliy O.
full_name: Pinchuk, Anatoliy O.
last_name: Pinchuk
- first_name: George C.
full_name: Schatz, George C.
last_name: Schatz
- first_name: Bartosz A.
full_name: Grzybowski, Bartosz A.
last_name: Grzybowski
citation:
ama: Klajn R, Pinchuk AO, Schatz GC, Grzybowski BA. Synthesis of heterodimeric sphere–prism
nanostructures via metastable gold supraspheres. Angewandte Chemie International
Edition. 2007;46(44):8363-8367. doi:10.1002/anie.200702570
apa: Klajn, R., Pinchuk, A. O., Schatz, G. C., & Grzybowski, B. A. (2007). Synthesis
of heterodimeric sphere–prism nanostructures via metastable gold supraspheres.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.200702570
chicago: Klajn, Rafal, Anatoliy O. Pinchuk, George C. Schatz, and Bartosz A. Grzybowski.
“Synthesis of Heterodimeric Sphere–Prism Nanostructures via Metastable Gold Supraspheres.”
Angewandte Chemie International Edition. Wiley, 2007. https://doi.org/10.1002/anie.200702570.
ieee: R. Klajn, A. O. Pinchuk, G. C. Schatz, and B. A. Grzybowski, “Synthesis of
heterodimeric sphere–prism nanostructures via metastable gold supraspheres,” Angewandte
Chemie International Edition, vol. 46, no. 44. Wiley, pp. 8363–8367, 2007.
ista: Klajn R, Pinchuk AO, Schatz GC, Grzybowski BA. 2007. Synthesis of heterodimeric
sphere–prism nanostructures via metastable gold supraspheres. Angewandte Chemie
International Edition. 46(44), 8363–8367.
mla: Klajn, Rafal, et al. “Synthesis of Heterodimeric Sphere–Prism Nanostructures
via Metastable Gold Supraspheres.” Angewandte Chemie International Edition,
vol. 46, no. 44, Wiley, 2007, pp. 8363–67, doi:10.1002/anie.200702570.
short: R. Klajn, A.O. Pinchuk, G.C. Schatz, B.A. Grzybowski, Angewandte Chemie International
Edition 46 (2007) 8363–8367.
date_created: 2023-08-01T10:31:08Z
date_published: 2007-11-12T00:00:00Z
date_updated: 2023-08-08T11:17:57Z
day: '12'
doi: 10.1002/anie.200702570
extern: '1'
external_id:
pmid:
- '17902083'
intvolume: ' 46'
issue: '44'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '11'
oa_version: None
page: 8363-8367
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: Synthesis of heterodimeric sphere–prism nanostructures via metastable gold
supraspheres
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 46
year: '2007'
...
---
_id: '13429'
abstract:
- lang: eng
text: 'The fruitful core: Organic syntheses reported in the literature from 1850
to 2004 are analyzed with mathematical tools from network theory and statistical
physics. There is a set of substances (the core) from which the majority of other
organic compounds can be made (see picture; red: core, blue: periphery, green:
islands). Search algorithms are used to identify small optimal sets of maximally
useful chemicals.'
article_processing_charge: No
article_type: original
author:
- first_name: Kyle J. M.
full_name: Bishop, Kyle J. M.
last_name: Bishop
- first_name: Rafal
full_name: Klajn, Rafal
id: 8e84690e-1e48-11ed-a02b-a1e6fb8bb53b
last_name: Klajn
- first_name: Bartosz A.
full_name: Grzybowski, Bartosz A.
last_name: Grzybowski
citation:
ama: Bishop KJM, Klajn R, Grzybowski BA. The core and most useful molecules in organic
chemistry. Angewandte Chemie International Edition. 2006;45(32):5348-5354.
doi:10.1002/anie.200600881
apa: Bishop, K. J. M., Klajn, R., & Grzybowski, B. A. (2006). The core and most
useful molecules in organic chemistry. Angewandte Chemie International Edition.
Wiley. https://doi.org/10.1002/anie.200600881
chicago: Bishop, Kyle J. M., Rafal Klajn, and Bartosz A. Grzybowski. “The Core and
Most Useful Molecules in Organic Chemistry.” Angewandte Chemie International
Edition. Wiley, 2006. https://doi.org/10.1002/anie.200600881.
ieee: K. J. M. Bishop, R. Klajn, and B. A. Grzybowski, “The core and most useful
molecules in organic chemistry,” Angewandte Chemie International Edition,
vol. 45, no. 32. Wiley, pp. 5348–5354, 2006.
ista: Bishop KJM, Klajn R, Grzybowski BA. 2006. The core and most useful molecules
in organic chemistry. Angewandte Chemie International Edition. 45(32), 5348–5354.
mla: Bishop, Kyle J. M., et al. “The Core and Most Useful Molecules in Organic Chemistry.”
Angewandte Chemie International Edition, vol. 45, no. 32, Wiley, 2006,
pp. 5348–54, doi:10.1002/anie.200600881.
short: K.J.M. Bishop, R. Klajn, B.A. Grzybowski, Angewandte Chemie International
Edition 45 (2006) 5348–5354.
date_created: 2023-08-01T10:37:16Z
date_published: 2006-08-11T00:00:00Z
date_updated: 2023-08-08T11:31:27Z
day: '11'
doi: 10.1002/anie.200600881
extern: '1'
external_id:
pmid:
- '16835857'
intvolume: ' 45'
issue: '32'
keyword:
- General Chemistry
- Catalysis
language:
- iso: eng
month: '08'
oa_version: None
page: 5348-5354
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: The core and most useful molecules in organic chemistry
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 45
year: '2006'
...