---
OA_type: closed access
_id: '17917'
abstract:
- lang: eng
text: A single-molecule method has been developed based on the scanning tunneling
microscope (STM) to selectively couple a series of aniline derivatives and create
azobenzenes. The Au-catalyzed oxidative coupling is driven by the local electrochemical
potential at the nanostructured Au STM tip. The products are detected in situ
by measuring the conductance and molecular junction elongation and compared with
analogous measurements of the expected azobenzene derivatives prepared ex situ.
This single-molecule approach is robust, and it can quickly and reproducibly create
reactions for a variety of anilines. We further demonstrate the selective synthesis
of geometric isomers and the assembly of complex molecular architectures by sequential
coupling of complementary anilines, demonstrating unprecedented control over bond
formation at the nanoscale.
article_processing_charge: No
article_type: original
author:
- first_name: Yaping
full_name: Zang, Yaping
last_name: Zang
- first_name: Ilana
full_name: Stone, Ilana
last_name: Stone
- first_name: Michael S.
full_name: Inkpen, Michael S.
last_name: Inkpen
- first_name: Fay
full_name: Ng, Fay
last_name: Ng
- first_name: Tristan H.
full_name: Lambert, Tristan H.
last_name: Lambert
- first_name: Colin
full_name: Nuckolls, Colin
last_name: Nuckolls
- first_name: Michael L.
full_name: Steigerwald, Michael L.
last_name: Steigerwald
- first_name: Xavier
full_name: Roy, Xavier
last_name: Roy
- first_name: Latha
full_name: Venkataraman, Latha
id: 9ebb78a5-cc0d-11ee-8322-fae086a32caf
last_name: Venkataraman
orcid: 0000-0002-6957-6089
citation:
ama: Zang Y, Stone I, Inkpen MS, et al. In situ coupling of single molecules driven
by gold‐catalyzed electrooxidation. Angewandte Chemie International Edition.
2019;58(45):16008-16012. doi:10.1002/anie.201906215
apa: Zang, Y., Stone, I., Inkpen, M. S., Ng, F., Lambert, T. H., Nuckolls, C., …
Venkataraman, L. (2019). In situ coupling of single molecules driven by gold‐catalyzed
electrooxidation. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201906215
chicago: Zang, Yaping, Ilana Stone, Michael S. Inkpen, Fay Ng, Tristan H. Lambert,
Colin Nuckolls, Michael L. Steigerwald, Xavier Roy, and Latha Venkataraman. “In
Situ Coupling of Single Molecules Driven by Gold‐catalyzed Electrooxidation.”
Angewandte Chemie International Edition. Wiley, 2019. https://doi.org/10.1002/anie.201906215.
ieee: Y. Zang et al., “In situ coupling of single molecules driven by gold‐catalyzed
electrooxidation,” Angewandte Chemie International Edition, vol. 58, no.
45. Wiley, pp. 16008–16012, 2019.
ista: Zang Y, Stone I, Inkpen MS, Ng F, Lambert TH, Nuckolls C, Steigerwald ML,
Roy X, Venkataraman L. 2019. In situ coupling of single molecules driven by gold‐catalyzed
electrooxidation. Angewandte Chemie International Edition. 58(45), 16008–16012.
mla: Zang, Yaping, et al. “In Situ Coupling of Single Molecules Driven by Gold‐catalyzed
Electrooxidation.” Angewandte Chemie International Edition, vol. 58, no.
45, Wiley, 2019, pp. 16008–12, doi:10.1002/anie.201906215.
short: Y. Zang, I. Stone, M.S. Inkpen, F. Ng, T.H. Lambert, C. Nuckolls, M.L. Steigerwald,
X. Roy, L. Venkataraman, Angewandte Chemie International Edition 58 (2019) 16008–16012.
date_created: 2024-09-09T07:41:47Z
date_published: 2019-11-04T00:00:00Z
date_updated: 2024-12-10T12:36:30Z
day: '04'
doi: 10.1002/anie.201906215
extern: '1'
external_id:
pmid:
- '31226235'
intvolume: ' 58'
issue: '45'
language:
- iso: eng
month: '11'
oa_version: None
page: 16008-16012
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: In situ coupling of single molecules driven by gold‐catalyzed electrooxidation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 58
year: '2019'
...
---
OA_type: closed access
_id: '17919'
abstract:
- lang: eng
text: The adsorption geometry and the electronic structure of a Blatter radical
derivative on a gold surface were investigated by a combination of high‐resolution
noncontact atomic force microscopy and scanning tunneling microscopy. While the
hybridization with the substrate hinders direct access to the molecular states,
we show that the unpaired‐electron orbital can be probed with Ångström resolution
by mapping the spatial distribution of the Kondo resonance. The Blatter derivative
features a peculiar delocalization of the unpaired‐electron orbital over some
but not all moieties of the molecule, such that the Kondo signature can be related
to the spatial fingerprint of the orbital. We observe a direct correspondence
between these two quantities, including a pronounced nodal plane structure. Finally,
we demonstrate that the spatial signature of the Kondo resonance also persists
upon noncovalent dimerization of molecules.
article_processing_charge: No
article_type: original
author:
- first_name: Laerte L.
full_name: Patera, Laerte L.
last_name: Patera
- first_name: Sophia
full_name: Sokolov, Sophia
last_name: Sokolov
- first_name: Jonathan Z.
full_name: Low, Jonathan Z.
last_name: Low
- first_name: Luis M.
full_name: Campos, Luis M.
last_name: Campos
- first_name: Latha
full_name: Venkataraman, Latha
id: 9ebb78a5-cc0d-11ee-8322-fae086a32caf
last_name: Venkataraman
orcid: 0000-0002-6957-6089
- first_name: Jascha
full_name: Repp, Jascha
last_name: Repp
citation:
ama: Patera LL, Sokolov S, Low JZ, Campos LM, Venkataraman L, Repp J. Resolving
the unpaired‐electron orbital distribution in a stable organic radical by Kondo
resonance mapping. Angewandte Chemie International Edition. 2019;58(32):11063-11067.
doi:10.1002/anie.201904851
apa: Patera, L. L., Sokolov, S., Low, J. Z., Campos, L. M., Venkataraman, L., &
Repp, J. (2019). Resolving the unpaired‐electron orbital distribution in a stable
organic radical by Kondo resonance mapping. Angewandte Chemie International
Edition. Wiley. https://doi.org/10.1002/anie.201904851
chicago: Patera, Laerte L., Sophia Sokolov, Jonathan Z. Low, Luis M. Campos, Latha
Venkataraman, and Jascha Repp. “Resolving the Unpaired‐electron Orbital Distribution
in a Stable Organic Radical by Kondo Resonance Mapping.” Angewandte Chemie
International Edition. Wiley, 2019. https://doi.org/10.1002/anie.201904851.
ieee: L. L. Patera, S. Sokolov, J. Z. Low, L. M. Campos, L. Venkataraman, and J.
Repp, “Resolving the unpaired‐electron orbital distribution in a stable organic
radical by Kondo resonance mapping,” Angewandte Chemie International Edition,
vol. 58, no. 32. Wiley, pp. 11063–11067, 2019.
ista: Patera LL, Sokolov S, Low JZ, Campos LM, Venkataraman L, Repp J. 2019. Resolving
the unpaired‐electron orbital distribution in a stable organic radical by Kondo
resonance mapping. Angewandte Chemie International Edition. 58(32), 11063–11067.
mla: Patera, Laerte L., et al. “Resolving the Unpaired‐electron Orbital Distribution
in a Stable Organic Radical by Kondo Resonance Mapping.” Angewandte Chemie
International Edition, vol. 58, no. 32, Wiley, 2019, pp. 11063–67, doi:10.1002/anie.201904851.
short: L.L. Patera, S. Sokolov, J.Z. Low, L.M. Campos, L. Venkataraman, J. Repp,
Angewandte Chemie International Edition 58 (2019) 11063–11067.
date_created: 2024-09-09T07:43:21Z
date_published: 2019-08-05T00:00:00Z
date_updated: 2024-12-10T12:41:49Z
day: '05'
doi: 10.1002/anie.201904851
extern: '1'
external_id:
pmid:
- '31115954'
intvolume: ' 58'
issue: '32'
language:
- iso: eng
month: '08'
oa_version: None
page: 11063-11067
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: Resolving the unpaired‐electron orbital distribution in a stable organic radical
by Kondo resonance mapping
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 58
year: '2019'
...
---
_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: 2024-10-14T12:15:04Z
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'
...
---
OA_type: closed access
_id: '17936'
abstract:
- lang: eng
text: We report that the single‐molecule junction conductance of thiol‐terminated
silanes with Ag electrodes are higher than the conductance of those formed with
Au electrodes. These results are in contrast to the trends in the metal work function
Φ(Ag)<Φ(Au). As such, a better alignment of the Au Fermi level to the molecular
orbital of silane that mediates charge transport would be expected. This conductance
trend is reversed when we replace the thiols with amines, highlighting the impact
of metal–S covalent and metal–NH2 dative bonds in controlling
the molecular conductance. Density functional theory calculations elucidate the
crucial role of the chemical linkers in determining the level alignment when molecules
are attached to different metal contacts. We also demonstrate that conductance
of thiol‐terminated silanes with Pt electrodes is lower than the ones formed with
Au and Ag electrodes, again in contrast to the trends in the metal work‐functions.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Haixing
full_name: Li, Haixing
last_name: Li
- first_name: Timothy A.
full_name: Su, Timothy A.
last_name: Su
- first_name: María
full_name: Camarasa‐Gómez, María
last_name: Camarasa‐Gómez
- first_name: Daniel
full_name: Hernangómez‐Pérez, Daniel
last_name: Hernangómez‐Pérez
- first_name: Simon E.
full_name: Henn, Simon E.
last_name: Henn
- first_name: Vladislav
full_name: Pokorný, Vladislav
last_name: Pokorný
- first_name: Caravaggio D.
full_name: Caniglia, Caravaggio D.
last_name: Caniglia
- first_name: Michael S.
full_name: Inkpen, Michael S.
last_name: Inkpen
- first_name: Richard
full_name: Korytár, Richard
last_name: Korytár
- first_name: Michael L.
full_name: Steigerwald, Michael L.
last_name: Steigerwald
- first_name: Colin
full_name: Nuckolls, Colin
last_name: Nuckolls
- first_name: Ferdinand
full_name: Evers, Ferdinand
last_name: Evers
- first_name: Latha
full_name: Venkataraman, Latha
id: 9ebb78a5-cc0d-11ee-8322-fae086a32caf
last_name: Venkataraman
orcid: 0000-0002-6957-6089
citation:
ama: Li H, Su TA, Camarasa‐Gómez M, et al. Silver makes better eElectrical contacts
to thiol‐terminated silanes than Gold. Angewandte Chemie International Edition.
2017;56(45):14145-14148. doi:10.1002/anie.201708524
apa: Li, H., Su, T. A., Camarasa‐Gómez, M., Hernangómez‐Pérez, D., Henn, S. E.,
Pokorný, V., … Venkataraman, L. (2017). Silver makes better eElectrical contacts
to thiol‐terminated silanes than Gold. Angewandte Chemie International Edition.
Wiley. https://doi.org/10.1002/anie.201708524
chicago: Li, Haixing, Timothy A. Su, María Camarasa‐Gómez, Daniel Hernangómez‐Pérez,
Simon E. Henn, Vladislav Pokorný, Caravaggio D. Caniglia, et al. “Silver Makes
Better EElectrical Contacts to Thiol‐terminated Silanes than Gold.” Angewandte
Chemie International Edition. Wiley, 2017. https://doi.org/10.1002/anie.201708524.
ieee: H. Li et al., “Silver makes better eElectrical contacts to thiol‐terminated
silanes than Gold,” Angewandte Chemie International Edition, vol. 56, no.
45. Wiley, pp. 14145–14148, 2017.
ista: Li H, Su TA, Camarasa‐Gómez M, Hernangómez‐Pérez D, Henn SE, Pokorný V, Caniglia
CD, Inkpen MS, Korytár R, Steigerwald ML, Nuckolls C, Evers F, Venkataraman L.
2017. Silver makes better eElectrical contacts to thiol‐terminated silanes than
Gold. Angewandte Chemie International Edition. 56(45), 14145–14148.
mla: Li, Haixing, et al. “Silver Makes Better EElectrical Contacts to Thiol‐terminated
Silanes than Gold.” Angewandte Chemie International Edition, vol. 56, no.
45, Wiley, 2017, pp. 14145–48, doi:10.1002/anie.201708524.
short: H. Li, T.A. Su, M. Camarasa‐Gómez, D. Hernangómez‐Pérez, S.E. Henn, V. Pokorný,
C.D. Caniglia, M.S. Inkpen, R. Korytár, M.L. Steigerwald, C. Nuckolls, F. Evers,
L. Venkataraman, Angewandte Chemie International Edition 56 (2017) 14145–14148.
date_created: 2024-09-09T08:45:32Z
date_published: 2017-11-06T00:00:00Z
date_updated: 2024-12-17T10:06:36Z
day: '06'
doi: 10.1002/anie.201708524
extern: '1'
intvolume: ' 56'
issue: '45'
language:
- iso: eng
month: '11'
oa_version: None
page: 14145-14148
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: Silver makes better eElectrical contacts to thiol‐terminated silanes than Gold
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: 2024-10-14T12:17:36Z
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: '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'
...
---
OA_place: publisher
OA_type: free access
_id: '21102'
abstract:
- lang: eng
text: Racemates increase the chances of crystallization by allowing molecular contacts
to be formed in a greater number of ways. With the advent of protein synthesis,
the production of protein racemates and racemic‐protein crystallography are now
possible. Curiously, racemic DNA crystallography had not been investigated despite
the commercial availability of L- and D‐deoxyribo‐oligonucleotides. Here, we report
a study into racemic DNA crystallography showing the strong propensity of racemic
DNA mixtures to form racemic crystals. We describe racemic crystal structures
of various DNA sequences and folded conformations, including duplexes, quadruplexes,
and a four‐way junction, showing that the advantages of racemic crystallography
should extend to DNA.
article_processing_charge: No
article_type: original
author:
- first_name: Pradeep K
full_name: Mandal, Pradeep K
id: 6a3def15-d4b4-11ef-9fa9-a24c1f545ec3
last_name: Mandal
orcid: 0000-0001-5996-956X
- first_name: Gavin W.
full_name: Collie, Gavin W.
last_name: Collie
- first_name: Brice
full_name: Kauffmann, Brice
last_name: Kauffmann
- first_name: Ivan
full_name: Huc, Ivan
last_name: Huc
citation:
ama: Mandal PK, Collie GW, Kauffmann B, Huc I. Racemic DNA crystallography. Angewandte
Chemie International Edition. 2014;53(52):14424-14427. doi:10.1002/anie.201409014
apa: Mandal, P. K., Collie, G. W., Kauffmann, B., & Huc, I. (2014). Racemic
DNA crystallography. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201409014
chicago: Mandal, Pradeep K, Gavin W. Collie, Brice Kauffmann, and Ivan Huc. “Racemic
DNA Crystallography.” Angewandte Chemie International Edition. Wiley, 2014.
https://doi.org/10.1002/anie.201409014.
ieee: P. K. Mandal, G. W. Collie, B. Kauffmann, and I. Huc, “Racemic DNA crystallography,”
Angewandte Chemie International Edition, vol. 53, no. 52. Wiley, pp. 14424–14427,
2014.
ista: Mandal PK, Collie GW, Kauffmann B, Huc I. 2014. Racemic DNA crystallography.
Angewandte Chemie International Edition. 53(52), 14424–14427.
mla: Mandal, Pradeep K., et al. “Racemic DNA Crystallography.” Angewandte Chemie
International Edition, vol. 53, no. 52, Wiley, 2014, pp. 14424–27, doi:10.1002/anie.201409014.
short: P.K. Mandal, G.W. Collie, B. Kauffmann, I. Huc, Angewandte Chemie International
Edition 53 (2014) 14424–14427.
date_created: 2026-01-29T21:49:27Z
date_published: 2014-10-01T00:00:00Z
date_updated: 2026-02-23T09:12:57Z
doi: 10.1002/anie.201409014
extern: '1'
has_accepted_license: '1'
intvolume: ' 53'
issue: '52'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1002/anie.201409014
month: '10'
oa: 1
oa_version: Published Version
page: 14424-14427
publication: Angewandte Chemie International Edition
publication_identifier:
eissn:
- 1521-3773
issn:
- 1433-7851
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Racemic DNA crystallography
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 53
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'
...
---
OA_type: closed access
_id: '18003'
article_processing_charge: No
article_type: letter_note
author:
- first_name: Xavier
full_name: Roy, Xavier
last_name: Roy
- first_name: Christine L.
full_name: Schenck, Christine L.
last_name: Schenck
- first_name: Seokhoon
full_name: Ahn, Seokhoon
last_name: Ahn
- first_name: Roger A.
full_name: Lalancette, Roger A.
last_name: Lalancette
- first_name: Latha
full_name: Venkataraman, Latha
id: 9ebb78a5-cc0d-11ee-8322-fae086a32caf
last_name: Venkataraman
orcid: 0000-0002-6957-6089
- first_name: Colin
full_name: Nuckolls, Colin
last_name: Nuckolls
- first_name: Michael L.
full_name: Steigerwald, Michael L.
last_name: Steigerwald
citation:
ama: Roy X, Schenck CL, Ahn S, et al. Quantum soldering of individual quantum dots.
Angewandte Chemie International Edition. 2012;51(50):12473-12476. doi:10.1002/anie.201206301
apa: Roy, X., Schenck, C. L., Ahn, S., Lalancette, R. A., Venkataraman, L., Nuckolls,
C., & Steigerwald, M. L. (2012). Quantum soldering of individual quantum dots.
Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201206301
chicago: Roy, Xavier, Christine L. Schenck, Seokhoon Ahn, Roger A. Lalancette, Latha
Venkataraman, Colin Nuckolls, and Michael L. Steigerwald. “Quantum Soldering of
Individual Quantum Dots.” Angewandte Chemie International Edition. Wiley,
2012. https://doi.org/10.1002/anie.201206301.
ieee: X. Roy et al., “Quantum soldering of individual quantum dots,” Angewandte
Chemie International Edition, vol. 51, no. 50. Wiley, pp. 12473–12476, 2012.
ista: Roy X, Schenck CL, Ahn S, Lalancette RA, Venkataraman L, Nuckolls C, Steigerwald
ML. 2012. Quantum soldering of individual quantum dots. Angewandte Chemie International
Edition. 51(50), 12473–12476.
mla: Roy, Xavier, et al. “Quantum Soldering of Individual Quantum Dots.” Angewandte
Chemie International Edition, vol. 51, no. 50, Wiley, 2012, pp. 12473–76,
doi:10.1002/anie.201206301.
short: X. Roy, C.L. Schenck, S. Ahn, R.A. Lalancette, L. Venkataraman, C. Nuckolls,
M.L. Steigerwald, Angewandte Chemie International Edition 51 (2012) 12473–12476.
date_created: 2024-09-09T11:41:01Z
date_published: 2012-11-07T00:00:00Z
date_updated: 2025-01-03T08:58:55Z
day: '07'
doi: 10.1002/anie.201206301
extern: '1'
external_id:
pmid:
- '23135896'
intvolume: ' 51'
issue: '50'
language:
- iso: eng
month: '11'
oa_version: None
page: 12473-12476
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: Quantum soldering of individual quantum dots
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 51
year: '2012'
...
---
_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'
...