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Potential-driven molecular tiling of a charged polycyclic aromatic compound

Research output: Contribution to Journal/Magazine › Journal article › peer-review

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Potential-driven molecular tiling of a charged polycyclic aromatic compound. / Cui, K.; Ivasenko, O.; Mali, K.S. et al.
In: Chemical Communications, Vol. 50, No. 72, 2014, p. 10376-10378.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Cui, K, Ivasenko, O, Mali, KS, Wu, D, Feng, X, Müllen, K, De Feyter, S & Mertens, SFL 2014, 'Potential-driven molecular tiling of a charged polycyclic aromatic compound', Chemical Communications, vol. 50, no. 72, pp. 10376-10378. https://doi.org/10.1039/c4cc04189e

APA

Cui, K., Ivasenko, O., Mali, K. S., Wu, D., Feng, X., Müllen, K., De Feyter, S., & Mertens, S. F. L. (2014). Potential-driven molecular tiling of a charged polycyclic aromatic compound. Chemical Communications, 50(72), 10376-10378. https://doi.org/10.1039/c4cc04189e

Vancouver

Cui K, Ivasenko O, Mali KS, Wu D, Feng X, Müllen K et al. Potential-driven molecular tiling of a charged polycyclic aromatic compound. Chemical Communications. 2014;50(72):10376-10378. doi: 10.1039/c4cc04189e

Author

Cui, K. ; Ivasenko, O. ; Mali, K.S. et al. / Potential-driven molecular tiling of a charged polycyclic aromatic compound. In: Chemical Communications. 2014 ; Vol. 50, No. 72. pp. 10376-10378.

Bibtex

@article{61e108bb5d8f4f8abc7fdcd3df3d0005,
title = "Potential-driven molecular tiling of a charged polycyclic aromatic compound",
abstract = "Using in situ electrochemical scanning tunnelling microscopy (EC-STM), we demonstrate fully reversible tuning of molecular tiling between self-assembled structures with supramolecular motifs containing 2, 3, 4, 6 or 7 tectons. The structures can be explained by electrocompression of the cationic adlayer at the solid-liquid interface. This journal is {\textcopyright} the Partner Organisations 2014.",
keywords = "anthraquinonedisulfonate, organic compound, polycyclic aromatic compound, unclassified drug, anthraquinone derivative, anthraquinone-2,6-disulfonate, cation, electrolyte, gold, polycyclic aromatic hydrocarbon, addition reaction, article, chemical modification, chemical structure, cyclic potentiometry, electrochemical analysis, electrochemical scanning tunnelling microscopy, scanning electron microscopy, supramolecular chemistry, synthesis, chemistry, scanning tunneling microscopy, Anthraquinones, Cations, Electrochemical Techniques, Electrolytes, Gold, Microscopy, Scanning Tunneling, Polycyclic Hydrocarbons, Aromatic",
author = "K. Cui and O. Ivasenko and K.S. Mali and D. Wu and X. Feng and K. M{\"u}llen and {De Feyter}, S. and S.F.L. Mertens",
year = "2014",
doi = "10.1039/c4cc04189e",
language = "English",
volume = "50",
pages = "10376--10378",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "72",

}

RIS

TY - JOUR

T1 - Potential-driven molecular tiling of a charged polycyclic aromatic compound

AU - Cui, K.

AU - Ivasenko, O.

AU - Mali, K.S.

AU - Wu, D.

AU - Feng, X.

AU - Müllen, K.

AU - De Feyter, S.

AU - Mertens, S.F.L.

PY - 2014

Y1 - 2014

N2 - Using in situ electrochemical scanning tunnelling microscopy (EC-STM), we demonstrate fully reversible tuning of molecular tiling between self-assembled structures with supramolecular motifs containing 2, 3, 4, 6 or 7 tectons. The structures can be explained by electrocompression of the cationic adlayer at the solid-liquid interface. This journal is © the Partner Organisations 2014.

AB - Using in situ electrochemical scanning tunnelling microscopy (EC-STM), we demonstrate fully reversible tuning of molecular tiling between self-assembled structures with supramolecular motifs containing 2, 3, 4, 6 or 7 tectons. The structures can be explained by electrocompression of the cationic adlayer at the solid-liquid interface. This journal is © the Partner Organisations 2014.

KW - anthraquinonedisulfonate

KW - organic compound

KW - polycyclic aromatic compound

KW - unclassified drug

KW - anthraquinone derivative

KW - anthraquinone-2,6-disulfonate

KW - cation

KW - electrolyte

KW - gold

KW - polycyclic aromatic hydrocarbon

KW - addition reaction

KW - article

KW - chemical modification

KW - chemical structure

KW - cyclic potentiometry

KW - electrochemical analysis

KW - electrochemical scanning tunnelling microscopy

KW - scanning electron microscopy

KW - supramolecular chemistry

KW - synthesis

KW - chemistry

KW - scanning tunneling microscopy

KW - Anthraquinones

KW - Cations

KW - Electrochemical Techniques

KW - Electrolytes

KW - Gold

KW - Microscopy, Scanning Tunneling

KW - Polycyclic Hydrocarbons, Aromatic

U2 - 10.1039/c4cc04189e

DO - 10.1039/c4cc04189e

M3 - Journal article

VL - 50

SP - 10376

EP - 10378

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 72

ER -