TY - JOUR
T1 - Supramolecular assembly through interactions between molecular dipoles and alkali metal ions
AU - Shimizu, Tomoko K.
AU - Jung, Jaehoon
AU - Imada, Hiroshi
AU - Kim, Yousoo
N1 - Publisher Copyright:
© 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2014/10/29
Y1 - 2014/10/29
N2 - Establishing a way to fabricate well-ordered molecular structures is a necessary step toward advancement in organic optoelectronic devices. Here, we propose to use interactions between electric dipoles of molecules and alkali metal ions to form a well-developed homogeneous monolayer of diarylethene molecules on the Cu(111) surface with the aid of NaCl co-deposition. Scanning tunneling microscopy and density functional theory calculation results indicate that the formation of a row-type structure occurs as a result of interactions between the Na+ ions and the diarylethene molecular dipoles, drastically changing the adsorption configuration from that without Na+.
AB - Establishing a way to fabricate well-ordered molecular structures is a necessary step toward advancement in organic optoelectronic devices. Here, we propose to use interactions between electric dipoles of molecules and alkali metal ions to form a well-developed homogeneous monolayer of diarylethene molecules on the Cu(111) surface with the aid of NaCl co-deposition. Scanning tunneling microscopy and density functional theory calculation results indicate that the formation of a row-type structure occurs as a result of interactions between the Na+ ions and the diarylethene molecular dipoles, drastically changing the adsorption configuration from that without Na+.
KW - Density functional calculations
KW - Diarylethene
KW - Scanning probe microscopy
KW - Supramolecular chemistry
UR - http://www.scopus.com/inward/record.url?scp=84918799944&partnerID=8YFLogxK
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U2 - 10.1002/anie.201407555
DO - 10.1002/anie.201407555
M3 - Article
AN - SCOPUS:84918799944
SN - 1433-7851
VL - 53
SP - 13729
EP - 13733
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 50
ER -