Two dimensional chiral networks emerging from the aryl-FH hydrogen-bond-driven self-assembly of partially fluorinated rigid molecular structures

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Mu, Zhongcheng [1 ]
Shu, Lijin [2 ]
Fuchs, Harald [1 ]
Mayor, Marcel [2 ,3 ]
Chi, Lifeng [1 ]
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[1] Physikalisches Institut, Westfälische Wilhelms-Universität Münster, Wilhelm-Klemm-Str. 10, 48149 Münster, Germany
[2] Institute for Nanotechnology, Forschungszentrum Karlsruhe GmbH, Postfach 3640, 76021 Karlsruhe, Germany
[3] Department of Chemistry, University of Basel, St. Johannsring 19, 4056 Basel, Switzerland
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Self-assembly of the partially fluorinated rigid molecules physisorbed at solution/graphite interface has been investigated by scanning tunneling microscopy. Upon adsorption; both the branched star-shaped compound 1 and the angulate rod 2 compromising diacetylene and acetylene interlinked benzene and pentafluorobezene formed two-dimensional chiral porous networks. The spontaneous formation of these architectures is likely attributed to the two effects: the compensation of the dipole moments of the branches and the formation of Ar-HF hydrogen bonds. These results demonstrate that the immobilization of molecules at the liquid/solid interface can be driven by these weak intermolecular interactions instead of van der Waals interactions between alkyl chains and substrate. Copyright © 2008 American Chemical Society;
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页码:10840 / 10841
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