Selection of conformational states in surface self-assembly for a molecule with eight possible pairs of surface enantiomers

A. Nuermaimaiti, V. S-Falk, J. L. Cramer, K. L. Svane, B. Hammer, K. V. Gothelf, T. R. Linderoth

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Self-assembly of a molecule with many distinct conformational states, resulting in eight possible pairs of surface enantiomers, is investigated on a Au(111) surface under UHV conditions. The complex molecule is equipped with alkyl and carboxyl moieties to promote controlled self-assembly of lamellae structures. From statistical analysis of Scanning Tunnelling Microscopy (STM) data we observe a clear selection of specific conformational states after self-assembly. Using Density Functional Theory (DFT) calculations we rationalise how this selection is correlated to the orientation of the alkyl moieties in mirror-image domains of the lamellae structures, leading to selection of three out of the eight possible enantiomeric pairs.
Original languageEnglish
JournalChemical Communications
Volume52
Issue number97
Pages (from-to)14023-14026
ISSN1359-7345
DOIs
Publication statusPublished - 2016
Externally publishedYes

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