Visualizing Chiral Interactions in Carbohydrates Adsorbed on Au(111) by High‐Resolution STM Imaging

Author:

Seibel Johannes123ORCID,Fittolani Giulio45ORCID,Mirhosseini Hossein6ORCID,Wu Xu1,Rauschenbach Stephan17ORCID,Anggara Kelvin1ORCID,Seeberger Peter H.45ORCID,Delbianco Martina4ORCID,Kühne Thomas D.68,Schlickum Uta12,Kern Klaus19

Affiliation:

1. Max Planck Institute for Solid State Research 70569 Stuttgart Germany

2. Institute of Applied Physics and Laboratory for Emerging Nanometrology Technische Universität Braunschweig 38104 Braunschweig Germany

3. Current address: Institute of Physical Chemistry Karlsruhe Institute of Technology (KIT) 76131 Karlsruhe Germany

4. Max Planck Institute of Colloids and Interfaces 14476 Potsdam Germany

5. Institute for Chemistry and Biochemistry Free University Berlin 14195 Berlin Germany

6. Dynamics of Condensed Matter and Center for Sustainable Systems Design, Chair of Theoretical Chemistry University of Paderborn 33098 Paderborn Germany

7. Department of Chemistry University of Oxford OX13TA Oxford UK

8. Center for Advanced Systems Understanding (CASUS) and Helmholtz Zentrum Dresden-Rossendorf 02826 Görlitz Germany

9. Institut de Physique École Polytechnique Fédérale de Lausanne 1015 Lausanne Switzerland

Abstract

AbstractCarbohydrates are the most abundant organic material on Earth and the structural “material of choice” in many living systems. Nevertheless, design and engineering of synthetic carbohydrate materials presently lag behind that for protein and nucleic acids. Bottom‐up engineering of carbohydrate materials demands an atomic‐level understanding of their molecular structures and interactions in condensed phases. Here, high‐resolution scanning tunneling microscopy (STM) is used to visualize at submolecular resolution the three‐dimensional structure of cellulose oligomers assembled on Au(1111) and the interactions that drive their assembly. The STM imaging, supported by ab initio calculations, reveals the orientation of all glycosidic bonds and pyranose rings in the oligomers, as well as details of intermolecular interactions between the oligomers. By comparing the assembly of D‐ and L‐oligomers, these interactions are shown to be enantioselective, capable of driving spontaneous enantioseparation of cellulose chains from its unnatural enantiomer and promoting the formation of engineered carbohydrate assemblies in the condensed phases.

Funder

Deutsche Forschungsgemeinschaft

Niedersächsisches Ministerium für Wissenschaft und Kultur

Bundesministerium für Bildung und Forschung

Publisher

Wiley

Subject

General Chemistry,Catalysis

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