On‐Surface Isomerization of Indigo within 1D Coordination Polymers

Author:

Xu Hongxiang1,Chakraborty Ritam2,Adak Abhishek Kumar23ORCID,Das Arpan2,Yang Biao14,Meier Dennis1ORCID,Riss Alexander1ORCID,Reichert Joachim1ORCID,Narasimhan Shobhana2ORCID,Barth Johannes V.1ORCID,Papageorgiou Anthoula C.15ORCID

Affiliation:

1. Technical University of Munich TUM School of Natural Sciences, Physics Department E20 James Franck Strasse 1 85748 Garching Germany

2. Theoretical Sciences Unit & School of Advanced Materials Jawaharlal Nehru Centre for Advanced Scientific Research Jakkur Bangalore 560054 India

3. Current address: The Abdus Salam International Centre for Theoretical Physics Strada Costiera 11 34151 Trieste Italy

4. Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices Soochow University Suzhou 215123 P. R. China

5. Laboratory of Physical Chemistry, Department of Chemistry National and Kapodistrian University of Athens Panepistimiopolis 15771 Athens Greece

Abstract

AbstractNatural products are attractive components to tailor environmentally friendly advanced new materials. We present surface‐confined metallosupramolecular engineering of coordination polymers using natural dyes as molecular building blocks: indigo and the related Tyrian purple. Both building blocks yield identical, well‐defined coordination polymers composed of (1 dehydroindigo : 1 Fe) repeat units on two different silver single crystal surfaces. These polymers are characterized atomically by submolecular resolution scanning tunnelling microscopy, bond‐resolving atomic force microscopy and X‐ray photoelectron spectroscopy. On Ag(100) and on Ag(111), the trans configuration of dehydroindigo results in N,O‐chelation in the polymer chains. On the more inert Ag(111) surface, the molecules additionally undergo thermally induced isomerization from the trans to the cis configuration and afford N,N‐ plus O,O‐chelation. Density functional theory calculations confirm that the coordination polymers of the cis‐isomers on Ag(111) and of the trans‐isomers on Ag(100) are energetically favoured. Our results demonstrate post‐synthetic linker isomerization in interfacial metal‐organic nanosystems.

Funder

Deutsche Forschungsgemeinschaft

China Scholarship Council

Institute for Advanced Study, Technische Universität München

Hellenic Foundation for Research and Innovation

Publisher

Wiley

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