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Transoid-to-Cisoid Conformation Changes of Single Molecules on Surfaces Triggered by Metal Coordination

[Image: see text] Conformational isomers are stereoisomers that can interconvert over low potential barriers by rotation around a single bond. However, such bond rotation is hampered by geometrical constraints when molecules are adsorbed on surfaces. Here, we show that the adsorption of 4,4′-bis(4-c...

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Detalles Bibliográficos
Autores principales: Freund, Sara, Pawlak, Rémy, Moser, Lucas, Hinaut, Antoine, Steiner, Roland, Marinakis, Nathalie, Constable, Edwin C., Meyer, Ernst, Housecroft, Catherine E., Glatzel, Thilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645055/
https://www.ncbi.nlm.nih.gov/pubmed/31458009
http://dx.doi.org/10.1021/acsomega.8b01792
Descripción
Sumario:[Image: see text] Conformational isomers are stereoisomers that can interconvert over low potential barriers by rotation around a single bond. However, such bond rotation is hampered by geometrical constraints when molecules are adsorbed on surfaces. Here, we show that the adsorption of 4,4′-bis(4-carboxyphenyl)-6,6′-dimethyl-2,2′-bipyridine molecules on surfaces leads to the appearance of prochiral single molecules on NiO(001) and to enantiopure supramolecular domains on Au(111) surfaces containing the transoid-molecule conformation. Upon additional Fe adatom deposition, molecules undergo a controlled interconversion from a transoid-to-cisoid conformation as a result of coordination of the Fe atoms to the 2,2′-bipyridine moieties. As confirmed by atomic force microscopy images and X-ray photoelectron spectroscopy measurements, the resulting molecular structures become irreversibly achiral.