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On-Surface Driven Formal Michael AdditionProduces m-PolyanilineOligomers on Pt (111)

Authors :
Ministerio de Economía y Competitividad (España)
European Research Council
Comunidad de Madrid
Ministerio de Ciencia, Innovación y Universidades (España)
Ruiz del Árbol, Nerea
Sánchez-Sánchez, Carlos
Otero, Gonzalo
Martínez, José I.
Andrés, Pedro L. de
Gómez-Herrero, Ana C.
Merino-Mateo, Pablo
Piantek, Marten
Serrate Donoso, David
Lacovig, Paolo
Lizzit, Silvano
Alemán, José
Ellis, Gary James
López, María Francisca
Martín-Gago, José A.
Ministerio de Economía y Competitividad (España)
European Research Council
Comunidad de Madrid
Ministerio de Ciencia, Innovación y Universidades (España)
Ruiz del Árbol, Nerea
Sánchez-Sánchez, Carlos
Otero, Gonzalo
Martínez, José I.
Andrés, Pedro L. de
Gómez-Herrero, Ana C.
Merino-Mateo, Pablo
Piantek, Marten
Serrate Donoso, David
Lacovig, Paolo
Lizzit, Silvano
Alemán, José
Ellis, Gary James
López, María Francisca
Martín-Gago, José A.
Publication Year :
2020

Abstract

[EN] On-surface synthesis is emerging as a highly rational bottom-up methodology for the synthesis of molecular structures that are unattainable or complex to obtain by wet chemistry. Here, oligomers of meta-polyaniline, a known ferromagnetic polymer, were synthesized from para-aminophenol building-blocks via an unexpected and highly specific on-surface formal 1, 4 Michael-type addition at the meta position, driven by the reduction of the aminophenol molecule. We rationalize this dehydrogenation and coupling reaction mechanism with a combination of in situ scanning tunneling and non-contact atomic force microscopies, high-resolution synchrotron-based X-ray photoemission spectroscopy and first-principles calculations. This study demonstrates the capability of surfaces to selectively modify local molecular conditions to redirect well-established synthetic routes, such as Michael coupling, towards the rational synthesis of new covalent nanostructures.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1286561100
Document Type :
Electronic Resource