On-surface synthesis of non-benzenoid conjugated polymers by selective atomic rearrangement of ethynylarenes
Metadatos
Mostrar el registro completo del ítemAutor
Jiménez Martín, Alejandro; Villalobos Romero, Federico; Cuerva Carvajal, Juan Manuel; González Campaña, AraceliEditorial
Royal Society of Chemistry
Fecha
2022-12-20Referencia bibliográfica
Chem. Sci., 2023, Advance Article. DOI: [10.1039/d2sc04722e]
Patrocinador
Operational Programme for Research, Development, and Education of the European Regional Development Fund CZ.02.1.01/0.0/0.0/16_019/0000754; European Research Council (ERC) 677023; Conocimiento y Universidades Ministerio de Universidades (Spain) FPU18/05938; Internal Student Grant Agency of the Palacky University in Olomouc, Czech Republic IGA_PrF_2022_026 IGA_PrF_2022_019; FEDER/Junta de Andalucia-Consejeria de Transformacion Economica, Industria, Conocimiento y Universidades B.FQM.428.UGR20; Grant Agency of the Czech Republic 20-13692X; Fischer ScholarshipResumen
Here, we report a new on-surface synthetic strategy to precisely introduce five-membered units into
conjugated polymers from specifically designed precursor molecules that give rise to low-bandgap
fulvalene-bridged bisanthene polymers. The selective formation of non-benzenoid units is finely
controlled by the annealing parameters, which govern the initiation of atomic rearrangements that
efficiently transform previously formed diethynyl bridges into fulvalene moieties. The atomically precise
structures and electronic properties have been unmistakably characterized by STM, nc-AFM, and STS and
the results are supported by DFT theoretical calculations. Interestingly, the fulvalene-bridged bisanthene
polymers exhibit experimental narrow frontier electronic gaps of 1.2 eV on Au(111) with fully conjugated
units. This on-surface synthetic strategy can potentially be extended to other conjugated polymers to
tune their optoelectronic properties by integrating five-membered rings at precise sites.