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Electrochromic Polycationic Organoboronium Macrocycles with Multiple Redox States.
Shimoyama, Daisuke; Baser-Kirazli, Nurcan; Lalancette, Roger A; Jäkle, Frieder.
Afiliación
  • Shimoyama D; Department of Chemistry, Rutgers University-Newark, 73 Warren Street, Newark, NJ, 07102, USA.
  • Baser-Kirazli N; Department of Chemistry, Rutgers University-Newark, 73 Warren Street, Newark, NJ, 07102, USA.
  • Lalancette RA; Department of Chemistry, Rutgers University-Newark, 73 Warren Street, Newark, NJ, 07102, USA.
  • Jäkle F; Department of Chemistry, Rutgers University-Newark, 73 Warren Street, Newark, NJ, 07102, USA.
Angew Chem Int Ed Engl ; 60(33): 17942-17946, 2021 Aug 09.
Article en En | MEDLINE | ID: mdl-34111328
ABSTRACT
Polycationic macrocycles are attractive as they display unique molecular switching capabilities arising from their redox properties. Although diverse polycationic macrocycles have been developed, those based on cationic boron systems remain very limited. We present herein the development of novel polycationic macrocycles by introducing organoboronium moieties into a conjugated organoboron macrocyclic framework. These macrocycles consist of four bipyridylboronium units that are connected by fluorene and either electron-deficient arylborane or electron-rich arylamine moieties. Electrochemical studies reveal that the macrocycles undergo reversible multi-step redox processes with transfer of up to 10 electrons. Switchable electrochromic behavior is demonstrated via spectroelectrochemical studies and the observed color changes are rationalized by correlation with computed electronic transitions using DFT methods.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos