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Assessing the Photoinduced Electron-Donating Behavior of Carbon Nanodots in Nanoconjugates.
Ferrer-Ruiz, Andrés; Scharl, Tobias; Rodríguez-Pérez, Laura; Cadranel, Alejandro; Herranz, M Ángeles; Martín, Nazario; Guldi, Dirk M.
Afiliación
  • Ferrer-Ruiz A; Department of Organic Chemistry, Faculty of Chemistry, Complutense University of Madrid, Avda. Complutense s/n, Ciudad Universitaria, E-28040 Madrid, Spain.
  • Scharl T; Department of Chemistry and Pharmacy, Interdisciplinary Center for Molecular Materials, Friedrich-Alexander Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058 Erlangen, Germany.
  • Rodríguez-Pérez L; Department of Organic Chemistry, Faculty of Chemistry, Complutense University of Madrid, Avda. Complutense s/n, Ciudad Universitaria, E-28040 Madrid, Spain.
  • Cadranel A; Department of Chemistry and Pharmacy, Interdisciplinary Center for Molecular Materials, Friedrich-Alexander Universität Erlangen-Nürnberg, Egerlandstraße 3, 91058 Erlangen, Germany.
  • Herranz MÁ; Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Química Inorgánica, Analítica y Química Física, Pabellón 2, Ciudad Universitaria, C1428EHA, Buenos Aires, Argentina.
  • Martín N; CONICET - Universidad de Buenos Aires. Instituto de Química Física de Materiales, Medio Ambiente y Energía (INQUIMAE), Pabellón 2, Ciudad Universitaria, C1428EHA, Buenos Aires, Argentina.
  • Guldi DM; Department of Organic Chemistry, Faculty of Chemistry, Complutense University of Madrid, Avda. Complutense s/n, Ciudad Universitaria, E-28040 Madrid, Spain.
J Am Chem Soc ; 2020 Nov 19.
Article en En | MEDLINE | ID: mdl-33211959
ABSTRACT
Carbon nanodots (CNDs) undergo electron transfer in different scenarios. Previous studies have mainly focused on the electron-accepting features of CNDs in covalently linked donor-acceptor nanoconjugates. In view of this, we decided to carry out in this study the formation of covalently linked nanoconjugates that feature electron-donating pressure synthesized carbon nanodots (pCNDs) and electron-accepting 11,11,12,12-tetracyano-9,10-anthra-p-quinodimethane (TCAQ) pCND-TCAQ. The stability of the one-electron reduced form of TCAQ renders it the acceptor of choice. Detailed structural and electrochemical investigations allowed the characterization of pCND-TCAQ. Furthermore, investigations regarding intramolecular interactions, by means of steady-state and pump-probe transient absorption spectroscopies, allowed detection and characterization of three excited state species, in general, and the pCND•+-TCAQ•- charge-separated state, in particular.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2020 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2020 Tipo del documento: Article País de afiliación: España