Your browser doesn't support javascript.
loading
Solid-State Emissive Aroyl-S,N-Ketene Acetals with Tunable Aggregation-Induced Emission Characteristics.
Biesen, Lukas; Nirmalananthan-Budau, Nithiya; Hoffmann, Katrin; Resch-Genger, Ute; Müller, Thomas J J.
Afiliación
  • Biesen L; Institut für Organische Chemie und Makromolekulare Chemie, Heinrich-Heine-Universität Düsseldorf, Universitätsstrasse 1, 40225, Düsseldorf, Germany.
  • Nirmalananthan-Budau N; Division Biophotonics, Bundesanstalt für Materialforschung und -prüfung (BAM), Department 1, Richard-Willstätter-Strasse 11, 12489, Berlin, Germany.
  • Hoffmann K; Institut für Chemie und Biochemie, Freie Universität Berlin, Takustrasse 3, 14195, Berlin, Germany.
  • Resch-Genger U; Division Biophotonics, Bundesanstalt für Materialforschung und -prüfung (BAM), Department 1, Richard-Willstätter-Strasse 11, 12489, Berlin, Germany.
  • Müller TJJ; Division Biophotonics, Bundesanstalt für Materialforschung und -prüfung (BAM), Department 1, Richard-Willstätter-Strasse 11, 12489, Berlin, Germany.
Angew Chem Int Ed Engl ; 59(25): 10037-10041, 2020 06 15.
Article en En | MEDLINE | ID: mdl-31990116
ABSTRACT
N-Benzyl aroyl-S,N-ketene acetals can be readily synthesized by condensation of aroyl chlorides and N-benzyl 2-methyl benzothiazolium salts in good to excellent yields, yielding a library of 35 chromophores with bright solid-state emission and aggregation-induced emission characteristics. Varying the substituent from electron-donating to electron-withdrawing enables the tuning of the solid-state emission color from deep blue to red.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2020 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2020 Tipo del documento: Article País de afiliación: Alemania