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Covalently linked thieno[2,3-b]thiophene-fullerene dimers: synthesis and physical characterization.
M Alazemi, Abdulrahman; BinSabt, Mohammad H; Al-Matar, Hamad M; Balch, Alan L; Shalaby, Mona A.
Afiliação
  • M Alazemi A; Chemistry Department, Faculty of Science, University of Kuwait, P.O. Box 5969, Safat 13060, Kuwait. a.alazmi@ku.edu.kw.
  • BinSabt MH; Chemistry Department, Faculty of Science, University of Kuwait, P.O. Box 5969, Safat 13060, Kuwait. a.alazmi@ku.edu.kw.
  • Al-Matar HM; Chemistry Department, Faculty of Science, University of Kuwait, P.O. Box 5969, Safat 13060, Kuwait. a.alazmi@ku.edu.kw.
  • Balch AL; Department of Chemistry, University of California at Davis, One Shields Avenue, Davis, California 95616, USA.
  • Shalaby MA; Chemistry Department, Faculty of Science, University of Kuwait, P.O. Box 5969, Safat 13060, Kuwait. a.alazmi@ku.edu.kw.
Org Biomol Chem ; 22(15): 2978-2984, 2024 Apr 17.
Article em En | MEDLINE | ID: mdl-38415501
ABSTRACT
Thienothiophene (TT) has received great attention in the fields of electronics and optoelectronics. Here we report a synthesis and characterization of fullerene-donor-fullerene triads linked to thieno[2,3-b]thiophene as a donor. The photophysical and electrochemical properties of the new dumbbells were investigated using UV-vis spectroscopy, fluorescence spectroscopy, cyclic voltammetry, and square wave voltammetry. The results showed that both compounds have higher LUMO energy levels than PC61BM, indicating that they can be used in photovoltaic applications. Furthermore, the powder was structurally and morphologically characterized via X-ray diffraction (XRD) and scanning electron microscopy (SEM). The SEM revealed the morphological characterization of the two derivatives as globular and urchin-like supramolecular assemblies.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article