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Syntheses and properties of thienyl-substituted dithienophenazines

A series of dithienophenazines with different lengths of the oligomeric thiophene units (quaterthiophenes and sexithiophenes) was synthesized. The thiophene and phenazine units act as electron donors and acceptors, respectively, resulting in characteristic absorption spectra. The optical spectra wer...

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Detalles Bibliográficos
Autores principales: Meyer, Annemarie, Sigmund, Eva, Luppertz, Friedhelm, Schnakenburg, Gregor, Gadaczek, Immanuel, Bredow, Thomas, Jester, Stefan-S, Höger, Sigurd
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001992/
https://www.ncbi.nlm.nih.gov/pubmed/21160561
http://dx.doi.org/10.3762/bjoc.6.135
Descripción
Sumario:A series of dithienophenazines with different lengths of the oligomeric thiophene units (quaterthiophenes and sexithiophenes) was synthesized. The thiophene and phenazine units act as electron donors and acceptors, respectively, resulting in characteristic absorption spectra. The optical spectra were calculated using time-dependent density functional theory at the B3LYP/TZVP level and verify the experimental data. Adsorption of the dithienophenazines on highly ordered pyrolytic graphite (HOPG) was investigated by scanning tunneling microscopy, showing that one of the compounds forms highly organized self-assembled monolayers.