Cargando…

Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes

The synthesis of novel (N−)acene‐based cyclooligomers is reported. Glaser‐Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel‐permeation chromatographies. For the diazatetracene, the use of sec‐butyl‐silylethynyl groups is necessar...

Descripción completa

Detalles Bibliográficos
Autores principales: Maier, Steffen, Hippchen, Nikolai, Rominger, Frank, Freudenberg, Jan, Bunz, Uwe H. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297893/
https://www.ncbi.nlm.nih.gov/pubmed/34612544
http://dx.doi.org/10.1002/chem.202103193
Descripción
Sumario:The synthesis of novel (N−)acene‐based cyclooligomers is reported. Glaser‐Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel‐permeation chromatographies. For the diazatetracene, the use of sec‐butyl‐silylethynyl groups is necessary to achieve solubility. Diazatetracene‐based cyclodimers and cyclotrimers were used as semiconductors in thin‐film transistors. Although their optoelectronic properties are quite similar, their electron mobilities in proof‐of‐concept thin‐film transistors differ by an order of magnitude.