A versatile route to polythiophenes with functional pendant groups using alkyne chemistry
A new versatile polythiophene building block, 3-(3,4-ethylenedioxythiophene)prop-1-yne (pyEDOT) (3), is prepared from glycidol in four steps in 28% overall yield. pyEDOT features an ethynyl group on its ethylenedioxy bridge, allowing further functionalization by alkyne chemistry. Its usefulness is d...
Main Authors: | Xiao Huang, Li Yang, Rikard Emanuelsson, Jonas Bergquist, Maria Strømme, Martin Sjödin, Adolf Gogoll |
---|---|
Format: | Article |
Language: | English |
Published: |
Beilstein-Institut
2016-12-01
|
Series: | Beilstein Journal of Organic Chemistry |
Subjects: | |
Online Access: | https://doi.org/10.3762/bjoc.12.265 |
Similar Items
-
Chiral Polythiophenes: Part I: Syntheses of Monomeric Precursors
by: Dorota Krasowska, et al.
Published: (2021-07-01) -
Structural and thermal properties of carboxylic acid functionalized polythiophenes
by: Ariane de França Mescoloto, et al.
Published: (2014-01-01) -
Probing the molecular orientation of chemically polymerized polythiophene-polyrotaxane via solid state NMR
by: Mujeeb Khan, et al.
Published: (2017-07-01) -
Synthesis, Characterization, and Electropolymerization of Extended Fused-Ring Thieno[3,4-b]pyrazine-Based Terthienyls
by: Kristine L. Konkol, et al.
Published: (2016-05-01) -
Synthesis, electropolymerization, and electrochromic performances of two novel tetrathiafulvalene–thiophene assemblies
by: Li Yuhao, et al.
Published: (2020-07-01)