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Direct (Hetero)arylation Polymerization: Trends and Perspectives
- Source :
- Journal of the American Chemical Society. 138:10056-10071
- Publication Year :
- 2016
- Publisher :
- American Chemical Society (ACS), 2016.
-
Abstract
- Conjugated polymers have attracted much attention in recent years, as they can combine the best features of metals or inorganic semiconducting materials (excellent electrical and optical properties) with those of synthetic polymers (mechanical flexibility, simple processing, and low-cost production), thereby creating altogether new scientific synergies and technological opportunities. In the search for more efficient synthetic methods for the preparation of conjugated polymers, this Perspective reports advances in the field of direct (hetero)arylation polymerization. This recently developed polymerization method encompasses the formation of carbon-carbon bonds between simple (hetero)arenes and (hetero)aryl halides, reducing both the number of synthetic steps and the production of organometallic byproducts. Along these lines, we describe the most general and adaptable reaction conditions for the preparation of high-molecular-weight, defect-free conjugated polymers. We also discuss the bottleneck presented by the utilization of certain brominated thiophene units and propose some potential solutions. It is, however, firmly believed that this polymerization method will become a versatile tool in the field of conjugated polymers by providing a desirable atom-economical alternative to standard cross-coupling polymerization reactions.
- Subjects :
- Reaction conditions
chemistry.chemical_classification
Aryl
Nanotechnology
02 engineering and technology
General Chemistry
Polymer
Conjugated system
010402 general chemistry
021001 nanoscience & nanotechnology
01 natural sciences
Biochemistry
Catalysis
0104 chemical sciences
chemistry.chemical_compound
Colloid and Surface Chemistry
chemistry
Polymerization
0210 nano-technology
Subjects
Details
- ISSN :
- 15205126 and 00027863
- Volume :
- 138
- Database :
- OpenAIRE
- Journal :
- Journal of the American Chemical Society
- Accession number :
- edsair.doi.dedup.....60c6dc977a337582b2dc64af17448da6
- Full Text :
- https://doi.org/10.1021/jacs.6b06237