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Lewis acidic organoboron polymers
- Source :
- Macromolecular Symposia. 196:337-345
- Publication Year :
- 2003
- Publisher :
- Wiley, 2003.
-
Abstract
- We have developed a highly efficient new method for the introduction of Lewis acidic boron centers into the side chains of organic polymers. Our methodology involves three steps: (i) the controlled polymerization of a functional monomer, (ii) the exchange of the functional group for Lewis acidic boron centers, and (iii) the fine-tuning of the Lewis acidity of the individual centers through substituent exchange reactions with nucleophiles. This approach gives access to a family of new well-defined organoboron polymers including moderately Lewis acidic poly(arylboronates) and the first examples of highly Lewis acidic fluorinated triarylborane polymers.
- Subjects :
- Polymers and Plastics
Organic Chemistry
Radical polymerization
Substituent
chemistry.chemical_element
Condensed Matter Physics
chemistry.chemical_compound
chemistry
Nucleophile
Polymerization
Functional group
Polymer chemistry
Materials Chemistry
Side chain
Organic chemistry
Lewis acids and bases
Boron
Subjects
Details
- ISSN :
- 15213900 and 10221360
- Volume :
- 196
- Database :
- OpenAIRE
- Journal :
- Macromolecular Symposia
- Accession number :
- edsair.doi...........648104543ff7e61512593d9276f8405a
- Full Text :
- https://doi.org/10.1002/masy.200390172