Controlled copolymerization of the functional 5-membered lactone monomer, α-bromo-γ-butyrolactone, via selective organocatalysis. (22nd March 2016)
- Record Type:
- Journal Article
- Title:
- Controlled copolymerization of the functional 5-membered lactone monomer, α-bromo-γ-butyrolactone, via selective organocatalysis. (22nd March 2016)
- Main Title:
- Controlled copolymerization of the functional 5-membered lactone monomer, α-bromo-γ-butyrolactone, via selective organocatalysis
- Authors:
- Undin, Jenny
Olsén, Peter
Godfrey, Jamie
Odelius, Karin
Albertsson, Ann-Christine - Abstract:
- Abstract: The selective nature of organic catalysts has been exploited to synthesize copolymers of the functional monomer, α-bromo-γ-butyrolactone (αBrγBL), with trimethylene carbonate (TMC), 2-allyloxymethyl-2-ethyl-trimethylene carbonate (AOMEC) and ε-caprolactone (εCL) with excellent control. The high control is attributed to high selectivity and reactivity at ambient reaction temperatures, which suppresses the degree of side reactions (e.g., transesterification) that inherently plague this class of co-monomers. In particular, good results were obtained using diphenyl phosphate (DPP) as a catalyst, resulting in copolymers with low dispersities (ÐM ) (i.e., approximately 1.08) and number average molecular weights (Mn ) of approximately 20, 000 g/mol. The high control opened the possibility to construct more complex polymeric structures, exemplified via the synthesis of a multifunctional triblock copolymer composed of AOMEC as the center block, flanked with a statistical copolymer consisting of ɛCL and αBrγBL. The subsequent grafting of methyl acrylate (MA) via Cu(0)-mediated CRP on the copolymers resulted in graft copolymers with a final ÐM of less than 1.2. Graphical abstract: Highlights: Copolymerization of the functional 5-membered lactone monomer, α-bromo-γ-butyrolactone (αBrγBL), with TMC, AOMEC and εCL. Copolymers with low dispersities (ÐM) were obtained when using diphenyl phosphate (DPP) as a catalyst. Grafting of MA via Cu(0)-mediated CRP on the copolymersAbstract: The selective nature of organic catalysts has been exploited to synthesize copolymers of the functional monomer, α-bromo-γ-butyrolactone (αBrγBL), with trimethylene carbonate (TMC), 2-allyloxymethyl-2-ethyl-trimethylene carbonate (AOMEC) and ε-caprolactone (εCL) with excellent control. The high control is attributed to high selectivity and reactivity at ambient reaction temperatures, which suppresses the degree of side reactions (e.g., transesterification) that inherently plague this class of co-monomers. In particular, good results were obtained using diphenyl phosphate (DPP) as a catalyst, resulting in copolymers with low dispersities (ÐM ) (i.e., approximately 1.08) and number average molecular weights (Mn ) of approximately 20, 000 g/mol. The high control opened the possibility to construct more complex polymeric structures, exemplified via the synthesis of a multifunctional triblock copolymer composed of AOMEC as the center block, flanked with a statistical copolymer consisting of ɛCL and αBrγBL. The subsequent grafting of methyl acrylate (MA) via Cu(0)-mediated CRP on the copolymers resulted in graft copolymers with a final ÐM of less than 1.2. Graphical abstract: Highlights: Copolymerization of the functional 5-membered lactone monomer, α-bromo-γ-butyrolactone (αBrγBL), with TMC, AOMEC and εCL. Copolymers with low dispersities (ÐM) were obtained when using diphenyl phosphate (DPP) as a catalyst. Grafting of MA via Cu(0)-mediated CRP on the copolymers resulted in graft copolymers with a final ÐM of less than 1.2. … (more)
- Is Part Of:
- Polymer. Volume 87(2016)
- Journal:
- Polymer
- Issue:
- Volume 87(2016)
- Issue Display:
- Volume 87, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 87
- Issue:
- 2016
- Issue Sort Value:
- 2016-0087-2016-0000
- Page Start:
- 17
- Page End:
- 25
- Publication Date:
- 2016-03-22
- Subjects:
- α-Bromo-γ-butyrolactone (αBrγBL) -- Diphenyl phosphate (DPP) -- CRP
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00323861 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.polymer.2016.01.067 ↗
- Languages:
- English
- ISSNs:
- 0032-3861
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2502.xml