1,2-Polybutadiene Latices by Catalytic Polymerization in Aqueous Emulsion

dc.contributor.authorMonteil, Vincentdeu
dc.contributor.authorBastero, Amaiadeu
dc.contributor.authorMecking, Stefan
dc.date.accessioned2011-03-24T18:14:23Zdeu
dc.date.issued2005deu
dc.description.abstractCatalytic aqueous polymerization of butadiene by the cobalt catalyst system [Co(C8H13)-(C4H6)]/CS2 affords colloidally stable latices of highly crystalline syndiotactic 1,2-polybutadiene (Tm = 190 °C, ∆Hc = 60 J/g, Mw ~ 100000 g/mol, 97% 1,2, 3% 1,4-cis). Catalyst modification with reagents containing electrophilic carbon atoms (e.g., aromatic formamides) strongly decreases polymer crystallinity (Tm = 60-100 °C, ∆Hc = 11 J/g, Mw ~ 8 X 10000 g/mol for 85% 1,2). Latices of typically 150-200 nm particles are prepared. During polymerization affording low crystalline polymers the number of particles stays constant. Microstructures were analyzed by 13C NMR of hydrogenated polymers. In all polymers the 1,4-units are largely isolated. Crystallinity decrease results from an increase of 1,4-insertion frequency and the resulting decrease of 1,2-block length. Considerations on the nature of the active species are discussed. Copolymerization of butadiene with isoprene by [Co(C8H13)(C4H6)]/CS2 affords low crystalline copolymers; styrene is not incorporated as a comonomer.eng
dc.description.versionpublished
dc.format.mimetypeapplication/pdfdeu
dc.identifier.citationFirst publ. in: Macromolecules ; 38 (2005), 13. - S. 5393-5399deu
dc.identifier.doi10.1021/ma050621i
dc.identifier.ppn287028062deu
dc.identifier.urihttp://kops.uni-konstanz.de/handle/123456789/9783
dc.language.isoengdeu
dc.legacy.dateIssued2008deu
dc.rightsAttribution-NonCommercial-NoDerivs 2.0 Generic
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/
dc.subject.ddc540deu
dc.title1,2-Polybutadiene Latices by Catalytic Polymerization in Aqueous Emulsioneng
dc.typeJOURNAL_ARTICLEdeu
dspace.entity.typePublication
kops.citation.bibtex
@article{Monteil200512Pol-9783,
  year={2005},
  doi={10.1021/ma050621i},
  title={1,2-Polybutadiene Latices by Catalytic Polymerization in Aqueous Emulsion},
  number={13},
  volume={38},
  issn={0024-9297},
  journal={Macromolecules},
  pages={5393--5399},
  author={Monteil, Vincent and Bastero, Amaia and Mecking, Stefan}
}
kops.citation.iso690MONTEIL, Vincent, Amaia BASTERO, Stefan MECKING, 2005. 1,2-Polybutadiene Latices by Catalytic Polymerization in Aqueous Emulsion. In: Macromolecules. 2005, 38(13), pp. 5393-5399. ISSN 0024-9297. eISSN 1520-5835. Available under: doi: 10.1021/ma050621ideu
kops.citation.iso690MONTEIL, Vincent, Amaia BASTERO, Stefan MECKING, 2005. 1,2-Polybutadiene Latices by Catalytic Polymerization in Aqueous Emulsion. In: Macromolecules. 2005, 38(13), pp. 5393-5399. ISSN 0024-9297. eISSN 1520-5835. Available under: doi: 10.1021/ma050621ieng
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    <dcterms:abstract xml:lang="eng">Catalytic aqueous polymerization of butadiene by the cobalt catalyst system [Co(C8H13)-(C4H6)]/CS2 affords colloidally stable latices of highly crystalline syndiotactic 1,2-polybutadiene (Tm = 190 °C, ∆Hc = 60 J/g, Mw ~ 100000 g/mol, 97% 1,2, 3% 1,4-cis). Catalyst modification with reagents containing electrophilic carbon atoms (e.g., aromatic formamides) strongly decreases polymer crystallinity (Tm = 60-100 °C, ∆Hc = 11 J/g, Mw ~ 8 X 10000 g/mol for 85% 1,2). Latices of typically 150-200 nm particles are prepared. During polymerization affording low crystalline polymers the number of particles stays constant. Microstructures were analyzed by 13C NMR of hydrogenated polymers. In all polymers the 1,4-units are largely isolated. Crystallinity decrease results from an increase of 1,4-insertion frequency and the resulting decrease of 1,2-block length. Considerations on the nature of the active species are discussed. Copolymerization of butadiene with isoprene by [Co(C8H13)(C4H6)]/CS2 affords low crystalline copolymers; styrene is not incorporated as a comonomer.</dcterms:abstract>
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kops.sourcefieldMacromolecules. 2005, <b>38</b>(13), pp. 5393-5399. ISSN 0024-9297. eISSN 1520-5835. Available under: doi: 10.1021/ma050621ideu
kops.sourcefield.plainMacromolecules. 2005, 38(13), pp. 5393-5399. ISSN 0024-9297. eISSN 1520-5835. Available under: doi: 10.1021/ma050621ideu
kops.sourcefield.plainMacromolecules. 2005, 38(13), pp. 5393-5399. ISSN 0024-9297. eISSN 1520-5835. Available under: doi: 10.1021/ma050621ieng
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