The limits of precision monomer placement in chain growth polymerization
Identifieur interne : 001566 ( Main/Exploration ); précédent : 001565; suivant : 001567The limits of precision monomer placement in chain growth polymerization
Auteurs : Guillaume Gody [Royaume-Uni] ; Per B. Zetterlund [Australie] ; Sébastien Perrier [Royaume-Uni, Australie] ; Simon Harrisson [France]Source :
- Nature Communications [ 2041-1723 ] ; 2016.
Abstract
Precise control over the location of monomers in a polymer chain has been described as the ‘Holy Grail' of polymer synthesis. Controlled chain growth polymerization techniques have brought this goal closer, allowing the preparation of multiblock copolymers with ordered sequences of functional monomers. Such structures have promising applications ranging from medicine to materials engineering. Here we show, however, that the statistical nature of chain growth polymerization places strong limits on the control that can be obtained. We demonstrate that monomer locations are distributed according to surprisingly simple laws related to the Poisson or beta distributions. The degree of control is quantified in terms of the yield of the desired structure and the standard deviation of the appropriate distribution, allowing comparison between different synthetic techniques. This analysis establishes experimental requirements for the design of polymeric chains with controlled sequence of functionalities, which balance precise control of structure with simplicity of synthesis.
Url:
DOI: 10.1038/ncomms10514
PubMed: 26830125
PubMed Central: 4740409
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>Precise control over the location of monomers in a polymer chain has been described as the ‘Holy Grail' of polymer synthesis. Controlled chain growth polymerization techniques have brought this goal closer, allowing the preparation of multiblock copolymers with ordered sequences of functional monomers. Such structures have promising applications ranging from medicine to materials engineering. Here we show, however, that the statistical nature of chain growth polymerization places strong limits on the control that can be obtained. We demonstrate that monomer locations are distributed according to surprisingly simple laws related to the Poisson or beta distributions. The degree of control is quantified in terms of the yield of the desired structure and the standard deviation of the appropriate distribution, allowing comparison between different synthetic techniques. This analysis establishes experimental requirements for the design of polymeric chains with controlled sequence of functionalities, which balance precise control of structure with simplicity of synthesis.</p>
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<biblStruct><analytic><author><name sortKey="Ferguson, C J" uniqKey="Ferguson C">C. J. Ferguson</name>
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<affiliations><list><country><li>Australie</li>
<li>France</li>
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<tree><country name="Royaume-Uni"><noRegion><name sortKey="Gody, Guillaume" sort="Gody, Guillaume" uniqKey="Gody G" first="Guillaume" last="Gody">Guillaume Gody</name>
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<name sortKey="Perrier, Sebastien" sort="Perrier, Sebastien" uniqKey="Perrier S" first="Sébastien" last="Perrier">Sébastien Perrier</name>
</country>
<country name="Australie"><noRegion><name sortKey="Zetterlund, Per B" sort="Zetterlund, Per B" uniqKey="Zetterlund P" first="Per B." last="Zetterlund">Per B. Zetterlund</name>
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<name sortKey="Perrier, Sebastien" sort="Perrier, Sebastien" uniqKey="Perrier S" first="Sébastien" last="Perrier">Sébastien Perrier</name>
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<country name="France"><noRegion><name sortKey="Harrisson, Simon" sort="Harrisson, Simon" uniqKey="Harrisson S" first="Simon" last="Harrisson">Simon Harrisson</name>
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