Heterotelechelic and In-Chain Polar Functionalized Stereoregular Poly(dienes)


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LEICHT, Hannes, Julia BAUER, Inigo GÖTTKER-SCHNETMANN, Stefan MECKING, 2018. Heterotelechelic and In-Chain Polar Functionalized Stereoregular Poly(dienes). In: Macromolecules. 51(3), pp. 763-770. ISSN 0024-9297. eISSN 1520-5835. Available under: doi: 10.1021/acs.macromol.7b02006

@article{Leicht2018-02-13Heter-41749, title={Heterotelechelic and In-Chain Polar Functionalized Stereoregular Poly(dienes)}, year={2018}, doi={10.1021/acs.macromol.7b02006}, number={3}, volume={51}, issn={0024-9297}, journal={Macromolecules}, pages={763--770}, author={Leicht, Hannes and Bauer, Julia and Göttker-Schnetmann, Inigo and Mecking, Stefan} }

2018-03-13T08:13:58Z Bauer, Julia Leicht, Hannes Bauer, Julia Heterotelechelic and In-Chain Polar Functionalized Stereoregular Poly(dienes) Stereoregular trans-poly(dienes) with three different types of functional groups were synthesized by insertion polymerization. The functional groups are located simultaneously in the polymer backbone and at both chain ends, yielding heterotelechelic and in-chain functionalized polymers. A combination of three compatible functionalization methods allows for the syntheses of these particular polymers. Nd(BH<sub>4</sub>)<sub>3</sub>·(THF)<sub>3 </sub>catalyzes, after activation with MgR<sub>2</sub>, the direct copolymerization of 1,3-butadiene or isoprene with polar functionalized dienes, thus enabling the functionalization of the polymer’s backbone. The use of functionalized organo-Mg compounds, e.g., (PhS-C<sub>5</sub>H<sub>10</sub>)<sub>2</sub>Mg, for the activation of Nd(BH<sub>4</sub>)<sub>3</sub>·(THF)<sub>3</sub> enables the functionalization of the initiating chain-end and quenching of the polymerization with suitable reagents; e.g., Si(OEt)<sub>4</sub> allows for the functionalization of the terminating chain-end. Mecking, Stefan 2018-02-13 Mecking, Stefan Göttker-Schnetmann, Inigo eng Leicht, Hannes 2018-03-13T08:13:58Z Göttker-Schnetmann, Inigo

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