Stereoselective Copolymerization of Butadiene and Functionalized 1,3-Dienes

Publikationstyp: Zeitschriftenartikel
Publikationsstatus: Published
Autor/innen: Leicht, Hannes; Göttker-Schnetmann, Inigo; Mecking, Stefan
Erscheinungsjahr: 2016
Erschienen in: ACS Macro Letters ; 5 (2016), 6. - S. 777-780. - ISSN 2161-1653. - eISSN 2161-1653
DOI (zitierfähiger Link): https://dx.doi.org/10.1021/acsmacrolett.6b00321
Zusammenfassung:
[(Mesitylene)nickel(allyl)+][BArF4–] (Ni-1) catalyzes the 1,4-cis selective copolymerization of isoprene and 1,3-butadiene with 15 (RO)3Si-, R2N-, RSO2-, RSO2NH-, and (RO)2B-functionalized 1,3-dienes. Incorporation of the functionalized 1,3-diene occurs very efficiently with high comonomer conversions, as observed, for example, for copolymerizations of 1,3-butadiene with (EtO)3Si(CH2)3C(═CH2)CH═CH2 (1), PhS(O)2(CH2)3C(═CH2)–CH═CH2 (7), or (pinB)C(═CH2)C(CH3)═CH2 (15), while copolymerization rates vary from strongly to slightly decreased when compared to butadiene homopolymerizations.
Fachgebiet (DDC): 540 Chemie
Universitätsbibliographie: Ja

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LEICHT, Hannes, Inigo GÖTTKER-SCHNETMANN, Stefan MECKING, 2016. Stereoselective Copolymerization of Butadiene and Functionalized 1,3-Dienes. In: ACS Macro Letters. 5(6), pp. 777-780. ISSN 2161-1653. eISSN 2161-1653. Available under: doi: 10.1021/acsmacrolett.6b00321

@article{Leicht2016-06-21Stere-34765, title={Stereoselective Copolymerization of Butadiene and Functionalized 1,3-Dienes}, year={2016}, doi={10.1021/acsmacrolett.6b00321}, number={6}, volume={5}, issn={2161-1653}, journal={ACS Macro Letters}, pages={777--780}, author={Leicht, Hannes and Göttker-Schnetmann, Inigo and Mecking, Stefan} }

Göttker-Schnetmann, Inigo Stereoselective Copolymerization of Butadiene and Functionalized 1,3-Dienes Leicht, Hannes Leicht, Hannes Mecking, Stefan Mecking, Stefan 2016-07-13T08:41:32Z Göttker-Schnetmann, Inigo eng 2016-06-21 [(Mesitylene)nickel(allyl)<sup>+</sup>][BAr<sup>F</sup><sub>4</sub>–] (Ni-1) catalyzes the 1,4-cis selective copolymerization of isoprene and 1,3-butadiene with 15 (RO)<sub>3</sub>Si-, R<sub>2</sub>N-, RSO<sub>2</sub>-, RSO2NH-, and (RO)<sub>2</sub>B-functionalized 1,3-dienes. Incorporation of the functionalized 1,3-diene occurs very efficiently with high comonomer conversions, as observed, for example, for copolymerizations of 1,3-butadiene with (EtO)<sub>3</sub>Si(CH<sub>2</sub>)<sub>3</sub>C(═CH2)CH═CH<sub>2</sub> (1), PhS(O)<sub>2</sub>(CH<sub>2</sub>)<sub>3</sub>C(═CH<sub>2</sub>)–CH═CH<sub>2</sub> (7), or (pinB)C(═CH<sub>2</sub>)C(CH<sub>3</sub>)═CH<sub>2</sub> (15), while copolymerization rates vary from strongly to slightly decreased when compared to butadiene homopolymerizations. 2016-07-13T08:41:32Z

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