Degradation of natural rubber via cross-metathesis with electron-deficient enes

Publikation: KonferenzbeitragPosterForschung

Abstract

Due to the high degree of substitution at its double bond, cross-metathesis of natural rubber (cis-1,4-polyisoprene, NR) with other enes is known to be a challenging task as the accessibility of the double bond is limited and self-metathesis of the other reaction partner prevails [1]. Cross metathesis of NR has been accomplished with several substrates [2] among them acrylates. In this case the degradation lead to semi-telechelic oligomers bearing an electron deficient enoate end group, which has been exploited for further functionalization [3] (see Figure below). However, cross metathesis with acrylates suffers from an additional deactivation pathway of the intermediate methylidene species by deprotonation by a strong base formed in the phospha-Michael addition of dissociated phosphine ligands with acrylates [4]. Consequently typically phosphine free catalysts are used for this and similar transformations.
Herein we present a screening of different catalysts and electron-deficient cross-metathesis partners for the degradation of NR and NR-waste. Emphasis is laid on testing cross-metathesis partners not producing a methylidene species in the catalytic cycle and finding conditions for allowing a further reduction of catalyst loadings for this reaction.
[1] A. K. Chatterjee, T.-L. Choi, D. P. Sanders, R. H. Grubbs, J. Am. Chem. Soc., 2003, 125, 11360-11370.
[2] S. Leimgruber, G. Trimmel, Monatsh. Chem., 2015, 146, 1081-1097.
[3] M. Abbas, M. Neubauer, C. Slugovc, Polym. Chem., 2018, 9, 1763-1766.
[4] G. A. Bailey, D. E. Fogg, J. Am. Chem. Soc., 2015, 137, 7318-7321.
Originalspracheenglisch
SeitenP54
PublikationsstatusVeröffentlicht - 30 Jun 2019
Veranstaltung23rd International Symposium on Olefin Metathesis and Related Chemistry - CASA CONVALESCÈNCIA Sant Antoni Mª Claret, 171, Barcelona, Spanien
Dauer: 30 Jun 20193 Jul 2019
https://www.isom2019bcn.com/

Konferenz

Konferenz23rd International Symposium on Olefin Metathesis and Related Chemistry
KurztitelISOM 23
LandSpanien
OrtBarcelona
Zeitraum30/06/193/07/19
Internetadresse

Fields of Expertise

  • Advanced Materials Science

Dies zitieren

Schallert, V., & Slugovc, C. (2019). Degradation of natural rubber via cross-metathesis with electron-deficient enes. P54. Postersitzung präsentiert bei 23rd International Symposium on Olefin Metathesis and Related Chemistry, Barcelona, Spanien.

Degradation of natural rubber via cross-metathesis with electron-deficient enes. / Schallert, Viktor; Slugovc, Christian.

2019. P54 Postersitzung präsentiert bei 23rd International Symposium on Olefin Metathesis and Related Chemistry, Barcelona, Spanien.

Publikation: KonferenzbeitragPosterForschung

Schallert, V & Slugovc, C 2019, 'Degradation of natural rubber via cross-metathesis with electron-deficient enes' 23rd International Symposium on Olefin Metathesis and Related Chemistry, Barcelona, Spanien, 30/06/19 - 3/07/19, S. P54.
Schallert V, Slugovc C. Degradation of natural rubber via cross-metathesis with electron-deficient enes. 2019. Postersitzung präsentiert bei 23rd International Symposium on Olefin Metathesis and Related Chemistry, Barcelona, Spanien.
Schallert, Viktor ; Slugovc, Christian. / Degradation of natural rubber via cross-metathesis with electron-deficient enes. Postersitzung präsentiert bei 23rd International Symposium on Olefin Metathesis and Related Chemistry, Barcelona, Spanien.
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N2 - Due to the high degree of substitution at its double bond, cross-metathesis of natural rubber (cis-1,4-polyisoprene, NR) with other enes is known to be a challenging task as the accessibility of the double bond is limited and self-metathesis of the other reaction partner prevails [1]. Cross metathesis of NR has been accomplished with several substrates [2] among them acrylates. In this case the degradation lead to semi-telechelic oligomers bearing an electron deficient enoate end group, which has been exploited for further functionalization [3] (see Figure below). However, cross metathesis with acrylates suffers from an additional deactivation pathway of the intermediate methylidene species by deprotonation by a strong base formed in the phospha-Michael addition of dissociated phosphine ligands with acrylates [4]. Consequently typically phosphine free catalysts are used for this and similar transformations.Herein we present a screening of different catalysts and electron-deficient cross-metathesis partners for the degradation of NR and NR-waste. Emphasis is laid on testing cross-metathesis partners not producing a methylidene species in the catalytic cycle and finding conditions for allowing a further reduction of catalyst loadings for this reaction. [1] A. K. Chatterjee, T.-L. Choi, D. P. Sanders, R. H. Grubbs, J. Am. Chem. Soc., 2003, 125, 11360-11370.[2] S. Leimgruber, G. Trimmel, Monatsh. Chem., 2015, 146, 1081-1097.[3] M. Abbas, M. Neubauer, C. Slugovc, Polym. Chem., 2018, 9, 1763-1766.[4] G. A. Bailey, D. E. Fogg, J. Am. Chem. Soc., 2015, 137, 7318-7321.

AB - Due to the high degree of substitution at its double bond, cross-metathesis of natural rubber (cis-1,4-polyisoprene, NR) with other enes is known to be a challenging task as the accessibility of the double bond is limited and self-metathesis of the other reaction partner prevails [1]. Cross metathesis of NR has been accomplished with several substrates [2] among them acrylates. In this case the degradation lead to semi-telechelic oligomers bearing an electron deficient enoate end group, which has been exploited for further functionalization [3] (see Figure below). However, cross metathesis with acrylates suffers from an additional deactivation pathway of the intermediate methylidene species by deprotonation by a strong base formed in the phospha-Michael addition of dissociated phosphine ligands with acrylates [4]. Consequently typically phosphine free catalysts are used for this and similar transformations.Herein we present a screening of different catalysts and electron-deficient cross-metathesis partners for the degradation of NR and NR-waste. Emphasis is laid on testing cross-metathesis partners not producing a methylidene species in the catalytic cycle and finding conditions for allowing a further reduction of catalyst loadings for this reaction. [1] A. K. Chatterjee, T.-L. Choi, D. P. Sanders, R. H. Grubbs, J. Am. Chem. Soc., 2003, 125, 11360-11370.[2] S. Leimgruber, G. Trimmel, Monatsh. Chem., 2015, 146, 1081-1097.[3] M. Abbas, M. Neubauer, C. Slugovc, Polym. Chem., 2018, 9, 1763-1766.[4] G. A. Bailey, D. E. Fogg, J. Am. Chem. Soc., 2015, 137, 7318-7321.

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