Iron-catalysed ring-opening metathesis polymerization of olefins and mechanistic studies

Satoshi Takebayashi; Mark A. Iron; Moran Feller; Orestes Rivada-Wheelaghan; Gregory Leitus; Yael Diskin-Posner; Linda J.W. Shimon; Liat Avram; Raanan Carmieli; Sharon G. Wolf; Ilit Cohen-Ofri; Rajashekharayya A. Sanguramath; Roy Shenhar; Moris Eisen; David Milstein

doi:10.1038/s41929-022-00793-4

Iron-catalysed ring-opening metathesis polymerization of olefins and mechanistic studies

Satoshi Takebayashi^*, Mark A. Iron, Moran Feller, Orestes Rivada-Wheelaghan, Gregory Leitus, Yael Diskin-Posner, Linda J.W. Shimon, Liat Avram, Raanan Carmieli, Sharon G. Wolf, Ilit Cohen-Ofri, Rajashekharayya A. Sanguramath, Roy Shenhar, Moris Eisen, David Milstein^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

17 Scopus citations

Abstract

The olefin metathesis reaction is among the most widely applicable catalytic reactions for carbon–carbon double bond formation. Currently, Mo– and Ru–carbene catalysts are the most common choices for this reaction. It has been suggested that an iron-based catalyst would be a desirable economical and biocompatible substitute of the Ru catalysts; however, practical solutions in this regard are still lacking. Here, we report the discovery and mechanistic studies of three-coordinate iron(II) catalysts for ring-opening metathesis polymerization of olefins. Remarkably, their reactivity enabled the formation of polynorbornene with stereoregularity and high molecular weight (>10⁷ g mol^–1). The polymerization in the presence of styrene revealed cross metathesis reactivity with iron catalysts. Mechanistic studies suggest the possible role of metal–ligand cooperation in formation of the productive catalyst. This work opens the door to the development of iron complexes that can be economical and biocompatible catalysts for olefin metathesis reactions. [Figure not available: see fulltext.]

Original language	English
Pages (from-to)	494-502
Number of pages	9
Journal	Nature Catalysis
Volume	5
Issue number	6
DOIs	https://doi.org/10.1038/s41929-022-00793-4
State	Published - Jun 2022
Externally published	Yes

Access to Document

10.1038/s41929-022-00793-4

Cite this

Takebayashi, S., Iron, M. A., Feller, M., Rivada-Wheelaghan, O., Leitus, G., Diskin-Posner, Y., Shimon, L. J. W., Avram, L., Carmieli, R., Wolf, S. G., Cohen-Ofri, I., Sanguramath, R. A., Shenhar, R., Eisen, M., & Milstein, D. (2022). Iron-catalysed ring-opening metathesis polymerization of olefins and mechanistic studies. Nature Catalysis, 5(6), 494-502. https://doi.org/10.1038/s41929-022-00793-4

@article{1afb51d3cb314c038182362669420892,

title = "Iron-catalysed ring-opening metathesis polymerization of olefins and mechanistic studies",

abstract = "The olefin metathesis reaction is among the most widely applicable catalytic reactions for carbon–carbon double bond formation. Currently, Mo– and Ru–carbene catalysts are the most common choices for this reaction. It has been suggested that an iron-based catalyst would be a desirable economical and biocompatible substitute of the Ru catalysts; however, practical solutions in this regard are still lacking. Here, we report the discovery and mechanistic studies of three-coordinate iron(II) catalysts for ring-opening metathesis polymerization of olefins. Remarkably, their reactivity enabled the formation of polynorbornene with stereoregularity and high molecular weight (>107 g mol–1). The polymerization in the presence of styrene revealed cross metathesis reactivity with iron catalysts. Mechanistic studies suggest the possible role of metal–ligand cooperation in formation of the productive catalyst. This work opens the door to the development of iron complexes that can be economical and biocompatible catalysts for olefin metathesis reactions. [Figure not available: see fulltext.]",

author = "Satoshi Takebayashi and Iron, {Mark A.} and Moran Feller and Orestes Rivada-Wheelaghan and Gregory Leitus and Yael Diskin-Posner and Shimon, {Linda J.W.} and Liat Avram and Raanan Carmieli and Wolf, {Sharon G.} and Ilit Cohen-Ofri and Sanguramath, {Rajashekharayya A.} and Roy Shenhar and Moris Eisen and David Milstein",

note = "Publisher Copyright: {\textcopyright} 2022, The Author(s), under exclusive licence to Springer Nature Limited.",

year = "2022",

month = jun,

doi = "10.1038/s41929-022-00793-4",

language = "英语",

volume = "5",

pages = "494--502",

journal = "Nature Catalysis",

issn = "2520-1158",

publisher = "Nature Publishing Group",

number = "6",

}

Takebayashi, S, Iron, MA, Feller, M, Rivada-Wheelaghan, O, Leitus, G, Diskin-Posner, Y, Shimon, LJW, Avram, L, Carmieli, R, Wolf, SG, Cohen-Ofri, I, Sanguramath, RA, Shenhar, R, Eisen, M & Milstein, D 2022, 'Iron-catalysed ring-opening metathesis polymerization of olefins and mechanistic studies', Nature Catalysis, vol. 5, no. 6, pp. 494-502. https://doi.org/10.1038/s41929-022-00793-4

TY - JOUR

T1 - Iron-catalysed ring-opening metathesis polymerization of olefins and mechanistic studies

AU - Takebayashi, Satoshi

AU - Iron, Mark A.

AU - Feller, Moran

AU - Rivada-Wheelaghan, Orestes

AU - Leitus, Gregory

AU - Diskin-Posner, Yael

AU - Shimon, Linda J.W.

AU - Avram, Liat

AU - Carmieli, Raanan

AU - Wolf, Sharon G.

AU - Cohen-Ofri, Ilit

AU - Sanguramath, Rajashekharayya A.

AU - Shenhar, Roy

AU - Eisen, Moris

AU - Milstein, David

PY - 2022/6

Y1 - 2022/6

N2 - The olefin metathesis reaction is among the most widely applicable catalytic reactions for carbon–carbon double bond formation. Currently, Mo– and Ru–carbene catalysts are the most common choices for this reaction. It has been suggested that an iron-based catalyst would be a desirable economical and biocompatible substitute of the Ru catalysts; however, practical solutions in this regard are still lacking. Here, we report the discovery and mechanistic studies of three-coordinate iron(II) catalysts for ring-opening metathesis polymerization of olefins. Remarkably, their reactivity enabled the formation of polynorbornene with stereoregularity and high molecular weight (>107 g mol–1). The polymerization in the presence of styrene revealed cross metathesis reactivity with iron catalysts. Mechanistic studies suggest the possible role of metal–ligand cooperation in formation of the productive catalyst. This work opens the door to the development of iron complexes that can be economical and biocompatible catalysts for olefin metathesis reactions. [Figure not available: see fulltext.]

AB - The olefin metathesis reaction is among the most widely applicable catalytic reactions for carbon–carbon double bond formation. Currently, Mo– and Ru–carbene catalysts are the most common choices for this reaction. It has been suggested that an iron-based catalyst would be a desirable economical and biocompatible substitute of the Ru catalysts; however, practical solutions in this regard are still lacking. Here, we report the discovery and mechanistic studies of three-coordinate iron(II) catalysts for ring-opening metathesis polymerization of olefins. Remarkably, their reactivity enabled the formation of polynorbornene with stereoregularity and high molecular weight (>107 g mol–1). The polymerization in the presence of styrene revealed cross metathesis reactivity with iron catalysts. Mechanistic studies suggest the possible role of metal–ligand cooperation in formation of the productive catalyst. This work opens the door to the development of iron complexes that can be economical and biocompatible catalysts for olefin metathesis reactions. [Figure not available: see fulltext.]

UR - http://www.scopus.com/inward/record.url?scp=85131333642&partnerID=8YFLogxK

U2 - 10.1038/s41929-022-00793-4

DO - 10.1038/s41929-022-00793-4

M3 - 文章

AN - SCOPUS:85131333642

SN - 2520-1158

VL - 5

SP - 494

EP - 502

JO - Nature Catalysis

JF - Nature Catalysis

IS - 6

ER -

Iron-catalysed ring-opening metathesis polymerization of olefins and mechanistic studies

Abstract

Access to Document

Other files and links

Fingerprint

Cite this