Catalyst speciation during ansa-Zirconocene-catalyzed polymerization of 1-Hexene Studied by UV-vis spectroscopy-formation and partial re-activation of Zr-Allyl intermediates

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Catalyst speciation during ansa-Zirconocene-catalyzed polymerization of 1-Hexene Studied by UV-vis spectroscopy-formation and partial re-activation of Zr-Allyl intermediates. / Panchenko, Valentina N.; Babushkin, Dmitrii E.; Bercaw, John E. et al.

In: Polymers, Vol. 11, No. 6, 936, 29.05.2019.

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

BibTeX

@article{5d214c1c49784fbaae46a1ebc2bd75ff,

title = "Catalyst speciation during ansa-Zirconocene-catalyzed polymerization of 1-Hexene Studied by UV-vis spectroscopy-formation and partial re-activation of Zr-Allyl intermediates",

abstract = "Catalyst speciation during polymerization of 1-hexene in benzene or toluene solutions of the catalyst precursor SBIZr(μ-Me)2AlMe2+ B(C6F5)4- (SBI = rac-dimethylsilyl-bis(1-indenyl)) at 23 °C is studied by following the accompanying UV-vis-spectral changes. These indicate that the onset of polymerization catalysis is associated with the concurrent formation of two distinct zirconocene species. One of these is proposed to consist of SBIZr-σ-polyhexenyl cations arising from SBIZr-Me+ (formed from SBIZr(μ-Me)2AlMe2+ by release of AlMe3) by repeated olefin insertions, while the other one is proposed to consist of SBIZr-η3-allyl cations of composition SBIZr-η3-(1-R-C3H4)+ (R = n-propyl), formed by σ-bond metathesis between SBIZr-Me+ and 1-hexene under release of methane. At later reaction stages, all zirconocene-σ-polymeryl cations appear to decay to yet another SBIZr-allyl species, i.e., to cations of the type SBIZr- η3-(x-R-(3-x)-pol-C3H3)+ (pol = i-polyhexenyl, x = 1 or 2). Renewed addition of excess 1-hexene is proposed to convert these sterically encumbered Zr-allyl cations back to catalytically active SBIZr-σ-polymeryl cations within a few seconds, presumably by initial 1-hexene insertion into the η1- isomer, followed by repeated additional insertions, while the initially formed, less crowded allyl cations, SBIZr-η3-(1-R-C3H4)+ appear to remain unchanged. Implications of these results with regard to the kinetics of zirconocene-catalyzed olefin polymerization are discussed.",

keywords = "Catalyst speciation, De-activation, Polymerization catalysis, Re-activation, UV-vis spectroscopy, Zirconocene-allyl cations, de-activation, ALKENE POLYMERIZATION, ION-PAIRS, METALLOCENE CATALYSTS, COMPLEXES, OLEFIN POLYMERIZATION, PROPYLENE POLYMERIZATION, catalyst speciation, BOND METATHESIS, polymerization catalysis, ROTATION AMBIGUITIES, MCR-ALS, PROPENE POLYMERIZATION, re-activation, zirconocene-allyl cations",

author = "Panchenko, {Valentina N.} and Babushkin, {Dmitrii E.} and Bercaw, {John E.} and Brintzinger, {Hans H.}",

note = "Publisher Copyright: {\textcopyright} 2019 by the authors.",

year = "2019",

month = may,

day = "29",

doi = "10.3390/polym11060936",

language = "English",

volume = "11",

journal = "Polymers",

issn = "2073-4360",

publisher = "MDPI AG",

number = "6",

}

RIS

TY - JOUR

T1 - Catalyst speciation during ansa-Zirconocene-catalyzed polymerization of 1-Hexene Studied by UV-vis spectroscopy-formation and partial re-activation of Zr-Allyl intermediates

AU - Panchenko, Valentina N.

AU - Babushkin, Dmitrii E.

AU - Bercaw, John E.

AU - Brintzinger, Hans H.

PY - 2019/5/29

Y1 - 2019/5/29

N2 - Catalyst speciation during polymerization of 1-hexene in benzene or toluene solutions of the catalyst precursor SBIZr(μ-Me)2AlMe2+ B(C6F5)4- (SBI = rac-dimethylsilyl-bis(1-indenyl)) at 23 °C is studied by following the accompanying UV-vis-spectral changes. These indicate that the onset of polymerization catalysis is associated with the concurrent formation of two distinct zirconocene species. One of these is proposed to consist of SBIZr-σ-polyhexenyl cations arising from SBIZr-Me+ (formed from SBIZr(μ-Me)2AlMe2+ by release of AlMe3) by repeated olefin insertions, while the other one is proposed to consist of SBIZr-η3-allyl cations of composition SBIZr-η3-(1-R-C3H4)+ (R = n-propyl), formed by σ-bond metathesis between SBIZr-Me+ and 1-hexene under release of methane. At later reaction stages, all zirconocene-σ-polymeryl cations appear to decay to yet another SBIZr-allyl species, i.e., to cations of the type SBIZr- η3-(x-R-(3-x)-pol-C3H3)+ (pol = i-polyhexenyl, x = 1 or 2). Renewed addition of excess 1-hexene is proposed to convert these sterically encumbered Zr-allyl cations back to catalytically active SBIZr-σ-polymeryl cations within a few seconds, presumably by initial 1-hexene insertion into the η1- isomer, followed by repeated additional insertions, while the initially formed, less crowded allyl cations, SBIZr-η3-(1-R-C3H4)+ appear to remain unchanged. Implications of these results with regard to the kinetics of zirconocene-catalyzed olefin polymerization are discussed.

AB - Catalyst speciation during polymerization of 1-hexene in benzene or toluene solutions of the catalyst precursor SBIZr(μ-Me)2AlMe2+ B(C6F5)4- (SBI = rac-dimethylsilyl-bis(1-indenyl)) at 23 °C is studied by following the accompanying UV-vis-spectral changes. These indicate that the onset of polymerization catalysis is associated with the concurrent formation of two distinct zirconocene species. One of these is proposed to consist of SBIZr-σ-polyhexenyl cations arising from SBIZr-Me+ (formed from SBIZr(μ-Me)2AlMe2+ by release of AlMe3) by repeated olefin insertions, while the other one is proposed to consist of SBIZr-η3-allyl cations of composition SBIZr-η3-(1-R-C3H4)+ (R = n-propyl), formed by σ-bond metathesis between SBIZr-Me+ and 1-hexene under release of methane. At later reaction stages, all zirconocene-σ-polymeryl cations appear to decay to yet another SBIZr-allyl species, i.e., to cations of the type SBIZr- η3-(x-R-(3-x)-pol-C3H3)+ (pol = i-polyhexenyl, x = 1 or 2). Renewed addition of excess 1-hexene is proposed to convert these sterically encumbered Zr-allyl cations back to catalytically active SBIZr-σ-polymeryl cations within a few seconds, presumably by initial 1-hexene insertion into the η1- isomer, followed by repeated additional insertions, while the initially formed, less crowded allyl cations, SBIZr-η3-(1-R-C3H4)+ appear to remain unchanged. Implications of these results with regard to the kinetics of zirconocene-catalyzed olefin polymerization are discussed.

KW - Catalyst speciation

KW - De-activation

KW - Polymerization catalysis

KW - Re-activation

KW - UV-vis spectroscopy

KW - Zirconocene-allyl cations

KW - de-activation

KW - ALKENE POLYMERIZATION

KW - ION-PAIRS

KW - METALLOCENE CATALYSTS

KW - COMPLEXES

KW - OLEFIN POLYMERIZATION

KW - PROPYLENE POLYMERIZATION

KW - catalyst speciation

KW - BOND METATHESIS

KW - polymerization catalysis

KW - ROTATION AMBIGUITIES

KW - MCR-ALS

KW - PROPENE POLYMERIZATION

KW - re-activation

KW - zirconocene-allyl cations

UR - http://www.scopus.com/inward/record.url?scp=85067336842&partnerID=8YFLogxK

U2 - 10.3390/polym11060936

DO - 10.3390/polym11060936

M3 - Article

C2 - 31146475

AN - SCOPUS:85067336842

VL - 11

JO - Polymers

JF - Polymers

SN - 2073-4360

IS - 6

M1 - 936

ER -

ID: 20588462