SYNTHESIS OF FUNCTIONAL POLYETHYLENE via COPOLYMERIZATION OF ETHYLENE AND SUBSTITUTED ALLENE USING BIS(β-ENAMINOKETONATO)TITANIUM CATALYSTS
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SYNTHESIS OF FUNCTIONAL POLYETHYLENE via COPOLYMERIZATION OF ETHYLENE AND SUBSTITUTED ALLENE USING BIS(β-ENAMINOKETONATO)TITANIUM CATALYSTS
Chinese Journal of Polymer ScienceVol. 29, Issue 6, Pages: 692-698(2011)
Affiliations:
a.State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
b.Graduate School of the Chinese Academy of Sciences, Changchun Branch, Changchun 130022, China
Miao Hong, Bai-xiang Li, Yue-sheng Li. SYNTHESIS OF FUNCTIONAL POLYETHYLENE via COPOLYMERIZATION OF ETHYLENE AND SUBSTITUTED ALLENE USING BIS(β-ENAMINOKETONATO)TITANIUM CATALYSTS[J]. Chinese Journal of Polymer Science, 2011, 29(6): 692-698. DOI: 10.1007/s10118-011-1081-3.
DOI:
Miao Hong, Bai-xiang Li, Yue-sheng Li. SYNTHESIS OF FUNCTIONAL POLYETHYLENE via COPOLYMERIZATION OF ETHYLENE AND SUBSTITUTED ALLENE USING BIS(β-ENAMINOKETONATO)TITANIUM CATALYSTS[J]. Chinese Journal of Polymer Science, 2011, 29(6): 692-698. DOI: 10.1007/s10118-011-1081-3.DOI:
SYNTHESIS OF FUNCTIONAL POLYETHYLENE via COPOLYMERIZATION OF ETHYLENE AND SUBSTITUTED ALLENE USING BIS(β-ENAMINOKETONATO)TITANIUM CATALYSTS
Novel copolymerization of ethylene with substituted allenes (CH
2
=C=CH—R
1
: R =
n
-butyl
2
: R =
n
-octyl) using bis(
β
-enaminoketonato)titanium catalysts [PhN=C(R
2
)CHC(R
1
)O]
2
TiCl
2
(
1a
: R
1
= CF
3
R
2
= CH
3
;
1b
: R
1
= Ph
R
2
= CF
3
) has been investigated. In the presence of modified methylaluminoxane
these catalysts can copolymerize ethylene with substituted allenes
affording copolymers with unimodal molecular weight distributions and homogeneous compositions. By varying the reaction conditions
the comonomer incorporation can be tuned in the range of 0-3.6 mol%.
1
H-NMR spectra reveal that the copolymerization proceeds through 1
2-insertion fashion of allene comonomer exclusively
and the regioselective nature maintains under various reaction conditions. The retained intra-chain double bond can be converted into the epoxy group under mild conditions.
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