

FOLLOWUS
a.CNR – Istituto di Scienze e Tecnologie Chimiche “G. Natta” (CNR-SCITEC), via Alfonso Corti 12, - 20133 Milano, Italy
b.Total Petrochemicals Research, Zone Industrielle C, B-7181 Feluy, Belgium
tritto@ismac.cnr.it
Received:28 June 2019,
Revised:2019-8-17,
Accepted:29 August 2019,
Online First:07 November 2019,
Published:2020-03
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Losio, S.; Boggioni, L.; Cornelio, M.; Razavi, A.; Tritto, I. Ethylene-propene copolymerization with , C,1-symmetric , ansa,-fluorenyl-zirconocene catalysts: effects of catalyst structure and comonomer on molar mass. Chinese J. Polym. Sci. 2020, 38, 220–230. DOI: 10.1007/s10118-020-2348-3.
Simona Losio, Laura Boggioni, Massimiliano Cornelio, et al. Ethylene-Propene Copolymerization with
Losio, S.; Boggioni, L.; Cornelio, M.; Razavi, A.; Tritto, I. Ethylene-propene copolymerization with , C,1-symmetric , ansa,-fluorenyl-zirconocene catalysts: effects of catalyst structure and comonomer on molar mass. Chinese J. Polym. Sci. 2020, 38, 220–230. DOI: 10.1007/s10118-020-2348-3. DOI:
Simona Losio, Laura Boggioni, Massimiliano Cornelio, et al. Ethylene-Propene Copolymerization with
Ethylene-propene copolymers have been synthesized by three
C
1
-symmetric metallocene molecules (
1
2
and
3
)
having
tert
-butyl substituents on the Cp moiety
on the fluorenyl moiety
or on both moieties
and methylaluminoxane (MAO) at different polymerization temperatures and monomer concentrations. Copolymers were investigated by
13
C-NMR
1
H-NMR
and SEC analyses. A relationship was found between [EEE]/[E]
ratios and copolymer molar masses in each series: the higher the [EEE]/[E]
ratio
the lower the copolymer molar mass. At parity of [EEE]/[E]
ratio
copolymer molar mass follows the order
1
>
>
3
>
2
. Chain end group analysis reveals that copolymers mainly terminate when propene is the last inserted unit
confirming that it is the greater facility of Mt-P-E-poly(E-
co
-P) to terminate that influences the copolymer molar mass. Among the catalysts considered
catalyst
1
which gives syndiospecific polypropene
gives greater activities
comonomer incorporation
and molar masses. Catalyst
3
which gives isospecific polypropene
in copolymerization performs better than
2
having the same bridge
with respect to activities
ethylene content
and molar masses. The good performance of this catalyst arises from the not necessity of polymer chain to back skip when ethylene is the last inserted unit.
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