

FOLLOWUS
Shanghai Key Laboratory of Functional Materials Chemistry and Laboratory of Organometallic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China
haiyanma@ecust.edu.cn
Received:07 December 2018,
Revised:2019-1-10,
Accepted:14 January 2019,
Online First:01 March 2019,
Published:2019-06
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Citation: Zhang, L.; Zhang, B.; Ma, H. Ethylene-bridged indenyl-fluorenyl metallocene complexes for efficient preparation of allyl-terminated propylene oligomers and polymers via selective β-methyl transfer. Chinese J. Polym. Sci. 2019, 37, 578–590
Lei Zhang, Bin Zhang, Haiyan Ma. Ethylene-bridged Indenyl-fluorenyl Metallocene Complexes for Efficient Preparation of Allyl-terminated Propylene Oligomers and Polymers
Citation: Zhang, L.; Zhang, B.; Ma, H. Ethylene-bridged indenyl-fluorenyl metallocene complexes for efficient preparation of allyl-terminated propylene oligomers and polymers via selective β-methyl transfer. Chinese J. Polym. Sci. 2019, 37, 578–590 DOI: 10.1007/s10118-019-2224-1.
Lei Zhang, Bin Zhang, Haiyan Ma. Ethylene-bridged Indenyl-fluorenyl Metallocene Complexes for Efficient Preparation of Allyl-terminated Propylene Oligomers and Polymers
Four
C
1
-symmetric
ansa
-metallocene complexes
C
2
H
4
(Ind)(2
7-
t
Bu
2
-Flu)ZrCl
2
(
4
)
C
2
H
4
(3-Bn-Ind)(2
7-
t
Bu
2
-Flu)ZrCl
2
(
5
)
C
2
H
4
(3-Bn-Ind)(3
6-
t
Bu
2
-Flu)ZrCl
2
(
6
)
and C
2
H
4
(3-Bn-Ind)(2
7-
t
Bu
2
-Flu)HfCl
2
(
7
)
were synthesized and characterized. The structures of complexes
4
5
and
7
were further determined
via
X-ray diffraction studies. Upon activation with modified methylaluminoxane (MMAO) or Al
i
Bu
3
/[Ph
3
C][B(C
6
F
5
)
4
] (TIBA/TrB)
most of these complexes showed high efficiency in catalyzing propylene oligomerization/polymerization to afford products dominantly with allyl terminals
via
selective
β
-methyl transfer (
β
-Me transfer). The introduction of 3-benzyl group on the indenyl ring of the complexes was found to be crucial in enabling highly selective
β
-Me transfer during the polymerization process
leading to selectivities up to 89% obtained by zirconocene complexes
5
and
6
and up to 91% obtained by hafnocene complex
7
. Detailed chain-end analysis by
1
H-NMR
13
C-NMR
and MALDI-TOF mass spectroscopy revealed that the allyl chain-ends of the polymeric products resulted from a selective
β
-Me transfer process after two successively primary insertions of the monomer. Further studies concerning the dependence of chain release selectivity as well as the molecular weight of products on monomer concentration suggested that both
β
-Me transfer (major) and
β
-hydrogen transfer (
β
-H transfer) (minor) mediated by
5
/MMAO and
6
/MMAO systems may mainly operate in a bimolecular pathway.
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