

FOLLOWUS
a.Guangdong Provincial Key Laboratory for High Performance Polymeric Composites, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China
b.Key Laboratory for Polymer Composite and Functional Materials of Ministry of Education, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China
Fang-ming Zhu (祝方明), E-mail:ceszfm@mail.sysu.edu.cn
Received:07 December 2016,
Revised:2017-1-3,
Accepted:14 January 2017,
Published:05 July 2017
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Hua-qing Liang, Qi-hua Zhou, Yong-jiang Long, et al. Synthesis of Isotactic Polystyrene-block-Polyethylene by the Combination of Sequential Monomer Addition and Hydrogenation of 1, 4-
Hua-qing Liang, Qi-hua Zhou, Yong-jiang Long, et al. Synthesis of Isotactic Polystyrene-block-Polyethylene by the Combination of Sequential Monomer Addition and Hydrogenation of 1, 4-
Herein
we demonstrate the synthesis of a well-defined diblock copolymer consisting of isotactic polystyrene (
i
PS) and linear polyethylene
isotactic polystyrene-block-polyethylene (
i
PS-
b
-PE)
by the combination of sequential monomer addition and hydrogenation. Isospecific living polymerization of styrene and living
trans
-1
4-polymerization of 1
3-butadiene were catalyzed by 1
4-dithiabutandiyl-2
2′-bis(6-cumenyl-4-methylphenoxy) titanium dichloride (complex 1) activated by triisobutyl aluminum modified methylaluminoxane (MMAO) at room temperature to provide highly isotactic polystyrene (
i
PS) and 1
4-
trans
-polybutadiene (1
4-
trans
-PBD) with narrow molecular weight distribution. Furthermore
the
i
PS-
b
-1
4-
trans
-PBD was synthesized
via
sequential monomer addition in the presence of complex 1 and MMAO. The hydrogenation of the 1
4-
trans
-PBD block was promoted by RuCl
2
(PPh
3
)
3
used as a catalyst to produce
i
PS-
b
-PE.
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