Preparation of Tethered Half-Titanocene Complex on Syndiotactic Poly(styrene-co-p-methylstyrene) for Using in Syndiospecific Polymerization of Styrene

被引:3
|
作者
Rahmani, Sohrab [1 ]
Entezami, A. A. [1 ]
机构
[1] Univ Tabriz, Lab Polymer, Fac Chem, Tabriz, Iran
关键词
Syndiotactic polystyrene; Tethered metallocene; Half-titanocene; Syndiotactic (styrene-co-p-methylstyrene); Functionalization; SUPPORTED RAC-PH2SI(IND)(2)ZRCL2 CATALYST; ETHYLENE POLYMERIZATION; METALLOCENE CATALYST; NASCENT MORPHOLOGY; MOLECULAR-WEIGHT; POLYSTYRENE; ALUMINOXANE; COPOLYMERS; MECHANISM;
D O I
10.1007/s10562-011-0706-z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work the syndiotactic polystyrene copolymer, poly (styrene-co-p-methylstyrene) was prepared by the copolymerization of styrene and p-methylstyrene with cyclopentadienyltitanium trichloride/methylaluminoxane catalyst. This copolymer was functionalized with silyl-hydride groups. The structure of copolymer and functionalized copolymer were characterized by FT-IR, (1)H-NMR and (13)C-NMR spectroscopy. The obtained results revealed that the functionalization reaction successfully proceeds at low temperatures. Tethering of half-titanocene complex on polymeric support was done by the hydrosilylation reaction of 1-allylindenyltrichlorotitanium with silyl-hydride functionalized copolymer in the presence of Karstedt catalyst as a coupling reagent. The polymer-supported catalyst was tested for syndiospecific polymerization of styrene using methylaluminoxane as a cocatalyst. The results of styrene polymerization showed that the polymer-supported catalyst exhibited high activity for syndiospecific polymerization of styrene. The polymer prepared with supported catalyst was characterized by carbon nuclear magnetic resonance ((13)C-NMR) and differential scanning calorimetry (DSC). The results confirmed the syndiotacticity of obtained polymers. X-ray diffraction (XRD) analysis showed the delta-form crystalline structure of obtained syndiotactic polystyrene.
引用
收藏
页码:1625 / 1634
页数:10
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