Homopolymerizations of butadiene (BD), isoprene (IP), and 2,3-dimethylbutadiene (DMBD) were carried out by a Gd(OCOCCl 3 ) 3 -based catalyst, to investigate the effects of the energy levels of the monomers or the sterical factor of the methyl substituents on the polymerizability and the cis-selectiv
Copolymerization of vinyl monomers with Gd(OCOCCl3)3-(i-Bu)3Al-Et2AlCl
β Scribed by Shojiro Kaita; Takako Otaki; Eiichi Kobayashi; Sadahito Aoshima; Junji Furukawa
- Book ID
- 101271142
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 157 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
The polymerization of polar monomers such as methyl methacrylate (MMA), methyl acrylate (MA), methacrylonitrile (MAN), and acrylonitrile (AN) was carried out with gadolinium-based Ziegler-Natta catalysts [Gd(OCOCCl 3 ) 3 -(i-Bu) 3 Al-Et 2 AlCl] in hexane at 50ΠC under N 2 to elucidate the effect of the monomer's HOMO (highest occupied moleculor orbital) and LUMO (lowest unoccupied molecular orbital) levels on the polymerizability. In the case of homopolymerization, all monomers were found to polymerize and the order of relative polymerizability was as follows: MMA ΓΊ MA ΓΊ MAN ΓΊ AN. On the other hand, the result of copolymerization of St with MMA shows that the values of the monomer reactivity ratios are r 1 Γ 0.06 and r 2 Γ 1.98 for St(M 1 )/MMA(M 2 ). The monomer reactivity ratios of styrene (St), pmethoxystyrene (PMOS), p-methylstyrene (PMS), and p-chlorostyrene (PCS) evaluated as r 1 Γ 0.55 and r 2 Γ 1.07 for St(M 1 )/PMOS(M 2 ), r 1 Γ 0.38 and r 2 Γ 0.51 for St(M 1 )/PMS(M 2 ), and r 1 Γ 0.72 and r 2 Γ 1.25 for St(M 1 )/PCS(M 2 ) were compared with those for St(M 1 )/MMA(M 2 ). The copolymerization behavior is apparently different from the titanium-based Ziegler-Natta catalyst, regarding a larger monomer reactivity ratio of PCS. The lower LUMO level of PCS and MMA may enhance a backdonation process from the metal catalyst, therefore resulting in high polymerizability. These results are discussed on the basis of the energy level of the gadolinium catalyst and the HOMO and LUMO levels of the monomers.
π SIMILAR VOLUMES
The polymerization of butadiene in toluene using Co(acac)3-(i-Bu)3Al-H~O catalyst system was studied. Presented are the effects of the addition order, aging time, and composition of catalysts on rates, polymer microstructure, and molecular weights. The polymerization was found to be initiated by the