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纸质出版日期:2008-3-20,
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李爱香, 鲁在君. 结构明确的梳形支化聚合物的合成与表征[J]. 高分子学报, 2008,(3):203-208.
LI Aixiang, LU Zaijun. Synthesis and Characterization of WellDefined CombLike Branched Polymers[J]. Acta Polymerica Sinica, 2008,(3):203-208.
李爱香, 鲁在君. 结构明确的梳形支化聚合物的合成与表征[J]. 高分子学报, 2008,(3):203-208. DOI: 10.3724/SP.J.1105.2008.00203.
LI Aixiang, LU Zaijun. Synthesis and Characterization of WellDefined CombLike Branched Polymers[J]. Acta Polymerica Sinica, 2008,(3):203-208. DOI: 10.3724/SP.J.1105.2008.00203.
通过活性聚苯乙烯(PS)和聚异戊二烯(PI)负离子与1
1-二苯基乙烯(DPE)侧基的聚苯乙烯(PSe)的偶联反应合成了结构明确的每个重复单元含一条侧链的梳形支化聚合物,其中,PSe是通过Se 单体的原子转移自由基聚合(ATRP)和Wittig 反应制得的.用IR、1H-NMR、GPC和SLS 等测试方法对所得梳形支化聚合物进行了详细表征,讨论了活性负离子链与PSe的DPE基团的配比对接枝率的影响.结果表明,活性负离子链与DPE基团的偶联反应是高效的,可以通过调节活性负离子链与DPE 基团的加料比来控制接枝率. 另外,还讨论了PSe 和活性负离子链的分子量.
Combining living anionic polymerization and atom transfer radical polymerization (ATRP)
well-defined comb-like branched polymers having one branch in each repeating unit were successfully synthesized by the coupling reaction of living PS and PI anions with 1
1-diphenylethenyl (DPE) groups along PS backbone.ATRP of 4-vinylbenzyloxy benzophenone (Sc) carried out in diphenyl ether at 130℃ using PhCH2Cl as an initiator and CuCl/2
2′-bipyridine complex as a catalyst led to PSc with benzophenone pendant groups.The molar ratio of PhCH2Cl
CuCl and 2
2--bipyridine used in ATRP was 1∶1∶3.The PSc was then converted to the corresponding PSe bearing DPE pendant groups viaWittig reaction
and PSe was used as a polymer backbone.Finally the coupling reaction of living PSLi or PILi prepared by the polymerization of styrene or isoprene via living anionic polymerization using n-BuLi as initiator in THF with DPE groups of PSe was carried out at -78℃ to form the desired comb-like branched polymers PSe-g-PS or PSe-g-PI.The resulting comb-like branched polymers and precursors were characterized by IR
1H-NMR
GPC and SLS measurements in detail.The peak at higher molecular weight ascribed to the comblike branched polymer in the GPC profile of crude comb-like branched polymer was sharp monodal and very narrow
suggesting a homogeneous and clean grafting.The apparent molecular weight of the comblike branched polymers determined by GPC was not reliable due to its branching structure.The absolute molecular weights of these polymers were therefore determined by SLS measurements.The values were much closed to the corresponding theoretical ones calculated assuming all the living chains were coupled with DPE groups (living chains were lack or equal) or all the DPE groups were consumed (living chains were excess)
suggesting that the grafting is nearly complete.The grafting efficiency could be calculated by comparing the molecular weights by SLS and the corresponding theoretical ones.Furthermore
the grafting efficiency was also proved to be almost quantitative by comparing 1H-NMR spectrum of comb-like branched PSe-g-PS and PSe.The effect of living chains and DPE groups molar ratio ([PSLi]0/[DPE]0) on grafting efficiency was discussed.When [PSLi]0/[DPE]0 varied from 0.7 to 1.2
the grafting efficiency increased from 65.5% to 101%.The results showed the coupling reaction of living chains and DPE groups was highly effective and proceeded until all the DPE groups were consumed
and the grafting efficiency could be controlled viachanging the feed molar ratios of living chains and DPE groups.Moreover
when excess living polymers were used
the effect of molecular weights of PSe and PSLi or PILi on graft efficiency was also discussed.When the Mw of PSe was smaller than 10000 s
and the Mw of PSLi varied from 4200 to 11200
almost quantitative grafting efficiency could also be achieved.When living chains was PILi
the similar results were obtained.In conclusion
all the results demonstrate that the method by coupling reaction of living polymer anion with DPE groups along backbone is very effective for the synthesis of well defined comb-like branched polymers.
原子转移自由基聚合活性负离子聚合偶联反应梳形支化聚合物
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