结构明确的梳形支化聚合物的合成与表征

通过活性聚苯乙烯(PS)和聚异戊二烯(PI)负离子与含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Sc单体的原子转移自由基聚合(ATRP)和Wittig反应制得的.用IR1、H-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对接枝率的影响.结果表明,在实验范围内当活性负离子链过量时可获得几乎定量的接枝率.

SYNTHESIS AND CHARACTERIZATION OF WELL-DEFINED COMB-LIKE BRANCHED POLYMERS

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 PhCH_2Cl as an initiator and CuCl/2,2′-bipyridine complex as a catalyst led to PSc with benzophenone pendant groups.The molar ratio of PhCH_2Cl,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 via Wittig 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 comb-like 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 comb-like 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(_0/_0) on grafting efficiency was discussed.When _0/_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 via changing 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 M_w of PSe was smaller than 10000 s,and the M_w 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.