Characterization of α, ω-dihydroxypolystyrene by gradient polymer elution chromatography and two-dimensional liquid chromatography

被引:22
作者
Gao, HF [1 ]
Siegwart, DJ [1 ]
Jahed, N [1 ]
Sarbu, T [1 ]
Matyjaszewski, K [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
基金
美国安德鲁·梅隆基金会; 美国国家科学基金会;
关键词
atom transfer radical polymerization (ATRP); atom transfer radical coupling (ATRC); gradient polymer elution chromatography (GPEC); two-dimensional liquid chromatography (2D-LC); click modification;
D O I
10.1163/156855505774597713
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Gradient polymer elution chromatography (GPEC) and GPEC x size-exclusion chromatography (SEC) two-dimensional liquid chromatography (2D-LC) techniques were employed to characterize functionality of hydroxy-telechelic polystyrene (polySt) prepared by two different methods. The first method involved the synthesis of hydroxy-functionalized polySt via atom transfer radical polymerization (ATRP) using a hydroxy-containing initiator and subsequent atom transfer radical coupling (ATRC). For the second method, alpha,omega-dibromo-polySt was synthesized by ATRP using a dibromo-containing initiator, followed by nucleophilic substitution with azide and click reactions. Utilizing GPEC analysis, the polymers were separated according to their hydroxy functionality. The polySt chains containing less hydroxy groups eluted faster. GPEC analysis successfully separated dihydroxy-polySt from monohydroxy- and nonhydroxy-polySt. For the hydroxy-telechelic polySt obtained from ATRC, GPEC analysis provided quantitative information of the termination by coupling during ATRP and the efficiency of ATRC. During the post-polymerization modification of bromo-telechelic polySt by nucleophilic substitution and click reactions, the chain-end functionality of the polySt was changed, while the molecular weight of the polymer remained constant. The powerful ability of GPEC was further demonstrated by sufficiently separating polymers with similar molecular weight but different hydroxy functionality.
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页码:533 / 546
页数:14
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