Conversion dependence of the structural units and the degree of branching of a hyperbranched polyester based on 4,4-bis-(4′-hydroxyphenyl)pentanoic acid determined by NMR spectroscopy

D. Schmaljohann, H. Komber, B. I. Voit
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引用次数: 31

Abstract

The hyperbranched polyester based on 4,4-bis-(4′-hydroxyphenyl)pentanoic acid was synthesized with different DP's. A complete 1H and 13C NMR assignment of the oligomers was carried out. Six different structural units were quantified by NMR analysis. The conversion dependence of the content of these structural units and of the degree of branching DB follows the theoretically derived equations. Furthermore, six different diads were quantified by 13C NMR spectroscopy. The conversion dependence of the diads was calculated and again the measured data agree well with the theory. The good fit between theoretical and measured data proves that the polycondensation of the 4,4-bis-(4′-hydroxyphenyl)pentanoic acid follows a random growth of the different units with equal reaction rates of all reaction steps. Finally, spin-lattice relaxation times (T1C) and nuclear Overhauser enhancements (NOE) were determined and discussed.

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基于4,4-双-(4′-羟基苯基)戊酸的超支化聚酯的结构单元和支化程度的转化依赖
以4,4-二-(4′-羟基苯基)戊酸为原料,用不同的DP合成了超支化聚酯。对低聚物进行了完整的1H和13C NMR分配。通过核磁共振分析确定了6个不同的结构单元。这些结构单元的含量和分支DB的程度的转换依赖关系遵循理论推导的方程。此外,通过13C NMR对6种不同的双聚体进行了定量分析。计算了双极的转换关系,实测数据与理论吻合较好。理论数据与实测数据吻合较好,证明了4,4-双-(4′-羟基苯基)戊酸的缩聚反应遵循不同单元的随机生长,各反应步骤的反应速率相等。最后,确定并讨论了自旋-晶格弛豫时间(T1C)和核超hauser增强(NOE)。
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