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分析策略用于测定聚甲基丙烯酸甲酯和聚甲基丙烯酸随机共聚物的分子量。

Analytical strategy for the molecular weight determination of random copolymers of poly(methyl methacrylate) and poly(methacrylic acid).

机构信息

Universités Aix-Marseille I, II, and III-CNRS, UMR 6264: Laboratoire Chimie Provence, Spectrométries Appliquées à la Chimie Structurale, Marseille, France.

出版信息

J Am Soc Mass Spectrom. 2010 Jun;21(6):1075-85. doi: 10.1016/j.jasms.2010.02.007. Epub 2010 Feb 10.

DOI:10.1016/j.jasms.2010.02.007
PMID:20202862
Abstract

Molecular weight characterization of random amphiphilic copolymers currently represents an analytical challenge. In particular, molecules composed of methacrylic acid (MAA) and methyl methacrylate (MMA) as the repeat units raise issues in commonly used techniques. The present study shows that when random copolymers cannot be properly ionized by MALDI, and hence detected and measured in MS, one possible analytical strategy is to transform them into homopolymers, which are more amenable to this ionization technique. Then, by combining the molecular weight of the so-obtained homopolymers, as measured by MS, with the relative molar proportion of the MMA and MMA units, as given by (1)H NMR spectrum, one can straightforwardly estimate the molecular weight of the initial copolymer. A methylation reaction was performed to transform MAA-MMA copolymer samples into PMMA homopolymers, using trimethylsilyldiazomethane as a derivatization agent. Weight average molecular weight (M(w)) parameters of the MAA-MMA copolymers could then be derived from M(w) values obtained for the methylated MAA-MMA molecules by MALDI, which were also validated by pulsed gradient spin echo (PGSE) NMR. An alkene function in one of the studied copolymer end-groups was also shown to react with the methylation agent, giving rise to MMA-like polymeric by-products characterized by tandem mass spectrometry and which could be avoided by adjusting the amount of the trimethylsilyldiazomethane in the reaction medium.

摘要

目前,随机两亲性共聚物的分子量表征是一项分析挑战。特别是由甲基丙烯酸(MAA)和甲基丙烯酸甲酯(MMA)作为重复单元组成的分子在常用技术中存在问题。本研究表明,当随机共聚物不能通过 MALDI 适当离子化,从而在 MS 中检测和测量时,一种可能的分析策略是将它们转化为更适合这种电离技术的均聚物。然后,通过将通过 MS 测量的如此获得的均聚物的分子量与(1)H NMR 光谱给出的 MMA 和 MMA 单元的相对摩尔比例相结合,可以直接估计初始共聚物的分子量。使用三甲基硅基重氮甲烷作为衍生化试剂,将 MAA-MMA 共聚物样品进行甲基化反应转化为 PMMA 均聚物。然后可以通过 MALDI 从甲基化的 MAA-MMA 分子获得的 M(w)值推导出 MAA-MMA 共聚物的重均分子量(M(w))参数,这些值也通过脉冲梯度自旋回波(PGSE)NMR 进行了验证。还表明,研究的共聚物端基之一中的一个烯烃官能团与甲基化试剂反应,生成类似于 MMA 的聚合物副产物,通过串联质谱法进行了表征,并通过调整反应介质中三甲基硅基重氮甲烷的量可以避免这种副产物。

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本文引用的文献

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2
Molecular weight determination of block copolymers by pulsed gradient spin echo NMR.通过脉冲梯度自旋回波核磁共振测定嵌段共聚物的分子量
Anal Chem. 2009 Oct 1;81(19):8054-60. doi: 10.1021/ac9018654.
3
Positive mode electrospray tandem mass spectrometry of poly(methacrylic acid) oligomers.
聚(甲基丙烯酸)低聚物的正模式电喷雾串联质谱分析
Rapid Commun Mass Spectrom. 2009 Jun;23(11):1557-62. doi: 10.1002/rcm.4040.
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Tandem mass spectrometry of poly(methacrylic Acid) oligomers produced by negative mode electrospray ionization.负离子模式电喷雾电离产生的聚(甲基丙烯酸)低聚物的串联质谱分析。
J Am Soc Mass Spectrom. 2009 Jan;20(1):25-33. doi: 10.1016/j.jasms.2008.09.019. Epub 2008 Sep 25.
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Influence of internal standard charge state on the accuracy of mass measurements in orthogonal acceleration time-of-flight mass spectrometers.内标电荷态对正交加速飞行时间质谱仪质量测量准确性的影响。
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