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工业上重要的聚醚多元醇的串联质谱-剩余物分析

Tandem Mass-Remainder Analysis of Industrially Important Polyether Polyols.

作者信息

Hashimov Mahir, Kuki Ákos, Nagy Tibor, Zsuga Miklós, Kéki Sándor

机构信息

Department of Applied Chemistry, Faculty of Science and Technology, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.

Doctoral School of Chemistry, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.

出版信息

Polymers (Basel). 2020 Nov 24;12(12):2768. doi: 10.3390/polym12122768.

Abstract

The characteristics of the polyalkylene oxide polyether polyols highly influence the properties of final polyurethane products. As a novel approach, in order to gain structural information, the recently invented data mining procedures, namely the Mass-remainder analysis (MARA) and the Multistep Mass-remainder analysis (M-MARA) are successfully applied for the processing of tandem mass spectrometry (MS/MS) data of various industrially important polyether polyols. M-MARA yields an ultra-simplified graphical representation of the MS/MS spectra and sorts the product ions based on their double bond equivalent (DBE) values. The maximum DBE values unambiguously differentiate among the various polyether polyols. Accordingly, the characteristic DBE values were 0, 1 for the linear diol polyethers, 0, 1, 2 for the three-arm, and 0, 1 2, 3, 4 for the six-arm polyether polyols. In addition, it was also found that the characteristic collision energy necessary for the optimum fragmentation yield depended linearly on the molecular weight of the polyols. This relationship offers an easy way for instrument tuning to gain structural information.

摘要

聚环氧烷聚醚多元醇的特性对最终聚氨酯产品的性能有很大影响。作为一种新方法,为了获取结构信息,最近发明的数据挖掘程序,即质量余数分析(MARA)和多步质量余数分析(M-MARA),已成功应用于处理各种具有工业重要性的聚醚多元醇的串联质谱(MS/MS)数据。M-MARA产生了MS/MS光谱的超简化图形表示,并根据其双键当量(DBE)值对产物离子进行分类。最大DBE值能明确区分各种聚醚多元醇。因此,线性二醇聚醚的特征DBE值为0、1,三臂聚醚多元醇的为0、1、2,六臂聚醚多元醇的为0、1、2、3、4。此外,还发现获得最佳碎片产率所需的特征碰撞能量与多元醇的分子量呈线性关系。这种关系为仪器调谐以获取结构信息提供了一种简便方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c6a/7761062/848eb2533437/polymers-12-02768-g001.jpg

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