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首页> 外文期刊>Journal of Molecular Structure >Microstructure determination of 2-hydroxy ethyl methacrylate and methyl acrylate copolymers by NMR spectroscopy
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Microstructure determination of 2-hydroxy ethyl methacrylate and methyl acrylate copolymers by NMR spectroscopy

机译:NMR光谱法测定甲基丙烯酸2-羟乙酯和丙烯酸甲酯共​​聚物的显微结构

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Copolymers of 2-Hydroxy ethyl methacrylate and methyl acrylate (H/M) of different compositions were synthesized by free radical bulk polymerization using azobisisobutyronitrile (AIBN) as an initiator under nitrogen atmosphere. The copolymers compositions were calculated from H-1 NMR spectra. The reactivity ratios for H/M copolymers obtained from a linear Kelen-Tudos method (KT) and non-linear error-in-variables method (EVM) are r(H) = 3.31 +/- 0.08, r(M) = 0.23 +/- 0.00 and r(H) = 3.32, r(M) = 0.23, respectively. The complete spectral assignment of methine, methylene, methyl and carbonyl carbon regions in terms of compositional and configurational sequences of H/M copolymers was done with the help of C-13 {H-1} NMR, distortionless enhancement by polarization transfer (DEPT), two-dimensional heteronuclear single quantum coherence (HSQC) along with total correlated spectroscopy (TOCSY). Further, the assignments of carbonyl region were made with the help of heteronuclear multiple bond coherence (HMBC) spectrum. (c) 2006 Elsevier B.V. All rights reserved.
机译:采用偶氮二异丁腈(AIBN)作为引发剂,在氮气氛下,通过自由基本体聚合法合成了不同组成的甲基丙烯酸2-羟基乙酯和丙烯酸甲酯(H / M)共聚物。由H-1 NMR光谱计算共聚物组成。通过线性Kelen-Tudos方法(KT)和非线性变量误差方法(EVM)获得的H / M共聚物的反应比为r(H)= 3.31 +/- 0.08,r(M)= 0.23 +/- 0.00和r(H)= 3.32,r(M)= 0.23。借助C-13 {H-1} NMR,通过极化转移(DEPT)进行无失真增强,完成了H / M共聚物的组成,构型方面的次甲基,亚甲基,甲基和羰基碳区域的完整光谱分配。 ,二维异核单量子相干(HSQC)以及总相关光谱(TOCSY)。此外,借助异核多键相干(HMBC)光谱对羰基区域进行分配。 (c)2006 Elsevier B.V.保留所有权利。

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