首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Comprehensive analysis of stereoregularity and sequence distribution in 2-N-carbazolylethyl acrylate and methyl methacrylate copolymers by 2D NMR spectroscopy and their thermal studies
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Comprehensive analysis of stereoregularity and sequence distribution in 2-N-carbazolylethyl acrylate and methyl methacrylate copolymers by 2D NMR spectroscopy and their thermal studies

机译:通过2D NMR光谱综合分析丙烯酸2-N-咔唑基乙酯和甲基丙烯酸甲酯共​​聚物的立构规整度和序列分布及其热学研究

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摘要

A series of 2-N-carbazolylethyl acrylate (C) and methyl methacrylate (M) copolymers with varying compositions were prepared in toluene at 60 deg C using AIBN as an initiator.The molar outfeed ratio (F_C) for various compositions was determined from ~1H NMR spectra.Reactivity ratios calculated using Kelen-Tudos (KT) and non-linear error in variable (RREVM) methods were found to be r_C=0.43+-0.8 and r_M=2.78+-0.52.Molecular weight distribution was determined by gel permeation chromatography (GPC).The methine carbon of C unit showed splitting up to the pentad level in ~(13)C{~1H} NMR spectra and was found to be sensitive to the variation in C/M copolymer compositions.The backbone methylene and carbonyl carbons of both M and C unit along with alpha-methyl carbon of the M unit showed both compositional and configurational sensitivity.Distortionless enhancement by polarization transfer (DEPT) helped in differentiating the methylene carbon signals from the methine and methyl carbon resonances.2D heteronuclear single quantum coherence (HSQC) and 2D total correlation spectroscopy (TOCSY) were used in tandem to deduce all spectral assignments.2D heteronuclear multiple bond coherence (HMBC) played an important role in studying the stereoregularity of the carbonyl carbon.The trend in variation of glass transition temperature (T_g) of various C/M copolymer compositions was also studied.
机译:使用AIBN作为引发剂,在60°C的甲苯中制备了一系列具有不同组成的2-N-咔唑基丙烯酸甲酯(C)和甲基丙烯酸甲酯(M)共聚物,由〜确定了各种组成的摩尔输出比(F_C) 1H NMR谱图,使用Kelen-Tudos(KT)计算的反应率和变量非线性误差(RREVM)为r_C = 0.43 + -0.8和r_M = 2.78 + -0.52。通过凝胶测定分子量分布在〜(13)C {〜1H} NMR光谱中,C单元的次甲基碳显示分裂到五单元组水平,并且对C / M共聚物组成的变化敏感。 M和C单元的羰基碳以及M单元的α-甲基碳都表现出组成和构型敏感性。极化转移(DEPT)的无失真增强有助于将亚甲基碳信号与次甲基和甲基碳共振区分开.2D异核单量子相干性(HSQC)和2D总相关光谱法(TOCSY)串联使用来推断所有光谱分配.2D异核多键相干性(HMBC)在研究羰基碳的立体规则性方面起着重要作用。还研究了各种C / M共聚物组合物的玻璃化转变温度(T_g)的变化。

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