Microstructural analysis of methyl methacrylate lauryl methacrylate copolymers using 13C NMR spectroscopy

被引:2
|
作者
Sannigrahi, B [1 ]
Garnaik, B [1 ]
机构
[1] Natl Chem Lab, Div Polymer Chem, Pune 411008, Maharashtra, India
关键词
Group Transfer Polymerization; C-13 nuclear magnetic resonance; polymer microstructure; methyl methacrylate; lauryl methacrylate; (1-methoxy-2-methyl-1-propenyl)oxytrimethylsilane; tetrabutylammonium bibenzoate; tetrahydrofuran;
D O I
10.1295/polymj.30.340
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
C-13 NMR spectra (75.5 MHz) of methyl methacrylate (M)-lauryl methacrylate (L) copolymers prepared by group transfer polymerization (GTP) were analyzed far sequence distribution and relative stereochemical configuration of monomer units along the macromolecular chains. The concentrations of M- and L-centered triads, determined experimentally from alpha-CH3 and C = O resonance signals, were in good agreement with those calculated statistically, taking into consideration the terminal copolymerization model and Bernoullian distribution of stereoregularity, with the statistical parameters P-ij determined from the reflectivity ratios r(M) = 1.38 +/- 0.11 and r(L) = 0.68 +/- 0.10 and the coisotacticity parameters sigma(MM) = 0.24, sigma(LL) = 0.27,sigma(ML) = sigma(LM) = sigma* = 0.30.
引用
收藏
页码:340 / 344
页数:5
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