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Study on the Isomerization and Dehydrobromination Mechanism of Brominated Butyl Rubber  

Wu, Yibo (Department of Material Science and Engineering, Beijing Institute of Petrochemical Technology)
Guo, Wenli (Department of Material Science and Engineering, Beijing Institute of Petrochemical Technology)
Li, Shuxin (Department of Material Science and Engineering, Beijing Institute of Petrochemical Technology)
Gong, Liangfa (Department of Material Science and Engineering, Beijing Institute of Petrochemical Technology)
Shang, Yuwei (Department of Material Science and Engineering, Beijing Institute of Petrochemical Technology)
Publication Information
Polymer(Korea) / v.34, no.1, 2010 , pp. 69-73 More about this Journal
Abstract
Effects of reaction time and temperature on the isomerization and dehydrobromination reactions of brominated butyl rubber were investigated. The structural composition of brominated butyl rubber was determined by Fourier transform infrared spectroscopy (FT-IR) and proton nuclear magnetic resonance spectroscopy($^1H$-NMR), Density functional theory (DFT) was used to study on the isomerization and dehydrobromination mechanisms of model compounds. The geometries for model compounds of 3-bromo-5,5,7,7-tetramethyl-2(2',2',4',4'-tetramethyl)pentyl-1-octylene (3BrOE), 1-bromo-5,5,7,7-tetramethyl-2(2',2',4',4'-tetramethyl)pentyl-2-octylene (1Br2OE) and 5,5,7,7-tetramethyl-2(2',2', 4',4'-tetramethyl)pentyl-1,3-octadiene (CD) had been optimized by using density functional theory at B3LYP/3-21G and B3LYP/6-31G levels. The predicted energy of 3BrOE lies higher than that of 1Br2OE which suggests that 1Br2OE configuration is more stable than the 3BrOE configuration. Compared with the energy barrier, the pathway of dehydrobromination is less competitive than that of isomerization. This is qualitatively consistent with the experimental results.
Keywords
brominated butyl rubber; isomerization; dehydrobromination; density functional theory;
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