Premium
Diphenylselenonium 2,3,4,5‐tetraphenylcyclopentadienylide‐initiated polymerization of styrene and acrylonitrile: Synthesis, characterization, reactivity ratios, and thermal properties
Author(s) -
Singh Anamika,
Kamal Meet,
Singh D. K.
Publication year - 2011
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.33792
Subject(s) - copolymer , acrylonitrile , reactivity (psychology) , polymer chemistry , styrene , thermogravimetric analysis , fourier transform infrared spectroscopy , differential scanning calorimetry , polymerization , materials science , radical polymerization , chemistry , organic chemistry , polymer , chemical engineering , medicine , alternative medicine , physics , pathology , engineering , thermodynamics
Solution copolymerization of styrene (Sty) and acrylonitrile (AN) was carried out in dioxane at 60 ± 1°C for 90 min using diphenylselenonium 2,3,4,5‐tetraphenylcyclopentadienylide (selenonium ylide) as radical initiator. The kinetic expression is as follows: R p ∼ [Ylide] 0.5 [Sty] 1.0 [AN] 1.0 . The overall activation energy is 28.72 kJ mol −1 . The composition of copolymer calculated from 1 H‐NMR and elemental analysis was used to evaluate reactivity ratio as r 1 (Sty) = 0.351 and r 2 (AN) = 0.0185, using kelen‐Tudos method. It confirmed the alternating nature of the copolymer. The copolymer was characterized using Fourier transform infrared (FTIR) spectroscopy, 1 H‐NMR, 13 C‐NMR, differential scanning calorimetry, and thermal gravimetric analysis. Electron spin resonance spectroscopy confirmed the presence of the phenyl radical responsible for initiation. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011