Volume 121, Issue 2 pp. 1052-1058

Diphenylselenonium 2,3,4,5-tetraphenylcyclopentadienylide-initiated polymerization of styrene and acrylonitrile: Synthesis, characterization, reactivity ratios, and thermal properties

Anamika Singh

Anamika Singh

Analytical Research Laboratory, Department of Chemistry, Harcourt Butler Technological Institute, Kanpur 208002, India

Search for more papers by this author
Meet Kamal

Meet Kamal

Department of Chemistry, Christ Church College, Kanpur 208001, India

Search for more papers by this author
D. K. Singh

Corresponding Author

D. K. Singh

Analytical Research Laboratory, Department of Chemistry, Harcourt Butler Technological Institute, Kanpur 208002, India

Analytical Research Laboratory, Department of Chemistry, Harcourt Butler Technological Institute, Kanpur 208002, India===Search for more papers by this author
First published: 25 February 2011
Citations: 3

Abstract

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: Rp ∼ [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 1H-NMR and elemental analysis was used to evaluate reactivity ratio as r1 (Sty) = 0.351 and r2 (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, 1H-NMR, 13C-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

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.