Poly(arylene ether)s with trifluoromethyl groups via meta-activated nitro displacement reaction

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New poly(arylene ether)s with pendent trifluoromethyl groups were synthesized from 2,2'-bis(trifluoromethyl)-4,4'-dinitro-1,1'-biphenyl with several bisphenols. The nitro leaving group activated by the trifluoromethyl group at meta position was quantitatively displaced with phenolate ions, resulting in high molecular weight polymers. The quantum mechanical calculation of the energy state suggested that the nitro displacement reaction activated by the trifluoromethyl group at meta position is an energetically favorable process. The polymers having weight average molecular weight of 42,100-95,000 g/mol and molecular weight distribution of 2.65-2.95 were obtained. The polymers were amorphous and dissolved in a wide range of organic solvents. Transparent and flexible films were obtained by solution casting. The resulting polymers are thermally stable, and T(g)s of the polymers are in the range of 176-199 degrees C depending on their molecular structure. All of the synthesized polymers show refractive indices in the range of 1.592-1.624 with low birefringence below 0.006. (C) 2010 Elsevier Ltd. All rights reserved.
Publisher
ELSEVIER SCI LTD
Issue Date
2010-09
Language
English
Article Type
Article
Keywords

AROMATIC-SUBSTITUTION REACTION; POLY(BIPHENYLENE OXIDE)S; UNSYMMETRICAL DIAMINE; PHYSICAL-PROPERTIES; SOLUBLE POLYIMIDES; PENDENT GROUP; MONOMER; POLYMERIZATION; POLYMERS; SULFONE)S

Citation

POLYMER, v.51, no.20, pp.4477 - 4483

ISSN
0032-3861
DOI
10.1016/j.polymer.2010.08.003
URI
http://hdl.handle.net/10203/98282
Appears in Collection
CH-Journal Papers(저널논문)
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