Oligomeric aliphatic–aromatic ether containing phthalonitrile resins

Abstract

A versatile synthetic method has been developed for oligomeric aliphatic–aromatic ether containing phthalonitrile (PN) resins and applied to the preparation of three unique resin systems. The oligomeric PN monomers were prepared from the reaction of an excess amount of bisphenol A with a dihalo‐aliphatic containing compound in the presence of K2CO3 in dimethylsulfoxide, followed by end‐capping with 4‐nitrophthalonitrile in a two‐step, one‐pot reaction. These PN resin systems exhibited excellent viscosities for molding various shaped articles after thermal curing to yield crosslinked polymers. These polymers offered more mechanical flexibility, when compared with an all aromatic backbone, while still maintaining good thermal stability, dielectric properties, and low water absorption. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 2186–2191

Document Details

Document Type
Pub Defense Publication
Publication Date
Apr 23, 2015
Source ID
10.1002/pola.27659

Entities

People

  • Andrew P. Saab
  • Arianna Neal
  • Holly L. Ricks‐laskoski
  • Matthew Laskoski
  • Mollie B. Schear
  • Teddy M. Keller

Organizations

  • Strategic Environmental Research and Development Program
  • United States Naval Research Laboratory

Tags

Fields of Study

  • Chemistry

Readers

  • Polymer Science and Engineering.