Abstract
Two series of new aromatic poly(ester-imide)s were prepared from 1,5-bis(4-aminobenzoyloxy)naphthalene (p-1) and 1,5-bis(3-aminobenzoyloxy) naphthalene (m-1), respectively, with six commercially available aromatic tetracarboxylic dianhydrides via a conventional two-stage synthesis that included ring-opening polyaddition to give poly(amic acid)s followed by chemical imidization to polyimides. The intermediate poly(amic acid)s obtained in the first stage had inherent viscosities of 0.41-0.84 and 0.66-1.37 dl/g, respectively. All the para-series and most of the meta-series poly(ester-imide)s were semicrystalline and showed less solubility. Two of the meta-series poly(ester-imide)s derived from less rigid dianhydrides were amorphous and readily soluble in polar aprotic solvents, and they could be solution-cast into transparent and tough films with good mechanical properties. The meta-series polymers derived from rigid dianhydrides were generally semicrystalline and showed less solubility. Except for one example, the meta-series poly(ester-imide)s displayed discernible Tgs in the range 239-273 °C by DSC. All of these two series poly(ester-imide)s did not show significant decomposition below 450 °C in nitrogen or in air.
| Original language | English |
|---|---|
| Pages (from-to) | 328-335 |
| Number of pages | 8 |
| Journal | European Polymer Journal |
| Volume | 42 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2006 |
Bibliographical note
Funding Information:The authors are grateful to the National Science Council of Taiwan for the financial support of this work.
Keywords
- Bis(ester-amine)s
- Naphthalene units
- Poly(ester-imide)s
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