Abstract
Polyimide oligomers (prepolymers) and resins of the PMR-15 type have been prepared from 5-norbornene-2,3-dicarboxylic half acid ester (NE), 3,3',4,4'-benzophenonetetracarboxylic diester (BTDE) and a series of diamines including, and related to, 3,3'-diaminobenzophenone, viz. 3,3'-diaminobenzhydrol, 3-[(m,m'-diamino)benzhydryloxy]propyne (MDA-OMA) and 3,3'-diaminodiphenyl-a,a'-difluoromethane (FMDA). The PMR synthetic pathway (monomers?prepolymer?resin) has been assessed by dynamic mechanical thermal analysis. The Tg values for resins incorporating BTDE are significantly lowered compared to that for PMR-15 itself. The fluorine-containing PMR-15 type of resin (from FMDA) is of higher thermal stability than PMR-15 itself. © 1994.
| Original language | English |
|---|---|
| Pages (from-to) | 2378-2384 |
| Number of pages | 7 |
| Journal | Polymer |
| Volume | 35 |
| Issue number | 11 |
| Publication status | Published - May 1994 |
Keywords
- diamino(diaryl)methanes
- PMR-type polyimide resins
- structure-property relations
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