Chemistry Reference
In-Depth Information
Table 6.
Solubility of various new poly(ether imide)s a
Solvent b
Polymer code
NMP
DMAc
DMF
Pyridine
Cyclohexanone THF Chloroform
m-tert
+ +
+ +
+ +
+ +
+
+ +
+ +
TP-tert
+ +
+ +
+ +
+ +
+ +
+ +
+ +
Tcardo-tert
+ +
+ +
+ +
+ +
+ +
+ +
+ +
TMA-tert
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+
-
+ +
+
+ +
Cyclo-tert
+ +
+ +
+ +
+ +
+
+ +
+ +
Phcardo-tert
m-m
+ +
+ +
+ +
+ +
+
+ -
+ -
TP-m
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
+ +
Tcardo-m
TMA-m
+ +
+ +
+ +
+ +
+ +
+ +
+ +
Cyclo-m
+ +
+ +
+
-
+ +
+ +
+ +
Phcardo-m
+ +
+ +
+ +
+ +
+
+ +
+ +
BPDA-m c
+
+
+ -
-
+
+ -
-
a. Solubiltiy: ++, soluble at room temperature; +, soluble on heating at 70 ° C; + -, partially solu-
ble; -, insoluble.
b. Abbreviations: NMP: N -methyl-2-pyrrolidinone; DMAc: N , N -dimethylacetamide; DMF: N,N -
dimethylformamide; DMSO: dimethylsulfoxide; THF: tetrahydrofuran.
c. Analogous polyimide BPDA-m:
Source : Refs. 38-43.
bility between these poly(ether imide)s indicated that poly(ether imide)s contain-
ing the isopropylidene, kink and tert-butylcyclohexane groups shown slightly bet-
ter solubility than the others. For comparison, polyimide BPDA-m, shown below,
containing biphenylene without pendent cyclododecylidene was prepared from
4,4'- bis(4-aminophenoxy)biphenyl with dianhydride. It was observed that poly-
imide (BPDA-m) was nearly insoluble in the test solvents and showed poorer
solubility than its analogous polymer (Cyclo-m, Scheme III). This may be due to
the presence of the bulky pendent group which decreases the inter-chain interac-
tion between rigid aromatic repeat units, resulting in enhanced solubility.
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