Abstract
The synthesis of an aromatic trisamine enabled the generation of long-chain branched poly(ether imide)s (LCB-PEIs). The nucleophilic aromatic substitution of 1-chloro-4-nitrobenzene with 1,1,1-tris(4-hydroxyphenyl)ethane resulted in tris((p-nitrophenoxy)phenyl)ethane, and a subsequent reduction afforded tris((p-aminophenoxy)phenyl)ethane (TAPE) in high yields (>90%). Introducing TAPE at low percentages with m-phenylenediamine and bisphenol A dianhydride enabled synthesis of high molecular weight, branched poly(ether imide)s with varied branch lengths. The stoichiometric imbalance and phthalic anhydride end-capping controlled molecular weights. Complementary 1H NMR spectroscopy and size exclusion chromatography (SEC) identified average branch length as a function of TAPE incorporation and provided comparisons in molecular weights and distributions. The melt viscosity and thermal stability at elevated temperatures (∼340 °C) probed the feasibility of melt processing of LCB-PEIs in comparison to linear analog...
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