## Abstract A new pentafunctional monomer (3a) was prepared by acylation of silylated 3,5‐diaminobenzoic acid (DABA) with 3,5‐bisacetoxybenzoyl chloride. The polycondensation of this monomer or its trimethylsilyl ester yielded a hyperbranched poly(ester‐amide) having a nearly alternating sequence o
New polymer syntheses, 81 . Poly(3-oxybenzoate) randomly branched with 3,5-dihydroxybenzoic acid or 5-hydroxyisophthalic acid
✍ Scribed by Hans R. Kricheldorf; Olaf Stöber; Dierk Lübbers
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 577 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Randomly branched (hyperbranched) Poly(3‐hydroxybenzoate), poly(3‐Hybe), was prepared by polycondensation of silylated 3‐acetoxybenzoic acid with either silylated 3,5‐diacetoxybenzoic acid or bis(trimethylsilyl) 5‐acetoxyisophthalate. The number of branching points was varied by changing the feed ratio of difunctional and trifunctional monomers. ^1^H NMR and ^13^C NMR spectroscopy proved the nearly random incorporation of the trifunctional “branching units”. Cocondensations with small amounts of acetylated bisphenol‐P allowed one to control the degree of polymerization (DP) and to determine the DP by ^1^H NMR spectroscopy. However, analogous copolycondensations with silylated 2‐(4‐tert‐butylphenoxy)terephthalic acid failed. According to GPC measurements, weight‐average molecular weights above 10^5^ were obtained. DSC measurements revealed that the glass transition temperatures (T~g~'s) vary largely with the degree of branching (DB) and with the nature of the end‐groups. In the case of phenolic OH and acetate end‐groups, the relationship T~g~ vs. number of branching points passes through a minimum.
📜 SIMILAR VOLUMES
## Abstract The reaction of 3‐acetoxybenzoyl chloride (4) with __N,N__′,__O__‐tris(trimethylsilyl)‐3,5‐diaminobenzoic acid (5) proceeds by highly selective and almost quantitative acylation of both amino groups. The resulting 3,5‐bis(3‐acetoxybenzamido)benzoic acid (6a), or its silylated derivative