1998
DOI: 10.1021/ma980786+
|View full text |Cite
|
Sign up to set email alerts
|

Successful Thermal Self-Polycondensation of AB2 Monomer to Form Hyperbranched Aromatic Polyamide

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

2
45
0

Year Published

2000
2000
2014
2014

Publication Types

Select...
6
3

Relationship

2
7

Authors

Journals

citations
Cited by 63 publications
(47 citation statements)
references
References 16 publications
2
45
0
Order By: Relevance
“…[14][15][16][17][18][19] Kim synthesized hyperbranched aromatic polyamides by self condensation of either 3,5-diaminobenzoyl chloride or 3-aminoisophthaloyl chloride, the latter showing birefringence in an amide solvent (NMP). [12,14] Both thermal and direct polymerization of AB 2 monomers have been used by Kakimoto et al [16,17] to prepare HB aromatic polyamides. Recently, hyperbranched aramids have been synthesized also from commercial A 2 (diamine) + B 3 (triacid) reagent pairs.…”
Section: Introductionmentioning
confidence: 99%
“…[14][15][16][17][18][19] Kim synthesized hyperbranched aromatic polyamides by self condensation of either 3,5-diaminobenzoyl chloride or 3-aminoisophthaloyl chloride, the latter showing birefringence in an amide solvent (NMP). [12,14] Both thermal and direct polymerization of AB 2 monomers have been used by Kakimoto et al [16,17] to prepare HB aromatic polyamides. Recently, hyperbranched aramids have been synthesized also from commercial A 2 (diamine) + B 3 (triacid) reagent pairs.…”
Section: Introductionmentioning
confidence: 99%
“…In the literature, the authors selected 3,5-bis(4-aminophenoxy)benzoic acid as an unprotected AB 2 building block, which was synthesized by them from 3,5-dihydroxybenzoic acid and 4-fluoronitrobenzene in the presence of sodium carbonate. 53 In this study, we selected 2, which was commercially available, as an unprotected AB 2 building block. Although the steric hindrance was higher in 2 than in 3,5-bis(4-aminophoxy)benzoic acid, the desired structures were still obtained through corresponding changes in the activation and reaction conditions.…”
Section: Synthesis Of the Dendronsmentioning
confidence: 99%
“…Miller and Neenan first reported the preparation of hyperbranched poly(aryl ether)s by a nucleophilic aromatic substitution 5. Hyperbranched poly(ether ketone)s,6–8 polyamides,9–15 polyimides,16–21 poly(phenylene oxide)s,22, 23 poly(phenylene sulfide)s,24, 25 and poly(ether sulfone)s26–28 have already been reported in the literature. It is reported that the introduction of branching points to the rigid aromatic polymers results in an improved solubility, low viscosity, and low crystallinity.…”
Section: Introductionmentioning
confidence: 99%