## Abstract Poly(amido‐amine)s carrying primary amino groups as side substituents have been obtained by polyaddition of __N__‐triphenylmethyl‐monosubstituted 1,2‐diaminoethane (TPHMAE) to 2,2‐bisacrylamido acetic acid or 1,4‐bisacryloylpiperazine and subsequent removal of the protecting triphenylme
Poly(amido-amine)s and poly(ester-amine)s based on aromatic amines containing carboxyl groups
✍ Scribed by Do Thi Bich Loan; Ilya B. Rashkov; Ivan M. Panayotov
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 326 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
The preparation of poly(amido‐amine)s and poly(ester‐amine)s via polyaddition between aromatic amines containing free or esterified carboxyl groups and compounds with activated double bounds [N,N′‐methylenebis(acrylamide), 1,4‐diacryloylpiperazine and 1,3‐propanediyl diacrylate] is described. The products obtained are typical polyelectrolytes, their solutions exhibiting anomalous viscosity behaviour.
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## Abstract Disulfide‐functionalized hyperbranched poly(amido amine)s (HPAMAMs) were synthesized by Michael addition polymerization of __N,N__'‐cystaminebisacrylamide and 1‐(2‐aminoethyl)piperazine. The novel HPAMAMs displayed bright fluorescence, and the emissions bands cover nearly the whole visi
## Abstract The synthesis of Ag particles stabilized poly (__N__,__N__′‐methylene bisacrylamide __N__‐aminoethyl piperazine) (MBA‐AEPZ) and poly(__N__,__N__′‐dodecyl diacrylamide __N__‐aminoethyl piperazine) (MDA‐AEPZ) was reported. The effects of hyperbranched polymer structures and hyperbranched
## Abstract Summary: Poly(arylene ether amine)s were synthesized by a nucleophilic aromatic substitution polycondensation of bis[4‐fluoro‐3‐(trifluoromethyl)phenyl]amine with several bisphenols. Even though the monomer has an electron‐donating diphenylamine moiety, which normally deactivates a nucl