Novel AB2 monomers and corresponding hyperbranched polyureas are prepared in a one-pot process. AB2 monomers are synthesized by a highly selective reaction of carbonyl biscaprolactam (CBC) with triamines comprising one secondary and two primary amino groups. Only the primary amines react with CBC, yielding blocked isocyanates. On heating, self-condensation of the obtained monomer solution takes place, yielding polymers with Mn up to 11 000 Da. Mark-Houwink exponents of 0.3 and branching frequencies of 0.3 demonstrate the hyperbranched topology. Each polymer molecule comprises one secondary amino group in the focal point and numerous active blocked isocyanates located at the end of the polymer branches. The polymers are fully characterized b...
The thesis aims to synthesize hyperbranched poly(urea-urethane) polymers (HPU) in one-pot method usi...
A series of tertiary amine-based hyperbranched poly(amine-ester)s have been synthesized by Michael a...
10.1002/pola.10545Journal of Polymer Science, Part A: Polymer Chemistry40244563-4569JPAC
Novel AB2 monomers and corresponding hyperbranched polyureas are prepared in a one-pot process. AB2 ...
This thesis is devoted to the studies of preparation, characterization and application of novel hype...
N,N'-disubstituted hyperbranched polyureas with methyl, benzyl, and allyl substitutents were synthes...
Here we report, for the first time to our knowledge, a method to synthesize AB(2) monomers, the corr...
A highly efficient synthetic route, based on the quantitative reaction between amine and isocyanate ...
The thermal decomposition of 3,5-dihydroxybenzoyl azide, to generate in situ the corresponding AB2-t...
A new method for syntheses of hyperbranched poly(ester-amide)s from commercially available A(2) and ...
A new method for synthesis of novel hyperbranched poly(ester-amide)s from commercially available AA'...
A series of novel hyperbranched poly(ester-amide)s (HBPEAs) based on neutral a-amino acids have been...
The thermal decomposition of 3,5-dihydroxybenzoyl azide, to generate in situ the corresponding $AB_2...
Hyperbranched polyurethanes, with varying oligoethyleneoxy spacer segments between the branching poi...
The thermal decomposition of 3,5-diaminobenzoyl azide, to generate in situ the corresponding 3,5-dia...
The thesis aims to synthesize hyperbranched poly(urea-urethane) polymers (HPU) in one-pot method usi...
A series of tertiary amine-based hyperbranched poly(amine-ester)s have been synthesized by Michael a...
10.1002/pola.10545Journal of Polymer Science, Part A: Polymer Chemistry40244563-4569JPAC
Novel AB2 monomers and corresponding hyperbranched polyureas are prepared in a one-pot process. AB2 ...
This thesis is devoted to the studies of preparation, characterization and application of novel hype...
N,N'-disubstituted hyperbranched polyureas with methyl, benzyl, and allyl substitutents were synthes...
Here we report, for the first time to our knowledge, a method to synthesize AB(2) monomers, the corr...
A highly efficient synthetic route, based on the quantitative reaction between amine and isocyanate ...
The thermal decomposition of 3,5-dihydroxybenzoyl azide, to generate in situ the corresponding AB2-t...
A new method for syntheses of hyperbranched poly(ester-amide)s from commercially available A(2) and ...
A new method for synthesis of novel hyperbranched poly(ester-amide)s from commercially available AA'...
A series of novel hyperbranched poly(ester-amide)s (HBPEAs) based on neutral a-amino acids have been...
The thermal decomposition of 3,5-dihydroxybenzoyl azide, to generate in situ the corresponding $AB_2...
Hyperbranched polyurethanes, with varying oligoethyleneoxy spacer segments between the branching poi...
The thermal decomposition of 3,5-diaminobenzoyl azide, to generate in situ the corresponding 3,5-dia...
The thesis aims to synthesize hyperbranched poly(urea-urethane) polymers (HPU) in one-pot method usi...
A series of tertiary amine-based hyperbranched poly(amine-ester)s have been synthesized by Michael a...
10.1002/pola.10545Journal of Polymer Science, Part A: Polymer Chemistry40244563-4569JPAC