1999
DOI: 10.1021/ma9900941
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Polymerizable Polyelectrolyte−Surfactant Complexes from Monomeric Ammonium Cations and Polystyrenesulfonate

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Cited by 19 publications
(14 citation statements)
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“…[63] Exploring the functions or uses of polyelectrolyte±surfactant complexes further, these systems have also been applied as templates for the directing the structure of polymer architectures. [64] Antonietti and co-workers used polyelectrolyte± surfactant complexes as templates for the directed polymerization of standard monomers towards nanostructures. [65] Instead of finding a direct replica of the templating mesophase, polymer nanoparticles with interesting anisotropic shapes were found.…”
Section: Polyelectrolyte±surfactant and Polyelectrolyte±lipid Complexesmentioning
confidence: 99%
“…[63] Exploring the functions or uses of polyelectrolyte±surfactant complexes further, these systems have also been applied as templates for the directing the structure of polymer architectures. [64] Antonietti and co-workers used polyelectrolyte± surfactant complexes as templates for the directed polymerization of standard monomers towards nanostructures. [65] Instead of finding a direct replica of the templating mesophase, polymer nanoparticles with interesting anisotropic shapes were found.…”
Section: Polyelectrolyte±surfactant and Polyelectrolyte±lipid Complexesmentioning
confidence: 99%
“…Dreja and Lennartz also reported polymerizable polyelectrolyte±surfactant complexes from monomeric ammonium cations and PSS. [77] By modifying the properties of the monomer units such as flexibility or functionalized tails, it will be promising to build up complexes with controlled mesoscopic properties and internal orders. The self-organization and dynamic mechanical behavior of the solid complexes formed by poly(4-vinylpyridine) (P4VP) or P4VP-containing block copolymers with surfactant-like pentadecylphenol (PDP) through hydrogen bonding have been reported.…”
Section: Polyelectrolyte±surfactant Complexes In the Solid Statementioning
confidence: 99%
“…A linear dependence was found, and its slope was 1.7. The increment per methylene (CH 2 ) unit, 1.7 Å, is larger than the theoretical value of 1.27 Å calculated from the fully extended and all‐trans conformation of the alkyl group 22–24. This is because d (Table 3) is larger than the theoretical layer spacing calculated from the fully extended and completely interdigitated side chain.…”
Section: Resultsmentioning
confidence: 80%